Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7265 |
| ensemblid | ENSG00000113312.12 |
| hgncid | 12391 |
| symbol | TTC1 |
| name | tetratricopeptide repeat domain 1 |
| refseq_nuc | NM_003314.3 |
| refseq_prot | NP_003305.1 |
| ensembl_nuc | ENST00000231238.10 |
| ensembl_prot | ENSP00000231238.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 160009139 |
| end | 160065543 |
| strand | + |
| ver | v1.2 |
| region | chr5:160009139-160065543 |
| region5000 | chr5:160004139-160070543 |
| regionname0 | TTC1_chr5_160009139_160065543 |
| regionname5000 | TTC1_chr5_160004139_160070543 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 292 | 375 | 77 | 62 | 187 | 11 | 36 | 143 | TTC1_chr5_160004139_160070543 | TTC1 | MGEKS others(287): Show |
chr5 | 160004139 | 160070543 |
| a0002 | 0/0 | 292 | 6 | 2 | 1 | 0 | 1 | 2 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | MGEKS others(287): Show |
chr5 | 160004139 | 160070543 |
| a0003 | 0/0 | 292 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | MGEKS others(287): Show |
chr5 | 160004139 | 160070543 |
| a0004 | 0/0 | 292 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | MGEKS others(287): Show |
chr5 | 160004139 | 160070543 |
| a0005 | 0/0 | 292 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | MGEKS others(287): Show |
chr5 | 160004139 | 160070543 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 876 | 375 | 77 | 62 | 187 | 11 | 36 | TTC1_chr5_160004139_160070543 | TTC1 | ATGGG others(871): Show |
chr5 | 160004139 | 160070543 | ||
| a0002c0002 | 0/0 | 876 | 6 | 2 | 1 | 0 | 1 | 2 | TTC1_chr5_160004139_160070543 | TTC1 | ATGGG others(871): Show |
chr5 | 160004139 | 160070543 | ||
| a0003c0003 | 0/0 | 876 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | ATGGG others(871): Show |
chr5 | 160004139 | 160070543 | ||
| a0004c0005 | 0/0 | 876 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | ATGGG others(871): Show |
chr5 | 160004139 | 160070543 | ||
| a0005c0004 | 0/0 | 876 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | ATGGG others(871): Show |
chr5 | 160004139 | 160070543 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1441 | 309 | 73 | 48 | 143 | 9 | 34 | TTC1_chr5_160004139_160070543 | TTC1 | GGAAG others(1436): Show |
chr5 | 160004139 | 160070543 |
| a0001c0001t0002 | 0/0 | 1441 | 61 | 1 | 14 | 42 | 2 | 2 | TTC1_chr5_160004139_160070543 | TTC1 | GGAAG others(1436): Show |
chr5 | 160004139 | 160070543 |
| a0001c0001t0003 | 0/0 | 1441 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | GGAAG others(1436): Show |
chr5 | 160004139 | 160070543 |
| a0001c0001t0004 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | GGAAG others(1436): Show |
chr5 | 160004139 | 160070543 |
| a0001c0001t0005 | 0/0 | 1441 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | GGAAG others(1436): Show |
chr5 | 160004139 | 160070543 |
| a0001c0001t0006 | 0/0 | 1441 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | GGAAG others(1436): Show |
chr5 | 160004139 | 160070543 |
| a0001c0001t0007 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | GGAAG others(1436): Show |
chr5 | 160004139 | 160070543 |
| a0002c0002t0001 | 0/0 | 1441 | 6 | 2 | 1 | 0 | 1 | 2 | TTC1_chr5_160004139_160070543 | TTC1 | GGAAG others(1436): Show |
chr5 | 160004139 | 160070543 |
| a0003c0003t0001 | 0/0 | 1441 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | GGAAG others(1436): Show |
chr5 | 160004139 | 160070543 |
| a0004c0005t0001 | 0/0 | 1441 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | GGAAG others(1436): Show |
chr5 | 160004139 | 160070543 |
| a0005c0004t0002 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | GGAAG others(1436): Show |
chr5 | 160004139 | 160070543 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0006g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0003c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0004c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| a0005c0004t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | GBR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | GBR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | FIN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00642 | hp2 | a0003 | c0003 | t0001 | g0125 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0329 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | CLM | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0293 | EUR | IBS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0242 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0357 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0331 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0328 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02056 | hp1 | a0001 | c0001 | t0007 | g0200 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | CDX | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0275 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0319 | AMR | PEL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0342 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0239 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0352 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0241 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0291 | SAS | STU | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0350 | SAS | BEB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0240 | SAS | STU | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | YRI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18959 | hp1 | a0005 | c0004 | t0002 | g0343 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | YRI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ASW | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ASW | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | TSI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0243 | EUR | TSI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | GIH | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | GIH | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0144 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02486 | hp2 | a0004 | c0005 | t0001 | g0023 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | USA | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | USA | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0038 | REF | REF | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0057 | REF | REF | TTC1_chr5_160004139_160070543 | TTC1 | chr5 | 160004139 | 160070543 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:160010614 | C | G | 2 | a0002 a0004 |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
missense_variant | MODERATE | c.86C>G | p.Ala29Gly | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/8 | 170/1441 | 86/879 | 29/292 | chr5 | 160010614 | |||
| chr5:160036712 | C | T | 1 | a0004 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.413C>T | p.Ser138Phe | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/8 | 497/1441 | 413/879 | 138/292 | chr5 | 160036712 | |||
| chr5:160036742 | C | T | 1 | a0005 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.443C>T | p.Ser148Phe | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/8 | 527/1441 | 443/879 | 148/292 | chr5 | 160036742 | |||
| chr5:160065034 | A | G | 1 | a0003 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.848A>G | p.Asn283Ser | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 8/8 | 932/1441 | 848/879 | 283/292 | chr5 | 160065034 |
| view | 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 |
|---|
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:160009154 | C | T | 2 | a0001c0001t0002 a0005c0004t0002 |
62 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(59): Show |
5_prime_UTR_variant | MODIFIER | c.-69C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/8 | 1375 | chr5 | 160009154 | ||||||
| chr5:160009176 | C | T | 1 | a0001c0001t0007 | 1 | HG02056.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-47C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/8 | chr5 | 160009176 | |||||||
| chr5:160065120 | A | T | 1 | a0001c0001t0006 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 8/8 | 55 | chr5 | 160065120 | ||||||
| chr5:160065211 | C | G | 1 | a0001c0001t0005 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 8/8 | 146 | chr5 | 160065211 | ||||||
| chr5:160065478 | C | T | 1 | a0001c0001t0004 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*413C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 8/8 | 413 | chr5 | 160065478 | ||||||
| chr5:160065486 | G | A | 1 | a0001c0001t0003 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 8/8 | 421 | chr5 | 160065486 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:160009472 | A | T | 1 | a0001c0001t0001g0357 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-30+279A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009472 | |||||||
| chr5:160009491 | A | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0355 a0001c0001t0001g0356 |
4 | NA18948.hp1 NA18954.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+298A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009491 | |||||||
| chr5:160009517 | C | G | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-30+324C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009517 | |||||||
| chr5:160009539 | C | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0347 a0001c0001t0001g0348 others(3): Show |
7 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+346C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009539 | |||||||
| chr5:160009597 | C | CATAA | 63 | a0001c0001t0001g0296 a0001c0001t0001g0308 a0001c0001t0001g0322 others(60): Show |
66 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.-30+422_-30+425dup others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 160009597 | ||||||
| chr5:160009606 | A | G | 1 | a0001c0001t0001g0346 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-30+413A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009606 | |||||||
| chr5:160009763 | G | A | 2 | a0002c0002t0001g0022 a0004c0005t0001g0023 |
2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-30+570G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009763 | |||||||
| chr5:160009816 | A | C | 116 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0244 others(113): Show |
122 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.-30+623A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009816 | |||||||
| chr5:160009862 | G | A | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-638G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009862 | |||||||
| chr5:160009899 | C | A | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-601C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009899 | |||||||
| chr5:160009918 | T | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-29-582T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160009918 | |||||||
| chr5:160010001 | G | T | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-499G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160010001 | |||||||
| chr5:160010113 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-29-387C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160010113 | |||||||
| chr5:160010124 | G | A | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-376G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160010124 | |||||||
| chr5:160010218 | A | ACTG | 4 | a0002c0002t0001g0240 a0002c0002t0001g0241 a0002c0002t0001g0242 others(1): Show |
4 | HG01928.hp1 HG03669.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-280_-29-278dup others(3): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 160010218 | ||||||
| chr5:160010257 | C | CA | 54 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0024 others(51): Show |
57 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.-29-221dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 160010257 | ||||||
| chr5:160010257 | CA | C | 11 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(8): Show |
11 | HG00609.hp1 HG02523.hp1 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29-221delA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 160010257 | ||||||
| chr5:160010282 | A | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-29-218A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160010282 | |||||||
| chr5:160010396 | C | T | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-104C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160010396 | |||||||
| chr5:160010414 | T | G | 1 | a0001c0001t0001g0039 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-29-86T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160010414 | |||||||
| chr5:160010459 | C | T | 111 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0244 others(108): Show |
117 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-29-41C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 1/7 | chr5 | 160010459 | |||||||
| chr5:160011088 | T | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.330+230T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160011088 | |||||||
| chr5:160011124 | G | T | 1 | a0002c0002t0001g0243 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.330+266G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160011124 | |||||||
| chr5:160011187 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.330+329G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160011187 | |||||||
| chr5:160011245 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.330+387A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160011245 | |||||||
| chr5:160011439 | A | G | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.330+581A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160011439 | |||||||
| chr5:160011863 | G | A | 1 | a0001c0001t0006g0275 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.330+1005G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160011863 | |||||||
| chr5:160012030 | A | C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0251 others(30): Show |
36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.330+1172A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012030 | |||||||
| chr5:160012193 | C | G | 1 | a0001c0001t0001g0228 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.330+1335C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012193 | |||||||
| chr5:160012209 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.330+1351C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012209 | |||||||
| chr5:160012290 | T | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0043 others(10): Show |
14 | HG01928.hp1 HG01981.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.330+1432T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012290 | |||||||
| chr5:160012359 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0043 others(2): Show |
6 | HG01981.hp1 HG02723.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+1501A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012359 | |||||||
| chr5:160012368 | A | AT | 16 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0042 others(13): Show |
18 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.330+1524dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160012368 | ||||||
| chr5:160012832 | G | C | 1 | a0001c0001t0001g0024 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.330+1974G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012832 | |||||||
| chr5:160012955 | C | T | 63 | a0001c0001t0001g0296 a0001c0001t0001g0308 a0001c0001t0001g0322 others(60): Show |
66 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.330+2097C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012955 | |||||||
| chr5:160012957 | A | G | 31 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0251 others(28): Show |
34 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.330+2099A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160012957 | |||||||
| chr5:160013010 | T | A | 66 | a0001c0001t0001g0296 a0001c0001t0001g0308 a0001c0001t0001g0322 others(63): Show |
69 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.330+2152T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013010 | |||||||
| chr5:160013013 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.330+2155T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013013 | |||||||
| chr5:160013306 | A | G | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+2448A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013306 | |||||||
| chr5:160013308 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+2450A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013308 | |||||||
| chr5:160013398 | T | TA | 8 | a0001c0001t0001g0232 a0002c0002t0001g0022 a0002c0002t0001g0239 others(5): Show |
8 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.330+2552dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160013398 | ||||||
| chr5:160013458 | G | A | 115 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(112): Show |
122 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.330+2600G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013458 | |||||||
| chr5:160013509 | C | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0043 others(8): Show |
12 | HG01928.hp1 HG01981.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.330+2651C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013509 | |||||||
| chr5:160013540 | C | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0251 others(30): Show |
36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.330+2682C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013540 | |||||||
| chr5:160013541 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.330+2683G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013541 | |||||||
| chr5:160013627 | C | G | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+2769C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013627 | |||||||
| chr5:160013658 | G | A | 2 | a0001c0001t0002g0289 a0001c0001t0002g0290 |
2 | HG01106.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.330+2800G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160013658 | |||||||
| chr5:160013742 | C | CA | 107 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0046 others(104): Show |
113 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.330+2901dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160013742 | ||||||
| chr5:160013742 | CAA | C | 10 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0006g0275 others(7): Show |
10 | HG01928.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.330+2900_330+2901d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160013742 | ||||||
| chr5:160014007 | A | G | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3149A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014007 | |||||||
| chr5:160014039 | A | C | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3181A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014039 | |||||||
| chr5:160014070 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.330+3212T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014070 | |||||||
| chr5:160014114 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG00099.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.330+3256A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014114 | |||||||
| chr5:160014171 | A | G | 1 | a0004c0005t0001g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.330+3313A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014171 | |||||||
| chr5:160014226 | C | T | 1 | a0001c0001t0002g0342 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.330+3368C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014226 | |||||||
| chr5:160014241 | G | C | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3383G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014241 | |||||||
| chr5:160014241 | G | T | 1 | a0001c0001t0001g0220 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.330+3383G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014241 | |||||||
| chr5:160014335 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.330+3477G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014335 | |||||||
| chr5:160014391 | A | G | 32 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0251 others(29): Show |
35 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.330+3533A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014391 | |||||||
| chr5:160014493 | G | A | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3635G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014493 | |||||||
| chr5:160014514 | T | A | 106 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0224 others(103): Show |
112 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.330+3656T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014514 | |||||||
| chr5:160014515 | T | A | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3657T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014515 | |||||||
| chr5:160014674 | G | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0251 others(30): Show |
36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.330+3816G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014674 | |||||||
| chr5:160014683 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.330+3825A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014683 | |||||||
| chr5:160014835 | A | G | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3977A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160014835 | |||||||
| chr5:160015305 | G | A | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+4447G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015305 | |||||||
| chr5:160015569 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.330+4711A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015569 | |||||||
| chr5:160015590 | G | A | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+4732G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015590 | |||||||
| chr5:160015593 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.330+4735G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015593 | |||||||
| chr5:160015628 | C | T | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+4770C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015628 | |||||||
| chr5:160015755 | A | G | 9 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0002c0002t0001g0022 others(6): Show |
9 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+4897A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015755 | |||||||
| chr5:160015910 | A | G | 66 | a0001c0001t0001g0296 a0001c0001t0001g0308 a0001c0001t0001g0322 others(63): Show |
69 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.330+5052A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015910 | |||||||
| chr5:160015927 | T | C | 9 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0002c0002t0001g0022 others(6): Show |
9 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+5069T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015927 | |||||||
| chr5:160015929 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0355 a0001c0001t0001g0356 |
4 | NA18948.hp1 NA18954.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+5071C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160015929 | |||||||
| chr5:160016056 | A | G | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0228 |
3 | HG00438.hp1 NA18999.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.330+5198A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016056 | |||||||
| chr5:160016073 | T | C | 3 | a0002c0002t0001g0240 a0002c0002t0001g0241 a0002c0002t0001g0242 |
3 | HG01928.hp1 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.330+5215T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016073 | |||||||
| chr5:160016080 | G | A | 3 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0006g0275 |
3 | HG02258.hp2 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.330+5222G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016080 | |||||||
| chr5:160016167 | C | T | 63 | a0001c0001t0001g0296 a0001c0001t0001g0308 a0001c0001t0001g0322 others(60): Show |
66 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.330+5309C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016167 | |||||||
| chr5:160016285 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.330+5427C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016285 | |||||||
| chr5:160016318 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.330+5460C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016318 | |||||||
| chr5:160016321 | A | T | 354 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(351): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.330+5463A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016321 | |||||||
| chr5:160016398 | A | T | 8 | a0001c0001t0002g0288 a0001c0001t0002g0335 a0001c0001t0002g0336 others(5): Show |
8 | NA18946.hp1 NA18956.hp2 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.330+5540A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016398 | |||||||
| chr5:160016403 | A | T | 1 | a0002c0002t0001g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.330+5545A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016403 | |||||||
| chr5:160016423 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.330+5565C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016423 | |||||||
| chr5:160016585 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+5727A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016585 | |||||||
| chr5:160016659 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0006g0275 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.330+5801T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016659 | |||||||
| chr5:160016799 | G | T | 111 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0246 others(108): Show |
117 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.330+5941G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016799 | |||||||
| chr5:160016918 | T | C | 4 | a0002c0002t0001g0240 a0002c0002t0001g0241 a0002c0002t0001g0242 others(1): Show |
4 | HG01928.hp1 HG03669.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+6060T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016918 | |||||||
| chr5:160016977 | A | T | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+6119A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160016977 | |||||||
| chr5:160016991 | C | CAA | 9 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0002c0002t0001g0022 others(6): Show |
9 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+6134_330+6135i others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160016991 | ||||||
| chr5:160017010 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.330+6152G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017010 | |||||||
| chr5:160017179 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.330+6321G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017179 | |||||||
| chr5:160017189 | A | G | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.330+6331A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017189 | |||||||
| chr5:160017192 | A | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0037 others(2): Show |
5 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+6334A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017192 | |||||||
| chr5:160017213 | T | G | 9 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0002c0002t0001g0022 others(6): Show |
9 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+6355T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017213 | |||||||
| chr5:160017221 | A | C | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+6363A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017221 | |||||||
| chr5:160017621 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0006g0275 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.330+6763A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017621 | |||||||
| chr5:160017629 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+6771C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017629 | |||||||
| chr5:160017681 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+6823A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017681 | |||||||
| chr5:160017858 | T | C | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+7000T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017858 | |||||||
| chr5:160017924 | G | A | 2 | a0001c0001t0001g0274 a0001c0001t0006g0275 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.330+7066G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160017924 | |||||||
| chr5:160018209 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.330+7351G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018209 | |||||||
| chr5:160018224 | C | T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0237 |
3 | HG02523.hp1 NA19010.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.330+7366C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018224 | |||||||
| chr5:160018239 | C | A | 1 | a0001c0001t0001g0277 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.330+7381C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018239 | |||||||
| chr5:160018303 | C | G | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+7445C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018303 | |||||||
| chr5:160018341 | A | G | 13 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(10): Show |
13 | HG00609.hp1 HG02074.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.330+7483A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018341 | |||||||
| chr5:160018452 | G | A | 5 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+7594G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018452 | |||||||
| chr5:160018618 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0007g0200 |
2 | HG02056.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.330+7760A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018618 | |||||||
| chr5:160018632 | A | G | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+7774A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018632 | |||||||
| chr5:160018654 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.330+7796C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018654 | |||||||
| chr5:160018772 | G | A | 1 | a0001c0001t0002g0291 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.330+7914G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018772 | |||||||
| chr5:160018795 | C | A | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+7937C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018795 | |||||||
| chr5:160018799 | A | G | 2 | a0001c0001t0002g0333 a0001c0001t0002g0334 |
2 | NA18941.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.330+7941A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018799 | |||||||
| chr5:160018822 | A | G | 111 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0244 others(108): Show |
117 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.330+7964A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018822 | |||||||
| chr5:160018874 | T | C | 116 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0244 others(113): Show |
122 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.330+8016T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018874 | |||||||
| chr5:160018923 | T | C | 1 | a0001c0001t0001g0254 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.330+8065T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018923 | |||||||
| chr5:160018928 | G | A | 1 | a0001c0001t0001g0352 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.330+8070G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018928 | |||||||
| chr5:160018970 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.330+8112C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018970 | |||||||
| chr5:160018974 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.330+8116A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018974 | |||||||
| chr5:160018977 | G | C | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
5 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+8119G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160018977 | |||||||
| chr5:160019107 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0196 a0001c0001t0001g0223 others(3): Show |
7 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+8249A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019107 | |||||||
| chr5:160019204 | A | C | 5 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+8346A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019204 | |||||||
| chr5:160019235 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.330+8377T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019235 | |||||||
| chr5:160019410 | A | G | 66 | a0001c0001t0001g0296 a0001c0001t0001g0308 a0001c0001t0001g0322 others(63): Show |
69 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.330+8552A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019410 | |||||||
| chr5:160019451 | A | G | 116 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0244 others(113): Show |
122 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.330+8593A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019451 | |||||||
| chr5:160019491 | T | G | 33 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0251 others(30): Show |
36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.330+8633T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019491 | |||||||
| chr5:160019492 | C | T | 110 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0244 others(107): Show |
116 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.330+8634C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019492 | |||||||
| chr5:160019495 | A | G | 1 | a0001c0001t0006g0275 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.330+8637A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019495 | |||||||
| chr5:160019533 | C | T | 2 | a0001c0001t0001g0352 a0001c0001t0001g0353 |
2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.330+8675C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019533 | |||||||
| chr5:160019545 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.330+8687C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019545 | |||||||
| chr5:160019580 | C | CT | 19 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0180 others(16): Show |
20 | HG01175.hp2 HG01192.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.330+8745dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160019580 | ||||||
| chr5:160019580 | CT | C | 10 | a0001c0001t0001g0026 a0001c0001t0001g0061 a0001c0001t0001g0062 others(7): Show |
10 | HG01952.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.330+8745delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160019580 | ||||||
| chr5:160019580 | CTT | C | 64 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0276 others(61): Show |
67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.330+8744_330+8745d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160019580 | ||||||
| chr5:160019580 | CTTT | C | 6 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0335 others(3): Show |
6 | HG01515.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.330+8743_330+8745d others(5): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160019580 | ||||||
| chr5:160019580 | CTTTT | C | 8 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(5): Show |
8 | HG01928.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+8742_330+8745d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160019580 | ||||||
| chr5:160019580 | CTTTTTTT others(7): Show |
C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0251 others(30): Show |
36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.330+8732_330+8745d others(16): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160019580 | ||||||
| chr5:160019644 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.330+8786G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019644 | |||||||
| chr5:160019669 | CCTCCGCC others(22): Show |
C | 1 | a0001c0001t0001g0179 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.330+8815_330+8843d others(31): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160019669 | ||||||
| chr5:160019722 | C | T | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+8864C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160019722 | |||||||
| chr5:160020055 | A | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.330+9197A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020055 | |||||||
| chr5:160020206 | A | G | 267 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(264): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.330+9348A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020206 | |||||||
| chr5:160020302 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.330+9444A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020302 | |||||||
| chr5:160020390 | C | T | 3 | a0002c0002t0001g0240 a0002c0002t0001g0241 a0002c0002t0001g0242 |
3 | HG01928.hp1 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.330+9532C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020390 | |||||||
| chr5:160020480 | G | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0251 others(30): Show |
36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.330+9622G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020480 | |||||||
| chr5:160020663 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.330+9805C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020663 | |||||||
| chr5:160020693 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+9835G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020693 | |||||||
| chr5:160020707 | T | A | 1 | a0001c0001t0001g0274 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.330+9849T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020707 | |||||||
| chr5:160020754 | C | G | 1 | a0001c0001t0001g0350 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.330+9896C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020754 | |||||||
| chr5:160020770 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.330+9912A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020770 | |||||||
| chr5:160020776 | A | G | 4 | a0001c0001t0002g0330 a0001c0001t0002g0344 a0001c0001t0002g0345 others(1): Show |
4 | NA18959.hp1 NA18969.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+9918A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020776 | |||||||
| chr5:160020912 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.330+10054C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160020912 | |||||||
| chr5:160021129 | C | T | 66 | a0001c0001t0001g0296 a0001c0001t0001g0308 a0001c0001t0001g0322 others(63): Show |
69 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.330+10271C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160021129 | |||||||
| chr5:160021508 | A | C | 66 | a0001c0001t0001g0296 a0001c0001t0001g0308 a0001c0001t0001g0322 others(63): Show |
69 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.330+10650A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160021508 | |||||||
| chr5:160021570 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+10712C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160021570 | |||||||
| chr5:160021620 | C | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0196 a0001c0001t0001g0223 others(3): Show |
7 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+10762C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160021620 | |||||||
| chr5:160021793 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+10935G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160021793 | |||||||
| chr5:160021834 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.330+10976A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160021834 | |||||||
| chr5:160021959 | T | A | 69 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0296 others(66): Show |
72 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.330+11101T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160021959 | |||||||
| chr5:160022068 | C | T | 1 | a0001c0001t0002g0329 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.330+11210C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160022068 | |||||||
| chr5:160022092 | CCT | C | 6 | a0001c0001t0001g0174 a0002c0002t0001g0239 a0002c0002t0001g0240 others(3): Show |
6 | HG01928.hp1 HG02723.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+11235_330+1123 others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160022092 | |||||||
| chr5:160022293 | T | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.330+11435T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160022293 | |||||||
| chr5:160022435 | A | G | 1 | a0001c0001t0001g0350 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.330+11577A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160022435 | |||||||
| chr5:160022677 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.330+11819A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160022677 | |||||||
| chr5:160022695 | G | C | 1 | a0001c0001t0002g0294 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.330+11837G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160022695 | |||||||
| chr5:160022978 | G | A | 16 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0066 others(13): Show |
17 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+12120G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160022978 | |||||||
| chr5:160023188 | G | A | 2 | a0002c0002t0001g0022 a0004c0005t0001g0023 |
2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.331-11952G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160023188 | |||||||
| chr5:160023255 | C | CA | 103 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0060 others(100): Show |
109 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.331-11869dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160023255 | ||||||
| chr5:160023255 | C | CAA | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-11870_331-1186 others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160023255 | ||||||
| chr5:160023351 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.331-11789A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160023351 | |||||||
| chr5:160023406 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.331-11734C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160023406 | |||||||
| chr5:160023428 | A | G | 1 | a0001c0001t0001g0025 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.331-11712A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160023428 | |||||||
| chr5:160023526 | T | C | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.331-11614T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160023526 | |||||||
| chr5:160023745 | T | G | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.331-11395T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160023745 | |||||||
| chr5:160024056 | C | CT | 9 | a0001c0001t0001g0068 a0001c0001t0001g0166 a0001c0001t0001g0167 others(6): Show |
9 | HG01981.hp2 HG02155.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-11083dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160024056 | ||||||
| chr5:160024203 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.331-10937C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160024203 | |||||||
| chr5:160024266 | A | G | 1 | a0004c0005t0001g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.331-10874A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160024266 | |||||||
| chr5:160024588 | A | T | 66 | a0001c0001t0001g0296 a0001c0001t0001g0308 a0001c0001t0001g0322 others(63): Show |
69 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.331-10552A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160024588 | |||||||
| chr5:160024589 | C | T | 111 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0244 others(108): Show |
117 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.331-10551C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160024589 | |||||||
| chr5:160024664 | AT | A | 67 | a0001c0001t0001g0246 a0001c0001t0001g0274 a0001c0001t0001g0276 others(64): Show |
70 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.331-10461delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160024664 | ||||||
| chr5:160024725 | G | A | 1 | a0002c0002t0001g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.331-10415G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160024725 | |||||||
| chr5:160024799 | C | CTTG | 33 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0251 others(30): Show |
36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.331-10340_331-1033 others(7): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160024799 | ||||||
| chr5:160025050 | C | T | 98 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0035 others(95): Show |
102 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.331-10090C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025050 | |||||||
| chr5:160025092 | A | G | 1 | a0004c0005t0001g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.331-10048A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025092 | |||||||
| chr5:160025265 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.331-9875C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025265 | |||||||
| chr5:160025316 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0103 a0001c0001t0001g0152 |
3 | HG01884.hp1 HG03927.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.331-9824C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025316 | |||||||
| chr5:160025371 | A | G | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.331-9769A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025371 | |||||||
| chr5:160025427 | G | A | 5 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
5 | HG01071.hp2 HG02055.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.331-9713G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025427 | |||||||
| chr5:160025575 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.331-9565A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025575 | |||||||
| chr5:160025898 | A | T | 1 | a0001c0001t0001g0214 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.331-9242A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160025898 | |||||||
| chr5:160026005 | A | C | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0284 |
3 | NA18946.hp2 NA18975.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.331-9135A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026005 | |||||||
| chr5:160026155 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0073 |
2 | NA18962.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.331-8985G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026155 | |||||||
| chr5:160026208 | G | C | 1 | a0001c0001t0001g0029 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.331-8932G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026208 | |||||||
| chr5:160026216 | G | A | 2 | a0001c0001t0001g0274 a0001c0001t0006g0275 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.331-8924G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026216 | |||||||
| chr5:160026219 | G | A | 63 | a0001c0001t0001g0296 a0001c0001t0001g0308 a0001c0001t0001g0322 others(60): Show |
66 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.331-8921G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026219 | |||||||
| chr5:160026291 | A | G | 1 | a0002c0002t0001g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.331-8849A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026291 | |||||||
| chr5:160026322 | T | G | 63 | a0001c0001t0001g0296 a0001c0001t0001g0308 a0001c0001t0001g0322 others(60): Show |
66 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.331-8818T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026322 | |||||||
| chr5:160026415 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0150 others(1): Show |
6 | HG00140.hp2 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-8725A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026415 | |||||||
| chr5:160026450 | A | G | 1 | a0002c0002t0001g0243 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.331-8690A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026450 | |||||||
| chr5:160026595 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.331-8545C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026595 | |||||||
| chr5:160026789 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.331-8351T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026789 | |||||||
| chr5:160026848 | T | G | 64 | a0001c0001t0001g0154 a0001c0001t0001g0296 a0001c0001t0001g0308 others(61): Show |
67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.331-8292T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160026848 | |||||||
| chr5:160027128 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.331-8012C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160027128 | |||||||
| chr5:160027541 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331-7599A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160027541 | |||||||
| chr5:160027561 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.331-7579C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160027561 | |||||||
| chr5:160027622 | C | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0244 others(44): Show |
50 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.331-7518C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160027622 | |||||||
| chr5:160027643 | A | G | 116 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0244 others(113): Show |
122 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.331-7497A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160027643 | |||||||
| chr5:160027879 | C | T | 5 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-7261C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160027879 | |||||||
| chr5:160028014 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.331-7126C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028014 | |||||||
| chr5:160028095 | C | G | 1 | a0001c0001t0001g0354 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.331-7045C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028095 | |||||||
| chr5:160028109 | C | T | 4 | a0001c0001t0002g0330 a0001c0001t0002g0344 a0001c0001t0002g0345 others(1): Show |
4 | NA18959.hp1 NA18969.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-7031C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028109 | |||||||
| chr5:160028293 | C | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(41): Show |
48 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.331-6847C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028293 | |||||||
| chr5:160028298 | C | CA | 77 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0075 others(74): Show |
80 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.331-6823dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160028298 | ||||||
| chr5:160028298 | CA | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0101 others(32): Show |
38 | HG00609.hp2 HG01433.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.331-6823delA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160028298 | ||||||
| chr5:160028460 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.331-6680C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028460 | |||||||
| chr5:160028510 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.331-6630G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028510 | |||||||
| chr5:160028512 | C | T | 29 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0035 others(26): Show |
30 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.331-6628C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028512 | |||||||
| chr5:160028646 | T | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.331-6494T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028646 | |||||||
| chr5:160028666 | G | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG00738.hp1 HG01975.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.331-6474G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028666 | |||||||
| chr5:160028672 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.331-6468C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160028672 | |||||||
| chr5:160029032 | C | G | 1 | a0001c0001t0001g0211 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.331-6108C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029032 | |||||||
| chr5:160029200 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.331-5940G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029200 | |||||||
| chr5:160029285 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.331-5855C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029285 | |||||||
| chr5:160029466 | A | AC | 66 | a0001c0001t0001g0120 a0001c0001t0001g0296 a0001c0001t0001g0308 others(63): Show |
69 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.331-5667dupC | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160029466 | ||||||
| chr5:160029481 | C | CA | 13 | a0001c0001t0001g0017 a0001c0001t0001g0080 a0001c0001t0001g0121 others(10): Show |
14 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.331-5641dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160029481 | ||||||
| chr5:160029481 | C | CAA | 48 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0018 others(45): Show |
52 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.331-5642_331-5641d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160029481 | ||||||
| chr5:160029481 | C | CAAA | 71 | a0001c0001t0001g0028 a0001c0001t0001g0107 a0001c0001t0001g0108 others(68): Show |
74 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.331-5643_331-5641d others(5): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160029481 | ||||||
| chr5:160029580 | T | A | 1 | a0001c0001t0001g0122 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.331-5560T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029580 | |||||||
| chr5:160029583 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.331-5557G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029583 | |||||||
| chr5:160029680 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.331-5460G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029680 | |||||||
| chr5:160029751 | AC | A | 4 | a0002c0002t0001g0240 a0002c0002t0001g0241 a0002c0002t0001g0242 others(1): Show |
4 | HG01928.hp1 HG03669.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-5387delC | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160029751 | ||||||
| chr5:160029771 | C | T | 1 | a0001c0001t0002g0321 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.331-5369C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029771 | |||||||
| chr5:160029980 | C | T | 1 | a0001c0001t0002g0320 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.331-5160C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160029980 | |||||||
| chr5:160030025 | A | C | 1 | a0004c0005t0001g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.331-5115A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030025 | |||||||
| chr5:160030090 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | NA18986.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.331-5050A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030090 | |||||||
| chr5:160030095 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.331-5045C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030095 | |||||||
| chr5:160030265 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.331-4875G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030265 | |||||||
| chr5:160030293 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.331-4847G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030293 | |||||||
| chr5:160030376 | G | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0046 others(27): Show |
31 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.331-4764G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030376 | |||||||
| chr5:160030392 | G | A | 6 | a0001c0001t0001g0276 a0002c0002t0001g0022 a0002c0002t0001g0240 others(3): Show |
6 | HG01928.hp1 HG02486.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.331-4748G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030392 | |||||||
| chr5:160030450 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.331-4690A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030450 | |||||||
| chr5:160030616 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.331-4524C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030616 | |||||||
| chr5:160030637 | G | C | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | NA18986.hp1 NA19057.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.331-4503G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030637 | |||||||
| chr5:160030836 | A | T | 4 | a0001c0001t0001g0155 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | NA18968.hp2 NA18993.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-4304A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030836 | |||||||
| chr5:160030868 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.331-4272T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030868 | |||||||
| chr5:160030980 | T | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.331-4160T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160030980 | |||||||
| chr5:160031040 | T | C | 1 | a0001c0001t0001g0259 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.331-4100T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031040 | |||||||
| chr5:160031048 | T | C | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-4092T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031048 | |||||||
| chr5:160031085 | A | G | 1 | a0002c0002t0001g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.331-4055A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031085 | |||||||
| chr5:160031152 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.331-3988C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031152 | |||||||
| chr5:160031165 | T | A | 57 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0018 others(54): Show |
61 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.331-3975T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031165 | |||||||
| chr5:160031622 | T | A | 1 | a0002c0002t0001g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.331-3518T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031622 | |||||||
| chr5:160031715 | A | T | 1 | a0001c0001t0001g0146 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.331-3425A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031715 | |||||||
| chr5:160031753 | A | G | 6 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00558.hp1 HG02027.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-3387A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160031753 | |||||||
| chr5:160032285 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0100 a0001c0001t0001g0232 |
4 | HG02165.hp1 NA18612.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-2855A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160032285 | |||||||
| chr5:160032427 | C | G | 1 | a0001c0001t0001g0031 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.331-2713C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160032427 | |||||||
| chr5:160032619 | T | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0156 |
2 | NA18966.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.331-2521T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160032619 | |||||||
| chr5:160032702 | C | CT | 63 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0017 others(60): Show |
67 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.331-2408dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | ||||||
| chr5:160032702 | C | CTT | 13 | a0001c0001t0001g0048 a0001c0001t0001g0080 a0001c0001t0001g0099 others(10): Show |
13 | HG02055.hp1 HG02135.hp1 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.331-2409_331-2408d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | ||||||
| chr5:160032702 | C | CTTT | 38 | a0001c0001t0001g0120 a0001c0001t0001g0185 a0001c0001t0001g0211 others(35): Show |
41 | HG00408.hp2 HG01081.hp1 HG01256.hp1 others(38): Show |
intron_variant | MODIFIER | c.331-2410_331-2408d others(5): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | ||||||
| chr5:160032702 | C | CTTTT | 18 | a0001c0001t0001g0322 a0001c0001t0002g0286 a0001c0001t0002g0288 others(15): Show |
18 | HG00597.hp2 HG01192.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.331-2411_331-2408d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | ||||||
| chr5:160032702 | C | CTTTTT | 10 | a0001c0001t0002g0285 a0001c0001t0002g0289 a0001c0001t0002g0290 others(7): Show |
10 | HG01106.hp2 HG01175.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.331-2412_331-2408d others(7): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | ||||||
| chr5:160032702 | CT | C | 18 | a0001c0001t0001g0030 a0001c0001t0001g0046 a0001c0001t0001g0069 others(15): Show |
18 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.331-2408delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | ||||||
| chr5:160032702 | CTT | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0115 others(10): Show |
16 | HG00423.hp2 HG00609.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.331-2409_331-2408d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | ||||||
| chr5:160032702 | CTTT | C | 18 | a0001c0001t0001g0180 a0001c0001t0001g0252 a0001c0001t0001g0254 others(15): Show |
18 | HG01175.hp2 HG01433.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.331-2410_331-2408d others(5): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | ||||||
| chr5:160032702 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.331-2422_331-2408d others(17): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032702 | ||||||
| chr5:160032754 | G | A | 5 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-2386G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160032754 | |||||||
| chr5:160032880 | AT | A | 124 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(121): Show |
131 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.331-2249delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160032880 | ||||||
| chr5:160032891 | T | G | 42 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0133 others(39): Show |
45 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.331-2249T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160032891 | |||||||
| chr5:160033281 | G | A | 72 | a0001c0001t0001g0120 a0001c0001t0001g0244 a0001c0001t0001g0245 others(69): Show |
75 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.331-1859G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160033281 | |||||||
| chr5:160033336 | T | C | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(265): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.331-1804T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160033336 | |||||||
| chr5:160033365 | C | G | 1 | a0001c0001t0002g0330 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.331-1775C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160033365 | |||||||
| chr5:160033484 | A | G | 64 | a0001c0001t0001g0120 a0001c0001t0001g0296 a0001c0001t0001g0308 others(61): Show |
67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.331-1656A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160033484 | |||||||
| chr5:160033550 | A | C | 1 | a0001c0001t0006g0275 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.331-1590A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160033550 | |||||||
| chr5:160033758 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0006g0275 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.331-1382C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160033758 | |||||||
| chr5:160033794 | C | T | 5 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-1346C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160033794 | |||||||
| chr5:160034126 | CT | C | 57 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0030 others(54): Show |
60 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.331-993delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160034126 | ||||||
| chr5:160034303 | C | T | 118 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0120 others(115): Show |
124 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.331-837C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160034303 | |||||||
| chr5:160034711 | A | AACTAAGG others(13): Show |
1 | a0001c0001t0001g0269 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.331-428_331-409dup others(20): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 160034711 | ||||||
| chr5:160034731 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.331-409C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160034731 | |||||||
| chr5:160034782 | G | C | 4 | a0002c0002t0001g0240 a0002c0002t0001g0241 a0002c0002t0001g0242 others(1): Show |
4 | HG01928.hp1 HG03669.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-358G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160034782 | |||||||
| chr5:160034883 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0006g0275 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.331-257T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160034883 | |||||||
| chr5:160034932 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.331-208T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160034932 | |||||||
| chr5:160034938 | C | A | 1 | a0001c0001t0002g0316 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.331-202C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160034938 | |||||||
| chr5:160034976 | T | C | 4 | a0001c0001t0002g0286 a0001c0001t0002g0293 a0001c0001t0002g0317 others(1): Show |
4 | HG01175.hp1 HG01192.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-164T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 2/7 | chr5 | 160034976 | |||||||
| chr5:160035413 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.391+213C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160035413 | |||||||
| chr5:160035415 | T | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0024 others(15): Show |
21 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.391+215T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160035415 | |||||||
| chr5:160035650 | C | A | 5 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+450C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160035650 | |||||||
| chr5:160035753 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.391+553G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160035753 | |||||||
| chr5:160035952 | G | GT | 23 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0028 others(20): Show |
24 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.392-726dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 160035952 | ||||||
| chr5:160035953 | T | G | 71 | a0001c0001t0001g0120 a0001c0001t0001g0244 a0001c0001t0001g0245 others(68): Show |
74 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.392-738T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160035953 | |||||||
| chr5:160035954 | T | G | 1 | a0005c0004t0002g0343 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.392-737T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160035954 | |||||||
| chr5:160036115 | A | C | 1 | a0001c0001t0001g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.392-576A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160036115 | |||||||
| chr5:160036357 | T | G | 1 | a0001c0001t0002g0327 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.392-334T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160036357 | |||||||
| chr5:160036358 | G | A | 1 | a0001c0001t0002g0327 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.392-333G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160036358 | |||||||
| chr5:160036400 | A | G | 1 | a0002c0002t0001g0243 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.392-291A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160036400 | |||||||
| chr5:160036534 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.392-157A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160036534 | |||||||
| chr5:160036549 | G | C | 72 | a0001c0001t0001g0120 a0001c0001t0001g0244 a0001c0001t0001g0245 others(69): Show |
75 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.392-142G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160036549 | |||||||
| chr5:160036680 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0135 a0001c0001t0001g0189 others(1): Show |
4 | HG01071.hp1 HG02109.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-11C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 3/7 | chr5 | 160036680 | |||||||
| chr5:160037163 | G | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.504+360G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160037163 | |||||||
| chr5:160037296 | A | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0127 |
3 | HG02258.hp1 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.504+493A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160037296 | |||||||
| chr5:160037666 | A | G | 72 | a0001c0001t0001g0120 a0001c0001t0001g0244 a0001c0001t0001g0245 others(69): Show |
75 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.504+863A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160037666 | |||||||
| chr5:160037742 | C | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | NA18986.hp1 NA19057.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.504+939C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160037742 | |||||||
| chr5:160037743 | G | T | 354 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(351): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.504+940G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160037743 | |||||||
| chr5:160037781 | G | GT | 11 | a0001c0001t0001g0060 a0001c0001t0001g0145 a0001c0001t0001g0219 others(8): Show |
11 | HG00099.hp2 HG02074.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.504+992dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160037781 | ||||||
| chr5:160037899 | G | T | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.504+1096G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160037899 | |||||||
| chr5:160037962 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.504+1159A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160037962 | |||||||
| chr5:160038013 | G | T | 116 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0120 others(113): Show |
122 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.504+1210G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038013 | |||||||
| chr5:160038016 | T | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0086 |
2 | HG01099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.504+1213T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038016 | |||||||
| chr5:160038044 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0347 a0001c0001t0001g0348 others(2): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+1241G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038044 | |||||||
| chr5:160038086 | G | GT | 16 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0044 others(13): Show |
16 | HG01981.hp1 HG01981.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.504+1295dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160038086 | ||||||
| chr5:160038317 | T | G | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.504+1514T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038317 | |||||||
| chr5:160038359 | C | T | 1 | a0001c0001t0002g0327 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.504+1556C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038359 | |||||||
| chr5:160038659 | C | CT | 72 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0053 others(69): Show |
75 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.504+1877dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160038659 | ||||||
| chr5:160038659 | C | CTT | 7 | a0001c0001t0001g0308 a0001c0001t0002g0285 a0001c0001t0002g0307 others(4): Show |
7 | HG01175.hp1 HG01978.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.504+1876_504+1877d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160038659 | ||||||
| chr5:160038659 | CT | C | 6 | a0001c0001t0001g0064 a0001c0001t0001g0103 a0001c0001t0001g0108 others(3): Show |
6 | HG02896.hp2 HG03041.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+1877delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160038659 | ||||||
| chr5:160038659 | CTTTTTTT | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(42): Show |
48 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.504+1871_504+1877d others(9): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160038659 | ||||||
| chr5:160038686 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.504+1883G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038686 | |||||||
| chr5:160038721 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.504+1918G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038721 | |||||||
| chr5:160038791 | T | G | 113 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0120 others(110): Show |
119 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.504+1988T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038791 | |||||||
| chr5:160038809 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.504+2006C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038809 | |||||||
| chr5:160038875 | C | T | 4 | a0002c0002t0001g0240 a0002c0002t0001g0241 a0002c0002t0001g0242 others(1): Show |
4 | HG01928.hp1 HG03669.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+2072C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038875 | |||||||
| chr5:160038882 | C | T | 4 | a0002c0002t0001g0240 a0002c0002t0001g0241 a0002c0002t0001g0242 others(1): Show |
4 | HG01928.hp1 HG03669.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+2079C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038882 | |||||||
| chr5:160038947 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.504+2144C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160038947 | |||||||
| chr5:160039050 | A | T | 1 | a0001c0001t0001g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.504+2247A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039050 | |||||||
| chr5:160039207 | T | C | 1 | a0002c0002t0001g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504+2404T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039207 | |||||||
| chr5:160039221 | AGTTTCAG others(48): Show |
A | 1 | a0001c0001t0001g0308 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.504+2419_504+2473d others(57): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039221 | |||||||
| chr5:160039247 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0006g0275 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.504+2444A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039247 | |||||||
| chr5:160039280 | C | CT | 31 | a0001c0001t0001g0180 a0001c0001t0001g0252 a0001c0001t0001g0254 others(28): Show |
31 | HG00423.hp2 HG00438.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.504+2494dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160039280 | ||||||
| chr5:160039280 | C | CTT | 8 | a0001c0001t0001g0018 a0001c0001t0001g0251 a0001c0001t0001g0257 others(5): Show |
9 | HG00609.hp2 NA18959.hp2 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.504+2493_504+2494d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160039280 | ||||||
| chr5:160039280 | CT | C | 20 | a0001c0001t0001g0017 a0001c0001t0001g0049 a0001c0001t0001g0087 others(17): Show |
21 | HG00639.hp1 HG01167.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.504+2494delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160039280 | ||||||
| chr5:160039306 | T | C | 5 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.504+2503T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039306 | |||||||
| chr5:160039386 | C | T | 46 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(43): Show |
49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.504+2583C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039386 | |||||||
| chr5:160039459 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.504+2656T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039459 | |||||||
| chr5:160039532 | C | T | 4 | a0001c0001t0001g0071 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG00597.hp1 NA18747.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+2729C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039532 | |||||||
| chr5:160039539 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.504+2736G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039539 | |||||||
| chr5:160039643 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.504+2840A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039643 | |||||||
| chr5:160039744 | T | C | 46 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(43): Show |
49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.504+2941T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039744 | |||||||
| chr5:160039794 | T | G | 70 | a0001c0001t0001g0017 a0001c0001t0001g0120 a0001c0001t0001g0196 others(67): Show |
74 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.504+2991T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160039794 | |||||||
| chr5:160040078 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.505-3055A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040078 | |||||||
| chr5:160040264 | A | G | 7 | a0001c0001t0001g0028 a0001c0001t0001g0107 a0001c0001t0001g0108 others(4): Show |
7 | HG01109.hp1 HG01943.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-2869A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040264 | |||||||
| chr5:160040265 | T | TAC | 7 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0150 others(4): Show |
9 | HG00140.hp2 HG01074.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.505-2852_505-2851d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160040265 | ||||||
| chr5:160040323 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.505-2810G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040323 | |||||||
| chr5:160040406 | T | C | 46 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(43): Show |
49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.505-2727T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040406 | |||||||
| chr5:160040434 | A | T | 64 | a0001c0001t0001g0120 a0001c0001t0001g0296 a0001c0001t0001g0308 others(61): Show |
67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.505-2699A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040434 | |||||||
| chr5:160040467 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.505-2666G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040467 | |||||||
| chr5:160040475 | G | A | 5 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
5 | HG01071.hp2 HG02055.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-2658G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040475 | |||||||
| chr5:160040482 | G | C | 5 | a0001c0001t0001g0056 a0001c0001t0001g0121 a0001c0001t0001g0126 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-2651G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040482 | |||||||
| chr5:160040494 | AACTTT | A | 6 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0002c0002t0001g0241 others(3): Show |
6 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-2638_505-2634d others(7): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040494 | |||||||
| chr5:160040768 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.505-2365C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040768 | |||||||
| chr5:160040806 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.505-2327T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040806 | |||||||
| chr5:160040870 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.505-2263G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160040870 | |||||||
| chr5:160040945 | AT | A | 51 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0068 others(48): Show |
54 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.505-2174delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160040945 | ||||||
| chr5:160041040 | A | T | 1 | a0001c0001t0001g0308 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.505-2093A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041040 | |||||||
| chr5:160041091 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.505-2042G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041091 | |||||||
| chr5:160041247 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.505-1886T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041247 | |||||||
| chr5:160041313 | C | CT | 102 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0025 others(99): Show |
107 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.505-1804dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160041313 | ||||||
| chr5:160041313 | C | CTT | 6 | a0001c0001t0001g0142 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
7 | HG00408.hp2 HG00673.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.505-1805_505-1804d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 160041313 | ||||||
| chr5:160041372 | G | A | 39 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(36): Show |
42 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.505-1761G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041372 | |||||||
| chr5:160041496 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.505-1637A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041496 | |||||||
| chr5:160041686 | A | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02055.hp1 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.505-1447A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041686 | |||||||
| chr5:160041800 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.505-1333C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041800 | |||||||
| chr5:160041827 | C | T | 1 | a0001c0001t0002g0337 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.505-1306C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041827 | |||||||
| chr5:160041851 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.505-1282C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160041851 | |||||||
| chr5:160042076 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.505-1057C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042076 | |||||||
| chr5:160042178 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.505-955C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042178 | |||||||
| chr5:160042216 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.505-917C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042216 | |||||||
| chr5:160042222 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.505-911G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042222 | |||||||
| chr5:160042261 | G | A | 5 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0274 others(2): Show |
5 | HG02258.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-872G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042261 | |||||||
| chr5:160042270 | T | A | 113 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0120 others(110): Show |
119 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.505-863T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042270 | |||||||
| chr5:160042368 | C | G | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.505-765C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042368 | |||||||
| chr5:160042440 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505-693C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042440 | |||||||
| chr5:160042678 | C | T | 2 | a0001c0001t0002g0299 a0001c0001t0002g0324 |
2 | NA18962.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.505-455C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042678 | |||||||
| chr5:160042993 | A | G | 9 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0055 others(6): Show |
10 | HG00621.hp2 HG02027.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.505-140A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160042993 | |||||||
| chr5:160043127 | T | C | 5 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0002c0002t0001g0241 others(2): Show |
5 | HG01928.hp1 HG02723.hp2 HG03669.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.505-6T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 4/7 | chr5 | 160043127 | |||||||
| chr5:160043240 | G | T | 1 | a0004c0005t0001g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.541+71G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043240 | |||||||
| chr5:160043354 | C | G | 1 | a0002c0002t0001g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.541+185C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043354 | |||||||
| chr5:160043408 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.541+239G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043408 | |||||||
| chr5:160043455 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.541+286T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043455 | |||||||
| chr5:160043542 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.541+373G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043542 | |||||||
| chr5:160043572 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.541+403A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043572 | |||||||
| chr5:160043876 | A | G | 1 | a0001c0001t0006g0275 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.541+707A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043876 | |||||||
| chr5:160043886 | TA | T | 3 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0006g0275 |
3 | HG02258.hp2 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.541+719delA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160043886 | ||||||
| chr5:160043932 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.541+763C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043932 | |||||||
| chr5:160043962 | G | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.541+793G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160043962 | |||||||
| chr5:160044052 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.541+883T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160044052 | |||||||
| chr5:160044053 | G | A | 124 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(121): Show |
131 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.541+884G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160044053 | |||||||
| chr5:160044575 | G | GTGGGGGA others(6): Show |
1 | a0001c0001t0001g0308 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.541+1411_541+1412i others(15): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160044575 | ||||||
| chr5:160044798 | G | A | 7 | a0002c0002t0001g0022 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.541+1629G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160044798 | |||||||
| chr5:160044804 | C | T | 6 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0002c0002t0001g0241 others(3): Show |
6 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.541+1635C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160044804 | |||||||
| chr5:160045124 | C | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0042 others(7): Show |
13 | HG00140.hp2 HG00642.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.541+1955C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045124 | |||||||
| chr5:160045163 | C | T | 32 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(29): Show |
35 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.541+1994C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045163 | |||||||
| chr5:160045241 | C | T | 1 | a0001c0001t0006g0275 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.541+2072C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045241 | |||||||
| chr5:160045402 | T | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0160 others(6): Show |
9 | HG00408.hp1 NA18949.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.541+2233T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045402 | |||||||
| chr5:160045438 | C | T | 70 | a0001c0001t0001g0120 a0001c0001t0001g0274 a0001c0001t0001g0276 others(67): Show |
73 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.541+2269C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045438 | |||||||
| chr5:160045443 | T | G | 1 | a0001c0001t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.541+2274T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045443 | |||||||
| chr5:160045449 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.541+2280A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045449 | |||||||
| chr5:160045450 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.541+2281C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045450 | |||||||
| chr5:160045452 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.541+2283C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045452 | |||||||
| chr5:160045454 | C | CCA | 16 | a0001c0001t0001g0055 a0001c0001t0001g0069 a0001c0001t0001g0070 others(13): Show |
16 | HG01943.hp2 HG02040.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.541+2344_541+2345d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | C | CCACA | 12 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0059 others(9): Show |
12 | HG00423.hp1 HG00609.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.541+2342_541+2345d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | C | CCACACA | 10 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0053 others(7): Show |
10 | HG00738.hp2 HG00741.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.541+2340_541+2345d others(8): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | C | CCACACAC others(1): Show |
6 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0068 others(3): Show |
6 | HG00735.hp2 HG01169.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.541+2338_541+2345d others(10): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | C | CCACACAC others(3): Show |
1 | a0001c0001t0001g0061 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.541+2336_541+2345d others(12): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | C | CCACACAC others(5): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0168 |
2 | HG01884.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.541+2334_541+2345d others(14): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | C | CCACACAC others(7): Show |
1 | a0001c0001t0001g0172 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.541+2332_541+2345d others(16): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | CCA | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(20): Show |
23 | HG00639.hp2 HG01071.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.541+2344_541+2345d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | CCACA | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(29): Show |
33 | HG00738.hp1 HG01071.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.541+2342_541+2345d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | CCACACA | C | 31 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0015 others(28): Show |
33 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.541+2340_541+2345d others(8): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | CCACACAC others(1): Show |
C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(23): Show |
27 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.541+2338_541+2345d others(10): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | CCACACAC others(3): Show |
C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(20): Show |
25 | HG00140.hp2 HG00621.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.541+2336_541+2345d others(12): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | CCACACAC others(5): Show |
C | 18 | a0001c0001t0001g0028 a0001c0001t0001g0065 a0001c0001t0001g0118 others(15): Show |
18 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(15): Show |
intron_variant | MODIFIER | c.541+2334_541+2345d others(14): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | CCACACAC others(7): Show |
C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0054 others(5): Show |
9 | HG01167.hp2 HG01169.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.541+2332_541+2345d others(16): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | CCACACAC others(9): Show |
C | 5 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0041 others(2): Show |
5 | HG01256.hp2 HG01258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+2330_541+2345d others(18): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | CCACACAC others(11): Show |
C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0347 |
2 | HG01515.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.541+2328_541+2345d others(20): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | CCACACAC others(13): Show |
C | 4 | a0001c0001t0001g0155 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | NA18968.hp2 NA18993.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+2326_541+2345d others(22): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | CCACACAC others(15): Show |
C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0245 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.541+2324_541+2345d others(24): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | CCACACAC others(17): Show |
C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0263 a0001c0001t0001g0277 others(5): Show |
9 | HG02717.hp2 HG02723.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.541+2322_541+2345d others(26): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | CCACACAC others(19): Show |
C | 31 | a0001c0001t0001g0005 a0001c0001t0001g0180 a0001c0001t0001g0244 others(28): Show |
33 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.541+2320_541+2345d others(28): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045454 | CCACACAC others(25): Show |
C | 1 | a0001c0001t0001g0352 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.541+2314_541+2345d others(34): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045454 | ||||||
| chr5:160045483 | C | T | 4 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0353 others(1): Show |
4 | HG02055.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+2314C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045483 | |||||||
| chr5:160045485 | C | T | 2 | a0001c0001t0002g0313 a0001c0001t0006g0275 |
2 | HG02258.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.541+2316C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045485 | |||||||
| chr5:160045486 | A | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.541+2317A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045486 | |||||||
| chr5:160045487 | C | T | 62 | a0001c0001t0001g0120 a0001c0001t0001g0296 a0001c0001t0001g0308 others(59): Show |
65 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.541+2318C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045487 | |||||||
| chr5:160045487 | CACACACA others(21): Show |
C | 2 | a0001c0001t0001g0353 a0001c0001t0001g0354 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.541+2325_541+2352d others(30): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045487 | ||||||
| chr5:160045489 | C | T | 1 | a0001c0001t0002g0344 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.541+2320C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045489 | |||||||
| chr5:160045491 | CACACACA others(17): Show |
C | 2 | a0001c0001t0001g0274 a0001c0001t0001g0276 |
2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.541+2329_541+2352d others(26): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045491 | ||||||
| chr5:160045493 | CACACACA others(15): Show |
C | 3 | a0002c0002t0001g0240 a0002c0002t0001g0241 a0002c0002t0001g0242 |
3 | HG01928.hp1 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.541+2331_541+2352d others(24): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045493 | ||||||
| chr5:160045494 | A | T | 1 | a0001c0001t0006g0275 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.541+2325A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045494 | |||||||
| chr5:160045496 | A | T | 3 | a0001c0001t0002g0292 a0001c0001t0002g0313 a0001c0001t0006g0275 |
3 | HG02258.hp2 NA19085.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.541+2327A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045496 | |||||||
| chr5:160045496 | ACACACAC others(19): Show |
A | 1 | a0001c0001t0002g0295 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.541+2329_541+2354d others(28): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045496 | ||||||
| chr5:160045497 | CACACACA others(11): Show |
C | 4 | a0001c0001t0002g0019 a0001c0001t0002g0313 a0001c0001t0002g0345 others(1): Show |
4 | NA18945.hp1 NA18959.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+2335_541+2352d others(20): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045497 | ||||||
| chr5:160045498 | A | T | 60 | a0001c0001t0001g0120 a0001c0001t0001g0296 a0001c0001t0001g0308 others(57): Show |
62 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.541+2329A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045498 | |||||||
| chr5:160045499 | CACACACA others(9): Show |
C | 23 | a0001c0001t0001g0323 a0001c0001t0002g0287 a0001c0001t0002g0288 others(20): Show |
23 | HG01175.hp1 HG01256.hp1 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.541+2337_541+2352d others(18): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045499 | ||||||
| chr5:160045500 | A | T | 38 | a0001c0001t0001g0120 a0001c0001t0001g0296 a0001c0001t0001g0308 others(35): Show |
40 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.541+2331A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045500 | |||||||
| chr5:160045501 | CACACACA others(7): Show |
C | 28 | a0001c0001t0001g0120 a0001c0001t0001g0296 a0001c0001t0001g0308 others(25): Show |
29 | HG00408.hp2 HG00597.hp2 HG01928.hp2 others(26): Show |
intron_variant | MODIFIER | c.541+2339_541+2352d others(16): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045501 | ||||||
| chr5:160045502 | A | T | 11 | a0001c0001t0002g0006 a0001c0001t0002g0286 a0001c0001t0002g0290 others(8): Show |
11 | HG01081.hp1 HG01106.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.541+2333A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045502 | |||||||
| chr5:160045503 | CACACACA others(5): Show |
C | 6 | a0001c0001t0002g0006 a0001c0001t0002g0286 a0001c0001t0002g0290 others(3): Show |
6 | HG01106.hp2 HG01192.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.541+2341_541+2352d others(14): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045503 | ||||||
| chr5:160045504 | A | T | 5 | a0001c0001t0002g0299 a0001c0001t0002g0300 a0001c0001t0002g0304 others(2): Show |
5 | HG01081.hp1 HG02148.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+2335A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045504 | |||||||
| chr5:160045505 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.541+2336C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045505 | |||||||
| chr5:160045505 | CACACACA others(3): Show |
C | 2 | a0001c0001t0001g0021 a0001c0001t0002g0300 |
2 | HG01081.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.541+2343_541+2352d others(12): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045505 | ||||||
| chr5:160045506 | A | T | 4 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0001t0002g0321 others(1): Show |
4 | HG02148.hp2 NA18972.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+2337A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045506 | |||||||
| chr5:160045508 | A | T | 3 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0001t0002g0321 |
3 | HG02148.hp2 NA19060.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.541+2339A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045508 | |||||||
| chr5:160045510 | A | T | 2 | a0001c0001t0002g0299 a0001c0001t0002g0304 |
2 | HG02148.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.541+2341A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045510 | |||||||
| chr5:160045511 | CACAT | C | 3 | a0001c0001t0001g0163 a0001c0001t0002g0299 a0001c0001t0002g0304 |
3 | HG02148.hp2 NA19005.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.541+2346_541+2349d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045511 | ||||||
| chr5:160045512 | ACATACAC others(5): Show |
A | 1 | a0001c0001t0001g0159 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.541+2345_541+2356d others(14): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045512 | ||||||
| chr5:160045515 | T | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0134 a0001c0001t0001g0152 others(4): Show |
7 | HG00280.hp1 HG00642.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+2346T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045515 | |||||||
| chr5:160045516 | A | T | 65 | a0001c0001t0001g0120 a0001c0001t0001g0274 a0001c0001t0001g0296 others(62): Show |
68 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.541+2347A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045516 | |||||||
| chr5:160045518 | A | T | 69 | a0001c0001t0001g0120 a0001c0001t0001g0274 a0001c0001t0001g0276 others(66): Show |
72 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.541+2349A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045518 | |||||||
| chr5:160045518 | ACACTCTC others(7): Show |
A | 1 | a0001c0001t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.541+2351_541+2364d others(16): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045518 | ||||||
| chr5:160045520 | A | ACT | 11 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0119 others(8): Show |
12 | HG02055.hp1 HG02109.hp1 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.541+2383_541+2384d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | ||||||
| chr5:160045520 | A | ACTCT | 37 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0025 others(34): Show |
40 | HG00609.hp2 HG01109.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.541+2381_541+2384d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | ||||||
| chr5:160045520 | A | ACTCTCT | 7 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0260 others(4): Show |
7 | HG00423.hp2 HG00438.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+2379_541+2384d others(8): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | ||||||
| chr5:160045520 | A | ACTCTCTC others(1): Show |
3 | a0001c0001t0001g0180 a0001c0001t0001g0257 a0001c0001t0001g0261 |
3 | HG01175.hp2 HG02135.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.541+2377_541+2384d others(10): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | ||||||
| chr5:160045520 | A | ACTCTCTC others(3): Show |
1 | a0001c0001t0001g0244 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.541+2375_541+2384d others(12): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | ||||||
| chr5:160045520 | A | ACTCTCTC others(9): Show |
2 | a0001c0001t0001g0245 a0002c0002t0001g0239 |
2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.541+2369_541+2384d others(18): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | ||||||
| chr5:160045520 | A | T | 74 | a0001c0001t0001g0060 a0001c0001t0001g0120 a0001c0001t0001g0134 others(71): Show |
77 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.541+2351A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045520 | |||||||
| chr5:160045520 | ACT | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0042 others(13): Show |
19 | HG00140.hp2 HG00642.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.541+2383_541+2384d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | ||||||
| chr5:160045520 | ACTCT | A | 13 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0055 others(10): Show |
13 | HG00673.hp1 HG01071.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.541+2381_541+2384d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | ||||||
| chr5:160045520 | ACTCTCTC others(1): Show |
A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0122 others(2): Show |
6 | HG00741.hp2 HG01952.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.541+2377_541+2384d others(10): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | ||||||
| chr5:160045520 | ACTCTCTC others(3): Show |
A | 1 | a0001c0001t0001g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.541+2375_541+2384d others(12): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045520 | ||||||
| chr5:160045522 | T | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG02027.hp1 HG03098.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+2353T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045522 | |||||||
| chr5:160045554 | C | T | 112 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0120 others(109): Show |
118 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.541+2385C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045554 | |||||||
| chr5:160045556 | C | T | 70 | a0001c0001t0001g0120 a0001c0001t0001g0274 a0001c0001t0001g0276 others(67): Show |
73 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.541+2387C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045556 | |||||||
| chr5:160045558 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.541+2389T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045558 | |||||||
| chr5:160045558 | TC | T | 7 | a0001c0001t0001g0296 a0001c0001t0002g0299 a0001c0001t0002g0319 others(4): Show |
7 | HG01952.hp2 HG01993.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.541+2393delC | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160045558 | ||||||
| chr5:160045560 | C | T | 1 | a0001c0001t0002g0326 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.541+2391C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045560 | |||||||
| chr5:160045570 | A | G | 31 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(28): Show |
34 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.541+2401A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045570 | |||||||
| chr5:160045682 | C | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(31): Show |
37 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.541+2513C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045682 | |||||||
| chr5:160045733 | T | C | 1 | a0001c0001t0001g0354 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.541+2564T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045733 | |||||||
| chr5:160045903 | C | T | 5 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0002c0002t0001g0241 others(2): Show |
5 | HG01928.hp1 HG02723.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+2734C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160045903 | |||||||
| chr5:160046087 | C | A | 70 | a0001c0001t0001g0120 a0001c0001t0001g0274 a0001c0001t0001g0276 others(67): Show |
73 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.541+2918C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046087 | |||||||
| chr5:160046117 | C | T | 1 | a0002c0002t0001g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.541+2948C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046117 | |||||||
| chr5:160046270 | C | T | 5 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+3101C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046270 | |||||||
| chr5:160046645 | T | C | 5 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.542-2869T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046645 | |||||||
| chr5:160046789 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.542-2725G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046789 | |||||||
| chr5:160046826 | T | G | 1 | a0002c0002t0001g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.542-2688T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046826 | |||||||
| chr5:160046877 | C | T | 37 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(34): Show |
40 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.542-2637C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046877 | |||||||
| chr5:160046883 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.542-2631G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160046883 | |||||||
| chr5:160047152 | CAACTCTG others(582): Show |
C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG00423.hp2 HG00438.hp2 |
intron_variant | MODIFIER | c.542-2360_542-1772d others(2): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160047152 | ||||||
| chr5:160047186 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.542-2328G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047186 | |||||||
| chr5:160047256 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.542-2258A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047256 | |||||||
| chr5:160047265 | C | A | 1 | a0001c0001t0001g0014 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.542-2249C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047265 | |||||||
| chr5:160047378 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.542-2136T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047378 | |||||||
| chr5:160047410 | T | G | 64 | a0001c0001t0001g0120 a0001c0001t0001g0296 a0001c0001t0001g0308 others(61): Show |
67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.542-2104T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047410 | |||||||
| chr5:160047597 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.542-1917T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047597 | |||||||
| chr5:160047672 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.542-1842C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047672 | |||||||
| chr5:160047779 | A | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG02615.hp1 HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.542-1735A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047779 | |||||||
| chr5:160047797 | C | G | 11 | a0001c0001t0002g0292 a0001c0001t0002g0299 a0001c0001t0002g0305 others(8): Show |
11 | HG02132.hp2 NA18951.hp1 NA18962.hp2 others(8): Show |
intron_variant | MODIFIER | c.542-1717C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047797 | |||||||
| chr5:160047858 | G | A | 64 | a0001c0001t0001g0120 a0001c0001t0001g0296 a0001c0001t0001g0308 others(61): Show |
67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.542-1656G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047858 | |||||||
| chr5:160047933 | G | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.542-1581G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160047933 | |||||||
| chr5:160048094 | G | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.542-1420G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048094 | |||||||
| chr5:160048126 | CTT | C | 22 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0117 others(19): Show |
24 | HG00423.hp1 HG01106.hp1 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.542-1353_542-1352d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048126 | ||||||
| chr5:160048126 | CTTT | C | 21 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0068 others(18): Show |
22 | HG00280.hp1 HG00673.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.542-1354_542-1352d others(5): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048126 | ||||||
| chr5:160048126 | CTTTTTTT others(1): Show |
C | 22 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0044 others(19): Show |
22 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.542-1359_542-1352d others(10): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048126 | ||||||
| chr5:160048126 | CTTTTTTT others(2): Show |
C | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(89): Show |
99 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.542-1360_542-1352d others(11): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048126 | ||||||
| chr5:160048126 | CTTTTTTT others(3): Show |
C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(172): Show |
192 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.542-1361_542-1352d others(12): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048126 | ||||||
| chr5:160048126 | CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0001g0053 a0001c0001t0001g0214 a0001c0001t0001g0223 others(3): Show |
6 | HG01081.hp1 HG01167.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.542-1362_542-1352d others(13): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048126 | ||||||
| chr5:160048126 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.542-1364_542-1352d others(15): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048126 | ||||||
| chr5:160048162 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.542-1352T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048162 | |||||||
| chr5:160048179 | T | C | 5 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.542-1335T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048179 | |||||||
| chr5:160048186 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.542-1328T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048186 | |||||||
| chr5:160048197 | G | A | 1 | a0001c0001t0002g0290 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.542-1317G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048197 | |||||||
| chr5:160048309 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.542-1205G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048309 | |||||||
| chr5:160048391 | T | C | 3 | a0001c0001t0002g0292 a0001c0001t0002g0309 a0001c0001t0002g0325 |
3 | NA18951.hp1 NA18967.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.542-1123T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048391 | |||||||
| chr5:160048459 | C | G | 6 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0002c0002t0001g0241 others(3): Show |
6 | HG01928.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.542-1055C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048459 | |||||||
| chr5:160048469 | A | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(228): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.542-1045A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048469 | |||||||
| chr5:160048529 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.542-985A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048529 | |||||||
| chr5:160048548 | G | A | 5 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0274 others(2): Show |
5 | HG02258.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.542-966G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048548 | |||||||
| chr5:160048667 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.542-847C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048667 | |||||||
| chr5:160048686 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0007g0200 |
2 | HG00558.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.542-828A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048686 | |||||||
| chr5:160048746 | C | G | 1 | a0004c0005t0001g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.542-768C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048746 | |||||||
| chr5:160048929 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(228): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.542-585T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048929 | |||||||
| chr5:160048937 | C | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(38): Show |
44 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.542-577C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160048937 | |||||||
| chr5:160048949 | TA | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(228): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.542-553delA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 160048949 | ||||||
| chr5:160049020 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(228): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.542-494T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160049020 | |||||||
| chr5:160049078 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.542-436C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160049078 | |||||||
| chr5:160049278 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(157): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.542-236G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160049278 | |||||||
| chr5:160049369 | A | G | 1 | a0001c0001t0001g0354 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.542-145A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160049369 | |||||||
| chr5:160049488 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0006g0275 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.542-26A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 5/7 | chr5 | 160049488 | |||||||
| chr5:160050161 | C | A | 46 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(43): Show |
49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.690+499C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050161 | |||||||
| chr5:160050185 | C | T | 46 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(43): Show |
49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.690+523C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050185 | |||||||
| chr5:160050193 | C | A | 46 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(43): Show |
49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.690+531C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050193 | |||||||
| chr5:160050214 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.690+552G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050214 | |||||||
| chr5:160050345 | G | A | 46 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(43): Show |
49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.690+683G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050345 | |||||||
| chr5:160050423 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.691-706G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050423 | |||||||
| chr5:160050474 | A | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0105 a0001c0001t0001g0154 |
3 | HG00741.hp1 HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.691-655A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050474 | |||||||
| chr5:160050510 | C | CATCTGAT others(4): Show |
1 | a0001c0001t0001g0207 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.691-615_691-605dup others(11): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 160050510 | ||||||
| chr5:160050510 | C | T | 1 | a0001c0001t0002g0287 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.691-619C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050510 | |||||||
| chr5:160050627 | C | CT | 60 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0197 others(57): Show |
63 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.691-482dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 160050627 | ||||||
| chr5:160050627 | C | CTT | 6 | a0001c0001t0001g0308 a0001c0001t0001g0322 a0001c0001t0001g0323 others(3): Show |
6 | HG01993.hp2 HG04115.hp2 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-483_691-482dup others(2): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 160050627 | ||||||
| chr5:160050627 | CT | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(211): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.691-482delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 160050627 | ||||||
| chr5:160050761 | G | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(31): Show |
37 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.691-368G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050761 | |||||||
| chr5:160050816 | G | C | 1 | a0001c0001t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.691-313G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050816 | |||||||
| chr5:160050905 | C | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(31): Show |
37 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.691-224C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160050905 | |||||||
| chr5:160050977 | G | GT | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(185): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.691-140dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 160050977 | ||||||
| chr5:160051082 | GT | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(244): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.691-31delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 160051082 | ||||||
| chr5:160051082 | GTT | G | 22 | a0001c0001t0001g0016 a0001c0001t0001g0090 a0001c0001t0001g0120 others(19): Show |
25 | HG01081.hp1 HG01106.hp2 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.691-32_691-31delTT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 160051082 | ||||||
| chr5:160051087 | T | G | 2 | a0001c0001t0001g0274 a0001c0001t0006g0275 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.691-42T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 6/7 | chr5 | 160051087 | |||||||
| chr5:160051331 | G | A | 5 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.745+148G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160051331 | |||||||
| chr5:160051427 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.745+244A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160051427 | |||||||
| chr5:160051534 | G | A | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(302): Show |
329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.745+351G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160051534 | |||||||
| chr5:160051633 | C | T | 48 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0118 others(45): Show |
51 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.745+450C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160051633 | |||||||
| chr5:160051769 | T | C | 1 | a0001c0001t0002g0302 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.745+586T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160051769 | |||||||
| chr5:160051969 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.745+786C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160051969 | |||||||
| chr5:160052059 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.745+876G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160052059 | |||||||
| chr5:160052168 | C | CA | 48 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0118 others(45): Show |
51 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.745+991dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052168 | ||||||
| chr5:160052235 | CG | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0104 |
3 | HG02135.hp1 HG03017.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.745+1054delG | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052235 | ||||||
| chr5:160052391 | ATGGGAGG others(6): Show |
A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0024 others(15): Show |
21 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+1211_745+1223d others(15): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052391 | ||||||
| chr5:160052548 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.745+1365C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160052548 | |||||||
| chr5:160052548 | C | CA | 38 | a0001c0001t0001g0056 a0001c0001t0001g0132 a0001c0001t0001g0133 others(35): Show |
38 | HG00642.hp1 HG00673.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.745+1391dupA | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | ||||||
| chr5:160052548 | C | CAA | 7 | a0001c0001t0001g0027 a0001c0001t0001g0141 a0001c0001t0001g0145 others(4): Show |
7 | HG00597.hp2 HG00642.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.745+1390_745+1391d others(4): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | ||||||
| chr5:160052548 | C | CAAA | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(110): Show |
122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.745+1389_745+1391d others(5): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | ||||||
| chr5:160052548 | C | CAAAA | 47 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
53 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.745+1388_745+1391d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | ||||||
| chr5:160052548 | C | CAAAAA | 14 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0043 others(11): Show |
16 | HG01243.hp2 HG01978.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.745+1387_745+1391d others(7): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | ||||||
| chr5:160052548 | CAAAAA | C | 6 | a0001c0001t0001g0180 a0001c0001t0001g0249 a0001c0001t0001g0269 others(3): Show |
6 | HG01175.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.745+1387_745+1391d others(7): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | ||||||
| chr5:160052548 | CAAAAAA | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0246 others(37): Show |
43 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.745+1386_745+1391d others(8): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | ||||||
| chr5:160052548 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0075 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.745+1380_745+1391d others(14): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160052548 | ||||||
| chr5:160052572 | A | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.745+1389A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160052572 | |||||||
| chr5:160052893 | C | T | 1 | a0002c0002t0001g0242 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.745+1710C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160052893 | |||||||
| chr5:160053151 | AT | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0118 others(45): Show |
51 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.745+1970delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160053151 | ||||||
| chr5:160053186 | A | G | 1 | a0001c0001t0004g0253 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.745+2003A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160053186 | |||||||
| chr5:160053463 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.745+2280C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160053463 | |||||||
| chr5:160053611 | G | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(235): Show |
259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.745+2428G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160053611 | |||||||
| chr5:160053691 | A | G | 32 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0046 others(29): Show |
33 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.745+2508A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160053691 | |||||||
| chr5:160054026 | G | A | 3 | a0001c0001t0001g0347 a0001c0001t0001g0348 a0001c0001t0001g0349 |
3 | HG02630.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.745+2843G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054026 | |||||||
| chr5:160054069 | G | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(31): Show |
37 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.745+2886G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054069 | |||||||
| chr5:160054075 | T | TTTTG | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0278 |
3 | HG01192.hp2 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.745+2913_745+2916d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160054075 | ||||||
| chr5:160054075 | TTTTG | T | 5 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0002c0002t0001g0241 others(2): Show |
5 | HG01928.hp1 HG02723.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.745+2913_745+2916d others(6): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160054075 | ||||||
| chr5:160054108 | C | G | 2 | a0001c0001t0001g0274 a0001c0001t0006g0275 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.745+2925C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054108 | |||||||
| chr5:160054287 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.745+3104A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054287 | |||||||
| chr5:160054408 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0351 |
3 | HG02280.hp2 HG02895.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.745+3225G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054408 | |||||||
| chr5:160054625 | A | T | 1 | a0004c0005t0001g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.745+3442A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054625 | |||||||
| chr5:160054743 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.745+3560A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054743 | |||||||
| chr5:160054777 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.745+3594G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054777 | |||||||
| chr5:160054925 | G | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0227 |
2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.745+3742G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160054925 | |||||||
| chr5:160055034 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0347 a0001c0001t0001g0348 others(3): Show |
7 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.745+3851G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055034 | |||||||
| chr5:160055080 | A | C | 1 | a0001c0001t0001g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+3897A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055080 | |||||||
| chr5:160055230 | T | G | 1 | a0001c0001t0001g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+4047T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055230 | |||||||
| chr5:160055493 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.745+4310A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055493 | |||||||
| chr5:160055573 | G | T | 48 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0118 others(45): Show |
51 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.745+4390G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055573 | |||||||
| chr5:160055604 | T | C | 1 | a0001c0001t0001g0351 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.745+4421T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055604 | |||||||
| chr5:160055735 | G | T | 1 | a0001c0001t0001g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+4552G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055735 | |||||||
| chr5:160055953 | A | G | 1 | a0001c0001t0002g0324 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.745+4770A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160055953 | |||||||
| chr5:160056015 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.745+4832G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056015 | |||||||
| chr5:160056119 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.745+4936C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056119 | |||||||
| chr5:160056134 | T | C | 48 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0118 others(45): Show |
51 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.745+4951T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056134 | |||||||
| chr5:160056354 | T | A | 1 | a0001c0001t0001g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+5171T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056354 | |||||||
| chr5:160056490 | C | A | 1 | a0001c0001t0001g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+5307C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056490 | |||||||
| chr5:160056567 | A | T | 1 | a0001c0001t0001g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+5384A>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056567 | |||||||
| chr5:160056568 | T | A | 1 | a0001c0001t0001g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+5385T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056568 | |||||||
| chr5:160056768 | A | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(235): Show |
259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.745+5585A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056768 | |||||||
| chr5:160056928 | A | C | 1 | a0001c0001t0001g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+5745A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056928 | |||||||
| chr5:160056929 | C | A | 1 | a0001c0001t0001g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.745+5746C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056929 | |||||||
| chr5:160056941 | C | T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0237 |
3 | HG02523.hp1 NA19010.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.745+5758C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160056941 | |||||||
| chr5:160057040 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.745+5857C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160057040 | |||||||
| chr5:160057358 | T | A | 1 | a0001c0001t0001g0033 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.745+6175T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160057358 | |||||||
| chr5:160057418 | T | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0118 others(45): Show |
51 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.745+6235T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160057418 | |||||||
| chr5:160057809 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.745+6626G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160057809 | |||||||
| chr5:160057884 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0006g0275 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.745+6701C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160057884 | |||||||
| chr5:160058047 | G | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(31): Show |
37 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.745+6864G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058047 | |||||||
| chr5:160058133 | G | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(189): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.746-6799G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058133 | |||||||
| chr5:160058219 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(242): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.746-6713T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058219 | |||||||
| chr5:160058240 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0227 |
2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.746-6692C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058240 | |||||||
| chr5:160058262 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.746-6670A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058262 | |||||||
| chr5:160058389 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.746-6543T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058389 | |||||||
| chr5:160058409 | C | CT | 17 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0031 others(14): Show |
20 | HG00140.hp2 HG00642.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.746-6504dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160058409 | ||||||
| chr5:160058409 | CT | C | 18 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0087 others(15): Show |
18 | HG01071.hp1 HG01167.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.746-6504delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160058409 | ||||||
| chr5:160058413 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0006g0275 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.746-6519T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058413 | |||||||
| chr5:160058414 | T | G | 5 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0274 others(2): Show |
5 | HG02258.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-6518T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058414 | |||||||
| chr5:160058486 | G | C | 1 | a0001c0001t0006g0275 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.746-6446G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058486 | |||||||
| chr5:160058579 | T | A | 18 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0035 others(15): Show |
19 | HG00408.hp1 HG00621.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.746-6353T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058579 | |||||||
| chr5:160058616 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(180): Show |
201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.746-6316G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058616 | |||||||
| chr5:160058691 | G | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(27): Show |
33 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.746-6241G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058691 | |||||||
| chr5:160058702 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.746-6230C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058702 | |||||||
| chr5:160058741 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(175): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.746-6191A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058741 | |||||||
| chr5:160058775 | T | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.746-6157T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058775 | |||||||
| chr5:160058795 | G | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(180): Show |
201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.746-6137G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058795 | |||||||
| chr5:160058891 | C | G | 5 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0274 others(2): Show |
5 | HG02258.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-6041C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058891 | |||||||
| chr5:160058928 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.746-6004T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160058928 | |||||||
| chr5:160059012 | G | A | 64 | a0001c0001t0001g0120 a0001c0001t0001g0296 a0001c0001t0001g0308 others(61): Show |
67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.746-5920G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059012 | |||||||
| chr5:160059084 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(169): Show |
189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.746-5848G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059084 | |||||||
| chr5:160059193 | GT | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(210): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.746-5735delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160059193 | ||||||
| chr5:160059252 | G | C | 1 | a0001c0001t0001g0217 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.746-5680G>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059252 | |||||||
| chr5:160059347 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(181): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.746-5585T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059347 | |||||||
| chr5:160059425 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.746-5507G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059425 | |||||||
| chr5:160059687 | G | T | 1 | a0004c0005t0001g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.746-5245G>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059687 | |||||||
| chr5:160059729 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(169): Show |
189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.746-5203G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059729 | |||||||
| chr5:160059809 | G | A | 5 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
5 | HG01071.hp2 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-5123G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059809 | |||||||
| chr5:160059962 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.746-4970G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160059962 | |||||||
| chr5:160060243 | C | T | 1 | a0001c0001t0002g0325 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.746-4689C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060243 | |||||||
| chr5:160060316 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(181): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.746-4616A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060316 | |||||||
| chr5:160060323 | T | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(175): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.746-4609T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060323 | |||||||
| chr5:160060372 | C | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(181): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.746-4560C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060372 | |||||||
| chr5:160060384 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.746-4548C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060384 | |||||||
| chr5:160060468 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.746-4464C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060468 | |||||||
| chr5:160060618 | T | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(181): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.746-4314T>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060618 | |||||||
| chr5:160060639 | T | G | 1 | a0002c0002t0001g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.746-4293T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060639 | |||||||
| chr5:160060832 | T | C | 1 | a0002c0002t0001g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.746-4100T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060832 | |||||||
| chr5:160060946 | G | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(181): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.746-3986G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160060946 | |||||||
| chr5:160061088 | C | T | 64 | a0001c0001t0001g0120 a0001c0001t0001g0296 a0001c0001t0001g0308 others(61): Show |
67 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.746-3844C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061088 | |||||||
| chr5:160061329 | C | T | 1 | a0004c0005t0001g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.746-3603C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061329 | |||||||
| chr5:160061345 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.746-3587C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061345 | |||||||
| chr5:160061358 | G | A | 44 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0118 others(41): Show |
47 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.746-3574G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061358 | |||||||
| chr5:160061550 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0276 |
2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.746-3382G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061550 | |||||||
| chr5:160061660 | CT | C | 46 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0118 others(43): Show |
49 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.746-3261delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160061660 | ||||||
| chr5:160061671 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.746-3261T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061671 | |||||||
| chr5:160061690 | G | A | 39 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0118 others(36): Show |
42 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.746-3242G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061690 | |||||||
| chr5:160061694 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0151 |
5 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-3238A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061694 | |||||||
| chr5:160061915 | C | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.746-3017C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061915 | |||||||
| chr5:160061921 | A | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.746-3011A>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061921 | |||||||
| chr5:160061964 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.746-2968C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160061964 | |||||||
| chr5:160062062 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | NA18963.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.746-2870T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062062 | |||||||
| chr5:160062203 | G | A | 2 | a0001c0001t0001g0257 a0001c0001t0001g0266 |
2 | HG00609.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.746-2729G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062203 | |||||||
| chr5:160062230 | C | T | 1 | a0004c0005t0001g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.746-2702C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062230 | |||||||
| chr5:160062448 | C | T | 27 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0035 others(24): Show |
28 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.746-2484C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062448 | |||||||
| chr5:160062543 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(219): Show |
243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.746-2389T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062543 | |||||||
| chr5:160062807 | GT | G | 35 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0180 others(32): Show |
38 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.746-2115delT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160062807 | ||||||
| chr5:160062863 | G | A | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.746-2069G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062863 | |||||||
| chr5:160062934 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.746-1998C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062934 | |||||||
| chr5:160062955 | C | T | 4 | a0001c0001t0001g0097 a0001c0001t0001g0101 a0001c0001t0001g0102 others(1): Show |
4 | HG01884.hp2 HG02572.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.746-1977C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160062955 | |||||||
| chr5:160063032 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0006g0275 |
2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.746-1900G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160063032 | |||||||
| chr5:160063240 | T | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.746-1692T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160063240 | |||||||
| chr5:160063317 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.746-1615A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160063317 | |||||||
| chr5:160063386 | T | G | 4 | a0002c0002t0001g0240 a0002c0002t0001g0241 a0002c0002t0001g0242 others(1): Show |
4 | HG01928.hp1 HG03669.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.746-1546T>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160063386 | |||||||
| chr5:160063622 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.746-1310T>C | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160063622 | |||||||
| chr5:160063748 | A | G | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.746-1184A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160063748 | |||||||
| chr5:160063966 | C | CT | 49 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0042 others(46): Show |
52 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.746-946dupT | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160063966 | ||||||
| chr5:160063966 | C | CTT | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(167): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.746-947_746-946dup others(2): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160063966 | ||||||
| chr5:160063966 | C | CTTT | 72 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0001g0050 others(69): Show |
75 | HG00408.hp2 HG00597.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.746-948_746-946dup others(3): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160063966 | ||||||
| chr5:160064053 | C | T | 1 | a0001c0001t0002g0295 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.746-879C>T | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160064053 | |||||||
| chr5:160064126 | C | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.746-806C>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160064126 | |||||||
| chr5:160064501 | C | G | 10 | a0001c0001t0002g0292 a0001c0001t0002g0299 a0001c0001t0002g0305 others(7): Show |
10 | HG02132.hp2 NA18951.hp1 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.746-431C>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160064501 | |||||||
| chr5:160064513 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(175): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.746-419A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160064513 | |||||||
| chr5:160064585 | G | A | 5 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0002c0002t0001g0241 others(2): Show |
5 | HG01928.hp1 HG02723.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.746-347G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160064585 | |||||||
| chr5:160064730 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.746-202G>A | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160064730 | |||||||
| chr5:160064761 | A | G | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | HG02055.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.746-171A>G | TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | chr5 | 160064761 | |||||||
| chr5:160064828 | A | AGATACTT others(263): Show |
1 | a0001c0001t0001g0145 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.746-88_746-87insTT others(268): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160064828 | ||||||
| chr5:160064828 | A | AGATACTT others(264): Show |
1 | a0001c0001t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.746-88_746-87insTT others(269): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160064828 | ||||||
| chr5:160064828 | A | AGATACTT others(265): Show |
1 | a0001c0001t0001g0141 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.746-88_746-87insTT others(270): Show |
TTC1 | ENSG00000113312.12 | transcript | ENST00000231238.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 160064828 |