Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 91978 |
| ensemblid | ENSG00000141933.9 |
| hgncid | 25058 |
| symbol | TPGS1 |
| name | tubulin polyglutamylase complex subunit 1 |
| refseq_nuc | NM_033513.3 |
| refseq_prot | NP_277048.2 |
| ensembl_nuc | ENST00000359315.6 |
| ensembl_prot | ENSP00000352265.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 507497 |
| end | 519654 |
| strand | + |
| ver | v1.2 |
| region | chr19:507497-519654 |
| region5000 | chr19:502497-524654 |
| regionname0 | TPGS1_chr19_507497_519654 |
| regionname5000 | TPGS1_chr19_502497_524654 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 290 | 318 | 90 | 63 | 114 | 15 | 34 | 81 | TPGS1_chr19_502497_524654 | TPGS1 | MAAVE others(285): Show |
chr19 | 502497 | 524654 |
| a0002 | 0/0 | 290 | 15 | 4 | 3 | 7 | 0 | 1 | 6 | TPGS1_chr19_502497_524654 | TPGS1 | MAAVE others(285): Show |
chr19 | 502497 | 524654 |
| a0003 | 0/0 | 290 | 10 | 0 | 2 | 6 | 1 | 1 | 4 | TPGS1_chr19_502497_524654 | TPGS1 | MAAVE others(285): Show |
chr19 | 502497 | 524654 |
| a0004 | 0/0 | 290 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | MAAVE others(285): Show |
chr19 | 502497 | 524654 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 870 | 252 | 68 | 41 | 98 | 15 | 28 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(865): Show |
chr19 | 502497 | 524654 | ||
| a0001c0002 | 0/0 | 870 | 45 | 4 | 20 | 16 | 0 | 5 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(865): Show |
chr19 | 502497 | 524654 | ||
| a0001c0005 | 0/0 | 870 | 5 | 5 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(865): Show |
chr19 | 502497 | 524654 | ||
| a0001c0007 | 0/0 | 870 | 3 | 0 | 2 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(865): Show |
chr19 | 502497 | 524654 | ||
| a0001c0008 | 0/0 | 870 | 3 | 3 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(865): Show |
chr19 | 502497 | 524654 | ||
| a0001c0009 | 0/0 | 870 | 3 | 3 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(865): Show |
chr19 | 502497 | 524654 | ||
| a0001c0010 | 0/0 | 870 | 2 | 2 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(865): Show |
chr19 | 502497 | 524654 | ||
| a0001c0011 | 0/0 | 870 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(865): Show |
chr19 | 502497 | 524654 | ||
| a0001c0012 | 0/0 | 870 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(865): Show |
chr19 | 502497 | 524654 | ||
| a0001c0013 | 0/0 | 870 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(865): Show |
chr19 | 502497 | 524654 | ||
| a0001c0014 | 0/0 | 870 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(865): Show |
chr19 | 502497 | 524654 | ||
| a0001c0017 | 0/0 | 870 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(865): Show |
chr19 | 502497 | 524654 | ||
| a0002c0003 | 0/0 | 871 | 11 | 2 | 2 | 6 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(866): Show |
chr19 | 502497 | 524654 | ||
| a0002c0006 | 0/0 | 871 | 3 | 1 | 1 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(866): Show |
chr19 | 502497 | 524654 | ||
| a0002c0016 | 0/0 | 871 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(866): Show |
chr19 | 502497 | 524654 | ||
| a0003c0004 | 0/0 | 870 | 10 | 0 | 2 | 6 | 1 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(865): Show |
chr19 | 502497 | 524654 | ||
| a0004c0015 | 0/0 | 870 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | ATGGC others(865): Show |
chr19 | 502497 | 524654 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1114 | 207 | 56 | 35 | 81 | 15 | 18 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0001c0001t0002 | 0/0 | 1114 | 14 | 0 | 2 | 5 | 0 | 7 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0001c0001t0003 | 0/0 | 1115 | 11 | 2 | 3 | 5 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1110): Show |
chr19 | 502497 | 524654 |
| a0001c0001t0004 | 0/0 | 1114 | 7 | 7 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0001c0001t0005 | 0/0 | 1114 | 2 | 2 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0001c0001t0006 | 0/0 | 1115 | 3 | 0 | 1 | 2 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1110): Show |
chr19 | 502497 | 524654 |
| a0001c0001t0007 | 0/0 | 1116 | 2 | 0 | 0 | 1 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1111): Show |
chr19 | 502497 | 524654 |
| a0001c0001t0008 | 0/0 | 1115 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1110): Show |
chr19 | 502497 | 524654 |
| a0001c0001t0009 | 0/0 | 1116 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1111): Show |
chr19 | 502497 | 524654 |
| a0001c0001t0010 | 0/0 | 1115 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1110): Show |
chr19 | 502497 | 524654 |
| a0001c0001t0012 | 0/0 | 1116 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1111): Show |
chr19 | 502497 | 524654 |
| a0001c0001t0013 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0001c0001t0014 | 0/0 | 1115 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1110): Show |
chr19 | 502497 | 524654 |
| a0001c0002t0001 | 0/0 | 1114 | 43 | 4 | 20 | 14 | 0 | 5 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0001c0002t0003 | 0/0 | 1115 | 2 | 0 | 0 | 2 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1110): Show |
chr19 | 502497 | 524654 |
| a0001c0005t0001 | 0/0 | 1114 | 5 | 5 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0001c0007t0001 | 0/0 | 1114 | 3 | 0 | 2 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0001c0008t0001 | 0/0 | 1114 | 3 | 3 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0001c0009t0001 | 0/0 | 1114 | 3 | 3 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0001c0010t0001 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0001c0010t0003 | 0/0 | 1115 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1110): Show |
chr19 | 502497 | 524654 |
| a0001c0011t0001 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0001c0012t0004 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0001c0013t0011 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1111): Show |
chr19 | 502497 | 524654 |
| a0001c0014t0004 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0001c0017t0001 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0002c0003t0001 | 0/0 | 1115 | 8 | 0 | 2 | 5 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1110): Show |
chr19 | 502497 | 524654 |
| a0002c0003t0002 | 0/0 | 1115 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1110): Show |
chr19 | 502497 | 524654 |
| a0002c0003t0004 | 0/0 | 1115 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1110): Show |
chr19 | 502497 | 524654 |
| a0002c0003t0005 | 0/0 | 1115 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1110): Show |
chr19 | 502497 | 524654 |
| a0002c0006t0001 | 0/0 | 1115 | 3 | 1 | 1 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1110): Show |
chr19 | 502497 | 524654 |
| a0002c0016t0004 | 0/0 | 1115 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1110): Show |
chr19 | 502497 | 524654 |
| a0003c0004t0001 | 0/0 | 1114 | 10 | 0 | 2 | 6 | 1 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1109): Show |
chr19 | 502497 | 524654 |
| a0004c0015t0008 | 0/0 | 1115 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | CTCAG others(1110): Show |
chr19 | 502497 | 524654 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 24 | 3 | 3 | 17 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0002 | 0/0 | 19 | 1 | 4 | 7 | 3 | 4 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0004 | 0/0 | 10 | 1 | 1 | 8 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 6 | 0 | 1 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0007 | 0/0 | 5 | 1 | 2 | 0 | 2 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0010 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0011 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0023 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0005g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0009g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0010g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0012g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0013g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0001t0014g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0003 | 0/0 | 13 | 0 | 6 | 7 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0005t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0005t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0005t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0007t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0007t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0008t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0008t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0008t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0009t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0009t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0009t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0010t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0010t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0011t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0012t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0013t0011g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0014t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0001c0017t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0002c0003t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0002c0003t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0002c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0002c0003t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0002c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0002c0003t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0002c0003t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0002c0003t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0002c0006t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0002c0006t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0002c0006t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0002c0016t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0003c0004t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0003c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0003c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0003c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0003c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0003c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0003c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0003c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0003c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| a0004c0015t0008g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0004 | t0001 | g0115 | EUR | GBR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | GBR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | GBR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00423 | hp2 | a0001 | c0001 | t0014 | g0173 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0085 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0110 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | CHS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00735 | hp2 | a0002 | c0003 | t0001 | g0153 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0111 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01081 | hp2 | a0003 | c0004 | t0001 | g0030 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0185 | AMR | PUR | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01256 | hp1 | a0001 | c0007 | t0001 | g0026 | AMR | CLM | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0113 | AMR | CLM | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01258 | hp2 | a0001 | c0007 | t0001 | g0026 | AMR | CLM | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | CLM | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0165 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01891 | hp2 | a0001 | c0005 | t0001 | g0013 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01952 | hp2 | a0003 | c0004 | t0001 | g0030 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01978 | hp1 | a0002 | c0003 | t0001 | g0093 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0160 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02056 | hp1 | a0001 | c0001 | t0010 | g0066 | EAS | KHV | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02074 | hp1 | a0002 | c0006 | t0001 | g0012 | EAS | KHV | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02080 | hp2 | a0001 | c0001 | t0008 | g0022 | EAS | KHV | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | KHV | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02132 | hp2 | a0003 | c0004 | t0001 | g0134 | EAS | KHV | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CDX | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CDX | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CDX | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02293 | hp2 | a0002 | c0006 | t0001 | g0003 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | PEL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02572 | hp2 | a0001 | c0012 | t0004 | g0216 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02622 | hp2 | a0002 | c0016 | t0004 | g0161 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02630 | hp1 | a0001 | c0008 | t0001 | g0162 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02630 | hp2 | a0001 | c0009 | t0001 | g0013 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02647 | hp2 | a0002 | c0006 | t0001 | g0047 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0081 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02895 | hp2 | a0001 | c0009 | t0001 | g0163 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02897 | hp2 | a0001 | c0009 | t0001 | g0164 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02922 | hp2 | a0001 | c0005 | t0001 | g0013 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02965 | hp2 | a0001 | c0013 | t0011 | g0202 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02976 | hp1 | a0001 | c0008 | t0001 | g0166 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02976 | hp2 | a0001 | c0017 | t0001 | g0158 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03098 | hp1 | a0001 | c0010 | t0001 | g0196 | AFR | MSL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03139 | hp2 | a0002 | c0003 | t0004 | g0188 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | MSL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03490 | hp1 | a0002 | c0003 | t0001 | g0121 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03516 | hp2 | a0002 | c0003 | t0005 | g0190 | AFR | ESN | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | STU | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | STU | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | BEB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | BEB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0176 | SAS | BEB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03927 | hp2 | a0001 | c0007 | t0001 | g0152 | SAS | BEB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG04184 | hp2 | a0001 | c0001 | t0009 | g0041 | SAS | BEB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0199 | SAS | STU | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | STU | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18522 | hp2 | a0001 | c0005 | t0001 | g0090 | AFR | YRI | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18747 | hp2 | a0003 | c0004 | t0001 | g0145 | EAS | CHB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | YRI | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18947 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18950 | hp2 | a0001 | c0001 | t0006 | g0065 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18954 | hp2 | a0003 | c0004 | t0001 | g0143 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18956 | hp1 | a0002 | c0003 | t0001 | g0072 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18956 | hp2 | a0002 | c0003 | t0002 | g0039 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18965 | hp2 | a0004 | c0015 | t0008 | g0148 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18966 | hp2 | a0003 | c0004 | t0001 | g0146 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18980 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18995 | hp1 | a0003 | c0004 | t0001 | g0147 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18995 | hp2 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18999 | hp2 | a0003 | c0004 | t0001 | g0142 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19000 | hp2 | a0001 | c0001 | t0012 | g0175 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | LWK | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19030 | hp2 | a0001 | c0008 | t0001 | g0159 | AFR | LWK | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0215 | AFR | LWK | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19059 | hp2 | a0001 | c0002 | t0003 | g0137 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19077 | hp1 | a0001 | c0001 | t0006 | g0104 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19090 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | YRI | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | GIH | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA20905 | hp2 | a0003 | c0004 | t0001 | g0060 | SAS | GIH | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02486 | hp1 | a0001 | c0010 | t0003 | g0195 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG02559 | hp2 | a0001 | c0011 | t0001 | g0126 | AFR | ACB | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03471 | hp1 | a0001 | c0014 | t0004 | g0211 | AFR | MSL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | MSL | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | USA | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | USA | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA18955 | hp2 | a0001 | c0001 | t0007 | g0103 | EAS | JPT | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | LWK | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0181 | AFR | LWK | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0102 | REF | REF | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0023 | REF | REF | TPGS1_chr19_502497_524654 | TPGS1 | chr19 | 502497 | 524654 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:518957 | C | A | 1 | a0003 | 10 | HG00099.hp1 HG01081.hp2 HG01952.hp2 others(7): Show |
missense_variant | MODERATE | c.407C>A | p.Pro136Gln | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 417/1114 | 407/873 | 136/290 | chr19 | 518957 | |||
| chr19:519017 | C | G | 1 | a0004 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.467C>G | p.Ala156Gly | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 477/1114 | 467/873 | 156/290 | chr19 | 519017 | |||
| chr19:519258 | G | GC | 1 | a0002 | 15 | HG00735.hp2 HG01978.hp1 HG02074.hp1 others(12): Show |
frameshift_variant | HIGH | c.711dupC | p.Ala238fs | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 722/1114 | 712/873 | 238/290 | INFO_REALIGN_3_PRIME | chr19 | 519258 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:507545 | G | A | 1 | a0001c0011 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.39G>A | p.Pro13Pro | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/2 | 49/1114 | 39/873 | 13/290 | chr19 | 507545 | |||
| chr19:507560 | G | A | 1 | a0001c0010 | 2 | HG02486.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.54G>A | p.Thr18Thr | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/2 | 64/1114 | 54/873 | 18/290 | chr19 | 507560 | |||
| chr19:507731 | C | T | 5 | a0001c0005 a0001c0008 a0001c0009 others(2): Show |
13 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
synonymous_variant | LOW | c.225C>T | p.Gly75Gly | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/2 | 235/1114 | 225/873 | 75/290 | chr19 | 507731 | |||
| chr19:518982 | C | T | 1 | a0001c0009 | 3 | HG02630.hp2 HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.432C>T | p.Ser144Ser | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 442/1114 | 432/873 | 144/290 | chr19 | 518982 | |||
| chr19:519018 | C | T | 2 | a0001c0007 a0001c0017 |
4 | HG01256.hp1 HG01258.hp2 HG02976.hp2 others(1): Show |
synonymous_variant | LOW | c.468C>T | p.Ala156Ala | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 478/1114 | 468/873 | 156/290 | chr19 | 519018 | |||
| chr19:519135 | G | C | 1 | a0001c0012 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.585G>C | p.Val195Val | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 595/1114 | 585/873 | 195/290 | chr19 | 519135 | |||
| chr19:519258 | G | C | 1 | a0001c0013 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.708G>C | p.Ala236Ala | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 718/1114 | 708/873 | 236/290 | chr19 | 519258 | |||
| chr19:519315 | G | A | 1 | a0001c0014 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.765G>A | p.Ala255Ala | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 775/1114 | 765/873 | 255/290 | chr19 | 519315 | |||
| chr19:519324 | C | T | 2 | a0001c0005 a0001c0009 |
8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
synonymous_variant | LOW | c.774C>T | p.Arg258Arg | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 784/1114 | 774/873 | 258/290 | chr19 | 519324 | |||
| chr19:519336 | G | A | 3 | a0001c0002 a0001c0013 a0002c0006 |
49 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(46): Show |
synonymous_variant | LOW | c.786G>A | p.Gly262Gly | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 796/1114 | 786/873 | 262/290 | chr19 | 519336 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:519433 | G | GC | 3 | a0001c0001t0009 a0001c0001t0010 a0001c0013t0011 |
3 | HG02056.hp1 HG02965.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12dupC | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 13 | INFO_REALIGN_3_PRIME | chr19 | 519433 | |||||
| chr19:519434 | C | A | 2 | a0001c0001t0005 a0002c0003t0005 |
3 | HG02451.hp2 HG02895.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 11 | chr19 | 519434 | ||||||
| chr19:519457 | T | TG | 6 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(3): Show |
18 | HG00597.hp1 HG01099.hp2 HG01256.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*40dupG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 41 | INFO_REALIGN_3_PRIME | chr19 | 519457 | |||||
| chr19:519575 | T | A | 1 | a0001c0001t0013 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152T>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 152 | chr19 | 519575 | ||||||
| chr19:519575 | T | TC | 4 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0014 others(1): Show |
7 | HG00423.hp2 HG00639.hp1 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*156dupC | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 157 | INFO_REALIGN_3_PRIME | chr19 | 519575 | |||||
| chr19:519586 | C | T | 5 | a0001c0001t0004 a0001c0012t0004 a0001c0014t0004 others(2): Show |
11 | HG02257.hp2 HG02572.hp2 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*163C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 163 | chr19 | 519586 | ||||||
| chr19:519592 | G | C | 2 | a0001c0001t0002 a0002c0003t0002 |
15 | HG00408.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*169G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 169 | chr19 | 519592 | ||||||
| chr19:519593 | G | GC | 3 | a0001c0001t0008 a0001c0001t0012 a0004c0015t0008 |
3 | HG02080.hp2 NA18965.hp2 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*172dupC | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 173 | INFO_REALIGN_3_PRIME | chr19 | 519593 | |||||
| chr19:519596 | G | C | 1 | a0001c0001t0014 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*173G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 173 | chr19 | 519596 | ||||||
| chr19:519597 | C | G | 1 | a0001c0001t0014 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*174C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 2/2 | 174 | chr19 | 519597 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:508067 | C | A | 10 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(7): Show |
12 | HG00408.hp2 HG02015.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.338+223C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 508067 | |||||||
| chr19:508073 | G | A | 4 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0205 others(1): Show |
4 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+229G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 508073 | |||||||
| chr19:508074 | G | C | 5 | a0001c0001t0001g0050 a0001c0001t0004g0048 a0001c0001t0004g0049 others(2): Show |
6 | HG01243.hp1 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.338+230G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 508074 | |||||||
| chr19:508193 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.338+349G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 508193 | |||||||
| chr19:508235 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.338+391T>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 508235 | |||||||
| chr19:508285 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.338+441G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 508285 | |||||||
| chr19:508421 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.338+577G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 508421 | |||||||
| chr19:508448 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.338+604A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 508448 | |||||||
| chr19:508566 | T | TG | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0042 others(32): Show |
43 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.338+732dupG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 508566 | ||||||
| chr19:508566 | T | TGG | 20 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(17): Show |
29 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.338+731_338+732dup others(2): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 508566 | ||||||
| chr19:508566 | TG | T | 31 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(28): Show |
43 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(40): Show |
intron_variant | MODIFIER | c.338+732delG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 508566 | ||||||
| chr19:508569 | G | C | 1 | a0001c0001t0004g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.338+725G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 508569 | |||||||
| chr19:508577 | T | G | 1 | a0001c0001t0003g0067 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.338+733T>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 508577 | |||||||
| chr19:508578 | C | T | 1 | a0001c0001t0003g0067 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.338+734C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 508578 | |||||||
| chr19:508626 | C | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(140): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.338+782C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 508626 | |||||||
| chr19:508637 | GC | G | 2 | a0001c0001t0001g0021 a0001c0001t0003g0067 |
3 | NA18973.hp1 NA18974.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.338+796delC | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 508637 | ||||||
| chr19:508714 | A | C | 2 | a0001c0001t0004g0215 a0001c0012t0004g0216 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.338+870A>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 508714 | |||||||
| chr19:508727 | G | A | 1 | a0001c0002t0001g0094 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.338+883G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 508727 | |||||||
| chr19:509090 | G | C | 5 | a0001c0001t0001g0050 a0001c0001t0004g0048 a0001c0001t0004g0049 others(2): Show |
6 | HG01243.hp1 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.338+1246G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509090 | |||||||
| chr19:509158 | G | C | 40 | a0001c0001t0001g0031 a0001c0001t0001g0079 a0001c0001t0001g0084 others(37): Show |
58 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.338+1314G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509158 | |||||||
| chr19:509303 | G | C | 1 | a0002c0003t0001g0153 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.338+1459G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509303 | |||||||
| chr19:509326 | G | A | 26 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0019 others(23): Show |
38 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.338+1482G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509326 | |||||||
| chr19:509378 | C | A | 5 | a0001c0001t0001g0050 a0001c0001t0004g0048 a0001c0001t0004g0049 others(2): Show |
6 | HG01243.hp1 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.338+1534C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509378 | |||||||
| chr19:509421 | G | A | 5 | a0001c0001t0001g0050 a0001c0001t0004g0048 a0001c0001t0004g0049 others(2): Show |
6 | HG01243.hp1 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.338+1577G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509421 | |||||||
| chr19:509433 | C | G | 2 | a0001c0001t0001g0050 a0001c0001t0004g0049 |
2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.338+1589C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509433 | |||||||
| chr19:509449 | T | A | 1 | a0001c0001t0002g0203 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.338+1605T>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509449 | |||||||
| chr19:509450 | A | T | 1 | a0001c0001t0002g0203 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.338+1606A>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509450 | |||||||
| chr19:509569 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.338+1725C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509569 | |||||||
| chr19:509578 | C | T | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(8): Show |
12 | HG01243.hp2 HG01978.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.338+1734C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509578 | |||||||
| chr19:509627 | G | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG02080.hp1 HG02080.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.338+1783G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509627 | |||||||
| chr19:509635 | G | A | 27 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0019 others(24): Show |
39 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.338+1791G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509635 | |||||||
| chr19:509640 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.338+1796C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509640 | |||||||
| chr19:509715 | C | T | 1 | a0001c0002t0001g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.338+1871C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509715 | |||||||
| chr19:509717 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(133): Show |
198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.338+1873C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509717 | |||||||
| chr19:509726 | G | A | 5 | a0001c0001t0001g0050 a0001c0001t0004g0048 a0001c0001t0004g0049 others(2): Show |
6 | HG01243.hp1 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.338+1882G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509726 | |||||||
| chr19:509843 | A | T | 1 | a0001c0001t0002g0203 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.338+1999A>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509843 | |||||||
| chr19:509897 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0025 others(15): Show |
29 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.338+2053G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509897 | |||||||
| chr19:509922 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.338+2078A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 509922 | |||||||
| chr19:510096 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.338+2252G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510096 | |||||||
| chr19:510124 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.338+2280A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510124 | |||||||
| chr19:510148 | C | T | 1 | a0001c0001t0003g0193 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.338+2304C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510148 | |||||||
| chr19:510155 | C | T | 1 | a0001c0001t0003g0193 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.338+2311C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510155 | |||||||
| chr19:510156 | A | G | 1 | a0001c0001t0003g0193 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.338+2312A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510156 | |||||||
| chr19:510169 | C | T | 12 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0002g0016 others(9): Show |
15 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.338+2325C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510169 | |||||||
| chr19:510185 | A | C | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0002c0003t0001g0093 |
3 | HG01978.hp1 HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.338+2341A>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510185 | |||||||
| chr19:510185 | A | G | 9 | a0001c0001t0001g0151 a0001c0002t0001g0129 a0001c0005t0001g0013 others(6): Show |
10 | HG01884.hp1 HG01891.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.338+2341A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510185 | |||||||
| chr19:510189 | C | A | 1 | a0001c0001t0003g0193 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.338+2345C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510189 | |||||||
| chr19:510189 | C | T | 2 | a0001c0008t0001g0162 a0002c0016t0004g0161 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.338+2345C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510189 | |||||||
| chr19:510190 | G | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(137): Show |
205 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.338+2346G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510190 | |||||||
| chr19:510201 | G | A | 2 | a0001c0001t0001g0141 a0003c0004t0001g0142 |
2 | HG00621.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.338+2357G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510201 | |||||||
| chr19:510209 | T | TAAAAATA others(186): Show |
1 | a0001c0001t0003g0193 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.338+2388_338+2389i others(195): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 510209 | ||||||
| chr19:510239 | G | A | 1 | a0002c0006t0001g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.338+2395G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510239 | |||||||
| chr19:510259 | G | C | 1 | a0001c0002t0001g0130 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.338+2415G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510259 | |||||||
| chr19:510266 | G | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(130): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.338+2422G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510266 | |||||||
| chr19:510290 | A | G | 2 | a0001c0001t0001g0114 a0002c0006t0001g0047 |
2 | HG02155.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.338+2446A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510290 | |||||||
| chr19:510305 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0013g0181 |
2 | HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.338+2461G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510305 | |||||||
| chr19:510315 | T | G | 5 | a0001c0001t0001g0056 a0001c0001t0002g0016 a0001c0001t0002g0045 others(2): Show |
6 | HG02647.hp2 HG03130.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.338+2471T>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510315 | |||||||
| chr19:510326 | T | G | 85 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0019 others(82): Show |
115 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.338+2482T>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510326 | |||||||
| chr19:510328 | G | A | 1 | a0003c0004t0001g0143 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.338+2484G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510328 | |||||||
| chr19:510329 | C | T | 1 | a0003c0004t0001g0115 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.338+2485C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510329 | |||||||
| chr19:510330 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.338+2486G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510330 | |||||||
| chr19:510335 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.338+2491T>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510335 | |||||||
| chr19:510345 | C | T | 1 | a0003c0004t0001g0115 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.338+2501C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510345 | |||||||
| chr19:510355 | A | G | 1 | a0003c0004t0001g0115 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.338+2511A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510355 | |||||||
| chr19:510359 | C | A | 1 | a0001c0001t0001g0097 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.338+2515C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510359 | |||||||
| chr19:510372 | C | CA | 6 | a0001c0001t0001g0098 a0001c0005t0001g0160 a0001c0008t0001g0159 others(3): Show |
6 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.338+2541dupA | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 510372 | ||||||
| chr19:510394 | C | A | 1 | a0001c0001t0004g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.338+2550C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510394 | |||||||
| chr19:510480 | C | A | 1 | a0001c0001t0004g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.338+2636C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510480 | |||||||
| chr19:510520 | C | A | 1 | a0001c0001t0002g0203 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.338+2676C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510520 | |||||||
| chr19:510530 | CTTTTGAG others(3): Show |
C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0052 others(7): Show |
17 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.338+2688_338+2697d others(12): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 510530 | ||||||
| chr19:510541 | T | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0052 others(7): Show |
17 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.338+2697T>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510541 | |||||||
| chr19:510543 | G | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0052 others(7): Show |
17 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.338+2699G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510543 | |||||||
| chr19:510555 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.338+2711C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510555 | |||||||
| chr19:510609 | G | A | 1 | a0001c0001t0013g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.338+2765G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510609 | |||||||
| chr19:510622 | C | G | 11 | a0001c0001t0001g0037 a0001c0001t0001g0123 a0001c0001t0001g0201 others(8): Show |
12 | HG01109.hp1 HG02055.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.338+2778C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510622 | |||||||
| chr19:510675 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0040 a0002c0003t0002g0039 |
4 | HG00408.hp2 HG02015.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+2831G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510675 | |||||||
| chr19:510703 | A | G | 3 | a0001c0001t0001g0050 a0001c0002t0001g0018 a0002c0006t0001g0047 |
4 | HG01243.hp1 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.338+2859A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510703 | |||||||
| chr19:510818 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0052 others(6): Show |
16 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.338+2974T>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510818 | |||||||
| chr19:510885 | A | G | 3 | a0001c0001t0005g0038 a0002c0003t0005g0190 a0002c0006t0001g0047 |
4 | HG02451.hp2 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+3041A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510885 | |||||||
| chr19:510908 | C | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0058 others(2): Show |
5 | HG01109.hp2 HG01256.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.338+3064C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 510908 | |||||||
| chr19:511089 | G | A | 5 | a0001c0001t0002g0017 a0001c0001t0002g0040 a0001c0001t0002g0092 others(2): Show |
6 | HG00408.hp2 HG02015.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.338+3245G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511089 | |||||||
| chr19:511105 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.338+3261G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511105 | |||||||
| chr19:511255 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.338+3411T>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511255 | |||||||
| chr19:511292 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0131 others(4): Show |
10 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.338+3448G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511292 | |||||||
| chr19:511304 | C | T | 1 | a0001c0002t0001g0140 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.338+3460C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511304 | |||||||
| chr19:511453 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.338+3609A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511453 | |||||||
| chr19:511468 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.338+3624G>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511468 | |||||||
| chr19:511572 | A | G | 1 | a0002c0016t0004g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.338+3728A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511572 | |||||||
| chr19:511700 | C | G | 1 | a0001c0002t0001g0113 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.338+3856C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511700 | |||||||
| chr19:511795 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.338+3951A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511795 | |||||||
| chr19:511796 | C | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(77): Show |
124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.338+3952C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511796 | |||||||
| chr19:511845 | C | A | 1 | a0002c0003t0005g0190 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.338+4001C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511845 | |||||||
| chr19:511881 | G | GT | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(81): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.338+4045dupT | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 511881 | ||||||
| chr19:511881 | G | GTT | 6 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0005g0038 others(3): Show |
7 | HG02132.hp2 HG02451.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.338+4044_338+4045d others(4): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 511881 | ||||||
| chr19:511911 | A | C | 1 | a0001c0001t0010g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.338+4067A>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511911 | |||||||
| chr19:511911 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(142): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.338+4067A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511911 | |||||||
| chr19:511933 | G | A | 1 | a0001c0001t0001g0015 | 3 | HG02647.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.338+4089G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511933 | |||||||
| chr19:511994 | C | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(75): Show |
121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.338+4150C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 511994 | |||||||
| chr19:512016 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(86): Show |
135 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.338+4172C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512016 | |||||||
| chr19:512017 | G | A | 12 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(9): Show |
15 | HG00408.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.338+4173G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512017 | |||||||
| chr19:512116 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.338+4272C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512116 | |||||||
| chr19:512134 | G | A | 8 | a0001c0001t0002g0017 a0001c0001t0002g0032 a0001c0001t0002g0040 others(5): Show |
10 | HG00408.hp2 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.338+4290G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512134 | |||||||
| chr19:512146 | C | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(77): Show |
124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.338+4302C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512146 | |||||||
| chr19:512359 | C | G | 31 | a0001c0001t0001g0116 a0001c0001t0001g0207 a0001c0001t0003g0003 others(28): Show |
47 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.338+4515C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512359 | |||||||
| chr19:512368 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.338+4524G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512368 | |||||||
| chr19:512432 | G | A | 2 | a0001c0001t0004g0215 a0001c0012t0004g0216 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.338+4588G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512432 | |||||||
| chr19:512568 | A | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(115): Show |
184 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.338+4724A>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512568 | |||||||
| chr19:512574 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0031 others(32): Show |
57 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.338+4730C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512574 | |||||||
| chr19:512620 | T | G | 1 | a0001c0001t0004g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.338+4776T>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512620 | |||||||
| chr19:512647 | G | A | 11 | a0001c0001t0001g0054 a0001c0001t0001g0079 a0001c0001t0001g0204 others(8): Show |
12 | HG00099.hp1 HG01081.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.338+4803G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512647 | |||||||
| chr19:512661 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.338+4817C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512661 | |||||||
| chr19:512686 | C | A | 1 | a0001c0001t0014g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.338+4842C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512686 | |||||||
| chr19:512742 | G | T | 1 | a0001c0014t0004g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.338+4898G>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512742 | |||||||
| chr19:512860 | G | A | 2 | a0001c0009t0001g0163 a0001c0009t0001g0164 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.338+5016G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512860 | |||||||
| chr19:512861 | C | A | 2 | a0001c0009t0001g0163 a0001c0009t0001g0164 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.338+5017C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512861 | |||||||
| chr19:512947 | G | C | 4 | a0001c0007t0001g0026 a0001c0007t0001g0152 a0001c0008t0001g0159 others(1): Show |
5 | HG01256.hp1 HG01258.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.338+5103G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512947 | |||||||
| chr19:512956 | C | CG | 6 | a0001c0001t0001g0074 a0001c0001t0001g0180 a0001c0001t0001g0191 others(3): Show |
6 | HG02055.hp1 HG02129.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.338+5117dupG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 512956 | ||||||
| chr19:512962 | A | T | 1 | a0001c0002t0001g0118 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.338+5118A>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 512962 | |||||||
| chr19:513163 | G | T | 1 | a0001c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.338+5319G>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513163 | |||||||
| chr19:513207 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0001g0169 others(2): Show |
8 | HG00280.hp2 HG00738.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.338+5363C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513207 | |||||||
| chr19:513273 | C | G | 1 | a0002c0006t0001g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.338+5429C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513273 | |||||||
| chr19:513289 | G | A | 1 | a0001c0001t0004g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.338+5445G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513289 | |||||||
| chr19:513295 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.338+5451C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513295 | |||||||
| chr19:513296 | G | A | 3 | a0001c0001t0005g0038 a0002c0003t0005g0190 a0002c0006t0001g0047 |
4 | HG02451.hp2 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+5452G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513296 | |||||||
| chr19:513339 | G | C | 12 | a0001c0001t0001g0054 a0001c0001t0001g0079 a0001c0001t0001g0204 others(9): Show |
13 | HG00099.hp1 HG01081.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.338+5495G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513339 | |||||||
| chr19:513350 | T | C | 33 | a0001c0001t0001g0116 a0001c0001t0001g0207 a0001c0001t0003g0003 others(30): Show |
50 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.338+5506T>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513350 | |||||||
| chr19:513367 | A | AGAGTTGA others(3): Show |
1 | a0001c0001t0001g0183 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.339-5520_339-5511d others(12): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 513367 | ||||||
| chr19:513379 | C | T | 28 | a0001c0001t0001g0116 a0001c0001t0003g0003 a0001c0002t0001g0003 others(25): Show |
44 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.339-5510C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513379 | |||||||
| chr19:513537 | G | A | 2 | a0001c0001t0004g0215 a0001c0012t0004g0216 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.339-5352G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513537 | |||||||
| chr19:513619 | C | CACCTACT others(25): Show |
64 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(61): Show |
89 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.339-5239_339-5238i others(34): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 513619 | ||||||
| chr19:513635 | GCCCAGCA others(26): Show |
G | 1 | a0001c0002t0001g0118 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.339-5251_339-5219d others(35): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 513635 | ||||||
| chr19:513639 | AGCATTAC others(25): Show |
A | 32 | a0001c0001t0001g0116 a0001c0001t0001g0207 a0001c0001t0003g0003 others(29): Show |
49 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.339-5238_339-5207d others(34): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 513639 | ||||||
| chr19:513651 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0031 others(46): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.339-5238C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513651 | |||||||
| chr19:513662 | T | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0031 others(46): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.339-5227T>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513662 | |||||||
| chr19:513665 | T | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0031 others(46): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.339-5224T>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513665 | |||||||
| chr19:513666 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0031 others(46): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.339-5223G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513666 | |||||||
| chr19:513669 | C | T | 8 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0001t0004g0055 others(5): Show |
8 | HG02572.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.339-5220C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513669 | |||||||
| chr19:513671 | T | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0031 others(47): Show |
73 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.339-5218T>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513671 | |||||||
| chr19:513671 | TGCATTAC others(25): Show |
T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0131 others(4): Show |
10 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.339-5122_339-5091d others(34): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 513671 | ||||||
| chr19:513683 | T | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0031 others(46): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.339-5206T>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513683 | |||||||
| chr19:513686 | C | G | 33 | a0001c0001t0001g0116 a0001c0001t0001g0207 a0001c0001t0003g0003 others(30): Show |
50 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.339-5203C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513686 | |||||||
| chr19:513694 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0031 others(46): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.339-5195C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513694 | |||||||
| chr19:513697 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(86): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.339-5192C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513697 | |||||||
| chr19:513698 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0031 others(46): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.339-5191A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513698 | |||||||
| chr19:513703 | A | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0031 others(46): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.339-5186A>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513703 | |||||||
| chr19:513715 | T | C | 33 | a0001c0001t0001g0116 a0001c0001t0001g0207 a0001c0001t0003g0003 others(30): Show |
50 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.339-5174T>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513715 | |||||||
| chr19:513726 | C | T | 33 | a0001c0001t0001g0116 a0001c0001t0001g0207 a0001c0001t0003g0003 others(30): Show |
50 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.339-5163C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513726 | |||||||
| chr19:513728 | C | T | 1 | a0001c0014t0004g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.339-5161C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513728 | |||||||
| chr19:513729 | C | T | 34 | a0001c0001t0001g0116 a0001c0001t0001g0207 a0001c0001t0001g0208 others(31): Show |
51 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.339-5160C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513729 | |||||||
| chr19:513730 | A | G | 33 | a0001c0001t0001g0116 a0001c0001t0001g0207 a0001c0001t0003g0003 others(30): Show |
50 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.339-5159A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513730 | |||||||
| chr19:513733 | C | T | 33 | a0001c0001t0001g0116 a0001c0001t0001g0207 a0001c0001t0003g0003 others(30): Show |
50 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.339-5156C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513733 | |||||||
| chr19:513735 | A | T | 33 | a0001c0001t0001g0116 a0001c0001t0001g0207 a0001c0001t0003g0003 others(30): Show |
50 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.339-5154A>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513735 | |||||||
| chr19:513928 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.339-4961C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 513928 | |||||||
| chr19:513997 | GCTGGCCC others(352): Show |
G | 1 | a0003c0004t0001g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.339-4862_339-4504d others(2): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 513997 | ||||||
| chr19:514052 | C | G | 2 | a0001c0001t0004g0215 a0001c0012t0004g0216 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.339-4837C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514052 | |||||||
| chr19:514183 | C | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0101 a0001c0001t0001g0107 others(3): Show |
6 | NA18965.hp1 NA18986.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.339-4706C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514183 | |||||||
| chr19:514212 | C | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0131 others(4): Show |
10 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.339-4677C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514212 | |||||||
| chr19:514326 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.339-4563G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514326 | |||||||
| chr19:514455 | CTGGCCCA others(11): Show |
C | 1 | a0001c0002t0001g0113 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.339-4433_339-4416d others(20): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514455 | |||||||
| chr19:514511 | G | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0031 others(25): Show |
49 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.339-4378G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514511 | |||||||
| chr19:514587 | G | A | 1 | a0003c0004t0001g0146 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.339-4302G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514587 | |||||||
| chr19:514622 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.339-4267G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514622 | |||||||
| chr19:514625 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0189 |
2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.339-4264G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514625 | |||||||
| chr19:514750 | TC | T | 7 | a0001c0001t0002g0017 a0001c0001t0002g0040 a0001c0001t0002g0092 others(4): Show |
8 | HG00408.hp2 HG02015.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.339-4136delC | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 514750 | ||||||
| chr19:514808 | A | G | 1 | a0003c0004t0001g0030 | 2 | HG01081.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.339-4081A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514808 | |||||||
| chr19:514809 | T | TG | 6 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0003g0109 others(3): Show |
11 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.339-4074dupG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 514809 | ||||||
| chr19:514812 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.339-4077G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514812 | |||||||
| chr19:514858 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(47): Show |
87 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.339-4031C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514858 | |||||||
| chr19:514859 | G | A | 2 | a0001c0001t0004g0215 a0001c0012t0004g0216 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.339-4030G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514859 | |||||||
| chr19:514860 | G | C | 1 | a0001c0002t0001g0118 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.339-4029G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514860 | |||||||
| chr19:514868 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.339-4021G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 514868 | |||||||
| chr19:515012 | C | T | 10 | a0001c0001t0005g0038 a0001c0005t0001g0013 a0001c0005t0001g0090 others(7): Show |
12 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.339-3877C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515012 | |||||||
| chr19:515098 | C | G | 1 | a0001c0001t0001g0108 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.339-3791C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515098 | |||||||
| chr19:515111 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.339-3778G>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515111 | |||||||
| chr19:515112 | C | G | 1 | a0001c0001t0001g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.339-3777C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515112 | |||||||
| chr19:515154 | T | A | 1 | a0001c0002t0001g0118 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.339-3735T>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515154 | |||||||
| chr19:515259 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.339-3630C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515259 | |||||||
| chr19:515261 | A | G | 12 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(9): Show |
15 | HG00408.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.339-3628A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515261 | |||||||
| chr19:515265 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.339-3624G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515265 | |||||||
| chr19:515315 | C | T | 1 | a0001c0001t0002g0032 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.339-3574C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515315 | |||||||
| chr19:515381 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.339-3508A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515381 | |||||||
| chr19:515400 | C | CA | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(48): Show |
73 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.339-3473dupA | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 515400 | ||||||
| chr19:515412 | A | G | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0167 |
3 | HG02145.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.339-3477A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515412 | |||||||
| chr19:515417 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.339-3472G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515417 | |||||||
| chr19:515464 | G | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0051 others(8): Show |
20 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.339-3425G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515464 | |||||||
| chr19:515551 | G | A | 50 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(47): Show |
72 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.339-3338G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515551 | |||||||
| chr19:515554 | A | G | 34 | a0001c0001t0001g0116 a0001c0001t0001g0207 a0001c0001t0003g0003 others(31): Show |
51 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.339-3335A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515554 | |||||||
| chr19:515559 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.339-3330G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515559 | |||||||
| chr19:515562 | A | C | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.339-3327A>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515562 | |||||||
| chr19:515580 | A | G | 50 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(47): Show |
72 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.339-3309A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515580 | |||||||
| chr19:515653 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.339-3236G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515653 | |||||||
| chr19:515753 | C | G | 1 | a0001c0001t0001g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.339-3136C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515753 | |||||||
| chr19:515757 | GCGCGGTG others(3): Show |
G | 1 | a0001c0001t0001g0183 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.339-3130_339-3121d others(12): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 515757 | ||||||
| chr19:515799 | G | A | 2 | a0001c0002t0001g0205 a0001c0002t0001g0206 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.339-3090G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515799 | |||||||
| chr19:515803 | C | T | 1 | a0001c0001t0003g0193 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.339-3086C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515803 | |||||||
| chr19:515822 | G | A | 52 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(49): Show |
75 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.339-3067G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515822 | |||||||
| chr19:515833 | C | T | 1 | a0001c0001t0001g0010 | 4 | HG01361.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.339-3056C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515833 | |||||||
| chr19:515846 | A | C | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.339-3043A>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515846 | |||||||
| chr19:515856 | C | A | 1 | a0001c0002t0001g0081 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.339-3033C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515856 | |||||||
| chr19:515860 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.339-3029G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515860 | |||||||
| chr19:515876 | C | CA | 12 | a0001c0001t0001g0054 a0001c0001t0001g0079 a0001c0001t0001g0204 others(9): Show |
13 | HG00099.hp1 HG01081.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.339-3007dupA | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 515876 | ||||||
| chr19:515981 | G | A | 12 | a0001c0001t0001g0054 a0001c0001t0001g0079 a0001c0001t0001g0204 others(9): Show |
13 | HG00099.hp1 HG01081.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.339-2908G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515981 | |||||||
| chr19:515994 | TG | T | 12 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(9): Show |
15 | HG00408.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.339-2894delG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 515994 | |||||||
| chr19:516031 | C | CA | 12 | a0001c0001t0001g0078 a0001c0001t0001g0149 a0001c0001t0001g0197 others(9): Show |
14 | HG01081.hp1 HG01106.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.339-2842dupA | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 516031 | ||||||
| chr19:516031 | CA | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0031 others(33): Show |
57 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.339-2842delA | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 516031 | ||||||
| chr19:516031 | CAAAA | C | 8 | a0001c0005t0001g0013 a0001c0005t0001g0090 a0001c0005t0001g0160 others(5): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.339-2845_339-2842d others(6): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 516031 | ||||||
| chr19:516041 | AAAAAAAG others(1): Show |
A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0019 others(17): Show |
32 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.339-2845_339-2838d others(10): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 516041 | ||||||
| chr19:516044 | A | G | 23 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0050 others(20): Show |
33 | HG01243.hp1 HG01256.hp1 HG01258.hp2 others(30): Show |
intron_variant | MODIFIER | c.339-2845A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516044 | |||||||
| chr19:516049 | G | A | 32 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0050 others(29): Show |
43 | HG01243.hp1 HG01256.hp1 HG01258.hp2 others(40): Show |
intron_variant | MODIFIER | c.339-2840G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516049 | |||||||
| chr19:516073 | A | C | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.339-2816A>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516073 | |||||||
| chr19:516076 | A | C | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.339-2813A>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516076 | |||||||
| chr19:516077 | C | A | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.339-2812C>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516077 | |||||||
| chr19:516078 | A | C | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.339-2811A>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516078 | |||||||
| chr19:516095 | A | G | 4 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0014t0004g0211 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-2794A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516095 | |||||||
| chr19:516298 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.339-2591C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516298 | |||||||
| chr19:516299 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.339-2590G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516299 | |||||||
| chr19:516305 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18955.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.339-2584C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516305 | |||||||
| chr19:516388 | C | CT | 55 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(52): Show |
77 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.339-2487dupT | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 516388 | ||||||
| chr19:516388 | C | CTT | 5 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0007t0001g0026 others(2): Show |
6 | HG00597.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.339-2488_339-2487d others(4): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 516388 | ||||||
| chr19:516388 | CT | C | 14 | a0001c0001t0001g0079 a0001c0001t0001g0132 a0001c0001t0001g0204 others(11): Show |
15 | HG00099.hp1 HG00673.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.339-2487delT | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 516388 | ||||||
| chr19:516400 | T | G | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.339-2489T>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516400 | |||||||
| chr19:516408 | G | A | 2 | a0001c0001t0004g0215 a0001c0012t0004g0216 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.339-2481G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516408 | |||||||
| chr19:516480 | G | A | 12 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(9): Show |
15 | HG00408.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.339-2409G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516480 | |||||||
| chr19:516516 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.339-2373C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516516 | |||||||
| chr19:516592 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.339-2297C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516592 | |||||||
| chr19:516632 | C | T | 52 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(49): Show |
74 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.339-2257C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516632 | |||||||
| chr19:516643 | A | G | 1 | a0001c0001t0004g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339-2246A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516643 | |||||||
| chr19:516730 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.339-2159T>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516730 | |||||||
| chr19:516777 | G | A | 34 | a0001c0001t0001g0116 a0001c0001t0001g0207 a0001c0001t0003g0003 others(31): Show |
51 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.339-2112G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516777 | |||||||
| chr19:516801 | A | T | 1 | a0001c0001t0001g0054 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.339-2088A>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516801 | |||||||
| chr19:516998 | C | T | 12 | a0001c0001t0001g0054 a0001c0001t0001g0079 a0001c0001t0001g0204 others(9): Show |
13 | HG00099.hp1 HG01081.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.339-1891C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 516998 | |||||||
| chr19:517007 | G | A | 3 | a0001c0007t0001g0026 a0001c0007t0001g0152 a0001c0017t0001g0158 |
4 | HG01256.hp1 HG01258.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.339-1882G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517007 | |||||||
| chr19:517011 | G | GT | 39 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(36): Show |
60 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.339-1878_339-1877i others(3): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517011 | |||||||
| chr19:517012 | C | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(36): Show |
60 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.339-1877C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517012 | |||||||
| chr19:517013 | C | G | 39 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(36): Show |
60 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.339-1876C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517013 | |||||||
| chr19:517069 | C | T | 2 | a0001c0001t0004g0215 a0001c0012t0004g0216 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.339-1820C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517069 | |||||||
| chr19:517125 | G | T | 1 | a0001c0001t0014g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.339-1764G>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517125 | |||||||
| chr19:517218 | A | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0154 others(1): Show |
7 | HG02109.hp2 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.339-1671A>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517218 | |||||||
| chr19:517222 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.339-1667G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517222 | |||||||
| chr19:517290 | C | T | 1 | a0002c0006t0001g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.339-1599C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517290 | |||||||
| chr19:517294 | C | T | 12 | a0001c0001t0001g0054 a0001c0001t0001g0079 a0001c0001t0001g0204 others(9): Show |
13 | HG00099.hp1 HG01081.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.339-1595C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517294 | |||||||
| chr19:517315 | G | A | 8 | a0003c0004t0001g0030 a0003c0004t0001g0060 a0003c0004t0001g0115 others(5): Show |
9 | HG00099.hp1 HG01081.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.339-1574G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517315 | |||||||
| chr19:517395 | G | GGGAGGCC others(137): Show |
1 | a0002c0006t0001g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.339-1452_339-1309d others(146): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 517395 | ||||||
| chr19:517409 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.339-1480G>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517409 | |||||||
| chr19:517422 | A | AG | 7 | a0001c0001t0001g0059 a0001c0001t0001g0179 a0001c0001t0001g0197 others(4): Show |
7 | HG00639.hp1 HG02258.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.339-1461dupG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 517422 | ||||||
| chr19:517429 | AGGCCAGG others(13): Show |
A | 1 | a0001c0001t0001g0210 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.339-1437_339-1418d others(22): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 517429 | ||||||
| chr19:517462 | T | G | 1 | a0001c0002t0001g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.339-1427T>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517462 | |||||||
| chr19:517468 | C | G | 1 | a0001c0001t0014g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.339-1421C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517468 | |||||||
| chr19:517469 | T | C | 1 | a0001c0001t0014g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.339-1420T>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517469 | |||||||
| chr19:517470 | G | T | 1 | a0001c0001t0014g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.339-1419G>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517470 | |||||||
| chr19:517471 | G | A | 1 | a0001c0002t0001g0094 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.339-1418G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517471 | |||||||
| chr19:517488 | A | C | 47 | a0001c0001t0001g0089 a0001c0001t0001g0207 a0001c0001t0002g0016 others(44): Show |
67 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.339-1401A>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517488 | |||||||
| chr19:517517 | A | C | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.339-1372A>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517517 | |||||||
| chr19:517541 | G | T | 1 | a0001c0005t0001g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.339-1348G>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517541 | |||||||
| chr19:517560 | G | A | 1 | a0004c0015t0008g0148 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.339-1329G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517560 | |||||||
| chr19:517561 | C | G | 1 | a0004c0015t0008g0148 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.339-1328C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517561 | |||||||
| chr19:517566 | A | AG | 11 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0070 others(8): Show |
11 | HG00423.hp2 HG01109.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.339-1317dupG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 517566 | ||||||
| chr19:517566 | A | G | 1 | a0004c0015t0008g0148 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.339-1323A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517566 | |||||||
| chr19:517570 | G | A | 1 | a0004c0015t0008g0148 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.339-1319G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517570 | |||||||
| chr19:517628 | A | AG | 11 | a0001c0001t0001g0057 a0001c0001t0001g0070 a0001c0001t0001g0071 others(8): Show |
11 | HG00741.hp2 HG01981.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.339-1255dupG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 517628 | ||||||
| chr19:517642 | G | C | 1 | a0001c0001t0002g0032 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.339-1247G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517642 | |||||||
| chr19:517664 | G | A | 12 | a0001c0001t0001g0054 a0001c0001t0001g0079 a0001c0001t0001g0204 others(9): Show |
13 | HG00099.hp1 HG01081.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.339-1225G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517664 | |||||||
| chr19:517690 | A | AG | 8 | a0001c0001t0001g0063 a0001c0001t0001g0071 a0001c0001t0001g0089 others(5): Show |
8 | HG00423.hp2 HG00597.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.339-1193dupG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 517690 | ||||||
| chr19:517711 | G | A | 33 | a0001c0001t0001g0207 a0001c0001t0003g0003 a0001c0002t0001g0003 others(30): Show |
50 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.339-1178G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517711 | |||||||
| chr19:517777 | C | CG | 4 | a0001c0001t0001g0125 a0001c0001t0001g0180 a0002c0003t0001g0093 others(1): Show |
4 | HG01978.hp1 HG02602.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-1108dupG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 517777 | ||||||
| chr19:517822 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
5 | HG02622.hp1 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.339-1067G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517822 | |||||||
| chr19:517829 | G | C | 12 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(9): Show |
15 | HG00408.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.339-1060G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517829 | |||||||
| chr19:517888 | GGGCTGGG others(24): Show |
G | 1 | a0001c0002t0001g0119 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.339-987_339-957del others(31): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 517888 | ||||||
| chr19:517896 | A | G | 1 | a0001c0001t0014g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.339-993A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517896 | |||||||
| chr19:517896 | AGGAGGAG others(42): Show |
A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0052 others(2): Show |
12 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-933_339-885del others(49): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 517896 | ||||||
| chr19:517897 | G | A | 1 | a0001c0001t0014g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.339-992G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517897 | |||||||
| chr19:517910 | G | C | 30 | a0001c0001t0001g0207 a0001c0001t0003g0003 a0001c0002t0001g0003 others(27): Show |
47 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.339-979G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517910 | |||||||
| chr19:517949 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.339-940G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517949 | |||||||
| chr19:517977 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0184 |
2 | HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.339-912G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 517977 | |||||||
| chr19:518023 | G | T | 1 | a0001c0002t0001g0080 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.339-866G>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518023 | |||||||
| chr19:518027 | A | G | 1 | a0001c0001t0014g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.339-862A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518027 | |||||||
| chr19:518028 | G | A | 1 | a0001c0001t0014g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.339-861G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518028 | |||||||
| chr19:518043 | GA | G | 78 | a0001c0001t0001g0021 a0001c0001t0001g0054 a0001c0001t0001g0079 others(75): Show |
102 | HG00099.hp1 HG00408.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.339-845delA | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518043 | |||||||
| chr19:518044 | A | AG | 7 | a0001c0001t0001g0031 a0001c0001t0001g0057 a0001c0001t0001g0070 others(4): Show |
7 | HG00408.hp1 HG01981.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.339-840dupG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 518044 | ||||||
| chr19:518044 | A | G | 2 | a0001c0002t0001g0117 a0001c0002t0001g0118 |
2 | HG00741.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.339-845A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518044 | |||||||
| chr19:518048 | G | C | 2 | a0001c0001t0004g0215 a0001c0012t0004g0216 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.339-841G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518048 | |||||||
| chr19:518085 | G | C | 1 | a0002c0003t0002g0039 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.339-804G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518085 | |||||||
| chr19:518086 | G | T | 1 | a0002c0003t0002g0039 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.339-803G>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518086 | |||||||
| chr19:518100 | C | T | 5 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0001t0004g0170 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.339-789C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518100 | |||||||
| chr19:518140 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0052 others(2): Show |
12 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-749G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518140 | |||||||
| chr19:518143 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0052 others(2): Show |
12 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-746A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518143 | |||||||
| chr19:518143 | AGCTGGGA others(158): Show |
A | 2 | a0001c0001t0004g0035 a0002c0003t0004g0188 |
3 | HG02257.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.339-657_339-493del | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 518143 | ||||||
| chr19:518165 | G | C | 1 | a0001c0001t0014g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.339-724G>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518165 | |||||||
| chr19:518166 | C | T | 1 | a0001c0001t0014g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.339-723C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518166 | |||||||
| chr19:518167 | T | G | 1 | a0001c0001t0014g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.339-722T>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518167 | |||||||
| chr19:518172 | G | A | 2 | a0001c0002t0001g0018 a0001c0002t0001g0185 |
3 | HG01243.hp2 HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.339-717G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518172 | |||||||
| chr19:518194 | A | G | 1 | a0001c0001t0014g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.339-695A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518194 | |||||||
| chr19:518233 | G | A | 5 | a0001c0001t0001g0062 a0001c0001t0002g0016 a0001c0001t0002g0045 others(2): Show |
6 | HG03239.hp2 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.339-656G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518233 | |||||||
| chr19:518318 | A | C | 1 | a0001c0001t0006g0104 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.339-571A>C | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518318 | |||||||
| chr19:518353 | G | A | 1 | a0001c0002t0001g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.339-536G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518353 | |||||||
| chr19:518354 | A | AG | 4 | a0001c0001t0006g0104 a0001c0001t0009g0041 a0001c0002t0001g0117 others(1): Show |
4 | HG02300.hp2 HG03704.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.339-531dupG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 518354 | ||||||
| chr19:518354 | A | G | 1 | a0001c0002t0001g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.339-535A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518354 | |||||||
| chr19:518355 | G | A | 1 | a0001c0002t0001g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.339-534G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518355 | |||||||
| chr19:518383 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.339-506G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518383 | |||||||
| chr19:518397 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.339-492G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518397 | |||||||
| chr19:518437 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.339-452G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518437 | |||||||
| chr19:518438 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.339-451A>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518438 | |||||||
| chr19:518468 | A | AG | 5 | a0001c0001t0007g0103 a0001c0002t0001g0206 a0001c0013t0011g0202 others(2): Show |
5 | HG01978.hp1 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.339-416dupG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 518468 | ||||||
| chr19:518559 | A | G | 1 | a0001c0002t0001g0080 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.339-330A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518559 | |||||||
| chr19:518560 | G | A | 1 | a0001c0002t0001g0080 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.339-329G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518560 | |||||||
| chr19:518597 | GGGGGGAG others(24): Show |
G | 2 | a0001c0001t0004g0215 a0001c0012t0004g0216 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.339-261_339-231del others(31): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 518597 | ||||||
| chr19:518598 | G | T | 4 | a0001c0001t0002g0016 a0001c0001t0002g0045 a0001c0001t0002g0046 others(1): Show |
5 | HG03239.hp2 HG03490.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.339-291G>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518598 | |||||||
| chr19:518613 | C | G | 1 | a0001c0001t0004g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339-276C>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518613 | |||||||
| chr19:518628 | T | G | 3 | a0001c0001t0013g0181 a0001c0007t0001g0026 a0001c0007t0001g0152 |
4 | HG01256.hp1 HG01258.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.339-261T>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518628 | |||||||
| chr19:518629 | GGGGGAGG others(24): Show |
G | 7 | a0001c0005t0001g0013 a0001c0005t0001g0090 a0001c0005t0001g0160 others(4): Show |
8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.339-244_339-214del others(31): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 518629 | ||||||
| chr19:518636 | G | T | 4 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0014t0004g0211 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-253G>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518636 | |||||||
| chr19:518644 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.339-245C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518644 | |||||||
| chr19:518645 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0021 others(3): Show |
8 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.339-244G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518645 | |||||||
| chr19:518674 | C | T | 1 | a0001c0001t0004g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.339-215C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518674 | |||||||
| chr19:518684 | A | AG | 3 | a0001c0001t0002g0091 a0001c0001t0009g0041 a0001c0002t0001g0081 |
3 | HG02738.hp2 HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.339-204dupG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 518684 | ||||||
| chr19:518686 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.339-203A>G | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518686 | |||||||
| chr19:518694 | C | CG | 8 | a0001c0001t0001g0021 a0001c0001t0001g0061 a0001c0001t0001g0098 others(5): Show |
9 | HG00438.hp2 HG00741.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.339-190dupG | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 518694 | ||||||
| chr19:518718 | G | A | 34 | a0001c0001t0001g0207 a0001c0001t0003g0003 a0001c0002t0001g0003 others(31): Show |
51 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.339-171G>A | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518718 | |||||||
| chr19:518737 | A | AGGGGAGG others(4): Show |
1 | a0001c0002t0001g0094 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.339-149_339-139dup others(11): Show |
TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | 518737 | ||||||
| chr19:518884 | C | T | 12 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0032 others(9): Show |
15 | HG00408.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
splice_region_variant&intron_variant | LOW | c.339-5C>T | TPGS1 | ENSG00000141933.9 | transcript | ENST00000359315.6 | protein_coding | 1/1 | chr19 | 518884 |