Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 158248 |
| ensemblid | ENSG00000167094.16 |
| hgncid | 26536 |
| symbol | TTC16 |
| name | tetratricopeptide repeat domain 16 |
| refseq_nuc | NM_144965.3 |
| refseq_prot | NP_659402.1 |
| ensembl_nuc | ENST00000373289.4 |
| ensembl_prot | ENSP00000362386.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 127716079 |
| end | 127731590 |
| strand | + |
| ver | v1.2 |
| region | chr9:127716079-127731590 |
| region5000 | chr9:127711079-127736590 |
| regionname0 | TTC16_chr9_127716079_127731590 |
| regionname5000 | TTC16_chr9_127711079_127736590 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 873 | 201 | 57 | 39 | 76 | 5 | 23 | 52 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0002 | 0/1 | 873 | 77 | 7 | 20 | 25 | 5 | 19 | 17 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0003 | 0/0 | 873 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0004 | 0/0 | 873 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0005 | 0/0 | 873 | 7 | 0 | 6 | 1 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0006 | 0/0 | 873 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0007 | 0/0 | 873 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0008 | 0/0 | 873 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0009 | 0/0 | 873 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0010 | 0/0 | 873 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0011 | 0/0 | 873 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0012 | 0/0 | 873 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0013 | 0/0 | 873 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0014 | 0/0 | 143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(138): Show |
chr9 | 127711079 | 127736590 |
| a0015 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0016 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0017 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0018 | 0/0 | 873 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0019 | 0/0 | 873 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0020 | 0/0 | 873 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0021 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0022 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0023 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| a0024 | 0/0 | 873 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | MTDSD others(868): Show |
chr9 | 127711079 | 127736590 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2619 | 122 | 17 | 28 | 59 | 4 | 13 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0001c0002 | 0/0 | 2619 | 77 | 38 | 11 | 17 | 1 | 10 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0001c0013 | 0/0 | 2619 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0002c0003 | 0/1 | 2619 | 72 | 3 | 20 | 24 | 5 | 19 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0002c0010 | 0/0 | 2619 | 3 | 3 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0002c0023 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0002c0024 | 0/0 | 2619 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0003c0004 | 0/0 | 2619 | 9 | 7 | 2 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0004c0005 | 0/0 | 2619 | 9 | 9 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0005c0006 | 0/0 | 2619 | 7 | 0 | 6 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0006c0007 | 0/0 | 2619 | 5 | 5 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0007c0008 | 0/0 | 2619 | 5 | 0 | 0 | 5 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0008c0009 | 0/0 | 2619 | 3 | 0 | 0 | 3 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0009c0011 | 0/0 | 2619 | 2 | 0 | 2 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0010c0012 | 0/0 | 2619 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0011c0025 | 0/0 | 2619 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0012c0028 | 0/0 | 2619 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0013c0020 | 0/0 | 2619 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0014c0026 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2603): Show |
chr9 | 127711079 | 127736590 | ||
| a0015c0017 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0016c0027 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0017c0015 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0018c0022 | 0/0 | 2619 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0019c0019 | 0/0 | 2619 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0020c0021 | 0/0 | 2619 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0021c0014 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0022c0029 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0023c0016 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 | ||
| a0024c0018 | 0/0 | 2619 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | ATGAC others(2614): Show |
chr9 | 127711079 | 127736590 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2874 | 122 | 17 | 28 | 59 | 4 | 13 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0001c0002t0001 | 0/0 | 2874 | 24 | 14 | 0 | 10 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0001c0002t0002 | 0/0 | 2874 | 53 | 24 | 11 | 7 | 1 | 10 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0001c0013t0001 | 0/0 | 2874 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0002c0003t0002 | 0/1 | 2874 | 72 | 3 | 20 | 24 | 5 | 19 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0002c0010t0002 | 0/0 | 2874 | 3 | 3 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0002c0023t0002 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0002c0024t0001 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0003c0004t0002 | 0/0 | 2874 | 9 | 7 | 2 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0004c0005t0001 | 0/0 | 2874 | 9 | 9 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0005c0006t0002 | 0/0 | 2874 | 7 | 0 | 6 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0006c0007t0001 | 0/0 | 2874 | 5 | 5 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0007c0008t0002 | 0/0 | 2874 | 5 | 0 | 0 | 5 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0008c0009t0001 | 0/0 | 2874 | 3 | 0 | 0 | 3 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0009c0011t0002 | 0/0 | 2874 | 2 | 0 | 2 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0010c0012t0001 | 0/0 | 2874 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0011c0025t0001 | 0/0 | 2874 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0012c0028t0001 | 0/0 | 2874 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0013c0020t0002 | 0/0 | 2874 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0014c0026t0002 | 0/0 | 2863 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2858): Show |
chr9 | 127711079 | 127736590 |
| a0015c0017t0001 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0016c0027t0001 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0017c0015t0002 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0018c0022t0002 | 0/0 | 2874 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0019c0019t0002 | 0/0 | 2874 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0020c0021t0002 | 0/0 | 2874 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0021c0014t0002 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0022c0029t0002 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0023c0016t0001 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| a0024c0018t0001 | 0/0 | 2874 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | AGCAA others(2869): Show |
chr9 | 127711079 | 127736590 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 3 | 9 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0013t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0001c0013t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0001 | 0/1 | 10 | 0 | 3 | 4 | 1 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0004 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0005 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0006 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0010t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0010t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0010t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0023t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0002c0024t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0003c0004t0002g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0003c0004t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0003c0004t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0003c0004t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0003c0004t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0003c0004t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0004c0005t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0004c0005t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0004c0005t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0004c0005t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0004c0005t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0004c0005t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0004c0005t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0005c0006t0002g0001 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0005c0006t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0005c0006t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0006c0007t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0006c0007t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0006c0007t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0006c0007t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0007c0008t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0007c0008t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0007c0008t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0007c0008t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0008c0009t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0008c0009t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0008c0009t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0009c0011t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0009c0011t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0010c0012t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0010c0012t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0011c0025t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0012c0028t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0013c0020t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0014c0026t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0015c0017t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0016c0027t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0017c0015t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0018c0022t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0019c0019t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0020c0021t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0021c0014t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0022c0029t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0023c0016t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| a0024c0018t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | GBR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00099 | hp2 | a0002 | c0003 | t0002 | g0004 | EUR | GBR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00280 | hp1 | a0002 | c0003 | t0002 | g0001 | EUR | FIN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | FIN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0008 | EUR | FIN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00323 | hp2 | a0002 | c0003 | t0002 | g0132 | EUR | FIN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00423 | hp2 | a0002 | c0003 | t0002 | g0074 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00438 | hp1 | a0002 | c0003 | t0002 | g0042 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00438 | hp2 | a0008 | c0009 | t0001 | g0213 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00544 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00597 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00621 | hp1 | a0002 | c0003 | t0002 | g0006 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00642 | hp1 | a0009 | c0011 | t0002 | g0064 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00673 | hp2 | a0002 | c0003 | t0002 | g0039 | EAS | CHS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00735 | hp2 | a0002 | c0003 | t0002 | g0004 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00738 | hp1 | a0002 | c0003 | t0002 | g0053 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0143 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01069 | hp2 | a0003 | c0004 | t0002 | g0007 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0144 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01099 | hp2 | a0003 | c0004 | t0002 | g0084 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0116 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01106 | hp2 | a0002 | c0003 | t0002 | g0062 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01109 | hp1 | a0011 | c0025 | t0001 | g0257 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01109 | hp2 | a0012 | c0028 | t0001 | g0108 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01169 | hp2 | a0002 | c0003 | t0002 | g0001 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01175 | hp1 | a0002 | c0003 | t0002 | g0061 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01243 | hp2 | a0002 | c0003 | t0002 | g0004 | AMR | PUR | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0259 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01256 | hp2 | a0002 | c0003 | t0002 | g0001 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01257 | hp1 | a0002 | c0003 | t0002 | g0004 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01258 | hp1 | a0002 | c0003 | t0002 | g0004 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01261 | hp1 | a0002 | c0003 | t0002 | g0016 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01346 | hp2 | a0002 | c0003 | t0002 | g0063 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01358 | hp1 | a0002 | c0003 | t0002 | g0036 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01361 | hp1 | a0002 | c0003 | t0002 | g0006 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01361 | hp2 | a0005 | c0006 | t0002 | g0001 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01433 | hp1 | a0002 | c0003 | t0002 | g0060 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0141 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0254 | EUR | IBS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01515 | hp2 | a0002 | c0003 | t0002 | g0051 | EUR | IBS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01517 | hp1 | a0002 | c0003 | t0002 | g0059 | EUR | IBS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | IBS | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01884 | hp1 | a0006 | c0007 | t0001 | g0019 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0160 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01891 | hp1 | a0004 | c0005 | t0001 | g0021 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0057 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01928 | hp1 | a0002 | c0003 | t0002 | g0044 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0161 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01943 | hp1 | a0013 | c0020 | t0002 | g0139 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01952 | hp1 | a0002 | c0003 | t0002 | g0066 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01975 | hp1 | a0002 | c0003 | t0002 | g0001 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01975 | hp2 | a0005 | c0006 | t0002 | g0001 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01978 | hp1 | a0002 | c0003 | t0002 | g0005 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01978 | hp2 | a0002 | c0003 | t0002 | g0049 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01981 | hp2 | a0005 | c0006 | t0002 | g0038 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01993 | hp1 | a0002 | c0003 | t0002 | g0005 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0164 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02015 | hp1 | a0008 | c0009 | t0001 | g0217 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02055 | hp1 | a0004 | c0005 | t0001 | g0109 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02083 | hp1 | a0002 | c0003 | t0002 | g0009 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02132 | hp2 | a0008 | c0009 | t0001 | g0028 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02148 | hp1 | a0005 | c0006 | t0002 | g0041 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | CDX | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | CDX | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02165 | hp2 | a0002 | c0003 | t0002 | g0075 | EAS | CDX | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0067 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0165 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0023 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02280 | hp2 | a0002 | c0010 | t0002 | g0001 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02293 | hp2 | a0009 | c0011 | t0002 | g0014 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0145 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02300 | hp2 | a0005 | c0006 | t0002 | g0001 | AMR | PEL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02451 | hp1 | a0003 | c0004 | t0002 | g0007 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02572 | hp1 | a0004 | c0005 | t0001 | g0105 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02602 | hp1 | a0002 | c0003 | t0002 | g0001 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02615 | hp2 | a0014 | c0026 | t0002 | g0085 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0134 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02622 | hp2 | a0003 | c0004 | t0002 | g0082 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0170 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0147 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02683 | hp2 | a0002 | c0003 | t0002 | g0079 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02698 | hp1 | a0002 | c0003 | t0002 | g0035 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0146 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0140 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02723 | hp2 | a0010 | c0012 | t0001 | g0153 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0137 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02735 | hp2 | a0002 | c0003 | t0002 | g0014 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02809 | hp2 | a0015 | c0017 | t0001 | g0155 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02818 | hp2 | a0002 | c0003 | t0002 | g0131 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02895 | hp1 | a0002 | c0010 | t0002 | g0077 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0142 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02922 | hp1 | a0002 | c0003 | t0002 | g0043 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02922 | hp2 | a0004 | c0005 | t0001 | g0107 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02965 | hp1 | a0003 | c0004 | t0002 | g0007 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02965 | hp2 | a0004 | c0005 | t0001 | g0020 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02976 | hp1 | a0006 | c0007 | t0001 | g0019 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03017 | hp1 | a0002 | c0003 | t0002 | g0045 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03017 | hp2 | a0002 | c0003 | t0002 | g0069 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03041 | hp1 | a0004 | c0005 | t0001 | g0020 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03041 | hp2 | a0002 | c0010 | t0002 | g0076 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03098 | hp1 | a0002 | c0023 | t0002 | g0087 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0158 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03139 | hp1 | a0004 | c0005 | t0001 | g0021 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0133 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03195 | hp2 | a0016 | c0027 | t0001 | g0110 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0169 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03225 | hp1 | a0001 | c0013 | t0001 | g0173 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0115 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0126 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03239 | hp2 | a0002 | c0003 | t0002 | g0006 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0168 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03453 | hp2 | a0003 | c0004 | t0002 | g0083 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03486 | hp1 | a0006 | c0007 | t0001 | g0103 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03491 | hp1 | a0002 | c0003 | t0002 | g0046 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03491 | hp2 | a0002 | c0003 | t0002 | g0013 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03492 | hp1 | a0002 | c0003 | t0002 | g0013 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03516 | hp1 | a0017 | c0015 | t0002 | g0171 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03516 | hp2 | a0010 | c0012 | t0001 | g0152 | AFR | ESN | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0166 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0125 | AFR | GWD | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03579 | hp2 | a0002 | c0003 | t0002 | g0123 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03654 | hp1 | a0018 | c0022 | t0002 | g0236 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03654 | hp2 | a0019 | c0019 | t0002 | g0135 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03669 | hp2 | a0002 | c0003 | t0002 | g0005 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03688 | hp1 | a0002 | c0003 | t0002 | g0015 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0138 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0163 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0117 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03831 | hp2 | a0002 | c0003 | t0002 | g0055 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03834 | hp2 | a0020 | c0021 | t0002 | g0024 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03927 | hp2 | a0002 | c0003 | t0002 | g0078 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG04115 | hp1 | a0002 | c0003 | t0002 | g0006 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG04184 | hp2 | a0002 | c0003 | t0002 | g0054 | SAS | BEB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG04199 | hp1 | a0002 | c0003 | t0002 | g0005 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG04204 | hp1 | a0002 | c0003 | t0002 | g0034 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG04204 | hp2 | a0002 | c0003 | t0002 | g0033 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0127 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | STU | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18522 | hp1 | a0004 | c0005 | t0001 | g0106 | AFR | YRI | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0148 | AFR | YRI | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18612 | hp2 | a0007 | c0008 | t0002 | g0009 | EAS | CHB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18906 | hp1 | a0021 | c0014 | t0002 | g0136 | AFR | YRI | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18943 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18952 | hp2 | a0002 | c0003 | t0002 | g0073 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18956 | hp2 | a0002 | c0003 | t0002 | g0086 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18963 | hp1 | a0002 | c0003 | t0002 | g0050 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18964 | hp2 | a0002 | c0003 | t0002 | g0210 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18966 | hp2 | a0002 | c0003 | t0002 | g0016 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18973 | hp1 | a0002 | c0003 | t0002 | g0052 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18978 | hp2 | a0002 | c0003 | t0002 | g0037 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18979 | hp1 | a0007 | c0008 | t0002 | g0040 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18982 | hp2 | a0002 | c0003 | t0002 | g0015 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18983 | hp2 | a0005 | c0006 | t0002 | g0001 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19004 | hp2 | a0002 | c0003 | t0002 | g0047 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19007 | hp2 | a0002 | c0003 | t0002 | g0048 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19030 | hp1 | a0003 | c0004 | t0002 | g0080 | AFR | LWK | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | LWK | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | LWK | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19043 | hp2 | a0001 | c0013 | t0001 | g0172 | AFR | LWK | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19054 | hp2 | a0002 | c0003 | t0002 | g0068 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19059 | hp1 | a0002 | c0024 | t0001 | g0032 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19060 | hp2 | a0007 | c0008 | t0002 | g0009 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19067 | hp1 | a0007 | c0008 | t0002 | g0070 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19075 | hp1 | a0007 | c0008 | t0002 | g0072 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19081 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19083 | hp2 | a0002 | c0003 | t0002 | g0058 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19084 | hp1 | a0002 | c0003 | t0002 | g0071 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19088 | hp2 | a0002 | c0003 | t0002 | g0065 | EAS | JPT | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0056 | AFR | YRI | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA19240 | hp2 | a0022 | c0029 | t0002 | g0101 | AFR | YRI | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ASW | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA20129 | hp2 | a0023 | c0016 | t0001 | g0002 | AFR | ASW | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0157 | SAS | GIH | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA20905 | hp2 | a0024 | c0018 | t0001 | g0201 | SAS | GIH | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG01123 | hp2 | a0005 | c0006 | t0002 | g0001 | AMR | CLM | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02109 | hp2 | a0006 | c0007 | t0001 | g0111 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG02486 | hp2 | a0003 | c0004 | t0002 | g0081 | AFR | ACB | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03471 | hp1 | a0004 | c0005 | t0001 | g0104 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0023 | AFR | MSL | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG06807 | hp1 | a0006 | c0007 | t0001 | g0102 | AFR | USA | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0247 | AFR | USA | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | USA | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0159 | AFR | USA | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| NA21309 | hp2 | a0003 | c0004 | t0002 | g0007 | AFR | LWK | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0002 | g0001 | REF | REF | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0243 | REF | REF | TTC16_chr9_127711079_127736590 | TTC16 | chr9 | 127711079 | 127736590 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127716911 | A | G | 4 | a0004 a0012 a0016 others(1): Show |
12 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
missense_variant | MODERATE | c.86A>G | p.Lys29Arg | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/14 | 153/2874 | 86/2622 | 29/873 | chr9 | 127716911 | |||
| chr9:127716931 | T | G | 1 | a0021 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.106T>G | p.Phe36Val | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/14 | 173/2874 | 106/2622 | 36/873 | chr9 | 127716931 | |||
| chr9:127717689 | G | A | 1 | a0016 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.343G>A | p.Ala115Thr | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/14 | 410/2874 | 343/2622 | 115/873 | chr9 | 127717689 | |||
| chr9:127717746 | C | T | 1 | a0008 | 3 | HG00438.hp2 HG02015.hp1 HG02132.hp2 |
missense_variant | MODERATE | c.400C>T | p.Arg134Cys | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/14 | 467/2874 | 400/2622 | 134/873 | chr9 | 127717746 | |||
| chr9:127720075 | CAGGGACA others(6): Show |
C | 1 | a0014 | 1 | HG02615.hp2 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.427-2_437delAGGGAC others(7): Show |
p.Gly143fs | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 5/14 | 427/2622 | 143/873 | chr9 | 127720075 | ||||
| chr9:127720162 | T | C | 1 | a0009 | 2 | HG00642.hp1 HG02293.hp2 |
missense_variant | MODERATE | c.511T>C | p.Cys171Arg | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 5/14 | 578/2874 | 511/2622 | 171/873 | chr9 | 127720162 | |||
| chr9:127723169 | G | C | 1 | a0014 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.708G>C | p.Lys236Asn | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/14 | 775/2874 | 708/2622 | 236/873 | chr9 | 127723169 | |||
| chr9:127723197 | A | C | 1 | a0003 | 9 | HG01069.hp2 HG01099.hp2 HG02451.hp1 others(6): Show |
missense_variant | MODERATE | c.736A>C | p.Lys246Gln | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/14 | 803/2874 | 736/2622 | 246/873 | chr9 | 127723197 | |||
| chr9:127724190 | G | T | 1 | a0011 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.943G>T | p.Val315Leu | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 8/14 | 1010/2874 | 943/2622 | 315/873 | chr9 | 127724190 | |||
| chr9:127724196 | G | A | 1 | a0010 | 2 | HG02723.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.949G>A | p.Glu317Lys | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 8/14 | 1016/2874 | 949/2622 | 317/873 | chr9 | 127724196 | |||
| chr9:127724854 | G | A | 4 | a0004 a0012 a0016 others(1): Show |
12 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
missense_variant | MODERATE | c.1216G>A | p.Gly406Ser | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/14 | 1283/2874 | 1216/2622 | 406/873 | chr9 | 127724854 | |||
| chr9:127724878 | T | G | 1 | a0006 | 5 | HG01884.hp1 HG02109.hp2 HG02976.hp1 others(2): Show |
missense_variant | MODERATE | c.1240T>G | p.Phe414Val | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/14 | 1307/2874 | 1240/2622 | 414/873 | chr9 | 127724878 | |||
| chr9:127726328 | G | A | 1 | a0005 | 7 | HG01123.hp2 HG01361.hp2 HG01975.hp2 others(4): Show |
missense_variant | MODERATE | c.1349G>A | p.Arg450Gln | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/14 | 1416/2874 | 1349/2622 | 450/873 | chr9 | 127726328 | |||
| chr9:127726352 | G | C | 1 | a0023 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1373G>C | p.Gly458Ala | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/14 | 1440/2874 | 1373/2622 | 458/873 | chr9 | 127726352 | |||
| chr9:127727281 | G | C | 1 | a0015 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1580G>C | p.Arg527Pro | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/14 | 1647/2874 | 1580/2622 | 527/873 | chr9 | 127727281 | |||
| chr9:127727358 | G | A | 1 | a0019 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.1657G>A | p.Glu553Lys | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/14 | 1724/2874 | 1657/2622 | 553/873 | chr9 | 127727358 | |||
| chr9:127727382 | A | T | 1 | a0012 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1681A>T | p.Ile561Phe | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/14 | 1748/2874 | 1681/2622 | 561/873 | chr9 | 127727382 | |||
| chr9:127727464 | A | G | 6 | a0002 a0003 a0005 others(3): Show |
100 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(97): Show |
missense_variant&splice_region_variant | MODERATE | c.1763A>G | p.Glu588Gly | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/14 | 1830/2874 | 1763/2622 | 588/873 | chr9 | 127727464 | |||
| chr9:127730725 | T | G | 1 | a0007 | 5 | NA18612.hp2 NA18979.hp1 NA19060.hp2 others(2): Show |
missense_variant | MODERATE | c.1942T>G | p.Ser648Ala | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 2009/2874 | 1942/2622 | 648/873 | chr9 | 127730725 | |||
| chr9:127730861 | G | A | 1 | a0013 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.2078G>A | p.Arg693Gln | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 2145/2874 | 2078/2622 | 693/873 | chr9 | 127730861 | |||
| chr9:127731182 | G | A | 1 | a0024 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.2399G>A | p.Arg800Gln | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 2466/2874 | 2399/2622 | 800/873 | chr9 | 127731182 | |||
| chr9:127731209 | A | G | 1 | a0018 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.2426A>G | p.Tyr809Cys | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 2493/2874 | 2426/2622 | 809/873 | chr9 | 127731209 | |||
| chr9:127731348 | C | A | 1 | a0020 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.2565C>A | p.Ser855Arg | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 2632/2874 | 2565/2622 | 855/873 | chr9 | 127731348 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127716954 | A | G | 1 | a0002c0010 | 3 | HG02280.hp2 HG02895.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.129A>G | p.Gln43Gln | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/14 | 196/2874 | 129/2622 | 43/873 | chr9 | 127716954 | |||
| chr9:127727279 | A | G | 19 | a0001c0002 a0001c0013 a0002c0003 others(16): Show |
188 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
synonymous_variant | LOW | c.1578A>G | p.Lys526Lys | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/14 | 1645/2874 | 1578/2622 | 526/873 | chr9 | 127727279 | |||
| chr9:127729589 | A | G | 1 | a0001c0013 | 2 | HG03225.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.1773A>G | p.Lys591Lys | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/14 | 1840/2874 | 1773/2622 | 591/873 | chr9 | 127729589 | |||
| chr9:127731192 | C | A | 1 | a0002c0023 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.2409C>A | p.Thr803Thr | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 2476/2874 | 2409/2622 | 803/873 | chr9 | 127731192 | |||
| chr9:127731234 | A | G | 19 | a0001c0002 a0001c0013 a0002c0003 others(16): Show |
188 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
synonymous_variant | LOW | c.2451A>G | p.Lys817Lys | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 2518/2874 | 2451/2622 | 817/873 | chr9 | 127731234 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127731445 | C | T | 16 | a0001c0002t0002 a0002c0003t0002 a0002c0010t0002 others(13): Show |
159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*40C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 14/14 | 40 | chr9 | 127731445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127716191 | AAGGCAGA others(51): Show |
A | 1 | a0001c0002t0002g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.18+29_18+86delAGGC others(54): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 1/13 | chr9 | 127716191 | |||||||
| chr9:127716240 | T | A | 1 | a0001c0002t0002g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.18+77T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 1/13 | chr9 | 127716240 | |||||||
| chr9:127716246 | C | T | 9 | a0001c0002t0001g0018 a0001c0002t0001g0092 a0001c0002t0001g0093 others(6): Show |
10 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.18+83C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 1/13 | chr9 | 127716246 | |||||||
| chr9:127716374 | G | A | 70 | a0001c0002t0002g0056 a0001c0002t0002g0057 a0001c0002t0002g0067 others(67): Show |
99 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.18+211G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 1/13 | chr9 | 127716374 | |||||||
| chr9:127716580 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | NA18956.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.19-264G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 1/13 | chr9 | 127716580 | |||||||
| chr9:127717080 | C | T | 1 | a0001c0002t0001g0258 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.191+64C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/13 | chr9 | 127717080 | |||||||
| chr9:127717139 | T | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0090 a0001c0001t0001g0091 |
4 | HG01123.hp1 HG01346.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+123T>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/13 | chr9 | 127717139 | |||||||
| chr9:127717168 | C | T | 1 | a0002c0023t0002g0087 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.191+152C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/13 | chr9 | 127717168 | |||||||
| chr9:127717209 | T | C | 1 | a0002c0024t0001g0032 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.192-125T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/13 | chr9 | 127717209 | |||||||
| chr9:127717229 | T | C | 9 | a0001c0002t0001g0018 a0001c0002t0001g0092 a0001c0002t0001g0093 others(6): Show |
10 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.192-105T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/13 | chr9 | 127717229 | |||||||
| chr9:127717299 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.192-35G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 2/13 | chr9 | 127717299 | |||||||
| chr9:127717500 | C | T | 1 | a0011c0025t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.282+76C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 3/13 | chr9 | 127717500 | |||||||
| chr9:127717534 | T | C | 1 | a0022c0029t0002g0101 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.283-95T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 3/13 | chr9 | 127717534 | |||||||
| chr9:127717602 | T | C | 24 | a0001c0002t0001g0018 a0001c0002t0001g0092 a0001c0002t0001g0093 others(21): Show |
28 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.283-27T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 3/13 | chr9 | 127717602 | |||||||
| chr9:127717961 | A | G | 9 | a0001c0002t0001g0018 a0001c0002t0001g0092 a0001c0002t0001g0093 others(6): Show |
10 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.426+189A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127717961 | |||||||
| chr9:127717969 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.426+197T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127717969 | |||||||
| chr9:127718043 | A | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0248 a0001c0001t0001g0249 others(7): Show |
12 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.426+271A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127718043 | |||||||
| chr9:127718087 | T | TTTA | 14 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(11): Show |
17 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.426+330_426+332dup others(3): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 127718087 | ||||||
| chr9:127718105 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.426+333T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127718105 | |||||||
| chr9:127718156 | C | T | 15 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(12): Show |
18 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.426+384C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127718156 | |||||||
| chr9:127718739 | G | A | 4 | a0002c0003t0002g0005 a0002c0003t0002g0033 a0002c0003t0002g0034 others(1): Show |
7 | HG01978.hp1 HG01993.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.426+967G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127718739 | |||||||
| chr9:127718864 | T | G | 1 | a0002c0024t0001g0032 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.426+1092T>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127718864 | |||||||
| chr9:127718867 | C | T | 1 | a0001c0002t0001g0247 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.426+1095C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127718867 | |||||||
| chr9:127719083 | T | C | 167 | a0001c0001t0001g0027 a0001c0001t0001g0124 a0001c0001t0001g0156 others(164): Show |
210 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.427-995T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719083 | |||||||
| chr9:127719123 | A | T | 1 | a0001c0002t0002g0174 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.427-955A>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719123 | |||||||
| chr9:127719210 | C | CA | 40 | a0001c0001t0001g0028 a0001c0001t0001g0112 a0001c0001t0001g0175 others(37): Show |
45 | HG00673.hp2 HG01106.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.427-853dupA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 127719210 | ||||||
| chr9:127719235 | TA | T | 3 | a0001c0001t0001g0246 a0002c0003t0002g0086 a0002c0024t0001g0032 |
3 | NA18956.hp2 NA18984.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.427-838delA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 127719235 | ||||||
| chr9:127719243 | A | C | 1 | a0001c0001t0001g0246 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.427-835A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719243 | |||||||
| chr9:127719291 | ATGTCCTG others(26): Show |
A | 1 | a0005c0006t0002g0041 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.427-786_427-754del others(33): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719291 | |||||||
| chr9:127719339 | C | A | 1 | a0002c0003t0002g0042 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.427-739C>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719339 | |||||||
| chr9:127719467 | T | A | 6 | a0001c0002t0001g0118 a0001c0002t0001g0119 a0001c0002t0001g0120 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-611T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719467 | |||||||
| chr9:127719557 | A | T | 1 | a0001c0001t0001g0089 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.427-521A>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719557 | |||||||
| chr9:127719562 | G | A | 1 | a0011c0025t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.427-516G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719562 | |||||||
| chr9:127719586 | A | G | 15 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(12): Show |
18 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.427-492A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719586 | |||||||
| chr9:127719876 | C | T | 1 | a0016c0027t0001g0110 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.427-202C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719876 | |||||||
| chr9:127719984 | T | A | 1 | a0001c0001t0001g0246 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.427-94T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 4/13 | chr9 | 127719984 | |||||||
| chr9:127720223 | C | T | 1 | a0003c0004t0002g0084 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.528-43C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 5/13 | chr9 | 127720223 | |||||||
| chr9:127720598 | A | T | 1 | a0001c0001t0001g0089 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.657+203A>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720598 | |||||||
| chr9:127720629 | C | A | 2 | a0016c0027t0001g0110 a0022c0029t0002g0101 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.657+234C>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720629 | |||||||
| chr9:127720636 | G | A | 1 | a0002c0003t0002g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.657+241G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720636 | |||||||
| chr9:127720687 | C | G | 168 | a0001c0001t0001g0027 a0001c0001t0001g0156 a0001c0001t0001g0162 others(165): Show |
211 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.657+292C>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720687 | |||||||
| chr9:127720705 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.657+310T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720705 | |||||||
| chr9:127720706 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.657+311G>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720706 | |||||||
| chr9:127720805 | T | A | 1 | a0001c0002t0002g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.657+410T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720805 | |||||||
| chr9:127720817 | T | C | 1 | a0002c0003t0002g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.657+422T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720817 | |||||||
| chr9:127720818 | C | T | 1 | a0002c0003t0002g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.657+423C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720818 | |||||||
| chr9:127720820 | T | C | 1 | a0002c0003t0002g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.657+425T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720820 | |||||||
| chr9:127720828 | G | C | 1 | a0001c0002t0002g0126 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.657+433G>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720828 | |||||||
| chr9:127720831 | T | TGCCCCGT others(514): Show |
1 | a0002c0003t0002g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.657+436_657+437ins others(521): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720831 | |||||||
| chr9:127720831 | T | TTCCCCCC others(597): Show |
1 | a0001c0002t0002g0127 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(604): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(414): Show |
1 | a0001c0002t0002g0126 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(421): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(515): Show |
1 | a0014c0026t0002g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(522): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(493): Show |
1 | a0001c0001t0001g0244 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(500): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(427): Show |
1 | a0001c0001t0001g0179 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(434): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(477): Show |
1 | a0001c0001t0001g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(484): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(440): Show |
1 | a0001c0001t0001g0181 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(447): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(456): Show |
1 | a0001c0001t0001g0182 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(463): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(426): Show |
1 | a0001c0001t0001g0183 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(433): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(888): Show |
1 | a0001c0002t0001g0128 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(895): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(490): Show |
1 | a0001c0002t0001g0092 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(497): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(566): Show |
1 | a0002c0003t0002g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(573): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(411): Show |
1 | a0001c0001t0001g0175 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(418): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(513): Show |
3 | a0001c0001t0001g0017 a0001c0001t0001g0090 a0001c0001t0001g0091 |
4 | HG01123.hp1 HG01346.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(520): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(491): Show |
1 | a0001c0001t0001g0245 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(498): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(454): Show |
1 | a0001c0001t0001g0184 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(461): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(426): Show |
1 | a0001c0001t0001g0248 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(433): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(405): Show |
1 | a0001c0001t0001g0089 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(412): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(390): Show |
2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(397): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(389): Show |
1 | a0001c0001t0001g0187 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(396): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(681): Show |
1 | a0001c0001t0001g0188 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(688): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(456): Show |
1 | a0001c0001t0001g0189 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(463): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(730): Show |
1 | a0001c0001t0001g0178 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(737): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(680): Show |
2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG00544.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(687): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(695): Show |
1 | a0001c0001t0001g0176 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(702): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(679): Show |
1 | a0001c0001t0001g0192 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(686): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(441): Show |
1 | a0001c0001t0001g0193 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(448): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(469): Show |
2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | NA18943.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(476): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(410): Show |
1 | a0001c0001t0001g0196 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(417): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(447): Show |
3 | a0001c0001t0001g0124 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02145.hp2 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(454): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(426): Show |
1 | a0001c0001t0001g0199 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(433): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(426): Show |
1 | a0001c0001t0001g0249 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(433): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(410): Show |
1 | a0001c0001t0001g0200 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(417): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(775): Show |
1 | a0024c0018t0001g0201 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(782): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(448): Show |
1 | a0001c0001t0001g0202 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(455): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(625): Show |
1 | a0001c0001t0001g0203 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(632): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(425): Show |
33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(30): Show |
55 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(432): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(440): Show |
1 | a0001c0001t0001g0031 | 2 | HG01069.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(447): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(455): Show |
2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA19004.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(462): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(468): Show |
1 | a0001c0001t0001g0221 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(475): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(380): Show |
1 | a0001c0002t0002g0022 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(387): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(395): Show |
2 | a0001c0002t0002g0133 a0001c0002t0002g0134 |
2 | HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(402): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(403): Show |
1 | a0001c0001t0001g0222 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(410): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(403): Show |
5 | a0001c0001t0001g0088 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG00609.hp1 HG02717.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(410): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(381): Show |
1 | a0001c0002t0002g0174 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(388): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(708): Show |
2 | a0001c0002t0001g0118 a0001c0002t0001g0119 |
2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(715): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(723): Show |
1 | a0001c0002t0001g0120 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(730): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(396): Show |
2 | a0001c0002t0001g0121 a0001c0002t0001g0247 |
2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(403): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(424): Show |
6 | a0001c0001t0001g0100 a0001c0001t0001g0177 a0001c0001t0001g0227 others(3): Show |
6 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(431): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(483): Show |
1 | a0001c0001t0001g0231 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(490): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(461): Show |
1 | a0001c0001t0001g0232 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(468): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(389): Show |
1 | a0001c0001t0001g0233 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(396): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(709): Show |
2 | a0006c0007t0001g0019 a0006c0007t0001g0102 |
3 | HG01884.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(716): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(425): Show |
1 | a0001c0001t0001g0234 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(432): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(424): Show |
1 | a0001c0001t0001g0235 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(431): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(723): Show |
1 | a0006c0007t0001g0103 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(730): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(822): Show |
1 | a0006c0007t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(829): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(582): Show |
1 | a0019c0019t0002g0135 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(589): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(522): Show |
3 | a0002c0003t0002g0044 a0002c0003t0002g0123 a0021c0014t0002g0136 |
3 | HG01928.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(529): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(666): Show |
1 | a0002c0003t0002g0045 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(673): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(492): Show |
1 | a0002c0024t0001g0032 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(499): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(381): Show |
1 | a0018c0022t0002g0236 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(388): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(419): Show |
1 | a0001c0001t0001g0237 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(426): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(418): Show |
1 | a0011c0025t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(425): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(396): Show |
1 | a0001c0001t0001g0112 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(403): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(360): Show |
1 | a0001c0002t0001g0099 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(367): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(338): Show |
1 | a0001c0001t0001g0238 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(345): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(359): Show |
1 | a0001c0002t0001g0093 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(366): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(410): Show |
4 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(1): Show |
4 | NA18947.hp1 NA18982.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(417): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(336): Show |
1 | a0001c0002t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(343): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(358): Show |
3 | a0001c0002t0001g0018 a0001c0002t0001g0095 a0001c0002t0001g0096 |
4 | HG02155.hp1 HG02165.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(365): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(512): Show |
2 | a0001c0002t0001g0097 a0001c0002t0001g0098 |
2 | NA18957.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(519): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(467): Show |
1 | a0002c0003t0002g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(474): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(563): Show |
1 | a0002c0003t0002g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(570): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(610): Show |
1 | a0001c0002t0002g0137 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(617): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(523): Show |
2 | a0002c0003t0002g0004 a0002c0003t0002g0046 |
6 | HG00099.hp2 HG00735.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(530): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(603): Show |
1 | a0002c0003t0002g0047 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(610): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(611): Show |
1 | a0001c0002t0002g0138 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(618): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(499): Show |
1 | a0002c0003t0002g0048 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(506): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(588): Show |
1 | a0013c0020t0002g0139 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(595): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(644): Show |
1 | a0002c0003t0002g0049 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(651): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(503): Show |
1 | a0002c0003t0002g0050 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(510): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(907): Show |
1 | a0002c0003t0002g0051 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(914): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(501): Show |
1 | a0001c0002t0002g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(508): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(582): Show |
1 | a0001c0002t0002g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(589): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(552): Show |
2 | a0001c0002t0002g0023 a0001c0002t0002g0141 |
3 | HG01496.hp2 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(559): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(537): Show |
1 | a0001c0002t0002g0142 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(544): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(709): Show |
1 | a0002c0003t0002g0052 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(716): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(522): Show |
1 | a0002c0003t0002g0053 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(529): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(508): Show |
1 | a0002c0003t0002g0037 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(515): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(508): Show |
1 | a0002c0003t0002g0054 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(515): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(485): Show |
1 | a0002c0003t0002g0055 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(492): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(598): Show |
1 | a0001c0002t0002g0143 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(605): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(596): Show |
5 | a0001c0002t0002g0008 a0001c0002t0002g0056 a0001c0002t0002g0116 others(2): Show |
8 | HG00323.hp1 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(603): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(582): Show |
1 | a0001c0002t0002g0057 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(589): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(510): Show |
1 | a0002c0003t0002g0058 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(517): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(908): Show |
1 | a0002c0003t0002g0059 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(915): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(909): Show |
1 | a0002c0003t0002g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(916): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(540): Show |
1 | a0005c0006t0002g0041 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(547): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(507): Show |
18 | a0001c0002t0002g0024 a0001c0002t0002g0067 a0002c0003t0002g0001 others(15): Show |
34 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(514): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(1071): Show |
1 | a0001c0002t0002g0146 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(1078): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(507): Show |
1 | a0002c0003t0002g0039 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(514): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(500): Show |
2 | a0001c0002t0002g0025 a0022c0029t0002g0101 |
3 | HG02258.hp1 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(507): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(511): Show |
1 | a0002c0003t0002g0068 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(518): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(507): Show |
1 | a0001c0002t0001g0258 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(514): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(536): Show |
1 | a0002c0003t0002g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(543): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(507): Show |
1 | a0007c0008t0002g0070 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(514): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(507): Show |
4 | a0002c0003t0002g0009 a0002c0003t0002g0042 a0007c0008t0002g0009 others(1): Show |
5 | HG00438.hp1 HG02083.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(514): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(506): Show |
1 | a0002c0003t0002g0071 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(513): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(507): Show |
1 | a0007c0008t0002g0072 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(514): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(506): Show |
1 | a0002c0003t0002g0016 | 2 | HG01261.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(513): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(506): Show |
1 | a0002c0003t0002g0073 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(513): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(506): Show |
1 | a0002c0003t0002g0074 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(513): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(552): Show |
1 | a0001c0002t0002g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(559): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(506): Show |
1 | a0002c0023t0002g0087 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(513): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(503): Show |
1 | a0002c0003t0002g0075 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(510): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(594): Show |
1 | a0001c0002t0002g0147 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(601): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(549): Show |
1 | a0002c0003t0002g0013 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(556): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(507): Show |
1 | a0003c0004t0002g0084 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(514): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(324): Show |
4 | a0004c0005t0001g0020 a0004c0005t0001g0104 a0004c0005t0001g0105 others(1): Show |
5 | HG02572.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(331): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(302): Show |
1 | a0004c0005t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(309): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(223): Show |
2 | a0004c0005t0001g0021 a0012c0028t0001g0108 |
3 | HG01109.hp2 HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.657+440_657+441ins others(230): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(464): Show |
3 | a0002c0003t0002g0005 a0002c0003t0002g0033 a0002c0003t0002g0035 |
6 | HG01978.hp1 HG01993.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(471): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(408): Show |
1 | a0001c0002t0002g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(415): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(284): Show |
1 | a0016c0027t0001g0110 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(291): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(397): Show |
1 | a0004c0005t0001g0109 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(404): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(479): Show |
1 | a0002c0010t0002g0076 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(486): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(475): Show |
1 | a0002c0010t0002g0077 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(482): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(535): Show |
1 | a0001c0002t0002g0149 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(542): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(535): Show |
1 | a0001c0002t0002g0150 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(542): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(534): Show |
2 | a0001c0002t0002g0026 a0001c0002t0002g0151 |
3 | NA18980.hp2 NA18984.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(541): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(492): Show |
1 | a0010c0012t0001g0153 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(499): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(883): Show |
1 | a0010c0012t0001g0152 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(890): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(493): Show |
1 | a0001c0002t0002g0154 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(500): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(537): Show |
1 | a0002c0003t0002g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(544): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(536): Show |
4 | a0001c0001t0001g0027 a0001c0001t0001g0156 a0002c0003t0002g0079 others(1): Show |
5 | HG02615.hp1 HG02683.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(543): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(479): Show |
1 | a0001c0002t0002g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(486): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(493): Show |
1 | a0001c0002t0002g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(500): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(514): Show |
2 | a0001c0002t0002g0159 a0001c0002t0002g0160 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(521): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(492): Show |
6 | a0001c0001t0001g0162 a0001c0002t0002g0161 a0001c0002t0002g0163 others(3): Show |
6 | HG01928.hp2 HG01993.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(499): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(477): Show |
1 | a0001c0002t0002g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.657+440_657+441ins others(484): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(535): Show |
1 | a0001c0001t0001g0167 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(542): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(438): Show |
1 | a0001c0002t0002g0168 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(445): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(479): Show |
1 | a0003c0004t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(486): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(478): Show |
6 | a0001c0002t0002g0169 a0001c0002t0002g0170 a0003c0004t0002g0007 others(3): Show |
9 | HG01069.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(485): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(474): Show |
1 | a0017c0015t0002g0171 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(481): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(22): Show |
2 | a0001c0013t0001g0172 a0001c0013t0001g0173 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.657+440_657+441ins others(29): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCCCT others(737): Show |
1 | a0001c0002t0001g0122 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(744): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720831 | T | TTCCCTTC others(467): Show |
1 | a0001c0001t0001g0246 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.657+441_657+442ins others(474): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720831 | ||||||
| chr9:127720832 | T | TCCCCCTT others(633): Show |
1 | a0001c0002t0002g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.657+440_657+441ins others(640): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720832 | ||||||
| chr9:127720835 | C | CCCT | 4 | a0001c0002t0001g0010 a0001c0002t0001g0114 a0001c0002t0001g0129 others(1): Show |
6 | HG02572.hp2 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+440_657+441ins others(3): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720835 | |||||||
| chr9:127720839 | T | TCCCTCCC others(443): Show |
3 | a0001c0002t0001g0010 a0001c0002t0001g0129 a0001c0002t0001g0130 |
5 | HG02572.hp2 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.657+448_657+449ins others(450): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720839 | ||||||
| chr9:127720839 | T | TCCCTCCC others(444): Show |
1 | a0001c0002t0001g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.657+448_657+449ins others(451): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720839 | ||||||
| chr9:127720847 | T | G | 1 | a0016c0027t0001g0110 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.657+452T>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720847 | |||||||
| chr9:127720874 | T | C | 1 | a0001c0002t0002g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.657+479T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720874 | |||||||
| chr9:127720881 | T | TCCCCTTT others(7): Show |
12 | a0001c0002t0001g0018 a0001c0002t0001g0092 a0001c0002t0001g0093 others(9): Show |
13 | HG01109.hp1 HG02135.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.657+492_657+493ins others(14): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720881 | ||||||
| chr9:127720881 | T | TCCCCTTT others(27): Show |
2 | a0001c0002t0001g0094 a0001c0002t0001g0095 |
2 | HG02165.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.657+492_657+493ins others(34): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127720881 | ||||||
| chr9:127720888 | C | T | 12 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(9): Show |
15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.657+493C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720888 | |||||||
| chr9:127720897 | T | C | 12 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(9): Show |
15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.657+502T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720897 | |||||||
| chr9:127720914 | C | T | 12 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(9): Show |
15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.657+519C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720914 | |||||||
| chr9:127720922 | T | TCCTCCC | 12 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(9): Show |
15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.657+527_657+528ins others(6): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720922 | |||||||
| chr9:127720934 | C | T | 13 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(10): Show |
16 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.657+539C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720934 | |||||||
| chr9:127720972 | C | T | 1 | a0006c0007t0001g0102 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.657+577C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127720972 | |||||||
| chr9:127721006 | A | G | 1 | a0001c0002t0002g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.657+611A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721006 | |||||||
| chr9:127721123 | G | A | 1 | a0002c0003t0002g0061 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.657+728G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721123 | |||||||
| chr9:127721263 | G | C | 14 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(11): Show |
17 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.657+868G>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721263 | |||||||
| chr9:127721283 | A | G | 1 | a0006c0007t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.657+888A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721283 | |||||||
| chr9:127721342 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.657+947C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721342 | |||||||
| chr9:127721413 | G | C | 9 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(6): Show |
11 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.657+1018G>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721413 | |||||||
| chr9:127721548 | C | T | 1 | a0001c0002t0001g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.657+1153C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721548 | |||||||
| chr9:127721552 | C | T | 172 | a0001c0001t0001g0027 a0001c0001t0001g0124 a0001c0001t0001g0156 others(169): Show |
215 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.657+1157C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721552 | |||||||
| chr9:127721649 | G | A | 2 | a0001c0013t0001g0172 a0001c0013t0001g0173 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.657+1254G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721649 | |||||||
| chr9:127721666 | T | A | 1 | a0001c0002t0002g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.657+1271T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721666 | |||||||
| chr9:127721667 | C | T | 1 | a0001c0002t0002g0259 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.657+1272C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721667 | |||||||
| chr9:127721738 | CTG | C | 9 | a0001c0002t0001g0018 a0001c0002t0001g0092 a0001c0002t0001g0093 others(6): Show |
10 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.657+1345_657+1346d others(4): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127721738 | ||||||
| chr9:127721791 | C | T | 6 | a0001c0002t0001g0118 a0001c0002t0001g0119 a0001c0002t0001g0120 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.658-1328C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127721791 | |||||||
| chr9:127722170 | C | T | 1 | a0001c0002t0001g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.658-949C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722170 | |||||||
| chr9:127722171 | T | G | 1 | a0001c0002t0001g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.658-948T>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722171 | |||||||
| chr9:127722243 | C | G | 2 | a0001c0002t0002g0067 a0014c0026t0002g0085 |
2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.658-876C>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722243 | |||||||
| chr9:127722263 | G | T | 2 | a0010c0012t0001g0152 a0010c0012t0001g0153 |
2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.658-856G>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722263 | |||||||
| chr9:127722378 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.658-741A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722378 | |||||||
| chr9:127722416 | T | G | 1 | a0001c0001t0001g0204 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.658-703T>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722416 | |||||||
| chr9:127722499 | T | C | 14 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(11): Show |
17 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.658-620T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722499 | |||||||
| chr9:127722749 | A | G | 1 | a0001c0013t0001g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.658-370A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722749 | |||||||
| chr9:127722807 | A | C | 1 | a0001c0002t0001g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.658-312A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722807 | |||||||
| chr9:127722816 | A | T | 1 | a0001c0002t0001g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.658-303A>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127722816 | |||||||
| chr9:127722967 | C | CA | 24 | a0001c0001t0001g0162 a0001c0001t0001g0178 a0001c0001t0001g0183 others(21): Show |
24 | HG01106.hp2 HG01243.hp1 HG01517.hp1 others(21): Show |
intron_variant | MODIFIER | c.658-137dupA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127722967 | ||||||
| chr9:127722967 | CA | C | 11 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(8): Show |
14 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.658-137delA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 127722967 | ||||||
| chr9:127723084 | T | C | 14 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(11): Show |
17 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.658-35T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | chr9 | 127723084 | |||||||
| chr9:127723339 | G | A | 122 | a0001c0002t0001g0258 a0001c0002t0002g0008 a0001c0002t0002g0022 others(119): Show |
158 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
splice_region_variant&intron_variant | LOW | c.872+6G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723339 | |||||||
| chr9:127723582 | G | A | 2 | a0001c0001t0001g0222 a0024c0018t0001g0201 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.872+249G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723582 | |||||||
| chr9:127723632 | C | G | 1 | a0006c0007t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.872+299C>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723632 | |||||||
| chr9:127723676 | G | A | 9 | a0001c0002t0001g0018 a0001c0002t0001g0092 a0001c0002t0001g0093 others(6): Show |
10 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.872+343G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723676 | |||||||
| chr9:127723794 | C | T | 1 | a0002c0003t0002g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.873-326C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723794 | |||||||
| chr9:127723838 | T | G | 3 | a0006c0007t0001g0019 a0006c0007t0001g0102 a0006c0007t0001g0103 |
4 | HG01884.hp1 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.873-282T>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723838 | |||||||
| chr9:127723842 | G | C | 4 | a0006c0007t0001g0019 a0006c0007t0001g0102 a0006c0007t0001g0103 others(1): Show |
5 | HG01884.hp1 HG02109.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.873-278G>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723842 | |||||||
| chr9:127723905 | C | CA | 127 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0194 others(124): Show |
163 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.873-202dupA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 127723905 | ||||||
| chr9:127723905 | C | CAA | 20 | a0001c0002t0001g0128 a0001c0002t0002g0022 a0001c0002t0002g0133 others(17): Show |
22 | HG01346.hp2 HG01358.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.873-203_873-202dup others(2): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 127723905 | ||||||
| chr9:127723905 | C | CAAAA | 8 | a0001c0002t0001g0018 a0001c0002t0001g0092 a0001c0002t0001g0093 others(5): Show |
9 | HG02155.hp1 HG02165.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.873-205_873-202dup others(4): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 127723905 | ||||||
| chr9:127723983 | A | G | 1 | a0002c0003t0002g0066 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.873-137A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127723983 | |||||||
| chr9:127724104 | A | ATG | 3 | a0001c0002t0002g0126 a0002c0003t0002g0036 a0022c0029t0002g0101 |
3 | HG01358.hp1 HG03239.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.873-16_873-15insTG | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127724104 | |||||||
| chr9:127724105 | C | T | 119 | a0001c0002t0001g0258 a0001c0002t0002g0008 a0001c0002t0002g0022 others(116): Show |
155 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.873-15C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127724105 | |||||||
| chr9:127724106 | G | C | 3 | a0001c0002t0002g0126 a0002c0003t0002g0036 a0022c0029t0002g0101 |
3 | HG01358.hp1 HG03239.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.873-14G>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | chr9 | 127724106 | |||||||
| chr9:127724106 | G | GC | 117 | a0001c0001t0001g0185 a0001c0001t0001g0233 a0001c0002t0001g0096 others(114): Show |
152 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
splice_region_variant&intron_variant | LOW | c.873-6dupC | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 127724106 | ||||||
| chr9:127724617 | A | T | 1 | a0011c0025t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1118-139A>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 8/13 | chr9 | 127724617 | |||||||
| chr9:127724636 | T | C | 148 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0092 others(145): Show |
187 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.1118-120T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 8/13 | chr9 | 127724636 | |||||||
| chr9:127724901 | C | T | 1 | a0002c0003t0002g0068 | 1 | NA19054.hp2 | splice_region_variant&intron_variant | LOW | c.1259+4C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127724901 | |||||||
| chr9:127724935 | C | T | 1 | a0002c0003t0002g0046 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1259+38C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127724935 | |||||||
| chr9:127724973 | C | T | 1 | a0001c0002t0002g0174 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1259+76C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127724973 | |||||||
| chr9:127724997 | C | G | 1 | a0001c0001t0001g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1259+100C>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127724997 | |||||||
| chr9:127725028 | C | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0234 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1259+131C>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725028 | |||||||
| chr9:127725115 | AATTTAAA others(6): Show |
A | 1 | a0001c0002t0002g0174 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1259+219_1259+231d others(15): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725115 | |||||||
| chr9:127725273 | C | CA | 24 | a0001c0001t0001g0090 a0001c0001t0001g0176 a0001c0001t0001g0177 others(21): Show |
24 | HG00544.hp1 HG00642.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1259+385dupA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 127725273 | ||||||
| chr9:127725411 | A | C | 1 | a0001c0002t0001g0129 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1259+514A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725411 | |||||||
| chr9:127725437 | G | A | 3 | a0001c0002t0001g0118 a0001c0002t0001g0119 a0001c0002t0001g0122 |
3 | HG02818.hp1 HG02896.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1259+540G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725437 | |||||||
| chr9:127725525 | C | G | 6 | a0004c0005t0001g0021 a0004c0005t0001g0105 a0004c0005t0001g0106 others(3): Show |
7 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1259+628C>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725525 | |||||||
| chr9:127725540 | G | A | 123 | a0001c0002t0001g0258 a0001c0002t0002g0008 a0001c0002t0002g0022 others(120): Show |
159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1259+643G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725540 | |||||||
| chr9:127725563 | C | CA | 38 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0091 others(35): Show |
42 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1260-653dupA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 127725563 | ||||||
| chr9:127725563 | CA | C | 16 | a0001c0001t0001g0031 a0001c0001t0001g0184 a0001c0002t0001g0018 others(13): Show |
20 | HG01069.hp1 HG01070.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1260-653delA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 127725563 | ||||||
| chr9:127725563 | CAA | C | 44 | a0001c0002t0001g0118 a0001c0002t0001g0128 a0001c0002t0001g0130 others(41): Show |
50 | HG00423.hp2 HG00621.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1260-654_1260-653d others(4): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 127725563 | ||||||
| chr9:127725563 | CAAA | C | 90 | a0001c0002t0001g0010 a0001c0002t0001g0119 a0001c0002t0001g0120 others(87): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1260-655_1260-653d others(5): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 127725563 | ||||||
| chr9:127725590 | T | G | 8 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(5): Show |
10 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1260-649T>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725590 | |||||||
| chr9:127725626 | G | A | 8 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(5): Show |
10 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1260-613G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725626 | |||||||
| chr9:127725906 | GCTTTTCT others(17): Show |
G | 1 | a0012c0028t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1260-330_1260-307d others(26): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 127725906 | ||||||
| chr9:127725932 | T | A | 1 | a0012c0028t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1260-307T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725932 | |||||||
| chr9:127725954 | T | A | 1 | a0012c0028t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1260-285T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127725954 | |||||||
| chr9:127726007 | C | T | 2 | a0004c0005t0001g0021 a0012c0028t0001g0108 |
3 | HG01109.hp2 HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1260-232C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127726007 | |||||||
| chr9:127726091 | G | A | 1 | a0011c0025t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1260-148G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127726091 | |||||||
| chr9:127726215 | C | T | 148 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0092 others(145): Show |
187 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.1260-24C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 9/13 | chr9 | 127726215 | |||||||
| chr9:127726614 | C | A | 9 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(6): Show |
11 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1425+210C>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726614 | |||||||
| chr9:127726643 | C | G | 9 | a0001c0002t0001g0018 a0001c0002t0001g0092 a0001c0002t0001g0093 others(6): Show |
10 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.1425+239C>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726643 | |||||||
| chr9:127726652 | G | A | 26 | a0001c0002t0001g0258 a0001c0002t0002g0008 a0001c0002t0002g0023 others(23): Show |
31 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1425+248G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726652 | |||||||
| chr9:127726712 | CG | C | 3 | a0001c0002t0001g0114 a0001c0002t0002g0149 a0012c0028t0001g0108 |
3 | HG01109.hp2 HG03098.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1426-255delG | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726712 | ||||||
| chr9:127726728 | C | T | 1 | a0002c0024t0001g0032 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1426-242C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726728 | |||||||
| chr9:127726766 | C | T | 13 | a0001c0002t0001g0010 a0001c0002t0001g0114 a0001c0002t0001g0118 others(10): Show |
15 | HG02572.hp2 HG02630.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.1426-204C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726766 | |||||||
| chr9:127726782 | T | A | 1 | a0012c0028t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1426-188T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726782 | |||||||
| chr9:127726787 | CA | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0028 others(43): Show |
53 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1426-149delA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726787 | ||||||
| chr9:127726787 | CAA | C | 35 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(32): Show |
51 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.1426-150_1426-149d others(4): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726787 | ||||||
| chr9:127726787 | CAAA | C | 6 | a0001c0001t0001g0027 a0001c0001t0001g0100 a0001c0001t0001g0180 others(3): Show |
7 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1426-151_1426-149d others(5): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726787 | ||||||
| chr9:127726787 | CAAAAA | C | 9 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(6): Show |
11 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1426-153_1426-149d others(7): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726787 | ||||||
| chr9:127726787 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0216 |
2 | HG00621.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1426-160_1426-149d others(14): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726787 | ||||||
| chr9:127726787 | CAAAAAAA others(6): Show |
C | 1 | a0008c0009t0001g0217 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1426-161_1426-149d others(15): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726787 | ||||||
| chr9:127726787 | CAAAAAAA others(16): Show |
C | 149 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0092 others(146): Show |
188 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1426-171_1426-149d others(25): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726787 | ||||||
| chr9:127726805 | A | C | 1 | a0011c0025t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1426-165A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726805 | |||||||
| chr9:127726807 | A | C | 1 | a0012c0028t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1426-163A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726807 | |||||||
| chr9:127726808 | A | C | 8 | a0004c0005t0001g0020 a0004c0005t0001g0021 a0004c0005t0001g0104 others(5): Show |
10 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1426-162A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726808 | |||||||
| chr9:127726817 | A | C | 160 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0092 others(157): Show |
201 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.1426-153A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726817 | |||||||
| chr9:127726890 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0256 |
2 | HG00099.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1426-80G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726890 | |||||||
| chr9:127726910 | C | T | 149 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0092 others(146): Show |
188 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1426-60C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | chr9 | 127726910 | |||||||
| chr9:127726953 | A | AC | 8 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0002t0002g0143 others(5): Show |
8 | HG00741.hp2 HG01358.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1426-12dupC | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 127726953 | ||||||
| chr9:127727482 | C | A | 1 | a0001c0002t0002g0174 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1764+17C>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727482 | |||||||
| chr9:127727498 | T | A | 1 | a0012c0028t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+33T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727498 | |||||||
| chr9:127727515 | G | T | 1 | a0012c0028t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+50G>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727515 | |||||||
| chr9:127727625 | G | A | 1 | a0002c0003t0002g0065 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1764+160G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727625 | |||||||
| chr9:127727701 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1764+236C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727701 | |||||||
| chr9:127727763 | A | T | 1 | a0012c0028t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+298A>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727763 | |||||||
| chr9:127727765 | T | A | 1 | a0002c0024t0001g0032 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1764+300T>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727765 | |||||||
| chr9:127727781 | C | T | 1 | a0001c0002t0002g0147 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1764+316C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727781 | |||||||
| chr9:127727797 | CA | C | 149 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0092 others(146): Show |
188 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1764+334delA | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr9 | 127727797 | ||||||
| chr9:127727821 | A | C | 1 | a0012c0028t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+356A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727821 | |||||||
| chr9:127727829 | G | A | 1 | a0002c0003t0002g0013 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1764+364G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727829 | |||||||
| chr9:127727845 | C | T | 4 | a0001c0002t0002g0145 a0001c0002t0002g0161 a0001c0002t0002g0164 others(1): Show |
4 | HG01928.hp2 HG01993.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1764+380C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727845 | |||||||
| chr9:127727846 | G | A | 1 | a0001c0002t0002g0141 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1764+381G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727846 | |||||||
| chr9:127727914 | C | A | 1 | a0012c0028t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+449C>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727914 | |||||||
| chr9:127727933 | G | A | 5 | a0001c0001t0001g0211 a0001c0001t0001g0215 a0001c0001t0001g0218 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1764+468G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127727933 | |||||||
| chr9:127728087 | A | C | 1 | a0012c0028t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+622A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728087 | |||||||
| chr9:127728112 | A | AC | 13 | a0001c0001t0001g0162 a0001c0001t0001g0205 a0001c0001t0001g0206 others(10): Show |
13 | HG00423.hp2 HG00438.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1764+649dupC | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr9 | 127728112 | ||||||
| chr9:127728113 | C | A | 2 | a0010c0012t0001g0152 a0010c0012t0001g0153 |
2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1764+648C>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728113 | |||||||
| chr9:127728115 | G | C | 1 | a0012c0028t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+650G>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728115 | |||||||
| chr9:127728134 | A | G | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1764+669A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728134 | |||||||
| chr9:127728229 | G | A | 12 | a0001c0001t0001g0214 a0001c0002t0001g0018 a0001c0002t0001g0092 others(9): Show |
13 | HG01934.hp1 HG02135.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.1764+764G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728229 | |||||||
| chr9:127728350 | T | C | 4 | a0001c0002t0002g0022 a0001c0002t0002g0133 a0001c0002t0002g0134 others(1): Show |
5 | HG02109.hp1 HG02622.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1764+885T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728350 | |||||||
| chr9:127728362 | C | T | 1 | a0001c0002t0001g0098 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1764+897C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728362 | |||||||
| chr9:127728381 | C | T | 1 | a0002c0003t0002g0035 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1764+916C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728381 | |||||||
| chr9:127728414 | TCTA | T | 13 | a0001c0002t0001g0010 a0001c0002t0001g0114 a0001c0002t0001g0118 others(10): Show |
15 | HG02572.hp2 HG02630.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.1764+952_1764+954d others(5): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr9 | 127728414 | ||||||
| chr9:127728639 | A | G | 1 | a0018c0022t0002g0236 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1765-942A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728639 | |||||||
| chr9:127728813 | A | G | 5 | a0001c0001t0001g0027 a0001c0001t0001g0156 a0001c0001t0001g0162 others(2): Show |
6 | HG02615.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1765-768A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728813 | |||||||
| chr9:127728958 | C | T | 9 | a0001c0002t0001g0018 a0001c0002t0001g0092 a0001c0002t0001g0093 others(6): Show |
10 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.1765-623C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127728958 | |||||||
| chr9:127729082 | G | A | 11 | a0001c0002t0001g0010 a0001c0002t0001g0114 a0001c0002t0001g0118 others(8): Show |
13 | HG02572.hp2 HG02630.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1765-499G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127729082 | |||||||
| chr9:127729204 | G | A | 145 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0092 others(142): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1765-377G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127729204 | |||||||
| chr9:127729259 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1765-322T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127729259 | |||||||
| chr9:127729260 | C | T | 1 | a0002c0003t0002g0035 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1765-321C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127729260 | |||||||
| chr9:127729354 | T | C | 164 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0002t0001g0010 others(161): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.1765-227T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127729354 | |||||||
| chr9:127729364 | C | T | 2 | a0001c0013t0001g0172 a0001c0013t0001g0173 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1765-217C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127729364 | |||||||
| chr9:127729447 | T | C | 149 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0092 others(146): Show |
188 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1765-134T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 12/13 | chr9 | 127729447 | |||||||
| chr9:127729719 | A | G | 149 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0092 others(146): Show |
188 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1852+51A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127729719 | |||||||
| chr9:127729760 | G | A | 124 | a0001c0002t0001g0258 a0001c0002t0002g0008 a0001c0002t0002g0022 others(121): Show |
160 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1852+92G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127729760 | |||||||
| chr9:127729782 | TG | T | 5 | a0001c0002t0001g0010 a0001c0002t0001g0114 a0001c0002t0001g0128 others(2): Show |
7 | HG02572.hp2 HG02630.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1852+117delG | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr9 | 127729782 | ||||||
| chr9:127729812 | G | A | 2 | a0001c0013t0001g0172 a0001c0013t0001g0173 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1852+144G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127729812 | |||||||
| chr9:127729924 | C | G | 1 | a0001c0002t0001g0098 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1852+256C>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127729924 | |||||||
| chr9:127730042 | G | C | 1 | a0016c0027t0001g0110 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1852+374G>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127730042 | |||||||
| chr9:127730105 | A | C | 1 | a0016c0027t0001g0110 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1852+437A>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127730105 | |||||||
| chr9:127730115 | A | G | 2 | a0010c0012t0001g0152 a0010c0012t0001g0153 |
2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1852+447A>G | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127730115 | |||||||
| chr9:127730299 | G | A | 11 | a0001c0002t0001g0010 a0001c0002t0001g0114 a0001c0002t0001g0118 others(8): Show |
13 | HG02572.hp2 HG02630.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1853-337G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127730299 | |||||||
| chr9:127730345 | G | A | 2 | a0006c0007t0001g0019 a0006c0007t0001g0102 |
3 | HG01884.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1853-291G>A | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127730345 | |||||||
| chr9:127730492 | C | T | 11 | a0001c0002t0001g0010 a0001c0002t0001g0114 a0001c0002t0001g0118 others(8): Show |
13 | HG02572.hp2 HG02630.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1853-144C>T | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127730492 | |||||||
| chr9:127730518 | T | C | 2 | a0001c0002t0002g0056 a0001c0002t0002g0057 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1853-118T>C | TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 13/13 | chr9 | 127730518 |