Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80222 |
| ensemblid | ENSG00000143374.18 |
| hgncid | 30740 |
| symbol | TARS2 |
| name | threonyl-tRNA synthetase 2, mitochondrial |
| refseq_nuc | NM_025150.5 |
| refseq_prot | NP_079426.2 |
| ensembl_nuc | ENST00000369064.8 |
| ensembl_prot | ENSP00000358060.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 150487419 |
| end | 150507602 |
| strand | + |
| ver | v1.2 |
| region | chr1:150487419-150507602 |
| region5000 | chr1:150482419-150512602 |
| regionname0 | TARS2_chr1_150487419_150507602 |
| regionname5000 | TARS2_chr1_150482419_150512602 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 718 | 398 | 90 | 68 | 180 | 14 | 44 | 137 | TARS2_chr1_150482419_150512602 | TARS2 | MALYQ others(713): Show |
chr1 | 150482419 | 150512602 |
| a0002 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | MALYQ others(713): Show |
chr1 | 150482419 | 150512602 |
| a0003 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | MALCQ others(713): Show |
chr1 | 150482419 | 150512602 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2154 | 346 | 73 | 57 | 157 | 14 | 43 | TARS2_chr1_150482419_150512602 | TARS2 | ATGGC others(2149): Show |
chr1 | 150482419 | 150512602 | ||
| a0001c0002 | 0/0 | 2154 | 39 | 10 | 7 | 22 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | ATGGC others(2149): Show |
chr1 | 150482419 | 150512602 | ||
| a0001c0003 | 0/0 | 2154 | 7 | 6 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | ATGGC others(2149): Show |
chr1 | 150482419 | 150512602 | ||
| a0001c0004 | 0/0 | 2154 | 5 | 0 | 3 | 1 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | ATGGC others(2149): Show |
chr1 | 150482419 | 150512602 | ||
| a0001c0006 | 0/0 | 2154 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | ATGGC others(2149): Show |
chr1 | 150482419 | 150512602 | ||
| a0002c0005 | 0/0 | 2154 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | ATGGC others(2149): Show |
chr1 | 150482419 | 150512602 | ||
| a0003c0007 | 0/0 | 2154 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | ATGGC others(2149): Show |
chr1 | 150482419 | 150512602 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2727 | 207 | 35 | 32 | 106 | 7 | 26 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2722): Show |
chr1 | 150482419 | 150512602 |
| a0001c0001t0002 | 0/0 | 2727 | 83 | 2 | 17 | 45 | 5 | 14 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2722): Show |
chr1 | 150482419 | 150512602 |
| a0001c0001t0004 | 0/0 | 2728 | 15 | 15 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2723): Show |
chr1 | 150482419 | 150512602 |
| a0001c0001t0005 | 0/0 | 2723 | 13 | 13 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2718): Show |
chr1 | 150482419 | 150512602 |
| a0001c0001t0006 | 0/0 | 2735 | 11 | 7 | 1 | 0 | 2 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2730): Show |
chr1 | 150482419 | 150512602 |
| a0001c0001t0007 | 0/1 | 2727 | 7 | 0 | 5 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2722): Show |
chr1 | 150482419 | 150512602 |
| a0001c0001t0010 | 0/0 | 2727 | 3 | 0 | 0 | 3 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2722): Show |
chr1 | 150482419 | 150512602 |
| a0001c0001t0011 | 0/0 | 2727 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2722): Show |
chr1 | 150482419 | 150512602 |
| a0001c0001t0012 | 0/0 | 2735 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2730): Show |
chr1 | 150482419 | 150512602 |
| a0001c0001t0013 | 0/0 | 2727 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2722): Show |
chr1 | 150482419 | 150512602 |
| a0001c0001t0014 | 0/0 | 2727 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2722): Show |
chr1 | 150482419 | 150512602 |
| a0001c0001t0015 | 0/0 | 2727 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2722): Show |
chr1 | 150482419 | 150512602 |
| a0001c0001t0016 | 0/0 | 2727 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2722): Show |
chr1 | 150482419 | 150512602 |
| a0001c0001t0017 | 0/0 | 2724 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | TGAGG others(2719): Show |
chr1 | 150482419 | 150512602 |
| a0001c0002t0003 | 0/0 | 2724 | 33 | 4 | 7 | 22 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | TGAGG others(2719): Show |
chr1 | 150482419 | 150512602 |
| a0001c0002t0009 | 0/0 | 2724 | 5 | 5 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | TGAGG others(2719): Show |
chr1 | 150482419 | 150512602 |
| a0001c0002t0018 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | TGAGG others(2719): Show |
chr1 | 150482419 | 150512602 |
| a0001c0003t0008 | 0/0 | 2727 | 7 | 6 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2722): Show |
chr1 | 150482419 | 150512602 |
| a0001c0004t0002 | 0/0 | 2727 | 4 | 0 | 3 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2722): Show |
chr1 | 150482419 | 150512602 |
| a0001c0004t0007 | 0/0 | 2727 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2722): Show |
chr1 | 150482419 | 150512602 |
| a0001c0006t0009 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | TGAGG others(2719): Show |
chr1 | 150482419 | 150512602 |
| a0002c0005t0001 | 0/0 | 2727 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2722): Show |
chr1 | 150482419 | 150512602 |
| a0003c0007t0001 | 0/0 | 2727 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | GTTTG others(2722): Show |
chr1 | 150482419 | 150512602 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 19 | 2 | 1 | 12 | 3 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 4 | 4 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0004 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0005g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0006g0037 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0006g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0007g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0007g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0007g0296 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0007g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0007g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0007g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0010g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0010g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0011g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0012g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0013g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0014g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0015g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0016g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0001t0017g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0009g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0009g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0002t0018g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0003t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0003t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0003t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0003t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0003t0008g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0003t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0003t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0004t0002g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0004t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0004t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0004t0007g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0001c0006t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0002c0005t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| a0003c0007t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0037 | EUR | GBR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0222 | EUR | GBR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0233 | EUR | GBR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | FIN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0189 | EAS | CHS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0191 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0013 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0295 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01167 | hp2 | a0001 | c0004 | t0002 | g0035 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0039 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01169 | hp2 | a0001 | c0004 | t0002 | g0248 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01175 | hp1 | a0001 | c0003 | t0008 | g0195 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0299 | AMR | PUR | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0297 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01257 | hp1 | a0001 | c0001 | t0007 | g0298 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0184 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01433 | hp2 | a0001 | c0001 | t0017 | g0174 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01496 | hp2 | a0001 | c0001 | t0014 | g0087 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0232 | EUR | IBS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01891 | hp1 | a0001 | c0002 | t0009 | g0181 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01928 | hp2 | a0001 | c0002 | t0003 | g0187 | AMR | PEL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0272 | AMR | PEL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01978 | hp1 | a0001 | c0002 | t0003 | g0192 | AMR | PEL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02004 | hp1 | a0001 | c0004 | t0002 | g0215 | AMR | PEL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02040 | hp1 | a0002 | c0005 | t0001 | g0120 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02056 | hp1 | a0001 | c0001 | t0013 | g0251 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02071 | hp2 | a0001 | c0001 | t0010 | g0090 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02135 | hp2 | a0001 | c0001 | t0016 | g0103 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02145 | hp1 | a0001 | c0002 | t0009 | g0175 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | CDX | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | CDX | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CDX | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0277 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0185 | AMR | PEL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02280 | hp2 | a0001 | c0002 | t0009 | g0182 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0281 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0285 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0266 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0289 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0286 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0263 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0264 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0265 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02630 | hp2 | a0001 | c0003 | t0008 | g0194 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02647 | hp1 | a0001 | c0003 | t0008 | g0041 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0269 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0290 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0274 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02809 | hp2 | a0001 | c0002 | t0018 | g0170 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02895 | hp1 | a0001 | c0003 | t0008 | g0197 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02896 | hp1 | a0001 | c0001 | t0012 | g0280 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02896 | hp2 | a0001 | c0003 | t0008 | g0042 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0294 | AFR | ESN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0262 | AFR | ESN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0278 | AFR | ESN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02970 | hp2 | a0001 | c0002 | t0003 | g0173 | AFR | ESN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02976 | hp1 | a0001 | c0003 | t0008 | g0196 | AFR | ESN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0275 | AFR | MSL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0268 | AFR | ESN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ESN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0270 | AFR | ESN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0292 | AFR | ESN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03209 | hp1 | a0001 | c0002 | t0009 | g0172 | AFR | MSL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03209 | hp2 | a0001 | c0003 | t0008 | g0193 | AFR | MSL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | MSL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0039 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0288 | AFR | MSL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0276 | AFR | MSL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0284 | AFR | MSL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0279 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | MSL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | BEB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | BEB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | BEB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG04199 | hp1 | a0001 | c0004 | t0002 | g0035 | SAS | STU | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG04228 | hp1 | a0001 | c0001 | t0011 | g0094 | SAS | STU | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | STU | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | YRI | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18942 | hp2 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18948 | hp2 | a0001 | c0002 | t0003 | g0013 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0178 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18956 | hp2 | a0001 | c0002 | t0003 | g0013 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18960 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18961 | hp2 | a0001 | c0002 | t0003 | g0180 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18964 | hp1 | a0001 | c0004 | t0007 | g0198 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18965 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18967 | hp2 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18969 | hp2 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18973 | hp2 | a0003 | c0007 | t0001 | g0002 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18974 | hp1 | a0001 | c0001 | t0015 | g0088 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18980 | hp2 | a0001 | c0001 | t0010 | g0111 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18983 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0179 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18999 | hp1 | a0001 | c0002 | t0003 | g0183 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19001 | hp2 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19003 | hp1 | a0001 | c0002 | t0003 | g0176 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19004 | hp1 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19005 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | LWK | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0282 | AFR | LWK | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19062 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19067 | hp2 | a0001 | c0002 | t0003 | g0190 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19070 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19087 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0028 | AFR | YRI | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0028 | AFR | ASW | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0037 | AFR | ASW | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0226 | EUR | TSI | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0223 | EUR | TSI | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0273 | EUR | TSI | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | GIH | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02109 | hp1 | a0001 | c0006 | t0009 | g0169 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02109 | hp2 | a0001 | c0002 | t0009 | g0171 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02486 | hp1 | a0001 | c0002 | t0003 | g0168 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0293 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0267 | AFR | MSL | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | USA | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0283 | AFR | USA | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0296 | REF | REF | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0076 | REF | REF | TARS2_chr1_150482419_150512602 | TARS2 | chr1 | 150482419 | 150512602 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:150487461 | A | G | 1 | a0003 | 1 | NA18973.hp2 | missense_variant | MODERATE | c.11A>G | p.Tyr4Cys | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 1/18 | 43/2727 | 11/2157 | 4/718 | chr1 | 150487461 | |||
| chr1:150498967 | G | A | 1 | a0002 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.1472G>A | p.Arg491His | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 12/18 | 1504/2727 | 1472/2157 | 491/718 | chr1 | 150498967 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:150487872 | C | T | 2 | a0001c0002 a0001c0006 |
40 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(37): Show |
synonymous_variant | LOW | c.81C>T | p.Thr27Thr | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 2/18 | 113/2727 | 81/2157 | 27/718 | chr1 | 150487872 | |||
| chr1:150497706 | A | G | 1 | a0001c0003 | 7 | HG01175.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
synonymous_variant | LOW | c.1197A>G | p.Thr399Thr | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/18 | 1229/2727 | 1197/2157 | 399/718 | chr1 | 150497706 | |||
| chr1:150498580 | C | T | 1 | a0001c0004 | 5 | HG01167.hp2 HG01169.hp2 HG02004.hp1 others(2): Show |
synonymous_variant | LOW | c.1317C>T | p.Ala439Ala | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 11/18 | 1349/2727 | 1317/2157 | 439/718 | chr1 | 150498580 | |||
| chr1:150507010 | G | A | 1 | a0001c0006 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.2103G>A | p.Gln701Gln | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 18/18 | 2135/2727 | 2103/2157 | 701/718 | chr1 | 150507010 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:150487425 | G | A | 1 | a0001c0001t0011 | 1 | HG04228.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 1/18 | 26 | chr1 | 150487425 | ||||||
| chr1:150487449 | A | G | 1 | a0001c0001t0016 | 1 | HG02135.hp2 | 5_prime_UTR_variant | MODIFIER | c.-2A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 1/18 | 2 | chr1 | 150487449 | ||||||
| chr1:150507271 | C | CA | 1 | a0001c0001t0004 | 15 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*216dupA | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 18/18 | 217 | INFO_REALIGN_3_PRIME | chr1 | 150507271 | |||||
| chr1:150507345 | G | A | 2 | a0001c0001t0012 a0001c0001t0013 |
2 | HG02056.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*281G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 18/18 | 281 | chr1 | 150507345 | ||||||
| chr1:150507366 | A | G | 3 | a0001c0002t0009 a0001c0002t0018 a0001c0006t0009 |
7 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*302A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 18/18 | 302 | chr1 | 150507366 | ||||||
| chr1:150507373 | C | T | 1 | a0001c0001t0010 | 3 | HG02071.hp2 NA18965.hp2 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*309C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 18/18 | 309 | chr1 | 150507373 | ||||||
| chr1:150507375 | C | T | 1 | a0001c0001t0017 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*311C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 18/18 | 311 | chr1 | 150507375 | ||||||
| chr1:150507425 | C | T | 4 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0015 others(1): Show |
89 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*361C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 18/18 | 361 | chr1 | 150507425 | ||||||
| chr1:150507438 | A | G | 1 | a0001c0003t0008 | 7 | HG01175.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*374A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 18/18 | 374 | chr1 | 150507438 | ||||||
| chr1:150507441 | C | T | 1 | a0001c0001t0014 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*377C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 18/18 | 377 | chr1 | 150507441 | ||||||
| chr1:150507501 | A | G | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(11): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*437A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 18/18 | 437 | chr1 | 150507501 | ||||||
| chr1:150507566 | C | CTAAATAA others(1): Show |
2 | a0001c0001t0006 a0001c0001t0012 |
12 | HG00099.hp1 HG01952.hp2 HG02258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*521_*528dupAATAAA others(2): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 18/18 | 529 | INFO_REALIGN_3_PRIME | chr1 | 150507566 | |||||
| chr1:150507566 | CTAAA | C | 1 | a0001c0001t0005 | 13 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*525_*528delAATA | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 18/18 | 525 | INFO_REALIGN_3_PRIME | chr1 | 150507566 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:150487577 | A | C | 1 | a0001c0001t0002g0304 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.66+61A>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 1/17 | chr1 | 150487577 | |||||||
| chr1:150487621 | G | A | 2 | a0001c0003t0008g0041 a0001c0003t0008g0042 |
2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.66+105G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 1/17 | chr1 | 150487621 | |||||||
| chr1:150487651 | T | TCTAA | 6 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0300 others(3): Show |
9 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+136_66+139dupCT others(2): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 150487651 | ||||||
| chr1:150487692 | A | G | 158 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0221 others(155): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.67-166A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 1/17 | chr1 | 150487692 | |||||||
| chr1:150487833 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.67-25C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 1/17 | chr1 | 150487833 | |||||||
| chr1:150487850 | C | A | 1 | a0001c0001t0001g0043 | 1 | NA18977.hp1 | splice_region_variant&intron_variant | LOW | c.67-8C>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 1/17 | chr1 | 150487850 | |||||||
| chr1:150488062 | G | T | 1 | a0001c0001t0001g0016 | 3 | HG02280.hp1 HG02970.hp1 HG03130.hp2 |
splice_region_variant&intron_variant | LOW | c.263+8G>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 2/17 | chr1 | 150488062 | |||||||
| chr1:150488218 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.263+164A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 2/17 | chr1 | 150488218 | |||||||
| chr1:150488366 | A | C | 41 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(38): Show |
46 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.263+312A>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 2/17 | chr1 | 150488366 | |||||||
| chr1:150488374 | C | T | 41 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(38): Show |
46 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.263+320C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 2/17 | chr1 | 150488374 | |||||||
| chr1:150488378 | GTCCTTTC others(3): Show |
G | 1 | a0001c0001t0001g0044 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.263+325_263+334del others(10): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 2/17 | chr1 | 150488378 | |||||||
| chr1:150488379 | T | G | 74 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(71): Show |
91 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.263+325T>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 2/17 | chr1 | 150488379 | |||||||
| chr1:150488462 | G | A | 11 | a0001c0001t0005g0015 a0001c0001t0005g0262 a0001c0001t0005g0263 others(8): Show |
13 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.263+408G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 2/17 | chr1 | 150488462 | |||||||
| chr1:150488469 | T | TTTCTCTC | 74 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(71): Show |
91 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.263+420_263+421ins others(7): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 150488469 | ||||||
| chr1:150488711 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-253A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 2/17 | chr1 | 150488711 | |||||||
| chr1:150488842 | A | G | 2 | a0001c0001t0002g0014 a0001c0001t0002g0036 |
5 | NA18951.hp1 NA18955.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-122A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 2/17 | chr1 | 150488842 | |||||||
| chr1:150489285 | AC | A | 30 | a0001c0001t0017g0174 a0001c0002t0003g0003 a0001c0002t0003g0013 others(27): Show |
41 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.387+199delC | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | chr1 | 150489285 | |||||||
| chr1:150489325 | A | G | 5 | a0001c0001t0007g0039 a0001c0001t0007g0295 a0001c0001t0007g0297 others(2): Show |
6 | HG01109.hp2 HG01168.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+238A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | chr1 | 150489325 | |||||||
| chr1:150489374 | G | A | 1 | a0001c0004t0007g0198 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.387+287G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | chr1 | 150489374 | |||||||
| chr1:150489397 | G | T | 5 | a0001c0001t0007g0039 a0001c0001t0007g0295 a0001c0001t0007g0297 others(2): Show |
6 | HG01109.hp2 HG01168.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+310G>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | chr1 | 150489397 | |||||||
| chr1:150489528 | C | T | 11 | a0001c0001t0001g0043 a0001c0001t0001g0155 a0001c0001t0001g0156 others(8): Show |
11 | HG00597.hp1 HG02027.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.387+441C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | chr1 | 150489528 | |||||||
| chr1:150489612 | C | G | 30 | a0001c0001t0017g0174 a0001c0002t0003g0003 a0001c0002t0003g0013 others(27): Show |
41 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.387+525C>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | chr1 | 150489612 | |||||||
| chr1:150489770 | C | T | 1 | a0001c0001t0002g0261 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.387+683C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | chr1 | 150489770 | |||||||
| chr1:150489858 | C | T | 1 | a0001c0001t0002g0260 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.388-743C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | chr1 | 150489858 | |||||||
| chr1:150489874 | G | A | 1 | a0001c0001t0007g0295 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.388-727G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | chr1 | 150489874 | |||||||
| chr1:150489921 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.388-680G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | chr1 | 150489921 | |||||||
| chr1:150490039 | G | A | 11 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(8): Show |
11 | NA18955.hp2 NA18957.hp1 NA18965.hp1 others(8): Show |
intron_variant | MODIFIER | c.388-562G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | chr1 | 150490039 | |||||||
| chr1:150490114 | C | CT | 22 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0026 others(19): Show |
27 | HG00673.hp1 HG00735.hp2 HG01981.hp1 others(24): Show |
intron_variant | MODIFIER | c.388-465dupT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 150490114 | ||||||
| chr1:150490114 | C | CTT | 79 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(76): Show |
97 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.388-466_388-465dup others(2): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 150490114 | ||||||
| chr1:150490114 | C | CTTT | 33 | a0001c0001t0002g0209 a0001c0001t0002g0253 a0001c0001t0002g0254 others(30): Show |
44 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.388-467_388-465dup others(3): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 150490114 | ||||||
| chr1:150490114 | C | CTTTT | 34 | a0001c0001t0002g0259 a0001c0001t0004g0038 a0001c0001t0004g0283 others(31): Show |
37 | HG00642.hp2 HG01891.hp2 HG01978.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-468_388-465dup others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 150490114 | ||||||
| chr1:150490114 | CT | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0046 a0001c0001t0001g0047 others(3): Show |
7 | HG02135.hp1 NA18961.hp1 NA18990.hp2 others(4): Show |
intron_variant | MODIFIER | c.388-465delT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 150490114 | ||||||
| chr1:150490315 | C | G | 7 | a0001c0003t0008g0041 a0001c0003t0008g0042 a0001c0003t0008g0193 others(4): Show |
7 | HG01175.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-286C>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | chr1 | 150490315 | |||||||
| chr1:150490335 | C | T | 152 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(149): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.388-266C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | chr1 | 150490335 | |||||||
| chr1:150490427 | T | A | 11 | a0001c0001t0005g0015 a0001c0001t0005g0262 a0001c0001t0005g0263 others(8): Show |
13 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.388-174T>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 3/17 | chr1 | 150490427 | |||||||
| chr1:150491026 | A | C | 1 | a0001c0001t0001g0141 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.512+301A>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 4/17 | chr1 | 150491026 | |||||||
| chr1:150491046 | CACTTTCT others(18): Show |
C | 1 | a0001c0001t0001g0050 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.512+323_513-322del others(25): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 150491046 | ||||||
| chr1:150491050 | T | C | 41 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(38): Show |
46 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.512+325T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 4/17 | chr1 | 150491050 | |||||||
| chr1:150491054 | C | CAA | 30 | a0001c0001t0017g0174 a0001c0002t0003g0003 a0001c0002t0003g0013 others(27): Show |
41 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.513-331_513-330dup others(2): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 150491054 | ||||||
| chr1:150491054 | CA | C | 42 | a0001c0001t0001g0005 a0001c0001t0004g0038 a0001c0001t0004g0275 others(39): Show |
47 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.513-330delA | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 150491054 | ||||||
| chr1:150491061 | AAAAC | A | 78 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(75): Show |
95 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.513-329_513-326del others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 150491061 | ||||||
| chr1:150491296 | C | G | 41 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(38): Show |
46 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.513-98C>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 4/17 | chr1 | 150491296 | |||||||
| chr1:150491734 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.695+72G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 6/17 | chr1 | 150491734 | |||||||
| chr1:150491792 | AT | A | 32 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0017g0174 others(29): Show |
43 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.695+142delT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 150491792 | ||||||
| chr1:150491817 | C | T | 7 | a0001c0003t0008g0041 a0001c0003t0008g0042 a0001c0003t0008g0193 others(4): Show |
7 | HG01175.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.695+155C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 6/17 | chr1 | 150491817 | |||||||
| chr1:150491835 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.695+173C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 6/17 | chr1 | 150491835 | |||||||
| chr1:150491855 | C | G | 5 | a0001c0001t0007g0039 a0001c0001t0007g0295 a0001c0001t0007g0297 others(2): Show |
6 | HG01109.hp2 HG01168.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+193C>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 6/17 | chr1 | 150491855 | |||||||
| chr1:150491961 | G | GT | 27 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0050 others(24): Show |
27 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.695+322dupT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 150491961 | ||||||
| chr1:150491961 | G | GTT | 80 | a0001c0001t0001g0049 a0001c0001t0001g0139 a0001c0001t0001g0221 others(77): Show |
99 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.695+321_695+322dup others(2): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 150491961 | ||||||
| chr1:150491961 | G | GTTT | 28 | a0001c0001t0002g0036 a0001c0001t0002g0207 a0001c0001t0002g0208 others(25): Show |
30 | HG00741.hp2 HG01081.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.695+320_695+322dup others(3): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 150491961 | ||||||
| chr1:150491961 | GT | G | 13 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(10): Show |
13 | HG00280.hp2 HG00438.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.695+322delT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 150491961 | ||||||
| chr1:150491961 | GTT | G | 22 | a0001c0001t0017g0174 a0001c0002t0003g0003 a0001c0002t0003g0013 others(19): Show |
33 | HG00642.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.695+321_695+322del others(2): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 150491961 | ||||||
| chr1:150491961 | GTTTTTTT others(3): Show |
G | 10 | a0001c0001t0006g0037 a0001c0001t0006g0272 a0001c0001t0006g0273 others(7): Show |
11 | HG00099.hp1 HG01952.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.695+313_695+322del others(10): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 150491961 | ||||||
| chr1:150492127 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(237): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.696-284A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 6/17 | chr1 | 150492127 | |||||||
| chr1:150492765 | G | A | 3 | a0001c0001t0004g0275 a0001c0001t0004g0276 a0001c0001t0004g0283 |
3 | HG03098.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.774+276G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150492765 | |||||||
| chr1:150492795 | G | A | 29 | a0001c0002t0003g0003 a0001c0002t0003g0013 a0001c0002t0003g0028 others(26): Show |
40 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.774+306G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150492795 | |||||||
| chr1:150492801 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.774+312G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150492801 | |||||||
| chr1:150492809 | C | CA | 25 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0045 others(22): Show |
28 | HG00609.hp2 HG01175.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.774+339dupA | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 150492809 | ||||||
| chr1:150492809 | C | CAAAAAAA | 9 | a0001c0001t0004g0038 a0001c0001t0004g0284 a0001c0001t0004g0291 others(6): Show |
11 | HG01109.hp2 HG01168.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.774+333_774+339dup others(7): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 150492809 | ||||||
| chr1:150492809 | C | CAAAAAAA others(1): Show |
18 | a0001c0001t0004g0275 a0001c0001t0004g0276 a0001c0001t0004g0286 others(15): Show |
19 | HG00099.hp1 HG01255.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.774+332_774+339dup others(8): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 150492809 | ||||||
| chr1:150492809 | CAAA | C | 11 | a0001c0001t0005g0015 a0001c0001t0005g0262 a0001c0001t0005g0263 others(8): Show |
13 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.774+337_774+339del others(3): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 150492809 | ||||||
| chr1:150492860 | C | T | 1 | a0001c0002t0003g0183 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.774+371C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150492860 | |||||||
| chr1:150492893 | T | A | 1 | a0001c0001t0002g0207 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.774+404T>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150492893 | |||||||
| chr1:150492917 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.774+428C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150492917 | |||||||
| chr1:150493039 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.774+550T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493039 | |||||||
| chr1:150493184 | C | G | 1 | a0001c0001t0002g0212 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.774+695C>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493184 | |||||||
| chr1:150493327 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.774+838G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493327 | |||||||
| chr1:150493331 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0154 |
2 | NA18993.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.774+842C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493331 | |||||||
| chr1:150493390 | G | A | 1 | a0001c0003t0008g0193 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.774+901G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493390 | |||||||
| chr1:150493421 | C | T | 11 | a0001c0001t0004g0038 a0001c0001t0004g0284 a0001c0001t0004g0286 others(8): Show |
12 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.774+932C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493421 | |||||||
| chr1:150493446 | A | G | 41 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(38): Show |
46 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.774+957A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493446 | |||||||
| chr1:150493477 | T | G | 74 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(71): Show |
91 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.774+988T>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493477 | |||||||
| chr1:150493491 | C | A | 1 | a0001c0004t0002g0215 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.774+1002C>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493491 | |||||||
| chr1:150493530 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0123 others(2): Show |
5 | HG02258.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+1041G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493530 | |||||||
| chr1:150493544 | G | A | 1 | a0001c0001t0006g0272 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.774+1055G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493544 | |||||||
| chr1:150493558 | G | A | 7 | a0001c0001t0004g0038 a0001c0001t0004g0284 a0001c0001t0004g0290 others(4): Show |
8 | HG01891.hp2 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+1069G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493558 | |||||||
| chr1:150493697 | G | A | 4 | a0001c0001t0002g0253 a0001c0001t0002g0254 a0001c0001t0002g0258 others(1): Show |
4 | HG00735.hp1 HG00738.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+1208G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493697 | |||||||
| chr1:150493798 | G | C | 19 | a0001c0002t0003g0003 a0001c0002t0003g0013 a0001c0002t0003g0029 others(16): Show |
29 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.774+1309G>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493798 | |||||||
| chr1:150493815 | G | A | 7 | a0001c0003t0008g0041 a0001c0003t0008g0042 a0001c0003t0008g0193 others(4): Show |
7 | HG01175.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.774+1326G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150493815 | |||||||
| chr1:150494082 | C | T | 41 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(38): Show |
46 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.774+1593C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494082 | |||||||
| chr1:150494141 | C | T | 5 | a0001c0001t0007g0039 a0001c0001t0007g0295 a0001c0001t0007g0297 others(2): Show |
6 | HG01109.hp2 HG01168.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.774+1652C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494141 | |||||||
| chr1:150494244 | G | A | 19 | a0001c0002t0003g0003 a0001c0002t0003g0013 a0001c0002t0003g0029 others(16): Show |
29 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.774+1755G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494244 | |||||||
| chr1:150494253 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.774+1764G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494253 | |||||||
| chr1:150494261 | A | G | 152 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(149): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.774+1772A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494261 | |||||||
| chr1:150494358 | G | A | 4 | a0001c0001t0004g0286 a0001c0001t0004g0287 a0001c0001t0004g0288 others(1): Show |
4 | HG02615.hp1 HG02615.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+1869G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494358 | |||||||
| chr1:150494370 | C | CA | 8 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0051 others(5): Show |
8 | HG01928.hp1 HG02145.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.774+1902dupA | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 150494370 | ||||||
| chr1:150494370 | CA | C | 38 | a0001c0001t0001g0044 a0001c0001t0001g0086 a0001c0001t0001g0121 others(35): Show |
42 | HG00558.hp2 HG00639.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.774+1902delA | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 150494370 | ||||||
| chr1:150494370 | CAA | C | 30 | a0001c0001t0017g0174 a0001c0002t0003g0003 a0001c0002t0003g0013 others(27): Show |
41 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.774+1901_774+1902d others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 150494370 | ||||||
| chr1:150494370 | CAAAAAAA others(6): Show |
C | 41 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(38): Show |
46 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.774+1890_774+1902d others(15): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 150494370 | ||||||
| chr1:150494449 | C | T | 71 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(68): Show |
87 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.774+1960C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494449 | |||||||
| chr1:150494480 | G | T | 2 | a0001c0001t0001g0119 a0002c0005t0001g0120 |
2 | HG02040.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.774+1991G>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494480 | |||||||
| chr1:150494489 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.775-1993C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494489 | |||||||
| chr1:150494513 | G | A | 1 | a0001c0003t0008g0042 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.775-1969G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494513 | |||||||
| chr1:150494527 | C | T | 11 | a0001c0001t0004g0038 a0001c0001t0004g0284 a0001c0001t0004g0286 others(8): Show |
12 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.775-1955C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494527 | |||||||
| chr1:150494587 | A | G | 81 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(78): Show |
98 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.775-1895A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494587 | |||||||
| chr1:150494620 | T | A | 3 | a0001c0001t0007g0297 a0001c0001t0007g0298 a0001c0001t0007g0299 |
3 | HG01243.hp2 HG01255.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.775-1862T>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494620 | |||||||
| chr1:150494737 | C | CA | 29 | a0001c0002t0003g0003 a0001c0002t0003g0013 a0001c0002t0003g0028 others(26): Show |
40 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.775-1739dupA | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 150494737 | ||||||
| chr1:150494809 | G | A | 1 | a0001c0002t0009g0181 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.775-1673G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494809 | |||||||
| chr1:150494820 | G | C | 81 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(78): Show |
98 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.775-1662G>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494820 | |||||||
| chr1:150494825 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.775-1657C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494825 | |||||||
| chr1:150494892 | C | T | 152 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(149): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.775-1590C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494892 | |||||||
| chr1:150494894 | A | C | 74 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(71): Show |
91 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.775-1588A>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494894 | |||||||
| chr1:150494917 | C | A | 81 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(78): Show |
98 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.775-1565C>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494917 | |||||||
| chr1:150494940 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.775-1542G>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494940 | |||||||
| chr1:150494963 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.775-1519T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150494963 | |||||||
| chr1:150495039 | C | G | 1 | a0002c0005t0001g0120 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.775-1443C>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495039 | |||||||
| chr1:150495137 | G | A | 41 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(38): Show |
46 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.775-1345G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495137 | |||||||
| chr1:150495159 | G | A | 1 | a0001c0006t0009g0169 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.775-1323G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495159 | |||||||
| chr1:150495172 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.775-1310C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495172 | |||||||
| chr1:150495206 | G | C | 1 | a0001c0001t0006g0273 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.775-1276G>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495206 | |||||||
| chr1:150495259 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.775-1223G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495259 | |||||||
| chr1:150495262 | G | A | 1 | a0001c0003t0008g0042 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.775-1220G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495262 | |||||||
| chr1:150495277 | G | A | 74 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(71): Show |
91 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.775-1205G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495277 | |||||||
| chr1:150495291 | G | A | 1 | a0001c0001t0002g0255 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.775-1191G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495291 | |||||||
| chr1:150495300 | G | A | 7 | a0001c0003t0008g0041 a0001c0003t0008g0042 a0001c0003t0008g0193 others(4): Show |
7 | HG01175.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.775-1182G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495300 | |||||||
| chr1:150495336 | T | TACAC | 29 | a0001c0001t0017g0174 a0001c0002t0003g0003 a0001c0002t0003g0013 others(26): Show |
40 | HG00642.hp2 HG01070.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.775-1133_775-1130d others(6): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 150495336 | ||||||
| chr1:150495338 | C | T | 41 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(38): Show |
46 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.775-1144C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495338 | |||||||
| chr1:150495341 | A | G | 41 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(38): Show |
46 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.775-1141A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495341 | |||||||
| chr1:150495634 | TCCAC | T | 74 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(71): Show |
91 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.775-842_775-839del others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 150495634 | ||||||
| chr1:150495844 | C | T | 1 | a0001c0002t0003g0188 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.775-638C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495844 | |||||||
| chr1:150495883 | T | C | 122 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(119): Show |
144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.775-599T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495883 | |||||||
| chr1:150495923 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.775-559T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150495923 | |||||||
| chr1:150496016 | G | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG03017.hp1 HG03654.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-466G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150496016 | |||||||
| chr1:150496052 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.775-430G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150496052 | |||||||
| chr1:150496057 | T | C | 1 | a0001c0001t0011g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.775-425T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150496057 | |||||||
| chr1:150496071 | G | T | 6 | a0001c0001t0001g0231 a0001c0001t0002g0210 a0001c0001t0002g0211 others(3): Show |
6 | HG00140.hp2 HG01243.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-411G>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150496071 | |||||||
| chr1:150496098 | C | T | 41 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(38): Show |
46 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.775-384C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150496098 | |||||||
| chr1:150496366 | A | G | 41 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(38): Show |
46 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.775-116A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 7/17 | chr1 | 150496366 | |||||||
| chr1:150496634 | GGAATTGG others(6): Show |
G | 1 | a0001c0001t0001g0158 | 1 | HG00597.hp1 | splice_region_variant&intron_variant | LOW | c.921+7_921+19delGAA others(10): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 8/17 | chr1 | 150496634 | |||||||
| chr1:150496748 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.922-62C>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 8/17 | chr1 | 150496748 | |||||||
| chr1:150496780 | G | T | 30 | a0001c0001t0017g0174 a0001c0002t0003g0003 a0001c0002t0003g0013 others(27): Show |
41 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.922-30G>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 8/17 | chr1 | 150496780 | |||||||
| chr1:150496939 | A | C | 1 | a0001c0001t0006g0274 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1020+31A>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 9/17 | chr1 | 150496939 | |||||||
| chr1:150497004 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(70): Show |
101 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1020+96C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 9/17 | chr1 | 150497004 | |||||||
| chr1:150497188 | G | A | 2 | a0001c0001t0002g0014 a0001c0001t0002g0036 |
5 | NA18951.hp1 NA18955.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+280G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 9/17 | chr1 | 150497188 | |||||||
| chr1:150497221 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1021-309G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 9/17 | chr1 | 150497221 | |||||||
| chr1:150497296 | A | G | 1 | a0001c0001t0004g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1021-234A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 9/17 | chr1 | 150497296 | |||||||
| chr1:150497774 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1238+27A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | chr1 | 150497774 | |||||||
| chr1:150497820 | G | A | 41 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(38): Show |
46 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1238+73G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | chr1 | 150497820 | |||||||
| chr1:150497846 | C | A | 82 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(79): Show |
99 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.1238+99C>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | chr1 | 150497846 | |||||||
| chr1:150497858 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1238+111G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | chr1 | 150497858 | |||||||
| chr1:150497862 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0116 |
4 | NA18950.hp2 NA18984.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1238+115C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | chr1 | 150497862 | |||||||
| chr1:150497955 | C | T | 1 | a0001c0001t0010g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1238+208C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | chr1 | 150497955 | |||||||
| chr1:150498002 | C | A | 82 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(79): Show |
99 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.1238+255C>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | chr1 | 150498002 | |||||||
| chr1:150498003 | T | G | 82 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0002g0004 others(79): Show |
99 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.1238+256T>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | chr1 | 150498003 | |||||||
| chr1:150498047 | C | T | 65 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(62): Show |
80 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.1238+300C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | chr1 | 150498047 | |||||||
| chr1:150498066 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1238+319C>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | chr1 | 150498066 | |||||||
| chr1:150498092 | C | CA | 6 | a0001c0001t0001g0062 a0001c0001t0001g0130 a0001c0001t0001g0153 others(3): Show |
6 | HG00639.hp1 HG00735.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1238+362dupA | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 150498092 | ||||||
| chr1:150498092 | CA | C | 6 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0002g0234 others(3): Show |
6 | HG01257.hp1 HG02015.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1238+362delA | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 150498092 | ||||||
| chr1:150498141 | GA | G | 3 | a0001c0001t0002g0235 a0001c0001t0002g0244 a0001c0001t0002g0245 |
3 | HG03490.hp1 HG03492.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1239-360delA | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | chr1 | 150498141 | |||||||
| chr1:150498148 | G | T | 1 | a0001c0001t0002g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1239-354G>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | chr1 | 150498148 | |||||||
| chr1:150498375 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1239-127A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | chr1 | 150498375 | |||||||
| chr1:150498488 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1239-14C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 10/17 | chr1 | 150498488 | |||||||
| chr1:150498680 | C | T | 9 | a0001c0001t0001g0301 a0001c0001t0004g0292 a0001c0001t0006g0037 others(6): Show |
10 | HG00099.hp1 HG01952.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1401+16C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 11/17 | chr1 | 150498680 | |||||||
| chr1:150498681 | T | A | 26 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0089 others(23): Show |
41 | HG01257.hp2 HG01258.hp2 HG02004.hp1 others(38): Show |
intron_variant | MODIFIER | c.1401+17T>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 11/17 | chr1 | 150498681 | |||||||
| chr1:150498718 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1401+54T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 11/17 | chr1 | 150498718 | |||||||
| chr1:150499056 | A | T | 1 | a0001c0001t0006g0279 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1539+22A>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 12/17 | chr1 | 150499056 | |||||||
| chr1:150499080 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1539+46T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 12/17 | chr1 | 150499080 | |||||||
| chr1:150499140 | T | C | 1 | a0001c0001t0005g0263 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1540-76T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 12/17 | chr1 | 150499140 | |||||||
| chr1:150499372 | A | AT | 154 | a0001c0001t0001g0050 a0001c0001t0001g0221 a0001c0001t0001g0303 others(151): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1617+90dupT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150499372 | ||||||
| chr1:150499459 | G | GT | 25 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(22): Show |
27 | HG00099.hp1 HG01891.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.1617+168dupT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150499459 | ||||||
| chr1:150499513 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1617+220G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150499513 | |||||||
| chr1:150499656 | G | A | 1 | a0001c0002t0009g0181 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1617+363G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150499656 | |||||||
| chr1:150499925 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1617+632G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150499925 | |||||||
| chr1:150499963 | AC | A | 5 | a0001c0001t0007g0039 a0001c0001t0007g0295 a0001c0001t0007g0297 others(2): Show |
6 | HG01109.hp2 HG01168.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617+671delC | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150499963 | |||||||
| chr1:150499970 | A | C | 8 | a0001c0001t0001g0138 a0001c0003t0008g0041 a0001c0003t0008g0042 others(5): Show |
8 | HG01175.hp1 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1617+677A>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150499970 | |||||||
| chr1:150499976 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1617+683A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150499976 | |||||||
| chr1:150500008 | C | CA | 8 | a0001c0001t0001g0050 a0001c0001t0001g0106 a0001c0001t0001g0125 others(5): Show |
8 | HG02572.hp1 HG02738.hp2 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1617+732dupA | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150500008 | ||||||
| chr1:150500147 | A | G | 1 | a0001c0001t0002g0242 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1617+854A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500147 | |||||||
| chr1:150500190 | C | T | 157 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0300 others(154): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1617+897C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500190 | |||||||
| chr1:150500305 | A | G | 80 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0014 others(77): Show |
97 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1617+1012A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500305 | |||||||
| chr1:150500393 | C | A | 73 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0014 others(70): Show |
90 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.1617+1100C>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500393 | |||||||
| chr1:150500401 | C | T | 1 | a0001c0003t0008g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1617+1108C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500401 | |||||||
| chr1:150500406 | G | A | 1 | a0001c0002t0018g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1617+1113G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500406 | |||||||
| chr1:150500423 | CT | C | 5 | a0001c0001t0007g0039 a0001c0001t0007g0295 a0001c0001t0007g0297 others(2): Show |
6 | HG01109.hp2 HG01168.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617+1131delT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500423 | |||||||
| chr1:150500498 | C | A | 1 | a0001c0001t0004g0292 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1617+1205C>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500498 | |||||||
| chr1:150500533 | C | T | 2 | a0001c0001t0005g0263 a0001c0001t0005g0268 |
2 | HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1617+1240C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500533 | |||||||
| chr1:150500608 | T | C | 157 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0300 others(154): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1617+1315T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500608 | |||||||
| chr1:150500613 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1617+1320G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500613 | |||||||
| chr1:150500663 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1617+1370G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500663 | |||||||
| chr1:150500689 | C | A | 1 | a0001c0001t0002g0217 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1617+1396C>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500689 | |||||||
| chr1:150500746 | C | T | 1 | a0001c0001t0017g0174 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1617+1453C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500746 | |||||||
| chr1:150500782 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1617+1489C>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500782 | |||||||
| chr1:150500843 | G | A | 11 | a0001c0001t0005g0015 a0001c0001t0005g0262 a0001c0001t0005g0263 others(8): Show |
13 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1617+1550G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150500843 | |||||||
| chr1:150501258 | T | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0132 |
2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1617+1965T>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501258 | |||||||
| chr1:150501293 | CAA | C | 17 | a0001c0001t0002g0032 a0001c0001t0002g0204 a0001c0001t0002g0205 others(14): Show |
19 | HG00099.hp1 HG02155.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.1617+2008_1617+200 others(6): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150501293 | ||||||
| chr1:150501300 | AAAT | A | 40 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0031 others(37): Show |
52 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1617+2008_1617+201 others(7): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501300 | |||||||
| chr1:150501300 | AAATT | A | 59 | a0001c0001t0002g0010 a0001c0001t0002g0033 a0001c0001t0002g0202 others(56): Show |
68 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.1617+2008_1617+201 others(8): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501300 | |||||||
| chr1:150501300 | AAATTT | A | 5 | a0001c0001t0002g0242 a0001c0001t0002g0246 a0001c0001t0007g0298 others(2): Show |
6 | HG01257.hp1 HG03704.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617+2008_1617+201 others(9): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501300 | |||||||
| chr1:150501300 | AAATTTTT others(5): Show |
A | 1 | a0001c0003t0008g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1617+2008_1617+201 others(16): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501300 | |||||||
| chr1:150501300 | AAATTTTT others(7): Show |
A | 6 | a0001c0003t0008g0042 a0001c0003t0008g0193 a0001c0003t0008g0194 others(3): Show |
6 | HG01175.hp1 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617+2008_1617+202 others(18): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501300 | |||||||
| chr1:150501301 | A | T | 20 | a0001c0001t0004g0286 a0001c0001t0004g0287 a0001c0002t0003g0003 others(17): Show |
29 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1617+2008A>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501301 | |||||||
| chr1:150501302 | A | AT | 43 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(40): Show |
49 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1617+2039dupT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150501302 | ||||||
| chr1:150501302 | A | T | 22 | a0001c0001t0004g0286 a0001c0001t0004g0287 a0001c0001t0006g0272 others(19): Show |
31 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1617+2009A>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501302 | |||||||
| chr1:150501302 | AT | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0016 others(10): Show |
15 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.1617+2039delT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150501302 | ||||||
| chr1:150501333 | A | C | 25 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(22): Show |
27 | HG00099.hp1 HG01891.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.1617+2040A>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501333 | |||||||
| chr1:150501333 | A | T | 125 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0014 others(122): Show |
156 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.1617+2040A>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501333 | |||||||
| chr1:150501334 | T | C | 142 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0014 others(139): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1617+2041T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501334 | |||||||
| chr1:150501334 | T | TC | 8 | a0001c0002t0003g0013 a0001c0002t0003g0177 a0001c0002t0003g0186 others(5): Show |
10 | HG00438.hp2 HG00642.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1617+2041_1617+204 others(5): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501334 | |||||||
| chr1:150501340 | C | T | 1 | a0001c0002t0003g0185 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1617+2047C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501340 | |||||||
| chr1:150501342 | A | G | 7 | a0001c0003t0008g0041 a0001c0003t0008g0042 a0001c0003t0008g0193 others(4): Show |
7 | HG01175.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1617+2049A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501342 | |||||||
| chr1:150501374 | G | A | 11 | a0001c0001t0005g0015 a0001c0001t0005g0262 a0001c0001t0005g0263 others(8): Show |
13 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1617+2081G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501374 | |||||||
| chr1:150501398 | AGCTCCGC others(14): Show |
A | 1 | a0001c0001t0001g0095 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1617+2106_1617+212 others(25): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501398 | |||||||
| chr1:150501418 | C | T | 1 | a0001c0001t0002g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1617+2125C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501418 | |||||||
| chr1:150501468 | CCCATCA | C | 155 | a0001c0001t0001g0022 a0001c0001t0001g0083 a0001c0001t0001g0146 others(152): Show |
189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1617+2186_1617+219 others(10): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150501468 | ||||||
| chr1:150501502 | C | CT | 17 | a0001c0001t0001g0050 a0001c0001t0001g0113 a0001c0001t0001g0115 others(14): Show |
19 | HG01109.hp2 HG02056.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1617+2224dupT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150501502 | ||||||
| chr1:150501502 | CT | C | 12 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0064 others(9): Show |
15 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1617+2224delT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150501502 | ||||||
| chr1:150501561 | C | T | 1 | a0001c0001t0006g0273 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1617+2268C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501561 | |||||||
| chr1:150501583 | G | A | 7 | a0001c0003t0008g0041 a0001c0003t0008g0042 a0001c0003t0008g0193 others(4): Show |
7 | HG01175.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1617+2290G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501583 | |||||||
| chr1:150501861 | G | A | 150 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0014 others(147): Show |
183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1618-2474G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501861 | |||||||
| chr1:150501882 | C | CT | 11 | a0001c0001t0004g0038 a0001c0001t0004g0284 a0001c0001t0004g0286 others(8): Show |
12 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1618-2445dupT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150501882 | ||||||
| chr1:150501882 | CTTTT | C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0060 others(4): Show |
8 | HG01255.hp1 HG01358.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1618-2448_1618-244 others(8): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150501882 | ||||||
| chr1:150501985 | TCACTGCA | T | 3 | a0001c0001t0004g0275 a0001c0001t0004g0276 a0001c0001t0004g0283 |
3 | HG03098.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1618-2349_1618-234 others(11): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501985 | |||||||
| chr1:150501993 | A | G | 3 | a0001c0001t0004g0275 a0001c0001t0004g0276 a0001c0001t0004g0283 |
3 | HG03098.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1618-2342A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150501993 | |||||||
| chr1:150502002 | T | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0300 others(3): Show |
9 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1618-2333T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150502002 | |||||||
| chr1:150502037 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0062 a0001c0001t0001g0080 others(4): Show |
8 | HG00280.hp1 HG00639.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1618-2298C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150502037 | |||||||
| chr1:150502215 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1618-2120G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150502215 | |||||||
| chr1:150502230 | G | GT | 151 | a0001c0001t0001g0050 a0001c0001t0002g0004 a0001c0001t0002g0010 others(148): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1618-2098dupT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150502230 | ||||||
| chr1:150502263 | G | A | 1 | a0001c0001t0011g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1618-2072G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150502263 | |||||||
| chr1:150502306 | CCACCTCC others(6): Show |
C | 1 | a0001c0001t0001g0067 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1618-2026_1618-201 others(17): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150502306 | ||||||
| chr1:150502357 | G | A | 1 | a0001c0003t0008g0193 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1618-1978G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150502357 | |||||||
| chr1:150502385 | A | AT | 6 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0062 others(3): Show |
6 | HG00639.hp1 HG01109.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.1618-1931dupT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150502385 | ||||||
| chr1:150502385 | A | T | 11 | a0001c0001t0005g0015 a0001c0001t0005g0262 a0001c0001t0005g0263 others(8): Show |
13 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1618-1950A>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150502385 | |||||||
| chr1:150502385 | AT | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(126): Show |
172 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.1618-1931delT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150502385 | ||||||
| chr1:150502426 | G | T | 1 | a0001c0001t0004g0289 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1618-1909G>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150502426 | |||||||
| chr1:150502577 | C | T | 19 | a0001c0002t0003g0003 a0001c0002t0003g0013 a0001c0002t0003g0029 others(16): Show |
29 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1618-1758C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150502577 | |||||||
| chr1:150502854 | G | C | 1 | a0001c0002t0009g0175 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1618-1481G>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150502854 | |||||||
| chr1:150502999 | C | A | 1 | a0001c0001t0012g0280 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1618-1336C>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150502999 | |||||||
| chr1:150503296 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0014 others(75): Show |
95 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1618-1039A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503296 | |||||||
| chr1:150503532 | A | G | 1 | a0001c0001t0002g0238 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1618-803A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503532 | |||||||
| chr1:150503545 | A | ATG | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(111): Show |
162 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.1618-758_1618-757d others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503545 | ||||||
| chr1:150503545 | A | ATGTG | 6 | a0001c0001t0001g0078 a0001c0001t0001g0098 a0001c0001t0001g0112 others(3): Show |
6 | HG01123.hp2 HG01167.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.1618-760_1618-757d others(6): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503545 | ||||||
| chr1:150503545 | ATG | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0068 a0001c0001t0001g0108 others(1): Show |
4 | HG00733.hp2 NA19062.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.1618-758_1618-757d others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503545 | ||||||
| chr1:150503547 | G | A | 149 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0014 others(146): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.1618-788G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503547 | |||||||
| chr1:150503555 | G | A | 1 | a0001c0001t0004g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1618-780G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503555 | |||||||
| chr1:150503567 | G | A | 6 | a0001c0001t0004g0038 a0001c0001t0004g0284 a0001c0001t0004g0290 others(3): Show |
7 | HG01891.hp2 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1618-768G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503567 | |||||||
| chr1:150503569 | G | A | 7 | a0001c0001t0002g0222 a0001c0001t0004g0038 a0001c0001t0004g0284 others(4): Show |
8 | HG00140.hp1 HG01891.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1618-766G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503569 | |||||||
| chr1:150503571 | G | A | 11 | a0001c0001t0002g0222 a0001c0001t0002g0304 a0001c0001t0004g0038 others(8): Show |
13 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1618-764G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503571 | |||||||
| chr1:150503573 | G | A | 82 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0014 others(79): Show |
100 | HG00140.hp1 HG00639.hp2 HG00673.hp2 others(97): Show |
intron_variant | MODIFIER | c.1618-762G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503573 | |||||||
| chr1:150503573 | G | GTATA | 5 | a0001c0001t0007g0039 a0001c0001t0007g0295 a0001c0001t0007g0297 others(2): Show |
6 | HG01109.hp2 HG01168.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1618-761_1618-760i others(6): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503573 | ||||||
| chr1:150503575 | G | A | 134 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0014 others(131): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1618-760G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503575 | |||||||
| chr1:150503577 | G | A | 153 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0301 others(150): Show |
189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1618-758G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503577 | |||||||
| chr1:150503577 | G | GTA | 6 | a0001c0001t0001g0091 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
6 | HG02055.hp2 HG02818.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1618-750_1618-749d others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503577 | ||||||
| chr1:150503579 | A | G | 14 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0027 others(11): Show |
18 | HG00673.hp1 HG01891.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1618-756A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503579 | |||||||
| chr1:150503581 | A | G | 6 | a0001c0001t0004g0038 a0001c0001t0004g0284 a0001c0001t0004g0290 others(3): Show |
7 | HG01891.hp2 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1618-754A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503581 | |||||||
| chr1:150503583 | A | ATG | 3 | a0001c0001t0006g0278 a0001c0001t0006g0282 a0001c0001t0006g0285 |
3 | HG02572.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1618-751_1618-750i others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503583 | ||||||
| chr1:150503583 | A | G | 7 | a0001c0001t0004g0038 a0001c0001t0004g0284 a0001c0001t0004g0290 others(4): Show |
8 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1618-752A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503583 | |||||||
| chr1:150503585 | A | ATATATGT others(1): Show |
5 | a0001c0001t0002g0227 a0001c0001t0002g0253 a0001c0001t0002g0258 others(2): Show |
5 | HG00738.hp2 HG01358.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1618-749_1618-748i others(10): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503585 | ||||||
| chr1:150503585 | A | ATATATGT others(5): Show |
2 | a0001c0002t0003g0028 a0001c0002t0003g0168 |
3 | HG02486.hp1 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1618-749_1618-748i others(14): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503585 | ||||||
| chr1:150503585 | A | ATATATGT others(7): Show |
1 | a0001c0002t0003g0173 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1618-749_1618-748i others(16): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503585 | ||||||
| chr1:150503585 | A | ATATG | 23 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0031 others(20): Show |
35 | HG01175.hp1 HG01257.hp2 HG01258.hp2 others(32): Show |
intron_variant | MODIFIER | c.1618-749_1618-748i others(6): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503585 | ||||||
| chr1:150503585 | A | ATATGTG | 32 | a0001c0001t0002g0010 a0001c0001t0002g0033 a0001c0001t0002g0210 others(29): Show |
36 | HG00140.hp2 HG00639.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1618-749_1618-748i others(8): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503585 | ||||||
| chr1:150503585 | A | ATATGTGT others(1): Show |
8 | a0001c0001t0002g0254 a0001c0002t0003g0029 a0001c0002t0003g0177 others(5): Show |
9 | HG00735.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1618-749_1618-748i others(10): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503585 | ||||||
| chr1:150503585 | A | ATATGTGT others(3): Show |
19 | a0001c0002t0003g0003 a0001c0002t0003g0013 a0001c0002t0003g0030 others(16): Show |
28 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1618-749_1618-748i others(12): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503585 | ||||||
| chr1:150503585 | A | ATGTG | 5 | a0001c0001t0002g0304 a0001c0001t0004g0288 a0001c0004t0002g0035 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1618-736_1618-733d others(6): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503585 | ||||||
| chr1:150503585 | A | ATGTGTG | 15 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(12): Show |
15 | HG03098.hp1 HG03453.hp2 HG06807.hp2 others(12): Show |
intron_variant | MODIFIER | c.1618-738_1618-733d others(8): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503585 | ||||||
| chr1:150503585 | A | G | 22 | a0001c0001t0001g0221 a0001c0001t0002g0222 a0001c0001t0004g0038 others(19): Show |
24 | HG00099.hp1 HG00140.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1618-750A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503585 | |||||||
| chr1:150503587 | G | A | 16 | a0001c0001t0001g0027 a0001c0001t0001g0107 a0001c0001t0001g0140 others(13): Show |
19 | HG00673.hp1 HG02451.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.1618-748G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503587 | |||||||
| chr1:150503589 | G | A | 12 | a0001c0001t0002g0228 a0001c0001t0005g0015 a0001c0001t0005g0262 others(9): Show |
14 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1618-746G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503589 | |||||||
| chr1:150503591 | G | A | 7 | a0001c0001t0005g0015 a0001c0001t0005g0262 a0001c0001t0005g0263 others(4): Show |
9 | HG02451.hp2 HG02622.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1618-744G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503591 | |||||||
| chr1:150503593 | G | A | 1 | a0001c0001t0005g0268 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1618-742G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503593 | |||||||
| chr1:150503601 | GTA | G | 3 | a0001c0001t0005g0267 a0001c0001t0005g0270 a0001c0001t0005g0271 |
3 | HG03139.hp2 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1618-732_1618-731d others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503601 | ||||||
| chr1:150503603 | A | G | 11 | a0001c0001t0002g0228 a0001c0001t0004g0293 a0001c0001t0005g0015 others(8): Show |
13 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1618-732A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503603 | |||||||
| chr1:150503605 | GTGTGTAT others(3): Show |
G | 1 | a0001c0003t0008g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1618-728_1618-719d others(12): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503605 | ||||||
| chr1:150503609 | GTA | G | 5 | a0001c0001t0001g0022 a0001c0001t0001g0083 a0001c0001t0001g0146 others(2): Show |
6 | HG01168.hp1 HG01169.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1618-718_1618-717d others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503609 | ||||||
| chr1:150503611 | A | G | 11 | a0001c0001t0005g0015 a0001c0001t0005g0262 a0001c0001t0005g0263 others(8): Show |
13 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1618-724A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503611 | |||||||
| chr1:150503613 | A | G | 11 | a0001c0001t0005g0015 a0001c0001t0005g0262 a0001c0001t0005g0263 others(8): Show |
13 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1618-722A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503613 | |||||||
| chr1:150503615 | A | G | 1 | a0001c0001t0005g0268 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1618-720A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503615 | |||||||
| chr1:150503617 | A | ACG | 8 | a0001c0001t0004g0275 a0001c0001t0004g0276 a0001c0001t0004g0283 others(5): Show |
8 | HG02451.hp1 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1618-718_1618-717i others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503617 | |||||||
| chr1:150503617 | A | ATG | 6 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0300 others(3): Show |
9 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1618-710_1618-709d others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503617 | ||||||
| chr1:150503617 | A | G | 18 | a0001c0001t0002g0209 a0001c0001t0002g0228 a0001c0001t0005g0015 others(15): Show |
20 | HG01175.hp1 HG02451.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.1618-718A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503617 | |||||||
| chr1:150503618 | T | C | 16 | a0001c0001t0004g0038 a0001c0001t0004g0284 a0001c0001t0004g0286 others(13): Show |
18 | HG00099.hp1 HG01891.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.1618-717T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503618 | |||||||
| chr1:150503619 | GTGTGTGT others(5): Show |
G | 17 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0031 others(14): Show |
29 | HG01257.hp2 HG01258.hp2 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.1618-708_1618-697d others(14): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503619 | ||||||
| chr1:150503621 | GTGTGTAT others(3): Show |
G | 6 | a0001c0001t0006g0037 a0001c0001t0006g0272 a0001c0001t0006g0273 others(3): Show |
7 | HG00099.hp1 HG01952.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1618-708_1618-699d others(12): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503621 | ||||||
| chr1:150503623 | G | A | 11 | a0001c0001t0002g0228 a0001c0001t0005g0015 a0001c0001t0005g0262 others(8): Show |
13 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1618-712G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503623 | |||||||
| chr1:150503625 | G | A | 14 | a0001c0001t0002g0228 a0001c0001t0004g0293 a0001c0001t0005g0015 others(11): Show |
16 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.1618-710G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503625 | |||||||
| chr1:150503627 | A | ATATGTGT others(3): Show |
6 | a0001c0003t0008g0041 a0001c0003t0008g0042 a0001c0003t0008g0193 others(3): Show |
6 | HG01175.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1618-705_1618-704i others(12): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503627 | ||||||
| chr1:150503627 | A | G | 107 | a0001c0001t0002g0010 a0001c0001t0002g0033 a0001c0001t0002g0199 others(104): Show |
125 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1618-708A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503627 | |||||||
| chr1:150503631 | A | G | 12 | a0001c0001t0002g0228 a0001c0001t0005g0015 a0001c0001t0005g0262 others(9): Show |
14 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1618-704A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503631 | |||||||
| chr1:150503633 | G | A | 6 | a0001c0003t0008g0041 a0001c0003t0008g0042 a0001c0003t0008g0193 others(3): Show |
6 | HG01175.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1618-702G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503633 | |||||||
| chr1:150503633 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0001g0302 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1618-660_1618-649d others(14): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503633 | ||||||
| chr1:150503633 | GTGTGTGT others(5): Show |
G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(47): Show |
75 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1618-660_1618-649d others(14): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503633 | ||||||
| chr1:150503633 | GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0001g0071 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1618-672_1618-649d others(26): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503633 | ||||||
| chr1:150503639 | GTA | G | 31 | a0001c0001t0001g0118 a0001c0001t0017g0174 a0001c0002t0003g0003 others(28): Show |
42 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1618-690_1618-689d others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503639 | ||||||
| chr1:150503642 | T | C | 6 | a0001c0001t0004g0038 a0001c0001t0004g0284 a0001c0001t0004g0290 others(3): Show |
7 | HG01891.hp2 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1618-693T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503642 | |||||||
| chr1:150503644 | T | C | 6 | a0001c0003t0008g0041 a0001c0003t0008g0042 a0001c0003t0008g0193 others(3): Show |
6 | HG01175.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1618-691T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503644 | |||||||
| chr1:150503644 | T | TATGTGTG others(5): Show |
54 | a0001c0001t0002g0010 a0001c0001t0002g0033 a0001c0001t0002g0199 others(51): Show |
59 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1618-680_1618-679i others(14): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503644 | ||||||
| chr1:150503645 | A | G | 26 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0031 others(23): Show |
39 | HG00099.hp1 HG01257.hp2 HG01258.hp2 others(36): Show |
intron_variant | MODIFIER | c.1618-690A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503645 | |||||||
| chr1:150503654 | T | C | 1 | a0001c0001t0004g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1618-681T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503654 | |||||||
| chr1:150503656 | T | C | 64 | a0001c0001t0004g0038 a0001c0001t0004g0275 a0001c0001t0004g0276 others(61): Show |
79 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(76): Show |
intron_variant | MODIFIER | c.1618-679T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503656 | |||||||
| chr1:150503668 | T | C | 25 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0031 others(22): Show |
38 | HG00099.hp1 HG01257.hp2 HG01258.hp2 others(35): Show |
intron_variant | MODIFIER | c.1618-667T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503668 | |||||||
| chr1:150503673 | GTGTATAT others(9): Show |
G | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1618-660_1618-645d others(18): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503673 | ||||||
| chr1:150503708 | TACAC | T | 11 | a0001c0001t0006g0037 a0001c0001t0006g0272 a0001c0001t0006g0273 others(8): Show |
12 | HG00099.hp1 HG01952.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1618-611_1618-608d others(6): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503708 | ||||||
| chr1:150503708 | TACACAC | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0025 others(13): Show |
24 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1618-613_1618-608d others(8): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503708 | ||||||
| chr1:150503710 | C | T | 127 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0014 others(124): Show |
150 | HG00140.hp2 HG00438.hp2 HG00639.hp2 others(147): Show |
intron_variant | MODIFIER | c.1618-625C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503710 | |||||||
| chr1:150503712 | C | T | 5 | a0001c0001t0007g0039 a0001c0001t0007g0295 a0001c0001t0007g0297 others(2): Show |
6 | HG01109.hp2 HG01168.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1618-623C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503712 | |||||||
| chr1:150503764 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG02083.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1618-571G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503764 | |||||||
| chr1:150503902 | C | CA | 26 | a0001c0001t0001g0057 a0001c0001t0001g0096 a0001c0001t0001g0104 others(23): Show |
28 | HG01109.hp2 HG02055.hp1 HG02056.hp1 others(25): Show |
intron_variant | MODIFIER | c.1618-415dupA | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 150503902 | ||||||
| chr1:150503930 | C | G | 156 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0300 others(153): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.1618-405C>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150503930 | |||||||
| chr1:150504040 | G | A | 73 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0014 others(70): Show |
90 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.1618-295G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150504040 | |||||||
| chr1:150504231 | G | A | 2 | a0001c0001t0006g0273 a0001c0001t0006g0274 |
2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1618-104G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150504231 | |||||||
| chr1:150504239 | G | T | 1 | a0001c0002t0003g0180 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1618-96G>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150504239 | |||||||
| chr1:150504306 | T | C | 1 | a0002c0005t0001g0120 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1618-29T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150504306 | |||||||
| chr1:150504310 | G | A | 19 | a0001c0002t0003g0003 a0001c0002t0003g0013 a0001c0002t0003g0029 others(16): Show |
29 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1618-25G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 13/17 | chr1 | 150504310 | |||||||
| chr1:150504572 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1719-60T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 14/17 | chr1 | 150504572 | |||||||
| chr1:150504585 | C | T | 72 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0014 others(69): Show |
89 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1719-47C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 14/17 | chr1 | 150504585 | |||||||
| chr1:150504612 | C | G | 1 | a0001c0002t0009g0182 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1719-20C>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 14/17 | chr1 | 150504612 | |||||||
| chr1:150504616 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1719-16C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 14/17 | chr1 | 150504616 | |||||||
| chr1:150504617 | C | A | 1 | a0001c0001t0001g0019 | 2 | NA18948.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1719-15C>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 14/17 | chr1 | 150504617 | |||||||
| chr1:150504774 | G | A | 7 | a0001c0003t0008g0041 a0001c0003t0008g0042 a0001c0003t0008g0193 others(4): Show |
7 | HG01175.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1820+41G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 15/17 | chr1 | 150504774 | |||||||
| chr1:150504876 | AT | A | 7 | a0001c0001t0004g0038 a0001c0001t0004g0284 a0001c0001t0004g0290 others(4): Show |
8 | HG01891.hp2 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1821-27delT | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 150504876 | ||||||
| chr1:150505087 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1893+109C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 16/17 | chr1 | 150505087 | |||||||
| chr1:150505349 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1894-242G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 16/17 | chr1 | 150505349 | |||||||
| chr1:150505364 | G | C | 4 | a0001c0001t0006g0037 a0001c0001t0006g0272 a0001c0001t0006g0273 others(1): Show |
5 | HG00099.hp1 HG01952.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1894-227G>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 16/17 | chr1 | 150505364 | |||||||
| chr1:150505741 | G | A | 1 | a0001c0002t0003g0186 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2008+36G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | chr1 | 150505741 | |||||||
| chr1:150505742 | C | T | 1 | a0001c0002t0003g0186 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2008+37C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | chr1 | 150505742 | |||||||
| chr1:150506062 | TGAG | T | 29 | a0001c0002t0003g0003 a0001c0002t0003g0013 a0001c0002t0003g0028 others(26): Show |
40 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.2008+361_2008+363d others(5): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506062 | ||||||
| chr1:150506147 | T | C | 150 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0014 others(147): Show |
183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.2008+442T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | chr1 | 150506147 | |||||||
| chr1:150506172 | A | G | 6 | a0001c0003t0008g0041 a0001c0003t0008g0042 a0001c0003t0008g0193 others(3): Show |
6 | HG01175.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2008+467A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | chr1 | 150506172 | |||||||
| chr1:150506278 | C | T | 1 | a0001c0002t0009g0181 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2008+573C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | chr1 | 150506278 | |||||||
| chr1:150506362 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2009-554G>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | chr1 | 150506362 | |||||||
| chr1:150506415 | G | A | 2 | a0001c0001t0002g0216 a0001c0001t0002g0223 |
2 | HG02683.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2009-501G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | chr1 | 150506415 | |||||||
| chr1:150506478 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0300 others(2): Show |
8 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2009-438A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | chr1 | 150506478 | |||||||
| chr1:150506484 | G | GCA | 9 | a0001c0001t0002g0230 a0001c0001t0002g0257 a0001c0001t0004g0287 others(6): Show |
10 | HG00099.hp1 HG00673.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.2009-431_2009-430i others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506484 | ||||||
| chr1:150506484 | G | GCACA | 64 | a0001c0001t0002g0010 a0001c0001t0002g0031 a0001c0001t0002g0033 others(61): Show |
70 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.2009-431_2009-430i others(6): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506484 | ||||||
| chr1:150506484 | G | GCACACA | 14 | a0001c0001t0001g0072 a0001c0001t0002g0004 a0001c0001t0002g0032 others(11): Show |
22 | HG00738.hp1 HG01257.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2009-431_2009-430i others(8): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506484 | ||||||
| chr1:150506484 | G | GCACACAC others(1): Show |
11 | a0001c0001t0002g0014 a0001c0001t0002g0036 a0001c0001t0002g0239 others(8): Show |
16 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2009-431_2009-430i others(10): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506484 | ||||||
| chr1:150506484 | G | GCACACAC others(5): Show |
3 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0301 |
6 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2009-431_2009-430i others(14): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506484 | ||||||
| chr1:150506484 | G | GCACACAC others(7): Show |
1 | a0001c0001t0001g0303 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2009-431_2009-430i others(16): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506484 | ||||||
| chr1:150506484 | GCGCACAC others(3): Show |
G | 1 | a0001c0001t0006g0273 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2009-430_2009-421d others(12): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506484 | ||||||
| chr1:150506486 | G | A | 111 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0072 others(108): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.2009-430G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | chr1 | 150506486 | |||||||
| chr1:150506486 | G | GCACA | 13 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0080 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2009-403_2009-400d others(6): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506486 | ||||||
| chr1:150506486 | GCA | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(149): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.2009-401_2009-400d others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506486 | ||||||
| chr1:150506486 | GCACA | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0149 |
3 | HG01168.hp1 HG01169.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2009-403_2009-400d others(6): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506486 | ||||||
| chr1:150506486 | GCACACA | G | 5 | a0001c0001t0007g0039 a0001c0001t0007g0295 a0001c0001t0007g0297 others(2): Show |
6 | HG01109.hp2 HG01168.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.2009-405_2009-400d others(8): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506486 | ||||||
| chr1:150506490 | A | G | 1 | a0001c0001t0011g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2009-426A>G | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | chr1 | 150506490 | |||||||
| chr1:150506491 | CACACACA others(76): Show |
C | 1 | a0001c0001t0004g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2009-399_2009-317d others(85): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506491 | ||||||
| chr1:150506493 | CACACACA others(74): Show |
C | 1 | a0001c0001t0004g0289 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2009-399_2009-319d others(83): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506493 | ||||||
| chr1:150506573 | TGACACA | T | 7 | a0001c0003t0008g0041 a0001c0003t0008g0042 a0001c0003t0008g0193 others(4): Show |
7 | HG01175.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2009-342_2009-337d others(8): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | chr1 | 150506573 | |||||||
| chr1:150506574 | G | GAC | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(15): Show |
18 | HG00280.hp1 HG00544.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2009-310_2009-309d others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506574 | ||||||
| chr1:150506574 | G | GACAC | 7 | a0001c0001t0001g0011 a0001c0001t0001g0096 a0001c0001t0001g0097 others(4): Show |
7 | HG00544.hp2 HG02040.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2009-312_2009-309d others(6): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506574 | ||||||
| chr1:150506574 | GAC | G | 19 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0100 others(16): Show |
24 | HG02145.hp2 HG02155.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.2009-310_2009-309d others(4): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506574 | ||||||
| chr1:150506574 | GACAC | G | 80 | a0001c0001t0001g0002 a0001c0001t0002g0004 a0001c0001t0002g0010 others(77): Show |
99 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.2009-312_2009-309d others(6): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506574 | ||||||
| chr1:150506574 | GACACAC | G | 16 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0123 others(13): Show |
17 | HG00099.hp1 HG01433.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.2009-314_2009-309d others(8): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506574 | ||||||
| chr1:150506578 | C | CACACACA others(76): Show |
4 | a0001c0001t0002g0212 a0001c0001t0002g0235 a0001c0001t0002g0244 others(1): Show |
4 | HG03490.hp1 HG03492.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009-313_2009-312i others(85): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506578 | ||||||
| chr1:150506578 | C | CACACACA others(76): Show |
5 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0241 others(2): Show |
5 | HG00733.hp1 HG00741.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.2009-313_2009-312i others(85): Show |
TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 150506578 | ||||||
| chr1:150506719 | C | T | 1 | a0001c0001t0002g0224 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2009-197C>T | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | chr1 | 150506719 | |||||||
| chr1:150506787 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2009-129G>A | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | chr1 | 150506787 | |||||||
| chr1:150506844 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2009-72T>C | TARS2 | ENSG00000143374.18 | transcript | ENST00000369064.8 | protein_coding | 17/17 | chr1 | 150506844 |