Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 123016 |
| ensemblid | ENSG00000165533.19 |
| hgncid | 20087 |
| symbol | TTC8 |
| name | tetratricopeptide repeat domain 8 |
| refseq_nuc | NM_144596.4 |
| refseq_prot | NP_653197.2 |
| ensembl_nuc | ENST00000380656.7 |
| ensembl_prot | ENSP00000370031.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 88824651 |
| end | 88877988 |
| strand | + |
| ver | v1.2 |
| region | chr14:88824651-88877988 |
| region5000 | chr14:88819651-88882988 |
| regionname0 | TTC8_chr14_88824651_88877988 |
| regionname5000 | TTC8_chr14_88819651_88882988 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 515 | 396 | 93 | 70 | 176 | 14 | 41 | 141 | TTC8_chr14_88819651_88882988 | TTC8 | MSSEM others(510): Show |
chr14 | 88819651 | 88882988 |
| a0002 | 0/0 | 515 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | MNSEM others(510): Show |
chr14 | 88819651 | 88882988 |
| a0003 | 0/0 | 515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | MSSEM others(510): Show |
chr14 | 88819651 | 88882988 |
| a0004 | 0/0 | 515 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | MSSEM others(510): Show |
chr14 | 88819651 | 88882988 |
| a0005 | 0/0 | 515 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | MSSEM others(510): Show |
chr14 | 88819651 | 88882988 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1545 | 393 | 92 | 68 | 176 | 14 | 41 | TTC8_chr14_88819651_88882988 | TTC8 | ATGAG others(1540): Show |
chr14 | 88819651 | 88882988 | ||
| a0001c0002 | 0/0 | 1545 | 2 | 1 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ATGAG others(1540): Show |
chr14 | 88819651 | 88882988 | ||
| a0001c0005 | 0/0 | 1545 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ATGAG others(1540): Show |
chr14 | 88819651 | 88882988 | ||
| a0002c0003 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ATGAA others(1540): Show |
chr14 | 88819651 | 88882988 | ||
| a0003c0007 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ATGAG others(1540): Show |
chr14 | 88819651 | 88882988 | ||
| a0004c0006 | 0/0 | 1545 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | ATGAG others(1540): Show |
chr14 | 88819651 | 88882988 | ||
| a0005c0004 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ATGAG others(1540): Show |
chr14 | 88819651 | 88882988 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2183 | 279 | 65 | 46 | 126 | 8 | 32 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0001c0001t0002 | 0/0 | 2183 | 92 | 9 | 22 | 46 | 6 | 9 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0001c0001t0003 | 0/0 | 2183 | 9 | 9 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0001c0001t0004 | 0/0 | 2183 | 3 | 3 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0001c0001t0005 | 0/0 | 2183 | 3 | 3 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0001c0001t0006 | 0/0 | 2183 | 2 | 2 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0001c0001t0007 | 0/0 | 2183 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0001c0001t0008 | 0/0 | 2183 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0001c0001t0009 | 0/0 | 2183 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0001c0001t0010 | 0/0 | 2183 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0001c0002t0003 | 0/0 | 2183 | 2 | 1 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0001c0005t0001 | 0/0 | 2183 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0002c0003t0001 | 0/0 | 2183 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0003c0007t0001 | 0/0 | 2183 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0004c0006t0001 | 0/0 | 2183 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| a0005c0004t0001 | 0/0 | 2183 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | ACTCC others(2178): Show |
chr14 | 88819651 | 88882988 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0010 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0296 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0331 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0004g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0005g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0007g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0008g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0001t0010g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0002t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0002t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0001c0005t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0002c0003t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0003c0007t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0004c0006t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| a0005c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0196 | EUR | GBR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0315 | EUR | GBR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0187 | EUR | FIN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0337 | EUR | FIN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0214 | EUR | FIN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | CHS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | CHS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | CHS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0292 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01261 | hp1 | a0001 | c0005 | t0001 | g0075 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0190 | EUR | IBS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | IBS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01891 | hp1 | a0003 | c0007 | t0001 | g0140 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02040 | hp2 | a0001 | c0001 | t0007 | g0037 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0293 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0090 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0272 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0268 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0291 | AFR | ESN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | ESN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | MSL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | MSL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03669 | hp1 | a0004 | c0006 | t0001 | g0305 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | BEB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | BEB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | STU | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0309 | SAS | BEB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | BEB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | STU | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | STU | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | STU | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | YRI | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | YRI | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18612 | hp2 | a0001 | c0001 | t0009 | g0179 | EAS | CHB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | CHB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | YRI | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0294 | AFR | YRI | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18944 | hp2 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18980 | hp2 | a0001 | c0001 | t0007 | g0037 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0290 | AFR | LWK | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | LWK | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | LWK | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0287 | AFR | LWK | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19072 | hp1 | a0005 | c0004 | t0001 | g0109 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ASW | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0345 | AFR | ASW | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | TSI | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0338 | EUR | TSI | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0314 | EUR | TSI | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0346 | EUR | TSI | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | CLM | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0241 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0289 | AFR | ACB | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0295 | AFR | USA | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | USA | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | USA | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0078 | AFR | USA | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | LWK | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0296 | REF | REF | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0331 | REF | REF | TTC8_chr14_88819651_88882988 | TTC8 | chr14 | 88819651 | 88882988 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:88824712 | G | A | 1 | a0002 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.5G>A | p.Ser2Asn | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/15 | 62/2183 | 5/1548 | 2/515 | chr14 | 88824712 | |||
| chr14:88839501 | A | G | 1 | a0003 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.194A>G | p.Asp65Gly | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 3/15 | 251/2183 | 194/1548 | 65/515 | chr14 | 88839501 | |||
| chr14:88840883 | A | G | 1 | a0004 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.284A>G | p.Lys95Arg | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 4/15 | 341/2183 | 284/1548 | 95/515 | chr14 | 88840883 | |||
| chr14:88840924 | G | A | 1 | a0005 | 1 | NA19072.hp1 | missense_variant | MODERATE | c.325G>A | p.Val109Ile | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 4/15 | 382/2183 | 325/1548 | 109/515 | chr14 | 88840924 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:88852988 | C | G | 1 | a0001c0005 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.642C>G | p.Ala214Ala | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/15 | 699/2183 | 642/1548 | 214/515 | chr14 | 88852988 | |||
| chr14:88875079 | G | A | 1 | a0001c0002 | 2 | HG00642.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.1401G>A | p.Pro467Pro | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/15 | 1458/2183 | 1401/1548 | 467/515 | chr14 | 88875079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:88824683 | G | A | 1 | a0001c0001t0006 | 2 | HG02572.hp1 NA20300.hp2 |
5_prime_UTR_variant | MODIFIER | c.-25G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/15 | 25 | chr14 | 88824683 | ||||||
| chr14:88877467 | C | T | 2 | a0001c0001t0007 a0001c0001t0010 |
3 | HG02040.hp2 HG02109.hp1 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*57C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 15/15 | 57 | chr14 | 88877467 | ||||||
| chr14:88877493 | A | G | 1 | a0001c0001t0007 | 2 | HG02040.hp2 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*83A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 15/15 | 83 | chr14 | 88877493 | ||||||
| chr14:88877502 | C | T | 1 | a0001c0001t0009 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*92C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 15/15 | 92 | chr14 | 88877502 | ||||||
| chr14:88877503 | G | A | 1 | a0001c0001t0004 | 3 | HG02559.hp1 HG03195.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*93G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 15/15 | 93 | chr14 | 88877503 | ||||||
| chr14:88877581 | A | G | 1 | a0001c0001t0008 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*171A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 15/15 | 171 | chr14 | 88877581 | ||||||
| chr14:88877648 | G | A | 3 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 |
94 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*238G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 15/15 | 238 | chr14 | 88877648 | ||||||
| chr14:88877882 | A | C | 3 | a0001c0001t0003 a0001c0001t0005 a0001c0002t0003 |
14 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*472A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 15/15 | 472 | chr14 | 88877882 | ||||||
| chr14:88877903 | T | C | 1 | a0001c0001t0005 | 3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*493T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 15/15 | 493 | chr14 | 88877903 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:88824960 | G | A | 2 | a0001c0001t0005g0011 a0001c0001t0005g0043 |
3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.114+139G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88824960 | |||||||
| chr14:88824981 | A | G | 2 | a0001c0001t0002g0345 a0001c0001t0002g0346 |
2 | NA20129.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.114+160A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88824981 | |||||||
| chr14:88825054 | T | C | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(293): Show |
345 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(342): Show |
intron_variant | MODIFIER | c.114+233T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88825054 | |||||||
| chr14:88825064 | C | T | 10 | a0001c0001t0003g0286 a0001c0001t0003g0287 a0001c0001t0003g0288 others(7): Show |
10 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+243C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88825064 | |||||||
| chr14:88825070 | C | T | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00408.hp1 NA19001.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+249C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88825070 | |||||||
| chr14:88825170 | G | A | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.114+349G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88825170 | |||||||
| chr14:88825391 | A | T | 6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0278 others(3): Show |
8 | HG00741.hp1 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+570A>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88825391 | |||||||
| chr14:88825623 | G | A | 10 | a0001c0001t0003g0286 a0001c0001t0003g0287 a0001c0001t0003g0288 others(7): Show |
10 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+802G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88825623 | |||||||
| chr14:88825969 | T | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
123 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.114+1148T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88825969 | |||||||
| chr14:88825977 | T | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
41 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.114+1156T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88825977 | |||||||
| chr14:88825985 | T | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
123 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.114+1164T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88825985 | |||||||
| chr14:88826051 | G | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.114+1230G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88826051 | |||||||
| chr14:88826069 | C | T | 10 | a0001c0001t0003g0286 a0001c0001t0003g0287 a0001c0001t0003g0288 others(7): Show |
10 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+1248C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88826069 | |||||||
| chr14:88826207 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.114+1386C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88826207 | |||||||
| chr14:88826246 | C | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0138 |
3 | HG02970.hp2 HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.114+1425C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88826246 | |||||||
| chr14:88826577 | G | T | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.114+1756G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88826577 | |||||||
| chr14:88826643 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.114+1822G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88826643 | |||||||
| chr14:88826660 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.114+1839C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88826660 | |||||||
| chr14:88826664 | A | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.114+1843A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88826664 | |||||||
| chr14:88826679 | C | G | 2 | a0001c0001t0002g0274 a0001c0001t0002g0275 |
2 | HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.114+1858C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88826679 | |||||||
| chr14:88826683 | A | G | 5 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0271 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+1862A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88826683 | |||||||
| chr14:88826916 | T | G | 94 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(91): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.114+2095T>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88826916 | |||||||
| chr14:88827054 | A | G | 11 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(8): Show |
11 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+2233A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88827054 | |||||||
| chr14:88827207 | A | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(293): Show |
345 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(342): Show |
intron_variant | MODIFIER | c.114+2386A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88827207 | |||||||
| chr14:88827265 | G | A | 2 | a0001c0001t0005g0011 a0001c0001t0005g0043 |
3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.114+2444G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88827265 | |||||||
| chr14:88827336 | G | T | 2 | a0001c0001t0005g0011 a0001c0001t0005g0043 |
3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.114+2515G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88827336 | |||||||
| chr14:88827339 | A | G | 94 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(91): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.114+2518A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88827339 | |||||||
| chr14:88827360 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.114+2539A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88827360 | |||||||
| chr14:88827862 | A | G | 94 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(91): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.114+3041A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88827862 | |||||||
| chr14:88827972 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.114+3151G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88827972 | |||||||
| chr14:88828179 | G | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0138 |
3 | HG02970.hp2 HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.114+3358G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88828179 | |||||||
| chr14:88828198 | AAT | A | 94 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(91): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.114+3378_114+3379d others(4): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88828198 | |||||||
| chr14:88828355 | C | T | 15 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0172 others(12): Show |
19 | HG00741.hp1 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.114+3534C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88828355 | |||||||
| chr14:88828609 | C | G | 68 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(65): Show |
78 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.114+3788C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88828609 | |||||||
| chr14:88828735 | G | C | 7 | a0001c0001t0001g0040 a0001c0001t0001g0297 a0001c0001t0001g0298 others(4): Show |
8 | HG00738.hp1 HG01358.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+3914G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88828735 | |||||||
| chr14:88828943 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.114+4122G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88828943 | |||||||
| chr14:88829185 | A | G | 73 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(70): Show |
90 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.114+4364A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88829185 | |||||||
| chr14:88829518 | A | G | 192 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(189): Show |
227 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.115-4175A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88829518 | |||||||
| chr14:88829998 | A | G | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.115-3695A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88829998 | |||||||
| chr14:88830028 | A | G | 2 | a0001c0001t0005g0011 a0001c0001t0005g0043 |
3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.115-3665A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88830028 | |||||||
| chr14:88830372 | A | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0168 |
3 | NA18961.hp2 NA18991.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.115-3321A>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88830372 | |||||||
| chr14:88830389 | C | T | 4 | a0001c0001t0003g0293 a0001c0001t0003g0295 a0001c0002t0003g0292 others(1): Show |
4 | HG00642.hp2 HG02145.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-3304C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88830389 | |||||||
| chr14:88830464 | T | A | 88 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0172 others(85): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.115-3229T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88830464 | |||||||
| chr14:88830839 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.115-2854A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88830839 | |||||||
| chr14:88830860 | G | T | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.115-2833G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88830860 | |||||||
| chr14:88830928 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.115-2765A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88830928 | |||||||
| chr14:88830976 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.115-2717G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88830976 | |||||||
| chr14:88831106 | T | A | 192 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(189): Show |
227 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.115-2587T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88831106 | |||||||
| chr14:88831145 | C | T | 2 | a0001c0001t0005g0011 a0001c0001t0005g0043 |
3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.115-2548C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88831145 | |||||||
| chr14:88831302 | T | C | 84 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(81): Show |
95 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.115-2391T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88831302 | |||||||
| chr14:88831419 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.115-2274G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88831419 | |||||||
| chr14:88831446 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
118 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.115-2247C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88831446 | |||||||
| chr14:88831656 | TA | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
40 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.115-2031delA | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 88831656 | ||||||
| chr14:88831824 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.115-1869G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88831824 | |||||||
| chr14:88831944 | T | A | 73 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(70): Show |
90 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.115-1749T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88831944 | |||||||
| chr14:88831964 | T | C | 1 | a0001c0001t0001g0013 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.115-1729T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88831964 | |||||||
| chr14:88832048 | A | C | 4 | a0001c0001t0001g0243 a0001c0001t0001g0265 a0001c0001t0001g0266 others(1): Show |
4 | HG02886.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-1645A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88832048 | |||||||
| chr14:88832303 | A | G | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.115-1390A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88832303 | |||||||
| chr14:88832396 | T | C | 192 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(189): Show |
227 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.115-1297T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88832396 | |||||||
| chr14:88832573 | A | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(30): Show |
39 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.115-1120A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88832573 | |||||||
| chr14:88832598 | G | C | 14 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0048 others(11): Show |
16 | HG02622.hp2 HG02738.hp1 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.115-1095G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88832598 | |||||||
| chr14:88832783 | CT | C | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | NA18969.hp2 NA18983.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-905delT | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 88832783 | ||||||
| chr14:88832958 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.115-735C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88832958 | |||||||
| chr14:88832959 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0228 a0001c0001t0001g0229 |
4 | HG02698.hp1 HG03491.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-734G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88832959 | |||||||
| chr14:88832983 | C | G | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.115-710C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88832983 | |||||||
| chr14:88833153 | T | C | 11 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(8): Show |
11 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-540T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88833153 | |||||||
| chr14:88833286 | G | A | 192 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(189): Show |
227 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.115-407G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88833286 | |||||||
| chr14:88833344 | G | A | 9 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(6): Show |
9 | HG02258.hp2 HG02486.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.115-349G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88833344 | |||||||
| chr14:88833525 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.115-168T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 1/14 | chr14 | 88833525 | |||||||
| chr14:88833983 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.144+261A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88833983 | |||||||
| chr14:88834223 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
40 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.144+501G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88834223 | |||||||
| chr14:88834280 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.144+558A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88834280 | |||||||
| chr14:88834393 | G | T | 1 | a0001c0001t0001g0302 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.144+671G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88834393 | |||||||
| chr14:88834468 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.144+746G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88834468 | |||||||
| chr14:88834557 | A | G | 105 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(102): Show |
127 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.144+835A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88834557 | |||||||
| chr14:88834698 | A | AT | 9 | a0001c0001t0001g0242 a0001c0001t0001g0342 a0001c0001t0001g0343 others(6): Show |
10 | HG00609.hp1 HG00639.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.144+987dupT | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 88834698 | ||||||
| chr14:88834698 | A | G | 1 | a0001c0001t0001g0344 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.144+976A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88834698 | |||||||
| chr14:88834793 | G | T | 1 | a0001c0001t0002g0273 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.144+1071G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88834793 | |||||||
| chr14:88834942 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.144+1220C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88834942 | |||||||
| chr14:88835036 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0057 a0001c0001t0001g0058 |
4 | HG02622.hp2 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+1314C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88835036 | |||||||
| chr14:88835056 | C | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
41 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.144+1334C>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88835056 | |||||||
| chr14:88835057 | T | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
41 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.144+1335T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88835057 | |||||||
| chr14:88835112 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.144+1390G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88835112 | |||||||
| chr14:88835567 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.144+1845T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88835567 | |||||||
| chr14:88835594 | T | A | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG00408.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.144+1872T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88835594 | |||||||
| chr14:88835968 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0007g0037 |
3 | HG02040.hp2 HG04204.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.144+2246T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88835968 | |||||||
| chr14:88836004 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
41 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.144+2282G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88836004 | |||||||
| chr14:88836156 | C | A | 49 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(46): Show |
54 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.144+2434C>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88836156 | |||||||
| chr14:88836180 | G | A | 3 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 |
3 | HG02056.hp1 NA18966.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.144+2458G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88836180 | |||||||
| chr14:88836239 | G | A | 9 | a0001c0001t0001g0278 a0001c0001t0003g0286 a0001c0001t0003g0289 others(6): Show |
9 | HG00642.hp2 HG00741.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.144+2517G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88836239 | |||||||
| chr14:88836280 | C | G | 29 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0244 others(26): Show |
33 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.144+2558C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88836280 | |||||||
| chr14:88836442 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.144+2720G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88836442 | |||||||
| chr14:88836472 | T | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.144+2750T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88836472 | |||||||
| chr14:88836490 | T | TA | 67 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(64): Show |
73 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.144+2786dupA | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 88836490 | ||||||
| chr14:88836490 | TA | T | 35 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(32): Show |
42 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.144+2786delA | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 88836490 | ||||||
| chr14:88836579 | T | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
40 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.144+2857T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88836579 | |||||||
| chr14:88836931 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | NA18954.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.145-2521C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88836931 | |||||||
| chr14:88836992 | C | T | 11 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(8): Show |
11 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.145-2460C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88836992 | |||||||
| chr14:88837173 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
7 | HG01109.hp2 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.145-2279C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88837173 | |||||||
| chr14:88837304 | T | C | 1 | a0001c0001t0004g0008 | 3 | HG02559.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.145-2148T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88837304 | |||||||
| chr14:88837333 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.145-2119C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88837333 | |||||||
| chr14:88837660 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
41 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.145-1792G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88837660 | |||||||
| chr14:88837758 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.145-1694G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88837758 | |||||||
| chr14:88837807 | G | C | 13 | a0001c0001t0001g0036 a0001c0001t0001g0228 a0001c0001t0001g0229 others(10): Show |
14 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.145-1645G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88837807 | |||||||
| chr14:88837949 | A | C | 1 | a0001c0001t0001g0339 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.145-1503A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88837949 | |||||||
| chr14:88837953 | C | T | 1 | a0001c0001t0002g0212 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.145-1499C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88837953 | |||||||
| chr14:88838093 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.145-1359A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88838093 | |||||||
| chr14:88838369 | C | A | 1 | a0001c0001t0002g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.145-1083C>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88838369 | |||||||
| chr14:88838458 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.145-994T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88838458 | |||||||
| chr14:88838505 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.145-947T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88838505 | |||||||
| chr14:88838566 | C | G | 2 | a0001c0001t0002g0274 a0001c0001t0002g0275 |
2 | HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.145-886C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88838566 | |||||||
| chr14:88838623 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.145-829G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88838623 | |||||||
| chr14:88838832 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.145-620C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88838832 | |||||||
| chr14:88838948 | AG | A | 129 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0020 others(126): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.145-503delG | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88838948 | |||||||
| chr14:88839093 | A | G | 1 | a0001c0001t0010g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.145-359A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88839093 | |||||||
| chr14:88839137 | T | C | 4 | a0001c0001t0001g0243 a0001c0001t0001g0265 a0001c0001t0001g0266 others(1): Show |
4 | HG02886.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.145-315T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88839137 | |||||||
| chr14:88839351 | T | C | 2 | a0001c0001t0001g0304 a0001c0001t0001g0344 |
2 | HG02027.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.145-101T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 2/14 | chr14 | 88839351 | |||||||
| chr14:88839580 | T | G | 1 | a0001c0001t0001g0070 | 1 | NA19000.hp1 | splice_region_variant&intron_variant | LOW | c.265+8T>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 3/14 | chr14 | 88839580 | |||||||
| chr14:88839642 | TA | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0338 a0001c0001t0001g0339 |
4 | HG00735.hp1 HG00735.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+71delA | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 3/14 | chr14 | 88839642 | |||||||
| chr14:88839671 | T | A | 2 | a0001c0001t0005g0011 a0001c0001t0005g0043 |
3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.265+99T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 3/14 | chr14 | 88839671 | |||||||
| chr14:88840206 | T | C | 143 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0020 others(140): Show |
173 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.265+634T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 3/14 | chr14 | 88840206 | |||||||
| chr14:88840212 | C | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
41 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.265+640C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 3/14 | chr14 | 88840212 | |||||||
| chr14:88840228 | T | G | 88 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0172 others(85): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.266-637T>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 3/14 | chr14 | 88840228 | |||||||
| chr14:88840280 | A | G | 49 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(46): Show |
54 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.266-585A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 3/14 | chr14 | 88840280 | |||||||
| chr14:88840398 | T | A | 1 | a0001c0001t0001g0169 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.266-467T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 3/14 | chr14 | 88840398 | |||||||
| chr14:88840445 | A | G | 192 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(189): Show |
227 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.266-420A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 3/14 | chr14 | 88840445 | |||||||
| chr14:88840528 | A | G | 192 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(189): Show |
227 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.266-337A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 3/14 | chr14 | 88840528 | |||||||
| chr14:88840687 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.266-178A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 3/14 | chr14 | 88840687 | |||||||
| chr14:88840781 | C | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(27): Show |
34 | HG00621.hp2 HG01074.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.266-84C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 3/14 | chr14 | 88840781 | |||||||
| chr14:88840783 | C | G | 17 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0113 others(14): Show |
20 | HG01074.hp1 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.266-82C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 3/14 | chr14 | 88840783 | |||||||
| chr14:88840956 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
5 | HG01109.hp2 HG02055.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.329+28C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 4/14 | chr14 | 88840956 | |||||||
| chr14:88840976 | T | C | 73 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(70): Show |
90 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.329+48T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 4/14 | chr14 | 88840976 | |||||||
| chr14:88841022 | T | A | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.330-15T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 4/14 | chr14 | 88841022 | |||||||
| chr14:88841373 | A | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0228 a0001c0001t0001g0229 |
4 | HG02698.hp1 HG03491.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-52A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 5/14 | chr14 | 88841373 | |||||||
| chr14:88841397 | C | G | 1 | a0001c0001t0002g0211 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.490-28C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 5/14 | chr14 | 88841397 | |||||||
| chr14:88841726 | T | C | 1 | a0004c0006t0001g0305 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.579+212T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88841726 | |||||||
| chr14:88841758 | A | G | 49 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(46): Show |
54 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.579+244A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88841758 | |||||||
| chr14:88841772 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.579+258G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88841772 | |||||||
| chr14:88842076 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.579+562A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88842076 | |||||||
| chr14:88842465 | A | G | 1 | a0001c0001t0002g0210 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.579+951A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88842465 | |||||||
| chr14:88842500 | T | G | 1 | a0001c0001t0009g0179 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.579+986T>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88842500 | |||||||
| chr14:88842664 | G | T | 11 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(8): Show |
11 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.580-1142G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88842664 | |||||||
| chr14:88842837 | C | G | 94 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(91): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.580-969C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88842837 | |||||||
| chr14:88842849 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.580-957C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88842849 | |||||||
| chr14:88842862 | A | C | 1 | a0001c0001t0001g0281 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.580-944A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88842862 | |||||||
| chr14:88842889 | C | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
41 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.580-917C>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88842889 | |||||||
| chr14:88842898 | T | C | 11 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(8): Show |
11 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.580-908T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88842898 | |||||||
| chr14:88842909 | G | C | 1 | a0003c0007t0001g0140 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.580-897G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88842909 | |||||||
| chr14:88842934 | A | G | 143 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0020 others(140): Show |
173 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.580-872A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88842934 | |||||||
| chr14:88842946 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.580-860G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88842946 | |||||||
| chr14:88842951 | GT | G | 129 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0020 others(126): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.580-844delT | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr14 | 88842951 | ||||||
| chr14:88842966 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.580-840G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88842966 | |||||||
| chr14:88842987 | T | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
41 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.580-819T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88842987 | |||||||
| chr14:88843143 | T | C | 3 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0007g0037 |
5 | HG02040.hp2 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-663T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88843143 | |||||||
| chr14:88843274 | A | T | 3 | a0001c0001t0003g0268 a0001c0001t0003g0287 a0001c0001t0003g0288 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.580-532A>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88843274 | |||||||
| chr14:88843296 | A | G | 143 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0020 others(140): Show |
173 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.580-510A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88843296 | |||||||
| chr14:88843384 | T | C | 2 | a0001c0001t0005g0011 a0001c0001t0005g0043 |
3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.580-422T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88843384 | |||||||
| chr14:88843403 | C | A | 3 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 |
3 | HG02056.hp1 NA18966.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.580-403C>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88843403 | |||||||
| chr14:88843597 | A | G | 1 | a0001c0001t0004g0008 | 3 | HG02559.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.580-209A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88843597 | |||||||
| chr14:88843761 | T | TA | 36 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(33): Show |
42 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.580-34dupA | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr14 | 88843761 | ||||||
| chr14:88843778 | C | A | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.580-28C>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 6/14 | chr14 | 88843778 | |||||||
| chr14:88843917 | A | G | 15 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0172 others(12): Show |
19 | HG00741.hp1 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.624+67A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88843917 | |||||||
| chr14:88843992 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.624+142C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88843992 | |||||||
| chr14:88844002 | T | C | 192 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(189): Show |
227 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.624+152T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88844002 | |||||||
| chr14:88844052 | A | T | 3 | a0001c0001t0003g0268 a0001c0001t0003g0287 a0001c0001t0003g0288 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.624+202A>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88844052 | |||||||
| chr14:88844295 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.624+445C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88844295 | |||||||
| chr14:88844350 | A | C | 1 | a0001c0001t0002g0209 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.624+500A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88844350 | |||||||
| chr14:88844378 | G | T | 1 | a0001c0001t0001g0263 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.624+528G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88844378 | |||||||
| chr14:88844578 | T | C | 1 | a0001c0002t0003g0292 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.624+728T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88844578 | |||||||
| chr14:88844613 | C | T | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | NA18951.hp2 NA18965.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.624+763C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88844613 | |||||||
| chr14:88844618 | C | T | 3 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0337 |
3 | HG00323.hp1 HG01256.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.624+768C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88844618 | |||||||
| chr14:88844650 | T | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
7 | HG01109.hp2 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.624+800T>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88844650 | |||||||
| chr14:88844711 | AT | A | 13 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(10): Show |
14 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.624+874delT | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr14 | 88844711 | ||||||
| chr14:88845048 | A | G | 1 | a0003c0007t0001g0140 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.624+1198A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88845048 | |||||||
| chr14:88845073 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0057 a0001c0001t0001g0058 |
4 | HG02622.hp2 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1223A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88845073 | |||||||
| chr14:88845175 | T | G | 144 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0020 others(141): Show |
174 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.624+1325T>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88845175 | |||||||
| chr14:88845259 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.624+1409G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88845259 | |||||||
| chr14:88845271 | CT | C | 3 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0004g0008 |
5 | HG02559.hp1 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.624+1422delT | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88845271 | |||||||
| chr14:88845393 | A | T | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.624+1543A>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88845393 | |||||||
| chr14:88845430 | G | A | 15 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0172 others(12): Show |
19 | HG00741.hp1 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.624+1580G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88845430 | |||||||
| chr14:88845473 | G | A | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
367 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.624+1623G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88845473 | |||||||
| chr14:88845632 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.624+1782A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88845632 | |||||||
| chr14:88845680 | T | C | 95 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(92): Show |
117 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.624+1830T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88845680 | |||||||
| chr14:88845926 | A | G | 11 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(8): Show |
11 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+2076A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88845926 | |||||||
| chr14:88846010 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.624+2160T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88846010 | |||||||
| chr14:88846259 | C | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
41 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.624+2409C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88846259 | |||||||
| chr14:88846331 | A | G | 50 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(47): Show |
55 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.624+2481A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88846331 | |||||||
| chr14:88846581 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.624+2731A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88846581 | |||||||
| chr14:88846925 | T | C | 50 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(47): Show |
55 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.624+3075T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88846925 | |||||||
| chr14:88847128 | C | T | 1 | a0001c0001t0002g0273 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.624+3278C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88847128 | |||||||
| chr14:88847210 | T | TTAAAAAC others(6098): Show |
1 | a0001c0001t0001g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.624+3369_624+3370i others(6107): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr14 | 88847210 | ||||||
| chr14:88847212 | A | G | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.624+3362A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88847212 | |||||||
| chr14:88847316 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.624+3466A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88847316 | |||||||
| chr14:88847337 | G | A | 9 | a0001c0001t0003g0268 a0001c0001t0003g0287 a0001c0001t0003g0288 others(6): Show |
10 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.624+3487G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88847337 | |||||||
| chr14:88847401 | C | T | 143 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0020 others(140): Show |
173 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.624+3551C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88847401 | |||||||
| chr14:88847424 | A | G | 1 | a0001c0001t0002g0211 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.624+3574A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88847424 | |||||||
| chr14:88847438 | T | C | 10 | a0001c0001t0003g0268 a0001c0001t0003g0287 a0001c0001t0003g0288 others(7): Show |
12 | HG00642.hp2 HG02040.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.624+3588T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88847438 | |||||||
| chr14:88847534 | G | A | 1 | a0001c0001t0001g0307 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.624+3684G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88847534 | |||||||
| chr14:88847557 | T | A | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.624+3707T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88847557 | |||||||
| chr14:88847625 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.624+3775A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88847625 | |||||||
| chr14:88847817 | A | G | 51 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0019 others(48): Show |
57 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.624+3967A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88847817 | |||||||
| chr14:88847885 | G | C | 1 | a0001c0001t0001g0332 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.624+4035G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88847885 | |||||||
| chr14:88847890 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.624+4040A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88847890 | |||||||
| chr14:88848078 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.624+4228G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88848078 | |||||||
| chr14:88848123 | C | CA | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0060 others(41): Show |
49 | HG00408.hp2 HG00741.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.624+4299dupA | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr14 | 88848123 | ||||||
| chr14:88848123 | C | CAA | 66 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
77 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.624+4298_624+4299d others(4): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr14 | 88848123 | ||||||
| chr14:88848123 | C | CAAA | 16 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0150 others(13): Show |
16 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.624+4297_624+4299d others(5): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr14 | 88848123 | ||||||
| chr14:88848302 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.624+4452G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88848302 | |||||||
| chr14:88848330 | A | C | 11 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(8): Show |
11 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+4480A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88848330 | |||||||
| chr14:88848424 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0251 |
2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.625-4547T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88848424 | |||||||
| chr14:88848517 | A | T | 1 | a0001c0001t0003g0288 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.625-4454A>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88848517 | |||||||
| chr14:88848532 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.625-4439A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88848532 | |||||||
| chr14:88848709 | A | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.625-4262A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88848709 | |||||||
| chr14:88848781 | A | G | 1 | a0001c0001t0002g0208 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.625-4190A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88848781 | |||||||
| chr14:88849153 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.625-3818G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88849153 | |||||||
| chr14:88849392 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.625-3579T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88849392 | |||||||
| chr14:88849531 | C | G | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
94 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.625-3440C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88849531 | |||||||
| chr14:88849555 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG01069.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.625-3416G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88849555 | |||||||
| chr14:88849661 | A | C | 1 | a0001c0001t0001g0049 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.625-3310A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88849661 | |||||||
| chr14:88849742 | G | A | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.625-3229G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88849742 | |||||||
| chr14:88849865 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.625-3106C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88849865 | |||||||
| chr14:88849956 | A | G | 2 | a0001c0001t0003g0293 a0001c0001t0003g0295 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.625-3015A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88849956 | |||||||
| chr14:88849984 | T | A | 4 | a0001c0001t0003g0286 a0001c0001t0003g0289 a0001c0001t0003g0290 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-2987T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88849984 | |||||||
| chr14:88850318 | A | G | 1 | a0001c0001t0002g0185 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.625-2653A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88850318 | |||||||
| chr14:88850418 | G | T | 1 | a0001c0001t0001g0328 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.625-2553G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88850418 | |||||||
| chr14:88850464 | G | C | 1 | a0001c0001t0002g0186 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.625-2507G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88850464 | |||||||
| chr14:88850692 | A | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.625-2279A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88850692 | |||||||
| chr14:88850731 | C | T | 13 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(10): Show |
14 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.625-2240C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88850731 | |||||||
| chr14:88851516 | G | A | 4 | a0001c0001t0001g0310 a0001c0001t0001g0314 a0001c0001t0001g0315 others(1): Show |
4 | HG00099.hp2 HG01071.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1455G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88851516 | |||||||
| chr14:88851583 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0057 a0001c0001t0001g0058 |
4 | HG02622.hp2 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1388T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88851583 | |||||||
| chr14:88851614 | A | G | 13 | a0001c0001t0001g0036 a0001c0001t0001g0228 a0001c0001t0001g0229 others(10): Show |
14 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.625-1357A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88851614 | |||||||
| chr14:88851742 | G | C | 2 | a0001c0001t0001g0334 a0001c0001t0001g0335 |
2 | NA18951.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.625-1229G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88851742 | |||||||
| chr14:88851808 | CTCAGCAT others(4): Show |
C | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
94 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.625-1159_625-1149d others(13): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr14 | 88851808 | ||||||
| chr14:88851885 | A | G | 4 | a0001c0001t0003g0293 a0001c0001t0003g0295 a0001c0002t0003g0292 others(1): Show |
4 | HG00642.hp2 HG02145.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-1086A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88851885 | |||||||
| chr14:88852231 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.625-740T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88852231 | |||||||
| chr14:88852546 | C | G | 1 | a0001c0001t0010g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.625-425C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88852546 | |||||||
| chr14:88852770 | A | G | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.625-201A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88852770 | |||||||
| chr14:88852854 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.625-117G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88852854 | |||||||
| chr14:88852890 | A | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
41 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.625-81A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88852890 | |||||||
| chr14:88852906 | T | C | 1 | a0001c0001t0001g0050 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.625-65T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 7/14 | chr14 | 88852906 | |||||||
| chr14:88853131 | G | C | 47 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(44): Show |
52 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.710+75G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88853131 | |||||||
| chr14:88853131 | G | T | 1 | a0001c0001t0001g0261 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.710+75G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88853131 | |||||||
| chr14:88853136 | G | A | 1 | a0001c0005t0001g0075 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.710+80G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88853136 | |||||||
| chr14:88853136 | G | C | 15 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(12): Show |
17 | HG00642.hp2 HG02040.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.710+80G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88853136 | |||||||
| chr14:88853636 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.710+580C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88853636 | |||||||
| chr14:88853644 | C | T | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(2): Show |
5 | HG00621.hp2 NA18951.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.710+588C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88853644 | |||||||
| chr14:88853776 | T | C | 1 | a0001c0001t0005g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.710+720T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88853776 | |||||||
| chr14:88853842 | A | G | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA19001.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.710+786A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88853842 | |||||||
| chr14:88854139 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.710+1083A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88854139 | |||||||
| chr14:88854218 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.710+1162A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88854218 | |||||||
| chr14:88854937 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.710+1881T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88854937 | |||||||
| chr14:88855041 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.710+1985T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88855041 | |||||||
| chr14:88855056 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.710+2000T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88855056 | |||||||
| chr14:88855194 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.711-1996A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88855194 | |||||||
| chr14:88855218 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.711-1972G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88855218 | |||||||
| chr14:88855253 | G | C | 1 | a0001c0001t0001g0342 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.711-1937G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88855253 | |||||||
| chr14:88855267 | G | A | 3 | a0001c0001t0002g0269 a0001c0001t0002g0271 a0001c0001t0002g0272 |
3 | HG01884.hp2 HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.711-1923G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88855267 | |||||||
| chr14:88855389 | A | G | 1 | a0001c0001t0006g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.711-1801A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88855389 | |||||||
| chr14:88855722 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.711-1468A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88855722 | |||||||
| chr14:88855791 | G | A | 11 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(8): Show |
11 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.711-1399G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88855791 | |||||||
| chr14:88855919 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
9 | HG01074.hp1 HG01106.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.711-1271G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88855919 | |||||||
| chr14:88855940 | T | C | 343 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(340): Show |
395 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.711-1250T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88855940 | |||||||
| chr14:88855985 | T | C | 15 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(12): Show |
17 | HG00642.hp2 HG02040.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.711-1205T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88855985 | |||||||
| chr14:88856011 | G | C | 1 | a0001c0001t0001g0013 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.711-1179G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88856011 | |||||||
| chr14:88856059 | G | C | 13 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(10): Show |
14 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.711-1131G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88856059 | |||||||
| chr14:88856407 | T | G | 2 | a0001c0002t0003g0292 a0001c0002t0003g0294 |
2 | HG00642.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.711-783T>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88856407 | |||||||
| chr14:88856526 | T | C | 13 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(10): Show |
14 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.711-664T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88856526 | |||||||
| chr14:88856571 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.711-619G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88856571 | |||||||
| chr14:88856587 | A | G | 1 | a0001c0001t0010g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.711-603A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88856587 | |||||||
| chr14:88856658 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.711-532G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88856658 | |||||||
| chr14:88856679 | A | G | 11 | a0001c0001t0002g0007 a0001c0001t0002g0032 a0001c0001t0002g0033 others(8): Show |
16 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.711-511A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88856679 | |||||||
| chr14:88856845 | C | CT | 4 | a0001c0001t0001g0244 a0001c0001t0001g0250 a0001c0001t0001g0260 others(1): Show |
4 | HG02683.hp1 HG03017.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.711-344dupT | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr14 | 88856845 | ||||||
| chr14:88856865 | C | T | 15 | a0001c0001t0001g0036 a0001c0001t0001g0228 a0001c0001t0001g0229 others(12): Show |
16 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.711-325C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 8/14 | chr14 | 88856865 | |||||||
| chr14:88857505 | T | C | 15 | a0001c0001t0001g0036 a0001c0001t0001g0228 a0001c0001t0001g0229 others(12): Show |
16 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.798+228T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88857505 | |||||||
| chr14:88857818 | AAG | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(27): Show |
36 | HG00423.hp1 HG00673.hp1 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.798+544_798+545del others(2): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88857818 | ||||||
| chr14:88858143 | G | A | 4 | a0001c0001t0003g0286 a0001c0001t0003g0289 a0001c0001t0003g0290 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+866G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88858143 | |||||||
| chr14:88858189 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.798+912C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88858189 | |||||||
| chr14:88858272 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.798+995A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88858272 | |||||||
| chr14:88858502 | G | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
7 | HG01109.hp2 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.798+1225G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88858502 | |||||||
| chr14:88858599 | T | C | 100 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(97): Show |
123 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.798+1322T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88858599 | |||||||
| chr14:88858754 | A | AT | 61 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(58): Show |
66 | HG00423.hp1 HG00642.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.798+1505dupT | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88858754 | ||||||
| chr14:88858754 | A | ATT | 15 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0089 others(12): Show |
16 | HG00621.hp2 HG01106.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+1504_798+1505d others(4): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88858754 | ||||||
| chr14:88858754 | AT | A | 23 | a0001c0001t0001g0036 a0001c0001t0001g0059 a0001c0001t0001g0061 others(20): Show |
24 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.798+1505delT | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88858754 | ||||||
| chr14:88858754 | ATT | A | 25 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0244 others(22): Show |
29 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.798+1504_798+1505d others(4): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88858754 | ||||||
| chr14:88858754 | ATTT | A | 20 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0172 others(17): Show |
25 | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.798+1503_798+1505d others(5): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88858754 | ||||||
| chr14:88858754 | ATTTT | A | 72 | a0001c0001t0001g0225 a0001c0001t0001g0279 a0001c0001t0002g0005 others(69): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.798+1502_798+1505d others(6): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88858754 | ||||||
| chr14:88858754 | ATTTTTTT others(11): Show |
A | 1 | a0005c0004t0001g0109 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.798+1488_798+1505d others(20): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88858754 | ||||||
| chr14:88858763 | T | A | 1 | a0001c0001t0002g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.798+1486T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88858763 | |||||||
| chr14:88858767 | T | A | 1 | a0001c0001t0002g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.798+1490T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88858767 | |||||||
| chr14:88858816 | G | C | 1 | a0001c0001t0001g0262 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.798+1539G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88858816 | |||||||
| chr14:88858839 | C | T | 5 | a0001c0001t0002g0031 a0001c0001t0002g0197 a0001c0001t0002g0198 others(2): Show |
6 | HG02132.hp2 NA18974.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+1562C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88858839 | |||||||
| chr14:88858872 | A | G | 113 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(110): Show |
137 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.798+1595A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88858872 | |||||||
| chr14:88859171 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.798+1894T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88859171 | |||||||
| chr14:88859257 | G | A | 9 | a0001c0001t0001g0172 a0001c0001t0001g0221 a0001c0001t0001g0222 others(6): Show |
11 | HG02280.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.799-1965G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88859257 | |||||||
| chr14:88859374 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.799-1848G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88859374 | |||||||
| chr14:88859505 | G | A | 99 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(96): Show |
121 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.799-1717G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88859505 | |||||||
| chr14:88859605 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.799-1617C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88859605 | |||||||
| chr14:88859634 | A | G | 50 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(47): Show |
53 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.799-1588A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88859634 | |||||||
| chr14:88859786 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.799-1436A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88859786 | |||||||
| chr14:88859841 | AAT | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0254 a0001c0001t0001g0263 |
5 | HG02280.hp1 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-1377_799-1376d others(4): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88859841 | ||||||
| chr14:88859849 | T | C | 1 | a0001c0001t0002g0205 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.799-1373T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88859849 | |||||||
| chr14:88859857 | C | CATATATA others(56): Show |
1 | a0001c0001t0010g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.799-1346_799-1345i others(65): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88859857 | ||||||
| chr14:88859857 | C | CATATATA others(49): Show |
1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.799-1346_799-1345i others(58): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88859857 | ||||||
| chr14:88859857 | C | CATATATA others(25): Show |
24 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(21): Show |
29 | HG00741.hp1 HG01109.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.799-1351_799-1320d others(34): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88859857 | ||||||
| chr14:88859857 | C | CATATATA others(82): Show |
1 | a0001c0001t0002g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.799-1320_799-1319i others(91): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88859857 | ||||||
| chr14:88859857 | C | CATATATA others(24): Show |
71 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(68): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.799-1345_799-1344i others(33): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88859857 | ||||||
| chr14:88859858 | A | ATATATAA others(18): Show |
1 | a0001c0001t0001g0013 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.799-1352_799-1328d others(27): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88859858 | ||||||
| chr14:88859883 | T | A | 84 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(81): Show |
96 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.799-1339T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88859883 | |||||||
| chr14:88859891 | TATATAAT others(3): Show |
T | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(45): Show |
53 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.799-1324_799-1315d others(12): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88859891 | ||||||
| chr14:88859896 | A | AATATAAA others(25): Show |
1 | a0001c0001t0001g0172 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.799-1320_799-1319i others(34): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88859896 | ||||||
| chr14:88859901 | A | AAATATAT others(24): Show |
1 | a0001c0001t0002g0274 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.799-1320_799-1319i others(33): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88859901 | ||||||
| chr14:88859956 | AATATAAT others(12): Show |
A | 4 | a0001c0001t0002g0183 a0001c0001t0002g0185 a0001c0001t0002g0195 others(1): Show |
4 | HG00099.hp1 HG01123.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-1255_799-1237d others(21): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88859956 | ||||||
| chr14:88859959 | A | G | 13 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(10): Show |
14 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.799-1263A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88859959 | |||||||
| chr14:88859976 | A | G | 1 | a0003c0007t0001g0140 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.799-1246A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88859976 | |||||||
| chr14:88860064 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.799-1158G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88860064 | |||||||
| chr14:88860191 | A | T | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.799-1031A>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88860191 | |||||||
| chr14:88860268 | C | T | 1 | a0001c0001t0001g0325 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.799-954C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88860268 | |||||||
| chr14:88860433 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.799-789G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88860433 | |||||||
| chr14:88860526 | A | G | 1 | a0001c0001t0010g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.799-696A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88860526 | |||||||
| chr14:88860527 | T | C | 15 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0172 others(12): Show |
19 | HG00741.hp1 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.799-695T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88860527 | |||||||
| chr14:88860610 | C | G | 1 | a0001c0001t0001g0264 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.799-612C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88860610 | |||||||
| chr14:88860611 | T | G | 1 | a0001c0001t0001g0264 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.799-611T>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88860611 | |||||||
| chr14:88860697 | A | G | 3 | a0001c0001t0002g0269 a0001c0001t0002g0271 a0001c0001t0002g0272 |
3 | HG01884.hp2 HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.799-525A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88860697 | |||||||
| chr14:88860730 | G | A | 1 | a0001c0001t0010g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.799-492G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88860730 | |||||||
| chr14:88860810 | C | CT | 47 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(44): Show |
52 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.799-399dupT | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 88860810 | ||||||
| chr14:88860828 | A | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
41 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.799-394A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 9/14 | chr14 | 88860828 | |||||||
| chr14:88861467 | A | G | 29 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0244 others(26): Show |
33 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.909+135A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88861467 | |||||||
| chr14:88861573 | A | G | 4 | a0001c0001t0001g0076 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | NA18961.hp1 NA18977.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+241A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88861573 | |||||||
| chr14:88861855 | A | G | 1 | a0001c0001t0010g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.909+523A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88861855 | |||||||
| chr14:88862085 | A | G | 197 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(194): Show |
232 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.909+753A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862085 | |||||||
| chr14:88862455 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.909+1123C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862455 | |||||||
| chr14:88862514 | A | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0138 a0001c0001t0002g0056 |
4 | HG02970.hp2 HG03041.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+1182A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862514 | |||||||
| chr14:88862538 | C | CTCCATAT others(28): Show |
1 | a0001c0001t0001g0300 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.909+1207_909+1241d others(37): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862538 | ||||||
| chr14:88862541 | C | CAT | 23 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0049 others(20): Show |
27 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(24): Show |
intron_variant | MODIFIER | c.909+1264_909+1265d others(4): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | C | CATAT | 40 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(37): Show |
48 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.909+1262_909+1265d others(6): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | C | CATATAT | 33 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0071 others(30): Show |
38 | HG00423.hp1 HG00733.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.909+1260_909+1265d others(8): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | C | CATATATA others(1): Show |
33 | a0001c0001t0001g0017 a0001c0001t0001g0041 a0001c0001t0001g0070 others(30): Show |
36 | HG00544.hp1 HG00621.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.909+1258_909+1265d others(10): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | C | CATATATA others(3): Show |
21 | a0001c0001t0001g0045 a0001c0001t0001g0068 a0001c0001t0001g0086 others(18): Show |
21 | HG00642.hp2 HG01109.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.909+1256_909+1265d others(12): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | C | CATATATA others(5): Show |
11 | a0001c0001t0001g0077 a0001c0001t0001g0112 a0001c0001t0001g0149 others(8): Show |
11 | HG00280.hp1 HG00639.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+1254_909+1265d others(14): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | C | CATATATA others(7): Show |
5 | a0001c0001t0001g0062 a0001c0001t0001g0113 a0001c0001t0001g0139 others(2): Show |
5 | HG02258.hp2 HG03654.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+1252_909+1265d others(16): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | C | CATATATA others(9): Show |
6 | a0001c0001t0001g0129 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | HG00323.hp2 HG01168.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.909+1250_909+1265d others(18): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | C | CATATATA others(11): Show |
2 | a0001c0001t0001g0085 a0001c0001t0001g0095 |
2 | NA18947.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.909+1248_909+1265d others(20): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | C | CATATATA others(21): Show |
1 | a0001c0001t0002g0188 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.909+1238_909+1265d others(30): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | C | CATATATA others(25): Show |
1 | a0001c0001t0001g0084 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.909+1234_909+1265d others(34): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | C | T | 2 | a0001c0001t0001g0327 a0001c0001t0001g0340 |
2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.909+1209C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862541 | |||||||
| chr14:88862541 | CAT | C | 19 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0088 others(16): Show |
22 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.909+1264_909+1265d others(4): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATAT | C | 15 | a0001c0001t0001g0057 a0001c0001t0001g0061 a0001c0001t0001g0067 others(12): Show |
18 | HG00609.hp1 HG00735.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.909+1262_909+1265d others(6): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATAT | C | 14 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0053 others(11): Show |
15 | HG00733.hp2 HG01255.hp2 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.909+1260_909+1265d others(8): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(1): Show |
C | 16 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0060 others(13): Show |
18 | HG00642.hp1 HG00741.hp2 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.909+1258_909+1265d others(10): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(3): Show |
C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(5): Show |
12 | HG02055.hp1 HG02486.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+1256_909+1265d others(12): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(5): Show |
C | 13 | a0001c0001t0001g0058 a0001c0001t0001g0097 a0001c0001t0001g0172 others(10): Show |
13 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.909+1254_909+1265d others(14): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(7): Show |
C | 6 | a0001c0001t0001g0036 a0001c0001t0001g0092 a0001c0001t0001g0338 others(3): Show |
9 | HG00438.hp1 HG02027.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.909+1252_909+1265d others(16): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(9): Show |
C | 13 | a0001c0001t0001g0038 a0001c0001t0001g0094 a0001c0001t0001g0167 others(10): Show |
17 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.909+1250_909+1265d others(18): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(11): Show |
C | 6 | a0001c0001t0001g0039 a0001c0001t0001g0083 a0001c0001t0001g0266 others(3): Show |
7 | HG01256.hp2 HG01257.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+1248_909+1265d others(20): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(13): Show |
C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0168 |
3 | NA18961.hp2 NA18991.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.909+1246_909+1265d others(22): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(15): Show |
C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0102 a0001c0001t0001g0341 |
4 | HG01361.hp2 HG02602.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+1244_909+1265d others(24): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(17): Show |
C | 4 | a0001c0001t0001g0330 a0001c0001t0002g0210 a0001c0001t0007g0037 others(1): Show |
5 | HG02040.hp1 HG02040.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+1242_909+1265d others(26): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(19): Show |
C | 1 | a0001c0001t0001g0240 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.909+1240_909+1265d others(28): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(21): Show |
C | 3 | a0001c0001t0001g0228 a0001c0001t0002g0030 a0001c0001t0002g0203 |
4 | HG00673.hp2 HG04204.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+1238_909+1265d others(30): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(23): Show |
C | 1 | a0001c0001t0001g0069 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.909+1236_909+1265d others(32): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(27): Show |
C | 2 | a0001c0001t0005g0011 a0001c0001t0005g0043 |
3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.909+1232_909+1265d others(36): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(31): Show |
C | 1 | a0001c0001t0001g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.909+1228_909+1265d others(40): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(33): Show |
C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0106 a0001c0001t0001g0107 |
4 | HG02970.hp2 HG03041.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+1226_909+1265d others(42): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(35): Show |
C | 1 | a0001c0001t0001g0250 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.909+1224_909+1265d others(44): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862541 | CATATATA others(37): Show |
C | 1 | a0001c0001t0001g0117 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.909+1222_909+1265d others(46): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862541 | ||||||
| chr14:88862586 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.909+1254A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862586 | |||||||
| chr14:88862586 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+1256_909+1266d others(13): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88862586 | ||||||
| chr14:88862597 | T | TATATATA | 3 | a0001c0001t0001g0073 a0001c0001t0001g0302 a0001c0001t0002g0199 |
3 | HG01496.hp1 HG03710.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.909+1265_909+1266i others(9): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862597 | |||||||
| chr14:88862597 | T | TATATATA others(4): Show |
1 | a0001c0001t0001g0145 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.909+1265_909+1266i others(13): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862597 | |||||||
| chr14:88862597 | T | TATATATA others(8): Show |
1 | a0001c0001t0001g0298 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.909+1265_909+1266i others(17): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862597 | |||||||
| chr14:88862597 | T | TATATATA others(10): Show |
1 | a0001c0001t0001g0128 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.909+1265_909+1266i others(19): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862597 | |||||||
| chr14:88862600 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.909+1268A>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862600 | |||||||
| chr14:88862624 | C | A | 1 | a0001c0001t0001g0051 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.909+1292C>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862624 | |||||||
| chr14:88862636 | G | T | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(45): Show |
53 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.909+1304G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862636 | |||||||
| chr14:88862841 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
7 | HG01109.hp2 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+1509C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862841 | |||||||
| chr14:88862850 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.909+1518C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862850 | |||||||
| chr14:88862865 | T | C | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.909+1533T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862865 | |||||||
| chr14:88862911 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.909+1579T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862911 | |||||||
| chr14:88862914 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.909+1582T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862914 | |||||||
| chr14:88862983 | T | C | 11 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(8): Show |
11 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.909+1651T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88862983 | |||||||
| chr14:88863079 | G | C | 1 | a0003c0007t0001g0140 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.909+1747G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88863079 | |||||||
| chr14:88863141 | G | A | 1 | a0001c0001t0010g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.909+1809G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88863141 | |||||||
| chr14:88863476 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.909+2144C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88863476 | |||||||
| chr14:88863573 | C | A | 1 | a0001c0001t0001g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.909+2241C>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88863573 | |||||||
| chr14:88863928 | G | A | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.909+2596G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88863928 | |||||||
| chr14:88863940 | C | T | 1 | a0001c0001t0003g0287 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.909+2608C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88863940 | |||||||
| chr14:88863947 | A | G | 114 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(111): Show |
138 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.909+2615A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88863947 | |||||||
| chr14:88864116 | A | C | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(45): Show |
53 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.909+2784A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88864116 | |||||||
| chr14:88864538 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.909+3206C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88864538 | |||||||
| chr14:88864558 | G | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00408.hp1 NA19001.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+3226G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88864558 | |||||||
| chr14:88864592 | C | T | 13 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(10): Show |
14 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.909+3260C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88864592 | |||||||
| chr14:88864666 | T | A | 1 | a0001c0001t0001g0341 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.909+3334T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88864666 | |||||||
| chr14:88864833 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.909+3501G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88864833 | |||||||
| chr14:88864835 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.909+3503C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88864835 | |||||||
| chr14:88865451 | C | G | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.909+4119C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88865451 | |||||||
| chr14:88865475 | C | A | 98 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(95): Show |
120 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.909+4143C>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88865475 | |||||||
| chr14:88865622 | C | T | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
94 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.909+4290C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88865622 | |||||||
| chr14:88865754 | ACTAAAAA others(4): Show |
A | 1 | a0001c0001t0002g0211 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.910-4304_910-4294d others(13): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88865754 | |||||||
| chr14:88866040 | A | G | 1 | a0001c0001t0004g0008 | 3 | HG02559.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.910-4019A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88866040 | |||||||
| chr14:88866116 | T | C | 2 | a0001c0001t0005g0011 a0001c0001t0005g0043 |
3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.910-3943T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88866116 | |||||||
| chr14:88866148 | T | C | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(45): Show |
53 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.910-3911T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88866148 | |||||||
| chr14:88866198 | A | G | 15 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0172 others(12): Show |
19 | HG00741.hp1 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.910-3861A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88866198 | |||||||
| chr14:88866353 | C | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | NA18973.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.910-3706C>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88866353 | |||||||
| chr14:88866382 | A | AAC | 118 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(115): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.910-3646_910-3645d others(4): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88866382 | ||||||
| chr14:88866382 | A | AACAC | 20 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0042 others(17): Show |
21 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.910-3648_910-3645d others(6): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88866382 | ||||||
| chr14:88866382 | A | AACACAC | 6 | a0001c0001t0003g0286 a0001c0001t0003g0289 a0001c0001t0003g0290 others(3): Show |
6 | HG00642.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-3650_910-3645d others(8): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88866382 | ||||||
| chr14:88866382 | A | AACACACA others(3): Show |
4 | a0001c0001t0003g0293 a0001c0001t0003g0295 a0001c0001t0005g0011 others(1): Show |
5 | HG02145.hp2 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-3654_910-3645d others(12): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88866382 | ||||||
| chr14:88866382 | A | AC | 4 | a0001c0001t0001g0098 a0001c0001t0001g0126 a0001c0001t0001g0129 others(1): Show |
4 | HG01952.hp1 NA18954.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-3677_910-3676i others(3): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88866382 | |||||||
| chr14:88866382 | A | ACAC | 3 | a0001c0001t0001g0313 a0001c0001t0002g0025 a0001c0001t0002g0056 |
3 | HG02071.hp1 NA18978.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.910-3677_910-3676i others(5): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88866382 | |||||||
| chr14:88866382 | AAC | A | 21 | a0001c0001t0001g0036 a0001c0001t0001g0103 a0001c0001t0001g0108 others(18): Show |
22 | HG01433.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.910-3646_910-3645d others(4): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88866382 | ||||||
| chr14:88866382 | AACAC | A | 66 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
75 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.910-3648_910-3645d others(6): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88866382 | ||||||
| chr14:88866415 | G | A | 1 | a0001c0001t0002g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.910-3644G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88866415 | |||||||
| chr14:88866415 | G | GCA | 4 | a0001c0001t0002g0269 a0001c0001t0002g0271 a0001c0001t0002g0272 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-3637_910-3636d others(4): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88866415 | ||||||
| chr14:88866462 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.910-3597C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88866462 | |||||||
| chr14:88866515 | A | G | 100 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(97): Show |
122 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.910-3544A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88866515 | |||||||
| chr14:88866559 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.910-3500C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88866559 | |||||||
| chr14:88866631 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.910-3428G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88866631 | |||||||
| chr14:88866741 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | NA18973.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.910-3318G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88866741 | |||||||
| chr14:88866768 | A | C | 1 | a0001c0001t0002g0211 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.910-3291A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88866768 | |||||||
| chr14:88867821 | C | T | 1 | a0001c0001t0003g0287 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.910-2238C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88867821 | |||||||
| chr14:88867822 | A | G | 195 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(192): Show |
230 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.910-2237A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88867822 | |||||||
| chr14:88867914 | A | C | 1 | a0001c0001t0001g0131 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.910-2145A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88867914 | |||||||
| chr14:88867933 | A | G | 197 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(194): Show |
232 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.910-2126A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88867933 | |||||||
| chr14:88868021 | T | A | 1 | a0001c0001t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.910-2038T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868021 | |||||||
| chr14:88868042 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.910-2017C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868042 | |||||||
| chr14:88868154 | C | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
7 | HG01109.hp2 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.910-1905C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868154 | |||||||
| chr14:88868169 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.910-1890T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868169 | |||||||
| chr14:88868242 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.910-1817T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868242 | |||||||
| chr14:88868355 | A | C | 1 | a0001c0001t0001g0323 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.910-1704A>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868355 | |||||||
| chr14:88868405 | C | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0235 |
2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.910-1654C>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868405 | |||||||
| chr14:88868412 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | NA18954.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.910-1647G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868412 | |||||||
| chr14:88868489 | T | C | 100 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(97): Show |
122 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.910-1570T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868489 | |||||||
| chr14:88868495 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.910-1564A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868495 | |||||||
| chr14:88868497 | T | C | 4 | a0001c0001t0001g0091 a0001c0001t0001g0311 a0001c0001t0001g0318 others(1): Show |
4 | NA18954.hp1 NA18959.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-1562T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868497 | |||||||
| chr14:88868655 | C | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
7 | HG01109.hp2 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.910-1404C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868655 | |||||||
| chr14:88868682 | TAGTCTGT others(31): Show |
T | 1 | a0001c0002t0003g0294 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.910-1374_910-1337d others(40): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 88868682 | ||||||
| chr14:88868743 | T | C | 1 | a0001c0001t0009g0179 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.910-1316T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868743 | |||||||
| chr14:88868754 | A | T | 101 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(98): Show |
124 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.910-1305A>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868754 | |||||||
| chr14:88868971 | A | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
41 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.910-1088A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88868971 | |||||||
| chr14:88869269 | T | C | 100 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(97): Show |
122 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.910-790T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88869269 | |||||||
| chr14:88869284 | A | G | 3 | a0001c0001t0001g0127 a0001c0001t0006g0078 a0001c0001t0006g0090 |
3 | HG02572.hp1 HG03017.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.910-775A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88869284 | |||||||
| chr14:88869287 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | NA18973.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.910-772G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88869287 | |||||||
| chr14:88869600 | C | T | 2 | a0001c0001t0007g0037 a0001c0001t0010g0241 |
3 | HG02040.hp2 HG02109.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.910-459C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88869600 | |||||||
| chr14:88869889 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0338 a0001c0001t0001g0339 |
4 | HG00735.hp1 HG00735.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-170T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88869889 | |||||||
| chr14:88870008 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.910-51T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 10/14 | chr14 | 88870008 | |||||||
| chr14:88870412 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0228 a0001c0001t0001g0229 |
4 | HG02698.hp1 HG03491.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1049+214C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 11/14 | chr14 | 88870412 | |||||||
| chr14:88870458 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1049+260T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 11/14 | chr14 | 88870458 | |||||||
| chr14:88870470 | A | G | 5 | a0001c0001t0001g0262 a0001c0001t0002g0269 a0001c0001t0002g0270 others(2): Show |
5 | HG01884.hp2 HG02572.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1049+272A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 11/14 | chr14 | 88870470 | |||||||
| chr14:88870501 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1049+303C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 11/14 | chr14 | 88870501 | |||||||
| chr14:88870698 | A | G | 11 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(8): Show |
11 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1049+500A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 11/14 | chr14 | 88870698 | |||||||
| chr14:88870758 | C | T | 2 | a0001c0001t0007g0037 a0001c0001t0010g0241 |
3 | HG02040.hp2 HG02109.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1049+560C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 11/14 | chr14 | 88870758 | |||||||
| chr14:88870917 | G | A | 13 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(10): Show |
14 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1050-632G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 11/14 | chr14 | 88870917 | |||||||
| chr14:88870992 | A | G | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(45): Show |
53 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1050-557A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 11/14 | chr14 | 88870992 | |||||||
| chr14:88871151 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1050-398C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 11/14 | chr14 | 88871151 | |||||||
| chr14:88871152 | G | A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0004g0008 |
5 | HG02559.hp1 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1050-397G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 11/14 | chr14 | 88871152 | |||||||
| chr14:88871247 | C | T | 1 | a0001c0001t0003g0291 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1050-302C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 11/14 | chr14 | 88871247 | |||||||
| chr14:88871379 | G | A | 1 | a0001c0001t0010g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1050-170G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 11/14 | chr14 | 88871379 | |||||||
| chr14:88871476 | A | AAT | 47 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(44): Show |
52 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1050-60_1050-59dup others(2): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 88871476 | ||||||
| chr14:88871766 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1224+43T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 12/14 | chr14 | 88871766 | |||||||
| chr14:88872275 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1225-55A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 12/14 | chr14 | 88872275 | |||||||
| chr14:88872815 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | NA18961.hp1 NA18977.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347+363C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88872815 | |||||||
| chr14:88872855 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1347+403A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88872855 | |||||||
| chr14:88872903 | C | A | 1 | a0001c0001t0001g0310 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1347+451C>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88872903 | |||||||
| chr14:88872932 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1347+480A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88872932 | |||||||
| chr14:88873025 | C | T | 2 | a0001c0001t0007g0037 a0001c0001t0010g0241 |
3 | HG02040.hp2 HG02109.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1347+573C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88873025 | |||||||
| chr14:88873040 | T | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(33): Show |
42 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.1347+588T>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88873040 | |||||||
| chr14:88873126 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1347+674G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88873126 | |||||||
| chr14:88873237 | G | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
7 | HG01109.hp2 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1347+785G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88873237 | |||||||
| chr14:88873375 | A | G | 1 | a0001c0001t0003g0290 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1347+923A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88873375 | |||||||
| chr14:88873495 | A | G | 1 | a0001c0001t0010g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1347+1043A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88873495 | |||||||
| chr14:88873584 | G | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0071 a0001c0001t0001g0087 others(4): Show |
8 | HG01099.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1347+1132G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88873584 | |||||||
| chr14:88873839 | G | C | 3 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0337 |
3 | HG00323.hp1 HG01256.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1348-1187G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88873839 | |||||||
| chr14:88874251 | A | T | 1 | a0001c0001t0007g0037 | 2 | HG02040.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1348-775A>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88874251 | |||||||
| chr14:88874430 | CA | C | 5 | a0001c0001t0001g0093 a0001c0001t0001g0255 a0001c0001t0001g0258 others(2): Show |
5 | HG02109.hp1 HG02135.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1348-586delA | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr14 | 88874430 | ||||||
| chr14:88874831 | C | A | 1 | a0001c0001t0001g0253 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1348-195C>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88874831 | |||||||
| chr14:88874844 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1348-182G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88874844 | |||||||
| chr14:88874891 | G | T | 2 | a0001c0001t0007g0037 a0001c0001t0010g0241 |
3 | HG02040.hp2 HG02109.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1348-135G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88874891 | |||||||
| chr14:88874949 | CAA | C | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(45): Show |
53 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1348-68_1348-67del others(2): Show |
TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr14 | 88874949 | ||||||
| chr14:88874969 | G | C | 1 | a0001c0001t0001g0320 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1348-57G>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 13/14 | chr14 | 88874969 | |||||||
| chr14:88875190 | A | G | 13 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(10): Show |
14 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1431+81A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88875190 | |||||||
| chr14:88875200 | C | G | 1 | a0001c0001t0001g0237 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1431+91C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88875200 | |||||||
| chr14:88875359 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1431+250G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88875359 | |||||||
| chr14:88875571 | A | G | 4 | a0001c0001t0001g0243 a0001c0001t0001g0265 a0001c0001t0001g0266 others(1): Show |
4 | HG02886.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1431+462A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88875571 | |||||||
| chr14:88875581 | C | T | 2 | a0001c0001t0007g0037 a0001c0001t0010g0241 |
3 | HG02040.hp2 HG02109.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1431+472C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88875581 | |||||||
| chr14:88875762 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1431+653A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88875762 | |||||||
| chr14:88875913 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1431+804C>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88875913 | |||||||
| chr14:88875964 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1431+855C>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88875964 | |||||||
| chr14:88876087 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
40 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.1431+978G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88876087 | |||||||
| chr14:88876229 | G | A | 191 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(188): Show |
226 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1432-1065G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88876229 | |||||||
| chr14:88876349 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1432-945G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88876349 | |||||||
| chr14:88876354 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1432-940T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88876354 | |||||||
| chr14:88876509 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0338 a0001c0001t0001g0339 |
4 | HG00735.hp1 HG00735.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1432-785A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88876509 | |||||||
| chr14:88876624 | A | G | 196 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(193): Show |
231 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1432-670A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88876624 | |||||||
| chr14:88876889 | G | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0080 others(2): Show |
7 | HG00423.hp2 NA18944.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1432-405G>T | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88876889 | |||||||
| chr14:88876977 | G | A | 100 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(97): Show |
123 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1432-317G>A | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88876977 | |||||||
| chr14:88877100 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1432-194A>G | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88877100 | |||||||
| chr14:88877282 | T | C | 13 | a0001c0001t0003g0268 a0001c0001t0003g0286 a0001c0001t0003g0287 others(10): Show |
14 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1432-12T>C | TTC8 | ENSG00000165533.19 | transcript | ENST00000380656.7 | protein_coding | 14/14 | chr14 | 88877282 |