| geneid | 8459 |
|---|---|
| ensemblid | ENSG00000128294.16 |
| hgncid | 12021 |
| symbol | TPST2 |
| name | tyrosylprotein sulfotransferase 2 |
| refseq_nuc | NM_003595.5 |
| refseq_prot | NP_003586.3 |
| ensembl_nuc | ENST00000338754.9 |
| ensembl_prot | ENSP00000339813.4 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 26521996 |
| end | 26590132 |
| strand | - |
| ver | v1.2 |
| region | chr22:26521996-26590132 |
| region5000 | chr22:26516996-26595132 |
| regionname0 | TPST2_chr22_26521996_26590132 |
| regionname5000 | TPST2_chr22_26516996_26595132 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 377 | 372 | 87 | 64 | 170 | 13 | 36 | 132 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002 | 0/0 | 130 | 26 | 6 | 6 | 12 | 0 | 2 | 8 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0003 | 0/0 | 377 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0004 | 0/0 | 377 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1134 | 275 | 49 | 40 | 150 | 9 | 26 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0002 | 0/0 | 1135 | 23 | 4 | 6 | 11 | 0 | 2 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0003 | 0/0 | 1134 | 23 | 21 | 2 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0004 | 0/0 | 1134 | 20 | 6 | 2 | 9 | 0 | 3 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0005 | 0/0 | 1134 | 17 | 7 | 7 | 1 | 1 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0006 | 0/0 | 1134 | 17 | 0 | 5 | 8 | 1 | 3 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0007 | 1/0 | 1134 | 6 | 0 | 3 | 0 | 0 | 2 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0008 | 0/0 | 1134 | 5 | 1 | 4 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0009 | 0/0 | 1134 | 2 | 0 | 0 | 0 | 1 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0010 | 0/0 | 1134 | 2 | 1 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0011 | 0/0 | 1135 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0012 | 0/0 | 1135 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0013 | 0/0 | 1135 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0014 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0015 | 0/0 | 1134 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0016 | 0/0 | 1134 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0017 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0018 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0019 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| c0020 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4522 | 71 | 8 | 7 | 46 | 0 | 10 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0002 | 0/0 | 4524 | 55 | 7 | 11 | 28 | 5 | 4 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0003 | 0/0 | 4488 | 50 | 0 | 7 | 33 | 1 | 9 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0004 | 0/1 | 4480 | 46 | 16 | 10 | 18 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0005 | 0/0 | 4512 | 33 | 0 | 16 | 13 | 2 | 2 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0006 | 0/0 | 4488 | 28 | 1 | 3 | 19 | 2 | 3 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0007 | 0/0 | 4521 | 26 | 0 | 9 | 12 | 0 | 5 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0008 | 0/0 | 4486 | 16 | 16 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0009 | 1/0 | 4520 | 8 | 3 | 2 | 0 | 0 | 2 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0010 | 0/0 | 4520 | 6 | 5 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0011 | 0/0 | 4512 | 6 | 6 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0012 | 0/0 | 4511 | 5 | 5 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0013 | 0/0 | 4480 | 4 | 4 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0014 | 0/0 | 4524 | 3 | 0 | 0 | 3 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0015 | 0/0 | 4508 | 3 | 0 | 0 | 3 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0016 | 0/0 | 4488 | 3 | 3 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0017 | 0/0 | 4480 | 3 | 3 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0018 | 0/0 | 4489 | 2 | 1 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0019 | 0/0 | 4512 | 2 | 2 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0020 | 0/0 | 4480 | 2 | 0 | 0 | 2 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0021 | 0/0 | 4512 | 2 | 2 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0022 | 0/0 | 4518 | 2 | 1 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0023 | 0/0 | 4488 | 2 | 0 | 1 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0024 | 0/0 | 4480 | 2 | 2 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0025 | 0/0 | 4480 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0026 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0027 | 0/0 | 4488 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0028 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0029 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0030 | 0/0 | 4522 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0031 | 0/0 | 4488 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0032 | 0/0 | 4488 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0033 | 0/0 | 4488 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0034 | 0/0 | 4521 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0035 | 0/0 | 4489 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0036 | 0/0 | 4520 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0037 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0038 | 0/0 | 4448 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0039 | 0/0 | 4512 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0040 | 0/0 | 4480 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0041 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0042 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0043 | 0/0 | 4488 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| t0044 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0015 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1134 | 275 | 49 | 40 | 150 | 9 | 26 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0003 | 0/0 | 1134 | 23 | 21 | 2 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0004 | 0/0 | 1134 | 20 | 6 | 2 | 9 | 0 | 3 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0005 | 0/0 | 1134 | 17 | 7 | 7 | 1 | 1 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0006 | 0/0 | 1134 | 17 | 0 | 5 | 8 | 1 | 3 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0007 | 1/0 | 1134 | 6 | 0 | 3 | 0 | 0 | 2 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0008 | 0/0 | 1134 | 5 | 1 | 4 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0009 | 0/0 | 1134 | 2 | 0 | 0 | 0 | 1 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0010 | 0/0 | 1134 | 2 | 1 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0014 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0016 | 0/0 | 1134 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0017 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0018 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0019 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0002 | 0/0 | 1135 | 23 | 4 | 6 | 11 | 0 | 2 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0011 | 0/0 | 1135 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0012 | 0/0 | 1135 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0013 | 0/0 | 1135 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0003c0015 | 0/0 | 1134 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0004c0020 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5655 | 51 | 0 | 3 | 39 | 0 | 9 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0002 | 0/0 | 5657 | 38 | 2 | 5 | 25 | 3 | 3 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0003 | 0/0 | 5621 | 44 | 0 | 6 | 30 | 0 | 8 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0004 | 0/1 | 5613 | 37 | 12 | 8 | 15 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0005 | 0/0 | 5645 | 15 | 0 | 9 | 5 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0006 | 0/0 | 5621 | 24 | 1 | 2 | 17 | 2 | 2 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0007 | 0/0 | 5654 | 17 | 0 | 4 | 12 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0008 | 0/0 | 5619 | 8 | 8 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0009 | 0/0 | 5653 | 3 | 3 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0010 | 0/0 | 5653 | 5 | 4 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0012 | 0/0 | 5644 | 4 | 4 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0013 | 0/0 | 5613 | 3 | 3 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0014 | 0/0 | 5657 | 3 | 0 | 0 | 3 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0016 | 0/0 | 5621 | 3 | 3 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0017 | 0/0 | 5613 | 3 | 3 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0018 | 0/0 | 5622 | 2 | 1 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0020 | 0/0 | 5613 | 2 | 0 | 0 | 2 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0023 | 0/0 | 5621 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0024 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0025 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0027 | 0/0 | 5621 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0029 | 0/0 | 5623 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0031 | 0/0 | 5621 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0032 | 0/0 | 5621 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0033 | 0/0 | 5621 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0034 | 0/0 | 5654 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0036 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0037 | 0/0 | 5645 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0001t0040 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0003t0001 | 0/0 | 5655 | 2 | 2 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0003t0002 | 0/0 | 5657 | 5 | 4 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0003t0004 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0003t0008 | 0/0 | 5619 | 7 | 7 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0003t0010 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0003t0021 | 0/0 | 5645 | 2 | 2 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0003t0022 | 0/0 | 5651 | 2 | 1 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0003t0039 | 0/0 | 5645 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0003t0041 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0003t0043 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0004t0001 | 0/0 | 5655 | 4 | 0 | 0 | 4 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0004t0003 | 0/0 | 5621 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0004t0004 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0004t0006 | 0/0 | 5621 | 3 | 0 | 0 | 2 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0004t0007 | 0/0 | 5654 | 4 | 0 | 2 | 0 | 0 | 2 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0004t0011 | 0/0 | 5645 | 6 | 6 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0004t0035 | 0/0 | 5622 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0005t0001 | 0/0 | 5655 | 5 | 3 | 2 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0005t0002 | 0/0 | 5657 | 5 | 0 | 3 | 1 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0005t0005 | 0/0 | 5645 | 2 | 0 | 2 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0005t0008 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0005t0019 | 0/0 | 5645 | 2 | 2 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0005t0030 | 0/0 | 5655 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0005t0038 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0006t0001 | 0/0 | 5655 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0006t0005 | 0/0 | 5645 | 15 | 0 | 5 | 7 | 1 | 2 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0006t0026 | 0/0 | 5645 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0007t0006 | 0/0 | 5621 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0007t0009 | 1/0 | 5653 | 5 | 0 | 2 | 0 | 0 | 2 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0008t0001 | 0/0 | 5655 | 3 | 1 | 2 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0008t0002 | 0/0 | 5657 | 2 | 0 | 2 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0009t0003 | 0/0 | 5621 | 2 | 0 | 0 | 0 | 1 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0010t0002 | 0/0 | 5657 | 2 | 1 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0014t0003 | 0/0 | 5621 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0016t0007 | 0/0 | 5654 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0017t0003 | 0/0 | 5621 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0018t0004 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0001c0019t0044 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0002t0001 | 0/0 | 5656 | 4 | 1 | 0 | 3 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0002t0002 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0002t0003 | 0/0 | 5622 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0002t0004 | 0/0 | 5614 | 3 | 0 | 2 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0002t0005 | 0/0 | 5646 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0002t0007 | 0/0 | 5655 | 4 | 0 | 2 | 0 | 0 | 2 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0002t0012 | 0/0 | 5645 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0002t0013 | 0/0 | 5614 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0002t0015 | 0/0 | 5642 | 3 | 0 | 0 | 3 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0002t0023 | 0/0 | 5622 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0002t0028 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0002t0042 | 0/0 | 5656 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0011t0004 | 0/0 | 5614 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0012t0004 | 0/0 | 5614 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0002c0013t0004 | 0/0 | 5614 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0003c0015t0002 | 0/0 | 5657 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| a0004c0020t0001 | 0/0 | 5655 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | copy fasta | chr22 | 26516996 | 26595132 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0002g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0004g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0005g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0005g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0006g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0007g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0008g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0008g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0010g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0010g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0010g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0012g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0012g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0013g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0013g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0013g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0014g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0014g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0014g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0016g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0016g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0016g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0017g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0017g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0017g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0018g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0018g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0020g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0020g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0023g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0024g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0024g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0025g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0027g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0029g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0031g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0032g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0033g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0034g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0036g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0037g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0001t0040g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0008g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0008g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0010g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0021g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0021g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0022g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0022g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0039g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0041g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0003t0043g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0006g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0007g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0007g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0007g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0007g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0011g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0011g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0011g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0011g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0004t0035g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0005g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0019g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0019g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0030g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0005t0038g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0005g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0005g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0005g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0005g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0006t0026g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0007t0006g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0007t0009g0015 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0007t0009g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0007t0009g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0007t0009g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0007t0009g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0008t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0008t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0008t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0008t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0008t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0009t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0009t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0010t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0010t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0014t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0016t0007g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0017t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0018t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0001c0019t0044g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0004g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0007g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0007g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0012g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0013g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0015g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0015g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0015g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0023g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0028g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0002t0042g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0011t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0012t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0002c0013t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0003c0015t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| a0004c0020t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0302 | EUR | GBR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00099 | hp2 | a0003 | c0015 | t0002 | g0169 | EUR | GBR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00140 | hp1 | a0001 | c0009 | t0003 | g0276 | EUR | GBR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00140 | hp2 | a0001 | c0006 | t0005 | g0104 | EUR | GBR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00323 | hp1 | a0001 | c0001 | t0027 | g0150 | EUR | FIN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0122 | EUR | FIN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00438 | hp1 | a0001 | c0001 | t0033 | g0314 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0304 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00597 | hp1 | a0001 | c0001 | t0006 | g0038 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00597 | hp2 | a0002 | c0002 | t0015 | g0152 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00639 | hp1 | a0001 | c0016 | t0007 | g0172 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00639 | hp2 | a0001 | c0008 | t0001 | g0167 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00673 | hp2 | a0002 | c0002 | t0042 | g0260 | EAS | CHS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00733 | hp1 | a0001 | c0006 | t0005 | g0163 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00733 | hp2 | a0001 | c0007 | t0009 | g0331 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00735 | hp1 | a0002 | c0002 | t0007 | g0157 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0342 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00738 | hp1 | a0001 | c0005 | t0002 | g0161 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00738 | hp2 | a0001 | c0006 | t0005 | g0318 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00741 | hp1 | a0002 | c0002 | t0023 | g0246 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0308 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0363 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0131 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0366 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0090 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0133 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0074 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0359 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0301 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01081 | hp1 | a0001 | c0005 | t0001 | g0184 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01099 | hp1 | a0001 | c0005 | t0002 | g0142 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01099 | hp2 | a0002 | c0002 | t0004 | g0380 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01109 | hp1 | a0001 | c0005 | t0001 | g0180 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0383 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0173 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01168 | hp1 | a0001 | c0005 | t0005 | g0158 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01168 | hp2 | a0001 | c0007 | t0006 | g0268 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01169 | hp2 | a0001 | c0005 | t0005 | g0159 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0130 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0333 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01192 | hp1 | a0002 | c0002 | t0007 | g0174 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01192 | hp2 | a0002 | c0002 | t0003 | g0287 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0175 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0185 | AMR | PUR | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01255 | hp1 | a0001 | c0004 | t0007 | g0047 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0285 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01256 | hp2 | a0001 | c0006 | t0005 | g0267 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01257 | hp1 | a0001 | c0006 | t0005 | g0006 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0360 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01258 | hp1 | a0001 | c0006 | t0005 | g0006 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01261 | hp1 | a0002 | c0002 | t0004 | g0121 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01261 | hp2 | a0001 | c0004 | t0007 | g0367 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01346 | hp1 | a0001 | c0008 | t0002 | g0053 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0340 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01358 | hp1 | a0001 | c0001 | t0034 | g0305 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01358 | hp2 | a0001 | c0008 | t0002 | g0201 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01433 | hp1 | a0001 | c0005 | t0002 | g0160 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0303 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01496 | hp2 | a0001 | c0003 | t0022 | g0362 | AMR | CLM | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0168 | EUR | IBS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0200 | EUR | IBS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01517 | hp1 | a0001 | c0005 | t0030 | g0179 | EUR | IBS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0171 | EUR | IBS | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01884 | hp1 | a0004 | c0020 | t0001 | g0139 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0372 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01891 | hp1 | a0001 | c0003 | t0002 | g0020 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0370 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0283 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0322 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01975 | hp1 | a0001 | c0008 | t0001 | g0207 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0329 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01981 | hp1 | a0001 | c0001 | t0018 | g0284 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01981 | hp2 | a0001 | c0007 | t0009 | g0358 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0098 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0271 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0272 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0324 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02040 | hp1 | a0001 | c0001 | t0014 | g0350 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0222 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02055 | hp1 | a0002 | c0002 | t0013 | g0385 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0120 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02071 | hp2 | a0001 | c0004 | t0003 | g0051 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02074 | hp2 | a0001 | c0006 | t0005 | g0141 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02129 | hp1 | a0001 | c0001 | t0006 | g0269 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02129 | hp2 | a0001 | c0004 | t0001 | g0049 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02135 | hp2 | a0001 | c0001 | t0007 | g0289 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02145 | hp1 | a0002 | c0002 | t0012 | g0011 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02145 | hp2 | a0001 | c0001 | t0010 | g0004 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02165 | hp1 | a0001 | c0017 | t0003 | g0275 | EAS | CDX | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02165 | hp2 | a0001 | c0004 | t0001 | g0237 | EAS | CDX | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02257 | hp1 | a0001 | c0003 | t0041 | g0379 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02257 | hp2 | a0001 | c0001 | t0024 | g0389 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02258 | hp2 | a0001 | c0010 | t0002 | g0339 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02280 | hp1 | a0001 | c0004 | t0011 | g0217 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0378 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0166 | AMR | PEL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02451 | hp1 | a0001 | c0001 | t0024 | g0390 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0146 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0354 | EAS | KHV | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02602 | hp2 | a0001 | c0004 | t0007 | g0044 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0266 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0382 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02622 | hp1 | a0002 | c0013 | t0004 | g0029 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02622 | hp2 | a0001 | c0001 | t0017 | g0138 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0348 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0262 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02647 | hp1 | a0001 | c0001 | t0013 | g0021 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0183 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02683 | hp1 | a0001 | c0007 | t0009 | g0321 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0310 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02698 | hp1 | a0001 | c0009 | t0003 | g0313 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0374 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02717 | hp2 | a0001 | c0005 | t0001 | g0376 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02735 | hp1 | a0001 | c0006 | t0005 | g0042 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02809 | hp1 | a0001 | c0004 | t0011 | g0265 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02809 | hp2 | a0001 | c0003 | t0008 | g0136 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02818 | hp1 | a0001 | c0005 | t0019 | g0190 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0213 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02886 | hp1 | a0001 | c0004 | t0011 | g0137 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0202 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0264 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0263 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02896 | hp1 | a0001 | c0003 | t0008 | g0113 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02896 | hp2 | a0001 | c0004 | t0011 | g0218 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0261 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02897 | hp2 | a0001 | c0003 | t0008 | g0114 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02922 | hp1 | a0001 | c0001 | t0016 | g0148 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02922 | hp2 | a0001 | c0005 | t0001 | g0375 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02965 | hp1 | a0001 | c0005 | t0008 | g0177 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0018 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02970 | hp1 | a0001 | c0001 | t0012 | g0009 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0004 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02976 | hp1 | a0001 | c0003 | t0021 | g0270 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0056 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0199 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0212 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03098 | hp1 | a0002 | c0002 | t0028 | g0388 | AFR | MSL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03098 | hp2 | a0001 | c0001 | t0037 | g0209 | AFR | MSL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03130 | hp1 | a0001 | c0003 | t0008 | g0214 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0365 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03139 | hp1 | a0001 | c0004 | t0011 | g0384 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03139 | hp2 | a0001 | c0001 | t0016 | g0346 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03195 | hp1 | a0001 | c0001 | t0017 | g0206 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03195 | hp2 | a0001 | c0004 | t0011 | g0216 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03209 | hp1 | a0001 | c0003 | t0039 | g0022 | AFR | MSL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03209 | hp2 | a0001 | c0001 | t0012 | g0013 | AFR | MSL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03225 | hp1 | a0002 | c0012 | t0004 | g0197 | AFR | MSL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03239 | hp1 | a0001 | c0006 | t0001 | g0195 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03239 | hp2 | a0001 | c0001 | t0032 | g0286 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03453 | hp1 | a0001 | c0001 | t0013 | g0019 | AFR | MSL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03453 | hp2 | a0001 | c0001 | t0017 | g0176 | AFR | MSL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0373 | AFR | MSL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03486 | hp2 | a0001 | c0003 | t0010 | g0211 | AFR | MSL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0134 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03490 | hp2 | a0001 | c0005 | t0002 | g0105 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0132 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0182 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0181 | AFR | ESN | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03540 | hp1 | a0001 | c0003 | t0008 | g0381 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03540 | hp2 | a0001 | c0003 | t0043 | g0066 | AFR | GWD | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0371 | AFR | MSL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03579 | hp2 | a0001 | c0005 | t0038 | g0215 | AFR | MSL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03654 | hp1 | a0002 | c0002 | t0007 | g0057 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0112 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0194 | SAS | STU | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03688 | hp2 | a0001 | c0007 | t0009 | g0351 | SAS | STU | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0325 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03831 | hp2 | a0001 | c0004 | t0007 | g0035 | SAS | BEB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03927 | hp2 | a0002 | c0002 | t0007 | g0041 | SAS | BEB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0295 | SAS | BEB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | BEB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | STU | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0023 | SAS | STU | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG04184 | hp1 | a0001 | c0004 | t0006 | g0249 | SAS | BEB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0165 | SAS | BEB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG04199 | hp1 | a0001 | c0006 | t0005 | g0178 | SAS | STU | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG04199 | hp2 | a0001 | c0001 | t0007 | g0081 | SAS | STU | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG04204 | hp1 | a0001 | c0001 | t0029 | g0124 | SAS | STU | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | STU | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0292 | SAS | STU | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | STU | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | YRI | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18522 | hp2 | a0001 | c0003 | t0002 | g0364 | AFR | YRI | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | CHB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | CHB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | CHB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18906 | hp1 | a0001 | c0005 | t0019 | g0186 | AFR | YRI | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18906 | hp2 | a0001 | c0003 | t0022 | g0347 | AFR | YRI | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18941 | hp1 | a0001 | c0006 | t0005 | g0188 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18942 | hp2 | a0001 | c0001 | t0006 | g0145 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18943 | hp2 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0323 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18950 | hp1 | a0001 | c0001 | t0007 | g0253 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18954 | hp2 | a0001 | c0004 | t0006 | g0054 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18956 | hp2 | a0001 | c0001 | t0006 | g0072 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18959 | hp1 | a0001 | c0001 | t0025 | g0129 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0337 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18964 | hp1 | a0002 | c0011 | t0004 | g0055 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0294 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18967 | hp1 | a0001 | c0001 | t0006 | g0073 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18970 | hp1 | a0001 | c0004 | t0006 | g0052 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18972 | hp1 | a0001 | c0006 | t0005 | g0258 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18972 | hp2 | a0001 | c0001 | t0007 | g0256 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18981 | hp2 | a0001 | c0001 | t0007 | g0255 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18983 | hp2 | a0001 | c0001 | t0007 | g0077 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18984 | hp1 | a0001 | c0001 | t0007 | g0096 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18985 | hp2 | a0001 | c0006 | t0005 | g0187 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18987 | hp1 | a0001 | c0001 | t0014 | g0369 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18987 | hp2 | a0002 | c0002 | t0015 | g0075 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18989 | hp1 | a0001 | c0001 | t0020 | g0086 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18989 | hp2 | a0001 | c0006 | t0026 | g0140 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18991 | hp1 | a0001 | c0001 | t0006 | g0071 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18992 | hp1 | a0001 | c0001 | t0007 | g0060 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18994 | hp1 | a0001 | c0004 | t0001 | g0076 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18994 | hp2 | a0001 | c0001 | t0007 | g0116 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0070 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18995 | hp2 | a0001 | c0006 | t0005 | g0257 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0361 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18998 | hp2 | a0001 | c0004 | t0001 | g0043 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19002 | hp2 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19004 | hp1 | a0001 | c0005 | t0002 | g0198 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19010 | hp2 | a0001 | c0004 | t0004 | g0046 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19011 | hp2 | a0002 | c0002 | t0004 | g0048 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19030 | hp1 | a0001 | c0003 | t0008 | g0135 | AFR | LWK | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19030 | hp2 | a0001 | c0001 | t0012 | g0014 | AFR | LWK | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0110 | AFR | LWK | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19043 | hp2 | a0001 | c0001 | t0040 | g0205 | AFR | LWK | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19054 | hp1 | a0001 | c0001 | t0006 | g0068 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19058 | hp2 | a0001 | c0001 | t0006 | g0085 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19062 | hp1 | a0001 | c0001 | t0006 | g0123 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19063 | hp2 | a0001 | c0001 | t0007 | g0254 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19064 | hp2 | a0001 | c0001 | t0020 | g0127 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19065 | hp1 | a0001 | c0014 | t0003 | g0298 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19066 | hp1 | a0001 | c0006 | t0005 | g0259 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19066 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19074 | hp1 | a0001 | c0001 | t0014 | g0368 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19078 | hp1 | a0001 | c0001 | t0007 | g0125 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19078 | hp2 | a0002 | c0002 | t0015 | g0155 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19080 | hp1 | a0001 | c0001 | t0006 | g0069 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19082 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19084 | hp1 | a0001 | c0004 | t0035 | g0250 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19084 | hp2 | a0001 | c0001 | t0006 | g0230 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19085 | hp1 | a0001 | c0001 | t0006 | g0251 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19085 | hp2 | a0001 | c0006 | t0005 | g0196 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19086 | hp1 | a0002 | c0002 | t0005 | g0143 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19090 | hp1 | a0001 | c0001 | t0006 | g0087 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19240 | hp1 | a0001 | c0001 | t0036 | g0119 | AFR | YRI | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA19240 | hp2 | a0001 | c0005 | t0001 | g0191 | AFR | YRI | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0115 | AFR | ASW | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ASW | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA20752 | hp1 | a0001 | c0001 | t0023 | g0341 | EUR | TSI | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0278 | EUR | TSI | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA20805 | hp1 | a0001 | c0010 | t0002 | g0338 | EUR | TSI | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA20805 | hp2 | a0001 | c0001 | t0031 | g0306 | EUR | TSI | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02109 | hp1 | a0001 | c0003 | t0004 | g0210 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02109 | hp2 | a0001 | c0001 | t0012 | g0010 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02486 | hp1 | a0001 | c0008 | t0001 | g0204 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02486 | hp2 | a0001 | c0003 | t0021 | g0387 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02559 | hp1 | a0001 | c0019 | t0044 | g0391 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0386 | AFR | ACB | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0203 | AFR | USA | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0355 | AFR | USA | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA20300 | hp1 | a0001 | c0001 | t0016 | g0377 | AFR | USA | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA20300 | hp2 | a0001 | c0001 | t0018 | g0277 | AFR | USA | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA21309 | hp1 | a0001 | c0003 | t0008 | g0345 | AFR | LWK | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| NA21309 | hp2 | a0001 | c0018 | t0004 | g0078 | AFR | LWK | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0059 | REF | REF | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| homoSapiens_grch38 | hp1 | a0001 | c0007 | t0009 | g0015 | REF | REF | TPST2_chr22_26516996_26595132 | TPST2 | chr22 | 26516996 | 26595132 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:26540862
|
C | T | 1 | a0003 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.769G>A | p.Gly257Ser | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/7 | 1009/5653 | 769/1134 | 257/377 | chr22 | 26540862 | ||
| chr22:26541248
|
A | AC | 1 | a0002 | 26 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(23): Show |
frameshift_variant | HIGH | c.382dupG | p.Val128fs | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/7 | 622/5653 | 382/1134 | 128/377 | chr22 | 26541248 | ||
| chr22:26541569
|
G | A | 1 | a0004 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.62C>T | p.Ala21Val | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/7 | 302/5653 | 62/1134 | 21/377 | chr22 | 26541569 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:26532710
|
C | T | 1 | a0001c0016 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.1077G>A | p.Leu359Leu | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/7 | 1317/5653 | 1077/1134 | 359/377 | chr22 | 26532710 | ||
| chr22:26536339
|
G | A | 1 | a0001c0017 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.990C>T | p.Asn330Asn | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/7 | 1230/5653 | 990/1134 | 330/377 | chr22 | 26536339 | ||
| chr22:26540800
|
G | A | 2 | a0001c0004a0002c0011 | 21 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(18): Show |
synonymous_variant | LOW | c.831C>T | p.Val277Val | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/7 | 1071/5653 | 831/1134 | 277/377 | chr22 | 26540800 | ||
| chr22:26540931
|
G | A | 5 | a0001c0005a0001c0008a0001c0010others(2): Show | 26 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(23): Show |
synonymous_variant | LOW | c.700C>T | p.Leu234Leu | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/7 | 940/5653 | 700/1134 | 234/377 | chr22 | 26540931 | ||
| chr22:26540962
|
G | C | 2 | a0001c0018a0002c0013 | 2 | HG02622.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.669C>G | p.Ala223Ala | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/7 | 909/5653 | 669/1134 | 223/377 | chr22 | 26540962 | ||
| chr22:26541031
|
C | T | 1 | a0001c0014 | 1 | NA19065.hp1 | synonymous_variant | LOW | c.600G>A | p.Ala200Ala | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/7 | 840/5653 | 600/1134 | 200/377 | chr22 | 26541031 | ||
| chr22:26541121
|
C | A | 1 | a0001c0006 | 17 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(14): Show |
synonymous_variant | LOW | c.510G>T | p.Ser170Ser | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/7 | 750/5653 | 510/1134 | 170/377 | chr22 | 26541121 | ||
| chr22:26541232
|
C | G | 1 | a0001c0009 | 2 | HG00140.hp1 HG02698.hp1 |
synonymous_variant | LOW | c.399G>C | p.Leu133Leu | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/7 | 639/5653 | 399/1134 | 133/377 | chr22 | 26541232 | ||
| chr22:26541355
|
G | A | 2 | a0001c0008a0001c0019 | 6 | HG00639.hp2 HG01346.hp1 HG01358.hp2 others(3): Show |
synonymous_variant | LOW | c.276C>T | p.Pro92Pro | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/7 | 516/5653 | 276/1134 | 92/377 | chr22 | 26541355 | ||
| chr22:26541361
|
C | A | 2 | a0001c0003a0001c0019 | 24 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(21): Show |
synonymous_variant | LOW | c.270G>T | p.Ala90Ala | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/7 | 510/5653 | 270/1134 | 90/377 | chr22 | 26541361 | ||
| chr22:26541361
|
C | G | 17 | a0001c0001a0001c0004a0001c0005others(14): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
synonymous_variant | LOW | c.270G>C | p.Ala90Ala | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/7 | 510/5653 | 270/1134 | 90/377 | chr22 | 26541361 | ||
| chr22:26541454
|
G | A | 1 | a0001c0010 | 2 | HG02258.hp2 NA20805.hp1 |
synonymous_variant | LOW | c.177C>T | p.His59His | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/7 | 417/5653 | 177/1134 | 59/377 | chr22 | 26541454 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:26522237
|
CCA | C | 11 | a0001c0001t0001a0001c0001t0029a0001c0003t0001others(8): Show | 74 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*4036_*4037delTG | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 5982 | chr22 | 26522237 | |||||
| chr22:26522245
|
G | A | 3 | a0001c0001t0012a0001c0001t0037a0002c0002t0012 | 6 | HG02109.hp2 HG02145.hp1 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4030C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 5976 | chr22 | 26522245 | |||||
| chr22:26522307
|
T | C | 1 | a0001c0001t0032 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3968A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 5914 | chr22 | 26522307 | |||||
| chr22:26522605
|
A | C | 1 | a0001c0003t0022 | 2 | HG01496.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3670T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 5616 | chr22 | 26522605 | |||||
| chr22:26522721
|
T | C | 2 | a0001c0001t0023a0002c0002t0023 | 2 | HG00741.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3554A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 5500 | chr22 | 26522721 | |||||
| chr22:26522724
|
T | C | 2 | a0001c0004t0011a0001c0005t0019 | 8 | HG02280.hp1 HG02809.hp1 HG02818.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3551A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 5497 | chr22 | 26522724 | |||||
| chr22:26522894
|
T | C | 14 | a0001c0001t0005a0001c0001t0012a0001c0001t0017others(11): Show | 55 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*3381A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 5327 | chr22 | 26522894 | |||||
| chr22:26522984
|
CCAGGAGT others(25): Show |
C | 40 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(37): Show | 169 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*3259_*3290delCAAA others(28): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 5205 | chr22 | 26522984 | |||||
| chr22:26522984
|
CCAGGAGT others(57): Show |
C | 1 | a0001c0005t0038 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3227_*3290delCAAA others(60): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 5173 | chr22 | 26522984 | |||||
| chr22:26523019
|
G | C | 1 | a0001c0001t0040 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3256C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 5202 | chr22 | 26523019 | |||||
| chr22:26523190
|
A | AAAAC | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0014others(17): Show | 133 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*3081_*3084dupGTTT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 5030 | chr22 | 26523190 | |||||
| chr22:26523334
|
C | T | 5 | a0001c0001t0012a0001c0001t0037a0001c0004t0011others(2): Show | 14 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2941G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 4887 | chr22 | 26523334 | |||||
| chr22:26523647
|
T | C | 56 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(53): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*2628A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 4574 | chr22 | 26523647 | |||||
| chr22:26523663
|
C | A | 1 | a0001c0001t0033 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2612G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 4558 | chr22 | 26523663 | |||||
| chr22:26523718
|
G | A | 1 | a0001c0003t0041 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2557C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 4503 | chr22 | 26523718 | |||||
| chr22:26523817
|
A | T | 13 | a0001c0001t0004a0001c0001t0020a0001c0001t0025others(10): Show | 53 | HG01069.hp1 HG01099.hp2 HG01109.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2458T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 4404 | chr22 | 26523817 | |||||
| chr22:26523983
|
A | AT | 6 | a0001c0001t0007a0001c0004t0007a0001c0004t0035others(3): Show | 30 | HG00597.hp2 HG00639.hp1 HG00735.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2291dupA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 4237 | chr22 | 26523983 | |||||
| chr22:26523992
|
T | G | 1 | a0001c0001t0036 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2283A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 4229 | chr22 | 26523992 | |||||
| chr22:26523993
|
T | G | 1 | a0001c0001t0036 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2282A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 4228 | chr22 | 26523993 | |||||
| chr22:26524082
|
T | C | 27 | a0001c0001t0004a0001c0001t0005a0001c0001t0012others(24): Show | 108 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2193A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 4139 | chr22 | 26524082 | |||||
| chr22:26524240
|
G | GA | 2 | a0001c0001t0018a0001c0001t0034 | 3 | HG01358.hp1 HG01981.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2034dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 3980 | chr22 | 26524240 | |||||
| chr22:26524265
|
A | G | 1 | a0001c0001t0016 | 3 | HG02922.hp1 HG03139.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2010T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 3956 | chr22 | 26524265 | |||||
| chr22:26524304
|
T | C | 37 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(34): Show | 148 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*1971A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 3917 | chr22 | 26524304 | |||||
| chr22:26524346
|
G | A | 28 | a0001c0001t0004a0001c0001t0005a0001c0001t0012others(25): Show | 111 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1929C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 3875 | chr22 | 26524346 | |||||
| chr22:26524347
|
A | G | 1 | a0002c0002t0015 | 3 | HG00597.hp2 NA18987.hp2 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1928T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 3874 | chr22 | 26524347 | |||||
| chr22:26524358
|
T | A | 2 | a0001c0001t0012a0002c0002t0012 | 5 | HG02109.hp2 HG02145.hp1 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1917A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 3863 | chr22 | 26524358 | |||||
| chr22:26524361
|
A | T | 28 | a0001c0001t0004a0001c0001t0005a0001c0001t0012others(25): Show | 111 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1914T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 3860 | chr22 | 26524361 | |||||
| chr22:26524362
|
A | T | 28 | a0001c0001t0004a0001c0001t0005a0001c0001t0012others(25): Show | 111 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1913T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 3859 | chr22 | 26524362 | |||||
| chr22:26524509
|
CACACACA others(1): Show |
C | 28 | a0001c0001t0004a0001c0001t0005a0001c0001t0012others(25): Show | 111 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1758_*1765delATGT others(4): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 3704 | chr22 | 26524509 | |||||
| chr22:26524949
|
TGATTTAT others(6): Show |
T | 1 | a0002c0002t0015 | 3 | HG00597.hp2 NA18987.hp2 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1313_*1325delCCCA others(9): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 3259 | chr22 | 26524949 | |||||
| chr22:26524997
|
G | A | 1 | a0001c0005t0030 | 1 | HG01517.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1278C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 3224 | chr22 | 26524997 | |||||
| chr22:26525146
|
A | C | 2 | a0001c0001t0012a0002c0002t0012 | 5 | HG02109.hp2 HG02145.hp1 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1129T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 3075 | chr22 | 26525146 | |||||
| chr22:26525249
|
G | A | 1 | a0001c0001t0040 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1026C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 2972 | chr22 | 26525249 | |||||
| chr22:26525293
|
C | A | 1 | a0001c0001t0020 | 2 | NA18989.hp1 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*982G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 2928 | chr22 | 26525293 | |||||
| chr22:26525335
|
T | C | 4 | a0001c0001t0012a0001c0003t0021a0001c0004t0011others(1): Show | 13 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*940A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 2886 | chr22 | 26525335 | |||||
| chr22:26525359
|
GCA | G | 6 | a0001c0001t0008a0001c0003t0008a0001c0003t0022others(3): Show | 20 | HG01496.hp2 HG02257.hp1 HG02258.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*914_*915delTG | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 2860 | chr22 | 26525359 | |||||
| chr22:26525416
|
G | A | 6 | a0001c0001t0008a0001c0003t0008a0001c0003t0022others(3): Show | 20 | HG01496.hp2 HG02257.hp1 HG02258.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*859C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 2805 | chr22 | 26525416 | |||||
| chr22:26525422
|
C | T | 1 | a0001c0001t0031 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*853G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 2799 | chr22 | 26525422 | |||||
| chr22:26525654
|
T | A | 1 | a0001c0001t0014 | 3 | HG02040.hp1 NA18987.hp1 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*621A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 2567 | chr22 | 26525654 | |||||
| chr22:26525747
|
A | G | 1 | a0002c0002t0028 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*528T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 2474 | chr22 | 26525747 | |||||
| chr22:26525759
|
A | G | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0014others(17): Show | 133 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*516T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 2462 | chr22 | 26525759 | |||||
| chr22:26525780
|
CT | C | 2 | a0001c0001t0012a0002c0002t0012 | 5 | HG02109.hp2 HG02145.hp1 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*494delA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 2440 | chr22 | 26525780 | |||||
| chr22:26526107
|
A | T | 1 | a0001c0001t0027 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*168T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 2114 | chr22 | 26526107 | |||||
| chr22:26526161
|
A | T | 1 | a0001c0006t0026 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 2060 | chr22 | 26526161 | |||||
| chr22:26526181
|
T | C | 1 | a0002c0002t0042 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*94A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 2040 | chr22 | 26526181 | |||||
| chr22:26526262
|
G | A | 9 | a0001c0001t0006a0001c0001t0012a0001c0001t0023others(6): Show | 42 | HG00597.hp1 HG00741.hp1 HG01074.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*13C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 7/7 | 1959 | chr22 | 26526262 | |||||
| chr22:26541685
|
C | T | 1 | a0001c0001t0025 | 1 | NA18959.hp1 | 5_prime_UTR_variant | MODIFIER | c.-55G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/7 | 55 | chr22 | 26541685 | |||||
| chr22:26590107
|
G | A | 2 | a0001c0001t0024a0001c0019t0044 | 3 | HG02257.hp2 HG02451.hp1 HG02559.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-215C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/7 | chr22 | 26590107 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:26526568
|
A | T | 3 | a0001c0008t0001g0167a0001c0008t0001g0204a0001c0008t0001g0207 | 3 | HG00639.hp2 HG01975.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.*8-301T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26526568 | ||||||
| chr22:26526579
|
A | C | 142 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0030others(139): Show | 148 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.*8-312T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26526579 | ||||||
| chr22:26526580
|
G | T | 1 | a0001c0001t0017g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.*8-313C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26526580 | ||||||
| chr22:26526728
|
G | A | 93 | a0001c0001t0002g0103a0001c0001t0002g0252a0001c0001t0002g0343others(90): Show | 95 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.*8-461C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26526728 | ||||||
| chr22:26526736
|
G | C | 6 | a0001c0001t0003g0223a0001c0001t0003g0224a0001c0001t0003g0288others(3): Show | 6 | HG01192.hp2 NA18747.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.*8-469C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26526736 | ||||||
| chr22:26526761
|
G | C | 1 | a0001c0001t0036g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*8-494C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26526761 | ||||||
| chr22:26526769
|
T | C | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.*8-502A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26526769 | ||||||
| chr22:26526803
|
T | C | 60 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0016others(57): Show | 62 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.*8-536A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26526803 | ||||||
| chr22:26526870
|
G | A | 1 | a0001c0004t0006g0054 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.*8-603C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26526870 | ||||||
| chr22:26526881
|
C | T | 4 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0021g0270others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.*8-614G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26526881 | ||||||
| chr22:26526929
|
T | G | 2 | a0001c0001t0003g0324a0001c0001t0003g0336 | 2 | HG02015.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.*8-662A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26526929 | ||||||
| chr22:26527098
|
T | C | 2 | a0001c0003t0001g0056a0001c0003t0001g0115 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.*8-831A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527098 | ||||||
| chr22:26527186
|
T | C | 2 | a0001c0003t0001g0056a0001c0003t0001g0115 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.*8-919A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527186 | ||||||
| chr22:26527187
|
G | A | 3 | a0001c0001t0014g0350a0001c0001t0014g0368a0001c0001t0014g0369 | 3 | HG02040.hp1 NA18987.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.*8-920C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527187 | ||||||
| chr22:26527189
|
T | C | 131 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0016others(128): Show | 134 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.*8-922A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527189 | ||||||
| chr22:26527308
|
A | G | 4 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0021g0270others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.*7+906T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527308 | ||||||
| chr22:26527353
|
C | T | 1 | a0001c0001t0010g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*7+861G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527353 | ||||||
| chr22:26527359
|
G | A | 139 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(136): Show | 140 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.*7+855C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527359 | ||||||
| chr22:26527376
|
C | T | 30 | a0001c0001t0007g0060a0001c0001t0007g0077a0001c0001t0007g0081others(27): Show | 30 | HG00597.hp2 HG00639.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.*7+838G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527376 | ||||||
| chr22:26527450
|
C | G | 138 | a0001c0001t0004g0008a0001c0001t0004g0149a0001c0001t0004g0162others(135): Show | 143 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.*7+764G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527450 | ||||||
| chr22:26527463
|
A | G | 4 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0021g0270others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.*7+751T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527463 | ||||||
| chr22:26527474
|
A | C | 15 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0001t0010g0182others(12): Show | 15 | HG01496.hp2 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.*7+740T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527474 | ||||||
| chr22:26527486
|
G | A | 4 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0021g0270others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.*7+728C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527486 | ||||||
| chr22:26527521
|
C | G | 56 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0016others(53): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.*7+693G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527521 | ||||||
| chr22:26527523
|
A | G | 1 | a0002c0002t0042g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.*7+691T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527523 | ||||||
| chr22:26527527
|
CA | C | 138 | a0001c0001t0004g0008a0001c0001t0004g0149a0001c0001t0004g0162others(135): Show | 143 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.*7+686delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527527 | ||||||
| chr22:26527545
|
C | G | 134 | a0001c0001t0004g0008a0001c0001t0004g0149a0001c0001t0004g0162others(131): Show | 139 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.*7+669G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527545 | ||||||
| chr22:26527768
|
C | T | 1 | a0001c0001t0003g0361 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.*7+446G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527768 | ||||||
| chr22:26527833
|
C | T | 4 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0021g0270others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.*7+381G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527833 | ||||||
| chr22:26527911
|
C | A | 6 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(3): Show | 6 | NA18956.hp1 NA18968.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.*7+303G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527911 | ||||||
| chr22:26527912
|
C | A | 6 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(3): Show | 6 | NA18956.hp1 NA18968.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.*7+302G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527912 | ||||||
| chr22:26527941
|
T | C | 180 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0244others(177): Show | 185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.*7+273A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26527941 | ||||||
| chr22:26528098
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.*7+116T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26528098 | ||||||
| chr22:26528173
|
C | G | 4 | a0001c0001t0017g0176a0001c0001t0017g0206a0001c0001t0024g0389others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.*7+41G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26528173 | ||||||
| chr22:26528183
|
C | T | 114 | a0001c0001t0004g0008a0001c0001t0004g0149a0001c0001t0004g0162others(111): Show | 117 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.*7+31G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26528183 | ||||||
| chr22:26528211
|
T | C | 1 | a0001c0004t0035g0250 | 1 | NA19084.hp1 | splice_region_variant&intron_variant | LOW | c.*7+3A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 6/6 | chr22 | 26528211 | ||||||
| chr22:26528346
|
C | T | 108 | a0001c0001t0004g0008a0001c0001t0004g0149a0001c0001t0004g0162others(105): Show | 111 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1093-84G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26528346 | ||||||
| chr22:26528370
|
C | T | 115 | a0001c0001t0004g0008a0001c0001t0004g0149a0001c0001t0004g0162others(112): Show | 118 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1093-108G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26528370 | ||||||
| chr22:26528424
|
C | T | 4 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0021g0270others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1093-162G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26528424 | ||||||
| chr22:26528490
|
G | A | 139 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(136): Show | 140 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.1093-228C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26528490 | ||||||
| chr22:26528554
|
G | A | 1 | a0001c0007t0009g0331 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1093-292C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26528554 | ||||||
| chr22:26528569
|
C | T | 75 | a0001c0001t0004g0008a0001c0001t0004g0149a0001c0001t0004g0162others(72): Show | 78 | HG00140.hp2 HG00597.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.1093-307G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26528569 | ||||||
| chr22:26528756
|
G | A | 1 | a0001c0001t0002g0192 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1093-494C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26528756 | ||||||
| chr22:26528785
|
C | T | 36 | a0001c0001t0007g0060a0001c0001t0007g0077a0001c0001t0007g0081others(33): Show | 36 | HG00597.hp2 HG00639.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1093-523G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26528785 | ||||||
| chr22:26528897
|
G | A | 5 | a0001c0001t0023g0341a0001c0001t0040g0205a0001c0003t0039g0022others(2): Show | 5 | HG00741.hp1 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1093-635C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26528897 | ||||||
| chr22:26528967
|
G | A | 2 | a0001c0001t0003g0279a0001c0001t0003g0311 | 2 | NA19057.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1093-705C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26528967 | ||||||
| chr22:26529001
|
C | A | 2 | a0001c0001t0003g0334a0001c0001t0004g0371 | 2 | HG03579.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.1093-739G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529001 | ||||||
| chr22:26529001
|
C | CA | 41 | a0001c0001t0004g0008a0001c0001t0004g0149a0001c0001t0004g0162others(38): Show | 43 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1093-740dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529001 | ||||||
| chr22:26529001
|
C | CAA | 95 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0016others(92): Show | 97 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1093-741_1093-740d others(4): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529001 | ||||||
| chr22:26529010
|
A | AC | 28 | a0001c0001t0006g0003a0001c0001t0006g0038a0001c0001t0006g0068others(25): Show | 29 | HG00597.hp1 HG01074.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.1093-749_1093-748i others(3): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529010 | ||||||
| chr22:26529029
|
A | G | 135 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0016others(132): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1093-767T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529029 | ||||||
| chr22:26529081
|
G | A | 1 | a0002c0013t0004g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1093-819C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529081 | ||||||
| chr22:26529283
|
C | A | 1 | a0001c0001t0005g0302 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1093-1021G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529283 | ||||||
| chr22:26529290
|
C | T | 2 | a0001c0001t0004g0225a0001c0001t0004g0337 | 2 | NA18961.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1093-1028G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529290 | ||||||
| chr22:26529339
|
C | T | 59 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0016others(56): Show | 61 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1093-1077G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529339 | ||||||
| chr22:26529452
|
C | T | 2 | a0001c0001t0007g0131a0001c0001t0007g0133 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1093-1190G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529452 | ||||||
| chr22:26529534
|
A | G | 42 | a0001c0001t0004g0008a0001c0001t0004g0149a0001c0001t0004g0162others(39): Show | 44 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1093-1272T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529534 | ||||||
| chr22:26529686
|
C | T | 30 | a0001c0001t0004g0089a0001c0001t0006g0003a0001c0001t0006g0038others(27): Show | 31 | HG00597.hp1 HG01074.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.1093-1424G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529686 | ||||||
| chr22:26529698
|
C | T | 15 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0001t0010g0182others(12): Show | 15 | HG01496.hp2 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1093-1436G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529698 | ||||||
| chr22:26529704
|
G | C | 5 | a0001c0001t0023g0341a0001c0001t0040g0205a0001c0003t0039g0022others(2): Show | 5 | HG00741.hp1 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1093-1442C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529704 | ||||||
| chr22:26529816
|
G | C | 42 | a0001c0001t0004g0008a0001c0001t0004g0149a0001c0001t0004g0162others(39): Show | 44 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1093-1554C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529816 | ||||||
| chr22:26529834
|
G | A | 4 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0021g0270others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1093-1572C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529834 | ||||||
| chr22:26529868
|
T | A | 54 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0016others(51): Show | 56 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1093-1606A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529868 | ||||||
| chr22:26529868
|
T | TA | 15 | a0001c0001t0002g0360a0001c0001t0008g0373a0001c0001t0008g0374others(12): Show | 15 | HG01257.hp2 HG01496.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1093-1607dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529868 | ||||||
| chr22:26529926
|
T | C | 6 | a0001c0004t0011g0137a0001c0004t0011g0216a0001c0004t0011g0217others(3): Show | 6 | HG02280.hp1 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1093-1664A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529926 | ||||||
| chr22:26529987
|
G | A | 30 | a0001c0001t0007g0060a0001c0001t0007g0077a0001c0001t0007g0081others(27): Show | 30 | HG00597.hp2 HG00639.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1093-1725C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26529987 | ||||||
| chr22:26530081
|
A | G | 193 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0016others(190): Show | 198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1093-1819T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530081 | ||||||
| chr22:26530186
|
A | G | 55 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0016others(52): Show | 57 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1093-1924T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530186 | ||||||
| chr22:26530394
|
T | C | 15 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0001t0010g0182others(12): Show | 15 | HG01496.hp2 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1093-2132A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530394 | ||||||
| chr22:26530443
|
A | C | 15 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0001t0010g0182others(12): Show | 15 | HG01496.hp2 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1093-2181T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530443 | ||||||
| chr22:26530588
|
C | T | 16 | a0001c0001t0003g0002a0001c0001t0003g0037a0001c0001t0003g0039others(13): Show | 17 | HG00438.hp1 HG01074.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1092+2107G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530588 | ||||||
| chr22:26530631
|
C | CAAAAAAA | 40 | a0001c0001t0004g0008a0001c0001t0004g0149a0001c0001t0004g0162others(37): Show | 42 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.1092+2057_1092+206 others(11): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530631 | ||||||
| chr22:26530631
|
C | CAAAAAAA others(1): Show |
29 | a0001c0001t0006g0003a0001c0001t0006g0038a0001c0001t0006g0068others(26): Show | 30 | HG00597.hp1 HG01074.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1092+2056_1092+206 others(12): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530631 | ||||||
| chr22:26530631
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0040g0205a0001c0003t0021g0270a0001c0003t0039g0022others(1): Show | 4 | HG02976.hp1 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092+2063_1092+206 others(18): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530631 | ||||||
| chr22:26530631
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0023g0341a0001c0003t0001g0056a0001c0003t0001g0115others(1): Show | 4 | HG00741.hp1 HG02976.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092+2063_1092+206 others(19): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530631 | ||||||
| chr22:26530631
|
C | CAAAAAAA others(9): Show |
27 | a0001c0001t0007g0077a0001c0001t0007g0096a0001c0001t0007g0116others(24): Show | 27 | HG00597.hp2 HG00639.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1092+2063_1092+206 others(20): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530631 | ||||||
| chr22:26530631
|
C | CAAAAAAA others(10): Show |
7 | a0001c0001t0003g0297a0001c0001t0003g0307a0001c0001t0007g0060others(4): Show | 7 | HG00323.hp1 HG04199.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1092+2063_1092+206 others(21): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530631 | ||||||
| chr22:26530631
|
C | CAAAAAAA others(11): Show |
51 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0003g0002others(48): Show | 53 | HG00140.hp1 HG00438.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1092+2063_1092+206 others(22): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530631 | ||||||
| chr22:26530631
|
C | CAAAAAAA others(12): Show |
8 | a0001c0001t0003g0106a0001c0001t0003g0164a0001c0001t0003g0288others(5): Show | 8 | HG00438.hp2 HG01074.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1092+2063_1092+206 others(23): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530631 | ||||||
| chr22:26530631
|
C | CAAAAAAA others(13): Show |
13 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0001t0032g0286others(10): Show | 13 | HG01496.hp2 HG02559.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1092+2063_1092+206 others(24): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530631 | ||||||
| chr22:26530631
|
C | CAAAAAAA others(14): Show |
3 | a0001c0001t0010g0182a0001c0001t0010g0183a0001c0003t0041g0379 | 3 | HG02257.hp1 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1092+2063_1092+206 others(25): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530631 | ||||||
| chr22:26530686
|
C | G | 1 | a0001c0001t0006g0145 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1092+2009G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530686 | ||||||
| chr22:26530739
|
G | T | 1 | a0001c0001t0006g0199 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1092+1956C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530739 | ||||||
| chr22:26530754
|
A | G | 1 | a0001c0001t0037g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1092+1941T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530754 | ||||||
| chr22:26530830
|
C | T | 2 | a0001c0001t0023g0341a0002c0002t0023g0246 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1092+1865G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530830 | ||||||
| chr22:26530989
|
A | G | 15 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0001t0010g0182others(12): Show | 15 | HG01496.hp2 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1092+1706T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26530989 | ||||||
| chr22:26531008
|
T | TCAAAAA | 30 | a0001c0001t0007g0060a0001c0001t0007g0077a0001c0001t0007g0081others(27): Show | 30 | HG00597.hp2 HG00639.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1092+1681_1092+168 others(10): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26531008 | ||||||
| chr22:26531033
|
C | A | 1 | a0001c0001t0004g0372 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1092+1662G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26531033 | ||||||
| chr22:26531037
|
A | G | 1 | a0001c0005t0002g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1092+1658T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26531037 | ||||||
| chr22:26531065
|
G | A | 6 | a0001c0004t0011g0137a0001c0004t0011g0216a0001c0004t0011g0217others(3): Show | 6 | HG02280.hp1 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1092+1630C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26531065 | ||||||
| chr22:26531148
|
C | A | 15 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0001t0010g0182others(12): Show | 15 | HG01496.hp2 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1092+1547G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26531148 | ||||||
| chr22:26531235
|
CATA | C | 3 | a0001c0001t0040g0205a0001c0003t0039g0022a0001c0003t0043g0066 | 3 | HG03209.hp1 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1092+1457_1092+145 others(7): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26531235 | ||||||
| chr22:26531255
|
T | C | 386 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(383): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1092+1440A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26531255 | ||||||
| chr22:26531381
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1092+1314C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26531381 | ||||||
| chr22:26531566
|
A | G | 1 | a0001c0001t0003g0194 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1092+1129T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26531566 | ||||||
| chr22:26531901
|
C | T | 2 | a0001c0001t0023g0341a0002c0002t0023g0246 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1092+794G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26531901 | ||||||
| chr22:26531962
|
T | G | 15 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0001t0010g0182others(12): Show | 15 | HG01496.hp2 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1092+733A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26531962 | ||||||
| chr22:26532025
|
T | C | 1 | a0001c0001t0007g0256 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1092+670A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26532025 | ||||||
| chr22:26532142
|
C | T | 3 | a0001c0001t0004g0181a0001c0001t0004g0370a0001c0001t0004g0372 | 3 | HG01884.hp2 HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1092+553G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26532142 | ||||||
| chr22:26532169
|
G | A | 30 | a0001c0001t0007g0060a0001c0001t0007g0077a0001c0001t0007g0081others(27): Show | 30 | HG00597.hp2 HG00639.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1092+526C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26532169 | ||||||
| chr22:26532323
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1092+372G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26532323 | ||||||
| chr22:26532354
|
C | T | 28 | a0001c0001t0004g0089a0001c0001t0006g0003a0001c0001t0006g0038others(25): Show | 29 | HG00597.hp1 HG01074.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.1092+341G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26532354 | ||||||
| chr22:26532442
|
G | A | 1 | a0001c0001t0036g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1092+253C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26532442 | ||||||
| chr22:26532480
|
C | T | 31 | a0001c0001t0004g0149a0001c0001t0004g0162a0001c0001t0005g0074others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1092+215G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26532480 | ||||||
| chr22:26532511
|
C | A | 4 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0021g0270others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092+184G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26532511 | ||||||
| chr22:26532647
|
G | A | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1092+48C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26532647 | ||||||
| chr22:26532660
|
A | G | 1 | a0001c0005t0002g0198 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1092+35T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 5/6 | chr22 | 26532660 | ||||||
| chr22:26532982
|
G | A | 15 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0001t0010g0182others(12): Show | 15 | HG01496.hp2 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1042-237C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26532982 | ||||||
| chr22:26533122
|
G | A | 62 | a0001c0001t0001g0062a0001c0001t0001g0151a0001c0001t0001g0156others(59): Show | 64 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1042-377C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533122 | ||||||
| chr22:26533207
|
C | G | 98 | a0001c0001t0001g0027a0001c0001t0001g0050a0001c0001t0001g0062others(95): Show | 99 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1042-462G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533207 | ||||||
| chr22:26533271
|
G | T | 106 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(103): Show | 107 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1042-526C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533271 | ||||||
| chr22:26533274
|
T | C | 7 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(4): Show | 7 | HG01243.hp2 HG01891.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042-529A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533274 | ||||||
| chr22:26533277
|
T | C | 1 | a0002c0002t0028g0388 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1042-532A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533277 | ||||||
| chr22:26533292
|
G | A | 7 | a0001c0001t0001g0344a0001c0001t0003g0002a0001c0001t0003g0039others(4): Show | 8 | HG02027.hp1 HG04204.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.1042-547C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533292 | ||||||
| chr22:26533333
|
T | C | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042-588A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533333 | ||||||
| chr22:26533374
|
C | T | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042-629G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533374 | ||||||
| chr22:26533390
|
A | C | 2 | a0001c0010t0002g0338a0001c0010t0002g0339 | 2 | HG02258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1042-645T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533390 | ||||||
| chr22:26533437
|
A | G | 4 | a0001c0001t0004g0181a0001c0001t0004g0370a0001c0001t0004g0371others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-692T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533437 | ||||||
| chr22:26533461
|
T | A | 1 | a0001c0001t0002g0355 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1042-716A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533461 | ||||||
| chr22:26533516
|
C | A | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042-771G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533516 | ||||||
| chr22:26533592
|
C | T | 53 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(50): Show | 53 | HG00438.hp2 HG01069.hp1 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.1042-847G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533592 | ||||||
| chr22:26533633
|
T | C | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042-888A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533633 | ||||||
| chr22:26533673
|
A | AT | 62 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0062others(59): Show | 62 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1042-929dupA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533673 | ||||||
| chr22:26533700
|
G | T | 3 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0328 | 3 | NA18949.hp1 NA19000.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1042-955C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533700 | ||||||
| chr22:26533805
|
G | C | 21 | a0001c0004t0001g0043a0001c0004t0001g0049a0001c0004t0001g0076others(18): Show | 21 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1042-1060C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533805 | ||||||
| chr22:26533815
|
T | C | 4 | a0001c0006t0005g0006a0001c0006t0005g0267a0001c0008t0001g0167others(1): Show | 5 | HG00639.hp2 HG01256.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-1070A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533815 | ||||||
| chr22:26533848
|
A | G | 144 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1042-1103T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533848 | ||||||
| chr22:26533944
|
G | A | 41 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(38): Show | 41 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.1042-1199C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26533944 | ||||||
| chr22:26534031
|
C | T | 1 | a0001c0001t0002g0355 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1042-1286G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26534031 | ||||||
| chr22:26534099
|
C | T | 144 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1042-1354G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26534099 | ||||||
| chr22:26534190
|
A | G | 62 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0062others(59): Show | 62 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1042-1445T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26534190 | ||||||
| chr22:26534330
|
C | T | 3 | a0001c0001t0008g0261a0001c0001t0008g0262a0001c0001t0008g0263 | 3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1042-1585G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26534330 | ||||||
| chr22:26534452
|
AC | A | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042-1708delG | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26534452 | ||||||
| chr22:26534581
|
C | A | 21 | a0001c0004t0001g0043a0001c0004t0001g0049a0001c0004t0001g0076others(18): Show | 21 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1041+1707G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26534581 | ||||||
| chr22:26534582
|
G | A | 2 | a0001c0004t0011g0265a0001c0004t0011g0384 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1041+1706C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26534582 | ||||||
| chr22:26534751
|
A | G | 2 | a0001c0001t0008g0373a0001c0001t0008g0374 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1041+1537T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26534751 | ||||||
| chr22:26534822
|
G | A | 11 | a0001c0006t0005g0006a0001c0006t0005g0042a0001c0006t0005g0141others(8): Show | 12 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1041+1466C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26534822 | ||||||
| chr22:26534932
|
G | A | 21 | a0001c0004t0001g0043a0001c0004t0001g0049a0001c0004t0001g0076others(18): Show | 21 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1041+1356C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26534932 | ||||||
| chr22:26535109
|
G | A | 2 | a0001c0001t0007g0253a0001c0001t0007g0256 | 2 | NA18950.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1041+1179C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26535109 | ||||||
| chr22:26535135
|
T | C | 1 | a0001c0001t0014g0350 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1041+1153A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26535135 | ||||||
| chr22:26535194
|
C | T | 1 | a0001c0001t0014g0350 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1041+1094G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26535194 | ||||||
| chr22:26535195
|
G | A | 1 | a0001c0003t0004g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1041+1093C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26535195 | ||||||
| chr22:26535237
|
T | C | 21 | a0001c0004t0001g0043a0001c0004t0001g0049a0001c0004t0001g0076others(18): Show | 21 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1041+1051A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26535237 | ||||||
| chr22:26535255
|
C | T | 141 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1041+1033G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26535255 | ||||||
| chr22:26535339
|
G | C | 24 | a0001c0001t0001g0226a0001c0001t0002g0097a0001c0001t0003g0106others(21): Show | 24 | HG00438.hp2 HG00544.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1041+949C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26535339 | ||||||
| chr22:26535363
|
A | G | 1 | a0001c0001t0004g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1041+925T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26535363 | ||||||
| chr22:26535415
|
C | T | 21 | a0001c0004t0001g0043a0001c0004t0001g0049a0001c0004t0001g0076others(18): Show | 21 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1041+873G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26535415 | ||||||
| chr22:26535454
|
C | G | 1 | a0001c0001t0003g0310 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1041+834G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26535454 | ||||||
| chr22:26535570
|
G | C | 18 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(15): Show | 19 | HG00597.hp1 HG02129.hp1 NA18950.hp2 others(16): Show |
intron_variant | MODIFIER | c.1041+718C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26535570 | ||||||
| chr22:26535662
|
G | A | 21 | a0001c0004t0001g0043a0001c0004t0001g0049a0001c0004t0001g0076others(18): Show | 21 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1041+626C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26535662 | ||||||
| chr22:26535700
|
G | A | 7 | a0001c0001t0001g0128a0001c0001t0001g0231a0001c0001t0001g0232others(4): Show | 7 | NA18944.hp2 NA18948.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1041+588C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26535700 | ||||||
| chr22:26535909
|
G | A | 21 | a0001c0004t0001g0043a0001c0004t0001g0049a0001c0004t0001g0076others(18): Show | 21 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1041+379C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26535909 | ||||||
| chr22:26536112
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1041+176G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26536112 | ||||||
| chr22:26536184
|
G | A | 144 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1041+104C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26536184 | ||||||
| chr22:26536227
|
A | C | 1 | a0001c0003t0002g0185 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1041+61T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 4/6 | chr22 | 26536227 | ||||||
| chr22:26536941
|
G | A | 18 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(15): Show | 19 | HG00597.hp1 HG02129.hp1 NA18950.hp2 others(16): Show |
intron_variant | MODIFIER | c.843-455C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26536941 | ||||||
| chr22:26536977
|
G | C | 1 | a0001c0001t0003g0326 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.843-491C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26536977 | ||||||
| chr22:26537055
|
C | CAA | 20 | a0001c0004t0001g0043a0001c0004t0001g0049a0001c0004t0001g0076others(17): Show | 20 | HG01255.hp1 HG01261.hp2 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.843-571_843-570dup others(2): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26537055 | ||||||
| chr22:26537229
|
C | A | 58 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0002g0312others(55): Show | 60 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.843-743G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26537229 | ||||||
| chr22:26537287
|
G | A | 30 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(27): Show | 30 | HG01243.hp2 HG01255.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.843-801C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26537287 | ||||||
| chr22:26537338
|
G | A | 21 | a0001c0004t0001g0043a0001c0004t0001g0049a0001c0004t0001g0076others(18): Show | 21 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.843-852C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26537338 | ||||||
| chr22:26537553
|
A | G | 1 | a0001c0001t0003g0299 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.843-1067T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26537553 | ||||||
| chr22:26537799
|
T | C | 24 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0154others(21): Show | 24 | HG00423.hp2 HG01255.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.843-1313A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26537799 | ||||||
| chr22:26537818
|
A | T | 21 | a0001c0004t0001g0043a0001c0004t0001g0049a0001c0004t0001g0076others(18): Show | 21 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.843-1332T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26537818 | ||||||
| chr22:26537834
|
G | T | 1 | a0001c0001t0001g0332 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.843-1348C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26537834 | ||||||
| chr22:26538448
|
A | T | 1 | a0001c0003t0039g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.843-1962T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26538448 | ||||||
| chr22:26538511
|
G | A | 2 | a0001c0001t0008g0373a0001c0001t0008g0374 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.843-2025C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26538511 | ||||||
| chr22:26538513
|
C | T | 2 | a0001c0001t0008g0373a0001c0001t0008g0374 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.843-2027G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26538513 | ||||||
| chr22:26538548
|
G | A | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.843-2062C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26538548 | ||||||
| chr22:26538667
|
T | G | 3 | a0001c0001t0017g0206a0001c0001t0024g0389a0001c0001t0024g0390 | 3 | HG02257.hp2 HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.842+2122A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26538667 | ||||||
| chr22:26538677
|
C | T | 1 | a0001c0001t0003g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.842+2112G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26538677 | ||||||
| chr22:26538754
|
C | T | 39 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0004t0001g0043others(36): Show | 40 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.842+2035G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26538754 | ||||||
| chr22:26538772
|
G | A | 23 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0004t0001g0043others(20): Show | 23 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.842+2017C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26538772 | ||||||
| chr22:26538775
|
A | T | 1 | a0002c0002t0028g0388 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.842+2014T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26538775 | ||||||
| chr22:26538780
|
A | G | 230 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(227): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.842+2009T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26538780 | ||||||
| chr22:26539037
|
T | C | 1 | a0001c0001t0002g0111 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.842+1752A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26539037 | ||||||
| chr22:26539307
|
G | A | 1 | a0001c0001t0037g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.842+1482C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26539307 | ||||||
| chr22:26539572
|
G | A | 1 | a0001c0001t0002g0342 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.842+1217C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26539572 | ||||||
| chr22:26539603
|
G | GA | 12 | a0001c0001t0004g0005a0001c0001t0004g0203a0001c0001t0004g0348others(9): Show | 13 | HG01243.hp2 HG01256.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.842+1185dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26539603 | ||||||
| chr22:26539603
|
GA | G | 10 | a0001c0001t0001g0239a0001c0001t0001g0344a0001c0001t0007g0131others(7): Show | 10 | HG00639.hp1 HG00735.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.842+1185delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26539603 | ||||||
| chr22:26539636
|
A | C | 193 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(190): Show | 196 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.842+1153T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26539636 | ||||||
| chr22:26539641
|
C | T | 2 | a0001c0001t0003g0308a0001c0001t0031g0306 | 2 | HG00741.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.842+1148G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26539641 | ||||||
| chr22:26539642
|
G | A | 1 | a0001c0001t0037g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.842+1147C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26539642 | ||||||
| chr22:26539698
|
G | A | 1 | a0001c0001t0002g0340 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.842+1091C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26539698 | ||||||
| chr22:26539759
|
ACCCTGT | A | 8 | a0001c0001t0004g0008a0001c0001t0004g0181a0001c0001t0004g0264others(5): Show | 9 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.842+1024_842+1029d others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26539759 | ||||||
| chr22:26539767
|
T | A | 8 | a0001c0001t0004g0008a0001c0001t0004g0181a0001c0001t0004g0264others(5): Show | 9 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.842+1022A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26539767 | ||||||
| chr22:26539768
|
C | G | 8 | a0001c0001t0004g0008a0001c0001t0004g0181a0001c0001t0004g0264others(5): Show | 9 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.842+1021G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26539768 | ||||||
| chr22:26539899
|
A | G | 8 | a0001c0001t0004g0382a0001c0001t0012g0009a0001c0001t0012g0010others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.842+890T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26539899 | ||||||
| chr22:26540003
|
C | T | 138 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(135): Show | 141 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.842+786G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26540003 | ||||||
| chr22:26540142
|
A | G | 19 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0001t0037g0209others(16): Show | 20 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.842+647T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26540142 | ||||||
| chr22:26540180
|
C | T | 24 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(21): Show | 24 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.842+609G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26540180 | ||||||
| chr22:26540532
|
C | T | 1 | a0001c0001t0002g0319 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.842+257G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26540532 | ||||||
| chr22:26540549
|
G | A | 1 | a0001c0001t0037g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.842+240C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26540549 | ||||||
| chr22:26540560
|
C | T | 40 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(37): Show | 40 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.842+229G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26540560 | ||||||
| chr22:26540581
|
A | G | 1 | a0001c0001t0006g0359 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.842+208T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26540581 | ||||||
| chr22:26540585
|
A | C | 1 | a0001c0003t0002g0364 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.842+204T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26540585 | ||||||
| chr22:26540596
|
G | A | 45 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(42): Show | 45 | HG01243.hp2 HG01255.hp1 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.842+193C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26540596 | ||||||
| chr22:26540757
|
G | A | 18 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(15): Show | 19 | HG00597.hp1 HG02129.hp1 NA18950.hp2 others(16): Show |
intron_variant | MODIFIER | c.842+32C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 3/6 | chr22 | 26540757 | ||||||
| chr22:26541731
|
G | A | 1 | a0001c0006t0005g0196 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-88-13C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26541731 | ||||||
| chr22:26541947
|
C | T | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-88-229G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26541947 | ||||||
| chr22:26542021
|
A | G | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0244 | 3 | HG00621.hp2 NA18944.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-88-303T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26542021 | ||||||
| chr22:26542059
|
C | T | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-88-341G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26542059 | ||||||
| chr22:26542074
|
T | C | 1 | a0001c0001t0003g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-88-356A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26542074 | ||||||
| chr22:26542214
|
C | T | 1 | a0001c0006t0005g0163 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-88-496G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26542214 | ||||||
| chr22:26542229
|
G | A | 2 | a0001c0001t0008g0373a0001c0001t0008g0374 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-88-511C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26542229 | ||||||
| chr22:26542240
|
T | TA | 150 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-88-523dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26542240 | ||||||
| chr22:26542240
|
T | TAA | 15 | a0001c0001t0001g0128a0001c0001t0002g0192a0001c0001t0004g0008others(12): Show | 16 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-88-524_-88-523dup others(2): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26542240 | ||||||
| chr22:26542240
|
TA | T | 19 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0005g0090others(16): Show | 20 | HG00597.hp1 HG01070.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.-88-523delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26542240 | ||||||
| chr22:26542259
|
G | T | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-88-541C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26542259 | ||||||
| chr22:26542267
|
T | C | 60 | a0001c0001t0001g0317a0001c0001t0001g0349a0001c0001t0002g0024others(57): Show | 61 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.-88-549A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26542267 | ||||||
| chr22:26543201
|
T | C | 3 | a0001c0001t0004g0005a0001c0001t0004g0203a0001c0001t0004g0348 | 4 | HG01256.hp1 HG01258.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89+1403A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26543201 | ||||||
| chr22:26543281
|
T | A | 1 | a0001c0001t0004g0348 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-89+1323A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26543281 | ||||||
| chr22:26543364
|
G | A | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-89+1240C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26543364 | ||||||
| chr22:26543596
|
C | A | 1 | a0001c0001t0003g0282 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-89+1008G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26543596 | ||||||
| chr22:26543597
|
G | A | 24 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(21): Show | 24 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.-89+1007C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26543597 | ||||||
| chr22:26543815
|
T | C | 206 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(203): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.-89+789A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26543815 | ||||||
| chr22:26544026
|
C | T | 140 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(137): Show | 143 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.-89+578G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26544026 | ||||||
| chr22:26544078
|
G | A | 24 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(21): Show | 24 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.-89+526C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26544078 | ||||||
| chr22:26544209
|
C | A | 1 | a0002c0002t0013g0385 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-89+395G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26544209 | ||||||
| chr22:26544229
|
A | G | 389 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(386): Show | 398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.-89+375T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26544229 | ||||||
| chr22:26544280
|
C | T | 8 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(5): Show | 8 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89+324G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26544280 | ||||||
| chr22:26544364
|
C | T | 2 | a0001c0001t0005g0074a0001c0001t0005g0090 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-89+240G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26544364 | ||||||
| chr22:26544375
|
G | A | 1 | a0001c0001t0004g0032 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-89+229C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26544375 | ||||||
| chr22:26544462
|
G | A | 27 | a0001c0001t0002g0221a0001c0005t0001g0180a0001c0005t0001g0184others(24): Show | 27 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.-89+142C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 2/6 | chr22 | 26544462 | ||||||
| chr22:26544770
|
G | A | 1 | a0001c0001t0002g0219 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-160-95C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26544770 | ||||||
| chr22:26544858
|
T | C | 1 | a0001c0001t0002g0354 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-160-183A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26544858 | ||||||
| chr22:26545210
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-160-535G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26545210 | ||||||
| chr22:26545218
|
C | T | 2 | a0001c0003t0008g0113a0001c0003t0008g0114 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-160-543G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26545218 | ||||||
| chr22:26545257
|
A | G | 101 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(98): Show | 104 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-160-582T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26545257 | ||||||
| chr22:26545294
|
G | C | 190 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(187): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.-160-619C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26545294 | ||||||
| chr22:26545398
|
T | A | 1 | a0004c0020t0001g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-160-723A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26545398 | ||||||
| chr22:26545419
|
T | C | 3 | a0001c0001t0002g0360a0001c0001t0002g0366a0001c0004t0035g0250 | 3 | HG01070.hp1 HG01257.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-160-744A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26545419 | ||||||
| chr22:26545802
|
T | G | 97 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(94): Show | 100 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.-160-1127A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26545802 | ||||||
| chr22:26545818
|
G | A | 1 | a0002c0002t0013g0385 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-160-1143C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26545818 | ||||||
| chr22:26545831
|
G | A | 28 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(25): Show | 28 | HG01255.hp1 HG01261.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.-160-1156C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26545831 | ||||||
| chr22:26545860
|
A | G | 217 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(214): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-160-1185T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26545860 | ||||||
| chr22:26545961
|
C | T | 1 | a0001c0001t0005g0302 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-160-1286G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26545961 | ||||||
| chr22:26546021
|
G | A | 3 | a0001c0001t0004g0005a0001c0001t0004g0203a0001c0001t0004g0348 | 4 | HG01256.hp1 HG01258.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-160-1346C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546021 | ||||||
| chr22:26546046
|
C | T | 17 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(14): Show | 18 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160-1371G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546046 | ||||||
| chr22:26546068
|
C | A | 2 | a0001c0001t0007g0131a0001c0001t0007g0133 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-160-1393G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546068 | ||||||
| chr22:26546092
|
G | A | 2 | a0001c0001t0001g0349a0002c0002t0015g0075 | 2 | NA18987.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-160-1417C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546092 | ||||||
| chr22:26546092
|
GA | G | 16 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(13): Show | 17 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(14): Show |
intron_variant | MODIFIER | c.-160-1418delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546092 | ||||||
| chr22:26546093
|
A | G | 1 | a0002c0002t0015g0075 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-160-1418T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546093 | ||||||
| chr22:26546102
|
A | C | 3 | a0001c0001t0004g0005a0001c0001t0004g0203a0001c0001t0004g0348 | 4 | HG01256.hp1 HG01258.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-160-1427T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546102 | ||||||
| chr22:26546146
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-160-1471G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546146 | ||||||
| chr22:26546161
|
A | G | 202 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(199): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-160-1486T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546161 | ||||||
| chr22:26546342
|
C | T | 9 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-160-1667G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546342 | ||||||
| chr22:26546385
|
C | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0156 | 2 | HG02698.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-160-1710G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546385 | ||||||
| chr22:26546395
|
A | G | 31 | a0001c0001t0004g0005a0001c0001t0004g0203a0001c0001t0004g0348others(28): Show | 32 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.-160-1720T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546395 | ||||||
| chr22:26546451
|
G | A | 31 | a0001c0001t0004g0005a0001c0001t0004g0203a0001c0001t0004g0348others(28): Show | 32 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.-160-1776C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546451 | ||||||
| chr22:26546561
|
C | T | 1 | a0001c0003t0039g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-160-1886G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546561 | ||||||
| chr22:26546581
|
A | C | 3 | a0001c0001t0004g0008a0001c0001t0004g0383a0002c0002t0004g0380 | 4 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-160-1906T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546581 | ||||||
| chr22:26546585
|
C | T | 219 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(216): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.-160-1910G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546585 | ||||||
| chr22:26546791
|
A | G | 6 | a0001c0005t0001g0191a0001c0005t0001g0375a0001c0005t0001g0376others(3): Show | 6 | HG02717.hp2 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-160-2116T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26546791 | ||||||
| chr22:26547047
|
G | A | 1 | a0001c0001t0003g0301 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-160-2372C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26547047 | ||||||
| chr22:26547492
|
A | G | 1 | a0001c0001t0003g0326 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-160-2817T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26547492 | ||||||
| chr22:26547679
|
G | A | 142 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(139): Show | 146 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.-160-3004C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26547679 | ||||||
| chr22:26547834
|
T | C | 1 | a0001c0004t0011g0216 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-160-3159A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26547834 | ||||||
| chr22:26547838
|
T | C | 1 | a0001c0001t0002g0356 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-160-3163A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26547838 | ||||||
| chr22:26547857
|
G | A | 1 | a0001c0004t0003g0051 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-160-3182C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26547857 | ||||||
| chr22:26548185
|
G | A | 1 | a0001c0003t0039g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-160-3510C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548185 | ||||||
| chr22:26548302
|
G | A | 142 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(139): Show | 146 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.-160-3627C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548302 | ||||||
| chr22:26548345
|
G | A | 142 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(139): Show | 146 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.-160-3670C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548345 | ||||||
| chr22:26548373
|
G | A | 9 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-160-3698C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548373 | ||||||
| chr22:26548399
|
T | C | 17 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(14): Show | 18 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160-3724A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548399 | ||||||
| chr22:26548545
|
GA | G | 390 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(387): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.-160-3871delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548545 | ||||||
| chr22:26548550
|
A | G | 142 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(139): Show | 146 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.-160-3875T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548550 | ||||||
| chr22:26548578
|
A | AAAGG | 24 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0005t0001g0180others(21): Show | 24 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.-160-3907_-160-390 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548578 | ||||||
| chr22:26548614
|
A | AG | 390 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(387): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.-160-3940_-160-393 others(5): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548614 | ||||||
| chr22:26548669
|
G | A | 7 | a0001c0001t0007g0131a0001c0001t0007g0133a0001c0001t0007g0166others(4): Show | 7 | HG00639.hp1 HG00735.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.-160-3994C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548669 | ||||||
| chr22:26548724
|
GGCT | G | 96 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0001g0095others(93): Show | 99 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-160-4052_-160-405 others(7): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548724 | ||||||
| chr22:26548739
|
C | G | 1 | a0001c0005t0002g0161 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-160-4064G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548739 | ||||||
| chr22:26548777
|
C | A | 17 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(14): Show | 18 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160-4102G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548777 | ||||||
| chr22:26548807
|
AT | A | 231 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(228): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.-160-4133delA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548807 | ||||||
| chr22:26548808
|
T | A | 2 | a0001c0001t0003g0290a0001c0001t0007g0060 | 2 | NA18992.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-160-4133A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548808 | ||||||
| chr22:26548809
|
T | A | 2 | a0001c0003t0008g0135a0001c0003t0008g0136 | 2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-160-4134A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26548809 | ||||||
| chr22:26549035
|
G | A | 17 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(14): Show | 18 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160-4360C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549035 | ||||||
| chr22:26549077
|
C | T | 77 | a0001c0001t0001g0088a0001c0001t0001g0317a0001c0001t0001g0349others(74): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.-160-4402G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549077 | ||||||
| chr22:26549136
|
C | T | 2 | a0001c0009t0003g0276a0001c0009t0003g0313 | 2 | HG00140.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-160-4461G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549136 | ||||||
| chr22:26549322
|
C | T | 60 | a0001c0001t0001g0317a0001c0001t0001g0349a0001c0001t0002g0024others(57): Show | 61 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.-160-4647G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549322 | ||||||
| chr22:26549355
|
C | T | 1 | a0001c0003t0010g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-160-4680G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549355 | ||||||
| chr22:26549396
|
C | T | 25 | a0001c0001t0004g0005a0001c0001t0004g0203a0001c0001t0004g0348others(22): Show | 26 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-160-4721G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549396 | ||||||
| chr22:26549526
|
G | A | 22 | a0001c0004t0001g0043a0001c0004t0001g0049a0001c0004t0001g0076others(19): Show | 22 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-160-4851C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549526 | ||||||
| chr22:26549575
|
T | C | 83 | a0001c0001t0001g0088a0001c0001t0001g0317a0001c0001t0001g0349others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.-160-4900A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549575 | ||||||
| chr22:26549590
|
G | A | 1 | a0001c0001t0017g0176 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-160-4915C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549590 | ||||||
| chr22:26549656
|
CA | C | 300 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(297): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-160-4982delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549656 | ||||||
| chr22:26549656
|
CAA | C | 8 | a0001c0001t0004g0227a0001c0001t0004g0363a0001c0001t0023g0341others(5): Show | 8 | HG01069.hp1 HG01168.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-160-4983_-160-498 others(6): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549656 | ||||||
| chr22:26549670
|
A | G | 1 | a0001c0001t0002g0366 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-160-4995T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549670 | ||||||
| chr22:26549672
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-160-4997T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549672 | ||||||
| chr22:26549691
|
A | C | 22 | a0001c0004t0001g0043a0001c0004t0001g0049a0001c0004t0001g0076others(19): Show | 22 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-160-5016T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549691 | ||||||
| chr22:26549715
|
A | G | 1 | a0001c0001t0003g0292 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-160-5040T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549715 | ||||||
| chr22:26549725
|
G | A | 9 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-160-5050C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549725 | ||||||
| chr22:26549736
|
C | T | 155 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0061others(152): Show | 158 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.-160-5061G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549736 | ||||||
| chr22:26549797
|
G | A | 3 | a0001c0001t0004g0005a0001c0001t0004g0203a0001c0001t0004g0348 | 4 | HG01256.hp1 HG01258.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-160-5122C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549797 | ||||||
| chr22:26549822
|
A | C | 1 | a0001c0005t0001g0191 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-160-5147T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549822 | ||||||
| chr22:26549858
|
C | A | 3 | a0001c0001t0001g0208a0001c0001t0001g0229a0001c0001t0001g0238 | 3 | HG00558.hp1 NA18960.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.-160-5183G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549858 | ||||||
| chr22:26549867
|
T | TA | 137 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0088others(134): Show | 142 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.-160-5193dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549867 | ||||||
| chr22:26549867
|
T | TAA | 6 | a0001c0001t0001g0109a0001c0001t0001g0231a0001c0001t0001g0245others(3): Show | 6 | HG00597.hp2 HG01243.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.-160-5194_-160-519 others(6): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549867 | ||||||
| chr22:26549867
|
TA | T | 10 | a0001c0001t0002g0111a0001c0001t0002g0170a0001c0001t0002g0171others(7): Show | 10 | HG00099.hp2 HG01081.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.-160-5193delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549867 | ||||||
| chr22:26549877
|
A | T | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-160-5202T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549877 | ||||||
| chr22:26549880
|
A | G | 1 | a0001c0001t0037g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-160-5205T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549880 | ||||||
| chr22:26549911
|
G | A | 10 | a0001c0001t0002g0153a0001c0001t0002g0221a0001c0001t0005g0001others(7): Show | 12 | HG00544.hp1 HG00597.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.-160-5236C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549911 | ||||||
| chr22:26549988
|
C | T | 6 | a0001c0004t0011g0137a0001c0004t0011g0216a0001c0004t0011g0217others(3): Show | 6 | HG02280.hp1 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-160-5313G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549988 | ||||||
| chr22:26549995
|
A | G | 189 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(186): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.-160-5320T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549995 | ||||||
| chr22:26549996
|
T | C | 220 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(217): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.-160-5321A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26549996 | ||||||
| chr22:26550039
|
C | CA | 62 | a0001c0001t0001g0058a0001c0001t0001g0317a0001c0001t0001g0349others(59): Show | 63 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.-160-5365dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26550039 | ||||||
| chr22:26550039
|
C | CAA | 17 | a0001c0001t0001g0088a0001c0001t0006g0003a0001c0001t0006g0038others(14): Show | 18 | HG00597.hp1 NA18956.hp2 NA18967.hp1 others(15): Show |
intron_variant | MODIFIER | c.-160-5366_-160-536 others(6): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26550039 | ||||||
| chr22:26550050
|
A | AAAC | 31 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0003t0001g0056others(28): Show | 31 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.-160-5376_-160-537 others(7): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26550050 | ||||||
| chr22:26550050
|
A | AAC | 109 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(106): Show | 113 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-160-5376_-160-537 others(6): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26550050 | ||||||
| chr22:26550051
|
C | A | 143 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(140): Show | 147 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.-160-5376G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26550051 | ||||||
| chr22:26550247
|
G | C | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-160-5572C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26550247 | ||||||
| chr22:26550276
|
A | G | 17 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(14): Show | 18 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160-5601T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26550276 | ||||||
| chr22:26550538
|
A | G | 1 | a0001c0003t0008g0345 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-160-5863T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26550538 | ||||||
| chr22:26550543
|
C | T | 2 | a0001c0001t0004g0005a0001c0001t0004g0203 | 3 | HG01256.hp1 HG01258.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-160-5868G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26550543 | ||||||
| chr22:26550624
|
G | A | 1 | a0001c0003t0039g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-160-5949C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26550624 | ||||||
| chr22:26550733
|
A | C | 389 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(386): Show | 398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.-160-6058T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26550733 | ||||||
| chr22:26550812
|
ACCT | A | 2 | a0001c0001t0004g0005a0001c0001t0004g0203 | 3 | HG01256.hp1 HG01258.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-160-6140_-160-613 others(7): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26550812 | ||||||
| chr22:26550909
|
G | C | 1 | a0001c0001t0003g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-160-6234C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26550909 | ||||||
| chr22:26551123
|
C | G | 159 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(156): Show | 164 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.-160-6448G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551123 | ||||||
| chr22:26551127
|
T | C | 159 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(156): Show | 164 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.-160-6452A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551127 | ||||||
| chr22:26551153
|
TA | T | 159 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(156): Show | 164 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.-160-6479delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551153 | ||||||
| chr22:26551390
|
T | C | 1 | a0001c0001t0003g0310 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-160-6715A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551390 | ||||||
| chr22:26551431
|
C | A | 1 | a0001c0001t0008g0262 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-160-6756G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551431 | ||||||
| chr22:26551662
|
G | A | 61 | a0001c0001t0001g0317a0001c0001t0001g0349a0001c0001t0002g0024others(58): Show | 62 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.-160-6987C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551662 | ||||||
| chr22:26551713
|
G | C | 18 | a0001c0001t0001g0128a0001c0001t0001g0220a0001c0001t0001g0231others(15): Show | 18 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160-7038C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551713 | ||||||
| chr22:26551872
|
CTTTTCTT others(6): Show |
C | 56 | a0001c0001t0002g0153a0001c0001t0003g0165a0001c0001t0004g0005others(53): Show | 57 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.-160-7210_-160-719 others(17): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551872 | ||||||
| chr22:26551872
|
CTTTTCTT others(7): Show |
C | 73 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(70): Show | 76 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-160-7211_-160-719 others(18): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551872 | ||||||
| chr22:26551872
|
CTTTTCTT others(8): Show |
C | 24 | a0001c0001t0001g0247a0001c0001t0002g0219a0001c0001t0004g0222others(21): Show | 24 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.-160-7212_-160-719 others(19): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551872 | ||||||
| chr22:26551872
|
CTTTTCTT others(9): Show |
C | 2 | a0001c0001t0037g0209a0001c0003t0002g0364 | 2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-160-7213_-160-719 others(20): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551872 | ||||||
| chr22:26551873
|
TTTTC | T | 6 | a0001c0001t0002g0111a0001c0001t0002g0168a0001c0001t0002g0170others(3): Show | 6 | HG00099.hp2 HG01081.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-160-7202_-160-719 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551873 | ||||||
| chr22:26551883
|
C | CT | 6 | a0001c0001t0001g0317a0001c0001t0003g0194a0001c0001t0006g0359others(3): Show | 6 | HG00438.hp1 HG01074.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.-160-7209dupA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551883 | ||||||
| chr22:26551883
|
C | CTT | 13 | a0001c0001t0002g0316a0001c0001t0002g0319a0001c0001t0002g0327others(10): Show | 14 | HG00140.hp2 HG00423.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-160-7210_-160-720 others(6): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551883 | ||||||
| chr22:26551883
|
C | CTTT | 6 | a0001c0006t0005g0042a0001c0006t0005g0141a0001c0006t0005g0178others(3): Show | 6 | HG02074.hp2 HG02735.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.-160-7211_-160-720 others(7): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551883 | ||||||
| chr22:26551883
|
CT | C | 74 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0062others(71): Show | 75 | HG00609.hp2 HG00621.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.-160-7209delA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551883 | ||||||
| chr22:26551883
|
CTT | C | 24 | a0001c0001t0001g0082a0001c0001t0002g0122a0001c0001t0005g0074others(21): Show | 24 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-160-7210_-160-720 others(6): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551883 | ||||||
| chr22:26551883
|
CTTTTT | C | 16 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(13): Show | 17 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(14): Show |
intron_variant | MODIFIER | c.-160-7213_-160-720 others(9): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551883 | ||||||
| chr22:26551890
|
T | C | 2 | a0001c0001t0017g0176a0002c0002t0007g0057 | 2 | HG03453.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-160-7215A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551890 | ||||||
| chr22:26551893
|
T | C | 3 | a0001c0001t0017g0206a0001c0001t0024g0389a0001c0001t0024g0390 | 3 | HG02257.hp2 HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-160-7218A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551893 | ||||||
| chr22:26551914
|
T | G | 390 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(387): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.-160-7239A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551914 | ||||||
| chr22:26551915
|
T | G | 172 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(169): Show | 177 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.-160-7240A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26551915 | ||||||
| chr22:26552040
|
G | A | 22 | a0001c0001t0001g0317a0001c0001t0002g0316a0001c0001t0002g0319others(19): Show | 23 | HG00140.hp2 HG00423.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-160-7365C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552040 | ||||||
| chr22:26552092
|
G | A | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-160-7417C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552092 | ||||||
| chr22:26552152
|
G | A | 172 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(169): Show | 177 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.-160-7477C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552152 | ||||||
| chr22:26552169
|
C | G | 1 | a0001c0001t0014g0350 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-160-7494G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552169 | ||||||
| chr22:26552212
|
T | C | 1 | a0001c0001t0003g0271 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-160-7537A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552212 | ||||||
| chr22:26552228
|
G | A | 1 | a0001c0003t0008g0345 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-160-7553C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552228 | ||||||
| chr22:26552252
|
C | T | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-160-7577G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552252 | ||||||
| chr22:26552255
|
G | A | 100 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(97): Show | 103 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-160-7580C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552255 | ||||||
| chr22:26552419
|
C | T | 1 | a0001c0001t0037g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-160-7744G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552419 | ||||||
| chr22:26552500
|
C | A | 172 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(169): Show | 177 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.-160-7825G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552500 | ||||||
| chr22:26552521
|
C | T | 155 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(152): Show | 159 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.-160-7846G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552521 | ||||||
| chr22:26552570
|
A | G | 2 | a0001c0003t0021g0270a0001c0003t0021g0387 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-160-7895T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552570 | ||||||
| chr22:26552622
|
G | C | 163 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(160): Show | 168 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.-160-7947C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552622 | ||||||
| chr22:26552638
|
C | T | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-160-7963G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552638 | ||||||
| chr22:26552656
|
C | T | 1 | a0001c0001t0040g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-160-7981G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552656 | ||||||
| chr22:26552724
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-160-8049A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552724 | ||||||
| chr22:26552725
|
C | T | 1 | a0001c0001t0006g0278 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-160-8050G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552725 | ||||||
| chr22:26552728
|
G | A | 163 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(160): Show | 168 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.-160-8053C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552728 | ||||||
| chr22:26552739
|
T | C | 1 | a0001c0001t0037g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-160-8064A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552739 | ||||||
| chr22:26552778
|
A | G | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-160-8103T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552778 | ||||||
| chr22:26552831
|
A | G | 24 | a0001c0001t0002g0122a0001c0001t0004g0059a0001c0001t0005g0074others(21): Show | 25 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.-160-8156T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552831 | ||||||
| chr22:26552834
|
A | C | 157 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(154): Show | 162 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.-160-8159T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552834 | ||||||
| chr22:26552885
|
C | A | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-160-8210G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552885 | ||||||
| chr22:26552918
|
C | G | 172 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(169): Show | 177 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.-160-8243G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552918 | ||||||
| chr22:26552921
|
A | G | 232 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(229): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.-160-8246T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552921 | ||||||
| chr22:26552969
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-160-8294T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552969 | ||||||
| chr22:26552976
|
C | A | 1 | a0001c0001t0006g0251 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-160-8301G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552976 | ||||||
| chr22:26552989
|
G | A | 1 | a0001c0008t0002g0053 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-160-8314C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552989 | ||||||
| chr22:26552991
|
C | T | 100 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(97): Show | 103 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-160-8316G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26552991 | ||||||
| chr22:26553060
|
C | CA | 41 | a0001c0001t0001g0058a0001c0001t0001g0088a0001c0001t0002g0024others(38): Show | 42 | HG00597.hp1 HG00735.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.-160-8386dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553060 | ||||||
| chr22:26553060
|
C | CAA | 7 | a0001c0001t0004g0089a0001c0001t0006g0072a0001c0001t0006g0085others(4): Show | 7 | HG02109.hp2 HG02970.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.-160-8387_-160-838 others(6): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553060 | ||||||
| chr22:26553060
|
CA | C | 76 | a0001c0001t0001g0050a0001c0001t0001g0151a0001c0001t0001g0208others(73): Show | 80 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-160-8386delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553060 | ||||||
| chr22:26553060
|
CAA | C | 85 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(82): Show | 86 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.-160-8387_-160-838 others(6): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553060 | ||||||
| chr22:26553095
|
C | T | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-160-8420G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553095 | ||||||
| chr22:26553167
|
A | C | 100 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(97): Show | 103 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-160-8492T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553167 | ||||||
| chr22:26553201
|
G | A | 1 | a0001c0001t0004g0098 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-160-8526C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553201 | ||||||
| chr22:26553250
|
C | T | 1 | a0001c0005t0038g0215 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-160-8575G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553250 | ||||||
| chr22:26553369
|
G | GT | 11 | a0001c0001t0004g0067a0001c0001t0004g0337a0001c0001t0004g0382others(8): Show | 11 | HG01175.hp1 HG02615.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-160-8695dupA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553369 | ||||||
| chr22:26553369
|
GT | G | 130 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(127): Show | 134 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.-160-8695delA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553369 | ||||||
| chr22:26553422
|
A | C | 1 | a0001c0001t0006g0072 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-160-8747T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553422 | ||||||
| chr22:26553440
|
C | T | 9 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-160-8765G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553440 | ||||||
| chr22:26553498
|
AAGTAGCT others(12): Show |
A | 1 | a0001c0001t0004g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-160-8842_-160-882 others(23): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553498 | ||||||
| chr22:26553546
|
A | ATTTTTGT others(138): Show |
1 | a0001c0004t0007g0044 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-160-8872_-160-887 others(149): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553546 | ||||||
| chr22:26553546
|
A | ATTTTTGT others(136): Show |
1 | a0001c0004t0011g0218 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-160-8872_-160-887 others(147): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553546 | ||||||
| chr22:26553546
|
A | ATTTTTGT others(136): Show |
1 | a0001c0004t0001g0043 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-160-8872_-160-887 others(147): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553546 | ||||||
| chr22:26553546
|
A | ATTTTTGT others(138): Show |
1 | a0001c0004t0007g0047 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-160-8872_-160-887 others(149): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553546 | ||||||
| chr22:26553546
|
A | ATTTTTGT others(137): Show |
5 | a0001c0004t0011g0137a0001c0004t0011g0216a0001c0004t0011g0217others(2): Show | 5 | HG02280.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-160-8872_-160-887 others(148): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553546 | ||||||
| chr22:26553546
|
A | ATTTTTGT others(137): Show |
4 | a0001c0004t0001g0049a0001c0004t0006g0054a0001c0004t0007g0367others(1): Show | 4 | HG01261.hp2 HG02129.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160-8872_-160-887 others(148): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553546 | ||||||
| chr22:26553546
|
A | ATTTTTGT others(138): Show |
7 | a0001c0004t0001g0076a0001c0004t0001g0237a0001c0004t0003g0051others(4): Show | 7 | HG02071.hp2 HG02165.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.-160-8872_-160-887 others(149): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553546 | ||||||
| chr22:26553546
|
A | ATTTTTGT others(134): Show |
2 | a0001c0001t0004g0005a0001c0001t0004g0203 | 3 | HG01256.hp1 HG01258.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-160-8872_-160-887 others(145): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553546 | ||||||
| chr22:26553546
|
A | ATTTTTGT others(132): Show |
1 | a0002c0002t0012g0011 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-160-8872_-160-887 others(143): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553546 | ||||||
| chr22:26553546
|
A | ATTTTTGT others(132): Show |
1 | a0001c0001t0012g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-160-8872_-160-887 others(143): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553546 | ||||||
| chr22:26553546
|
A | ATTTTTGT others(132): Show |
3 | a0001c0001t0012g0009a0001c0001t0012g0010a0002c0002t0001g0012 | 3 | HG02055.hp2 HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-160-8872_-160-887 others(143): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553546 | ||||||
| chr22:26553546
|
A | ATTTTTGT others(133): Show |
1 | a0001c0001t0012g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-160-8872_-160-887 others(144): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553546 | ||||||
| chr22:26553546
|
A | ATTTTTGT others(138): Show |
2 | a0001c0004t0004g0046a0002c0011t0004g0055 | 2 | NA18964.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-160-8872_-160-887 others(149): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553546 | ||||||
| chr22:26553559
|
C | T | 7 | a0001c0001t0001g0220a0001c0001t0001g0240a0001c0001t0001g0241others(4): Show | 7 | HG00609.hp1 HG00621.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.-160-8884G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553559 | ||||||
| chr22:26553592
|
G | A | 6 | a0001c0001t0002g0312a0001c0001t0002g0335a0001c0001t0003g0297others(3): Show | 6 | HG01358.hp1 HG01981.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.-160-8917C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553592 | ||||||
| chr22:26553684
|
G | A | 119 | a0001c0001t0001g0088a0001c0001t0001g0317a0001c0001t0001g0349others(116): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.-160-9009C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553684 | ||||||
| chr22:26553713
|
C | A | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-160-9038G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553713 | ||||||
| chr22:26553768
|
T | G | 1 | a0001c0001t0002g0221 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-160-9093A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553768 | ||||||
| chr22:26553780
|
G | A | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-160-9105C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553780 | ||||||
| chr22:26553864
|
T | C | 9 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-160-9189A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553864 | ||||||
| chr22:26553917
|
C | T | 60 | a0001c0001t0001g0317a0001c0001t0001g0349a0001c0001t0002g0024others(57): Show | 61 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.-160-9242G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553917 | ||||||
| chr22:26553990
|
G | C | 1 | a0001c0001t0001g0344 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-160-9315C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553990 | ||||||
| chr22:26553996
|
G | A | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-160-9321C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553996 | ||||||
| chr22:26553999
|
C | G | 217 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(214): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-160-9324G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26553999 | ||||||
| chr22:26554006
|
C | T | 3 | a0001c0001t0002g0153a0002c0002t0015g0152a0002c0002t0015g0155 | 3 | HG00597.hp2 NA18969.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-160-9331G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26554006 | ||||||
| chr22:26554063
|
C | T | 30 | a0001c0001t0004g0005a0001c0001t0004g0203a0001c0001t0012g0009others(27): Show | 31 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.-160-9388G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26554063 | ||||||
| chr22:26554092
|
G | A | 60 | a0001c0001t0001g0317a0001c0001t0001g0349a0001c0001t0002g0024others(57): Show | 61 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.-160-9417C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26554092 | ||||||
| chr22:26554523
|
C | G | 1 | a0001c0001t0002g0036 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-160-9848G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26554523 | ||||||
| chr22:26554638
|
C | A | 2 | a0001c0001t0002g0312a0001c0001t0002g0335 | 2 | NA18961.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-160-9963G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26554638 | ||||||
| chr22:26554641
|
G | A | 9 | a0001c0001t0002g0153a0001c0001t0005g0001a0001c0001t0005g0283others(6): Show | 11 | HG00544.hp1 HG00597.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-160-9966C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26554641 | ||||||
| chr22:26554772
|
T | C | 17 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(14): Show | 18 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160-10097A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26554772 | ||||||
| chr22:26554850
|
A | T | 59 | a0001c0001t0001g0317a0001c0001t0001g0349a0001c0001t0002g0024others(56): Show | 60 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.-160-10175T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26554850 | ||||||
| chr22:26554928
|
ACT | A | 100 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(97): Show | 103 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-160-10255_-160-10 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26554928 | ||||||
| chr22:26555046
|
C | T | 8 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(5): Show | 8 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-160-10371G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555046 | ||||||
| chr22:26555144
|
G | A | 2 | a0001c0003t0021g0270a0001c0003t0021g0387 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-160-10469C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555144 | ||||||
| chr22:26555161
|
T | A | 4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG03669.hp1 HG03704.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-160-10486A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555161 | ||||||
| chr22:26555171
|
G | A | 1 | a0001c0005t0002g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-160-10496C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555171 | ||||||
| chr22:26555219
|
C | G | 68 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0062others(65): Show | 68 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-160-10544G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555219 | ||||||
| chr22:26555249
|
T | C | 15 | a0001c0001t0004g0348a0001c0001t0008g0373a0001c0001t0008g0374others(12): Show | 15 | HG01496.hp2 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.-160-10574A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555249 | ||||||
| chr22:26555313
|
A | G | 1 | a0001c0001t0023g0341 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-160-10638T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555313 | ||||||
| chr22:26555351
|
A | G | 216 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(213): Show | 222 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.-160-10676T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555351 | ||||||
| chr22:26555404
|
G | A | 1 | a0001c0003t0039g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-160-10729C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555404 | ||||||
| chr22:26555463
|
C | T | 1 | a0002c0002t0015g0075 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-160-10788G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555463 | ||||||
| chr22:26555480
|
G | A | 15 | a0001c0001t0004g0348a0001c0001t0008g0373a0001c0001t0008g0374others(12): Show | 15 | HG01496.hp2 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.-160-10805C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555480 | ||||||
| chr22:26555623
|
G | A | 101 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(98): Show | 104 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-160-10948C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555623 | ||||||
| chr22:26555629
|
C | T | 2 | a0001c0001t0003g0297a0001c0001t0006g0085 | 2 | NA18612.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-160-10954G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555629 | ||||||
| chr22:26555720
|
C | T | 9 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-160-11045G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555720 | ||||||
| chr22:26555743
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-160-11068G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26555743 | ||||||
| chr22:26556005
|
T | G | 59 | a0001c0001t0001g0317a0001c0001t0001g0349a0001c0001t0002g0024others(56): Show | 60 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.-160-11330A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26556005 | ||||||
| chr22:26556022
|
T | C | 1 | a0002c0002t0015g0075 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-160-11347A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26556022 | ||||||
| chr22:26556024
|
C | T | 1 | a0002c0002t0015g0075 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-160-11349G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26556024 | ||||||
| chr22:26556130
|
T | C | 17 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(14): Show | 18 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160-11455A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26556130 | ||||||
| chr22:26556287
|
C | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0099 | 2 | NA19056.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-160-11612G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26556287 | ||||||
| chr22:26556313
|
C | T | 1 | a0001c0001t0009g0213 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-160-11638G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26556313 | ||||||
| chr22:26556343
|
A | C | 1 | a0002c0002t0015g0075 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-160-11668T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26556343 | ||||||
| chr22:26556368
|
G | A | 1 | a0001c0001t0006g0038 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-160-11693C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26556368 | ||||||
| chr22:26556397
|
A | G | 101 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(98): Show | 104 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-160-11722T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26556397 | ||||||
| chr22:26556518
|
C | T | 1 | a0001c0003t0008g0345 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-160-11843G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26556518 | ||||||
| chr22:26556542
|
A | G | 64 | a0001c0001t0001g0050a0001c0001t0001g0151a0001c0001t0001g0156others(61): Show | 66 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.-160-11867T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26556542 | ||||||
| chr22:26556781
|
G | A | 9 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0020others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-160-12106C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26556781 | ||||||
| chr22:26556841
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-160-12166T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26556841 | ||||||
| chr22:26556949
|
C | T | 1 | a0001c0004t0001g0043 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-160-12274G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26556949 | ||||||
| chr22:26557253
|
G | A | 1 | a0001c0004t0003g0051 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-160-12578C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557253 | ||||||
| chr22:26557343
|
T | C | 2 | a0001c0001t0010g0182a0001c0001t0010g0183 | 2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-160-12668A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557343 | ||||||
| chr22:26557358
|
T | C | 59 | a0001c0001t0001g0317a0001c0001t0001g0349a0001c0001t0002g0024others(56): Show | 60 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.-160-12683A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557358 | ||||||
| chr22:26557628
|
T | C | 1 | a0001c0001t0017g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-160-12953A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557628 | ||||||
| chr22:26557679
|
G | C | 1 | a0002c0002t0004g0121 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-160-13004C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557679 | ||||||
| chr22:26557687
|
T | C | 15 | a0001c0001t0004g0348a0001c0001t0008g0373a0001c0001t0008g0374others(12): Show | 15 | HG01496.hp2 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.-160-13012A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557687 | ||||||
| chr22:26557708
|
G | A | 1 | a0001c0003t0008g0345 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-160-13033C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557708 | ||||||
| chr22:26557749
|
C | CAAAGAAG others(303): Show |
1 | a0001c0005t0019g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-160-13075_-160-13 others(316): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557749 | ||||||
| chr22:26557749
|
C | CAAAGAAG others(310): Show |
3 | a0001c0001t0004g0149a0001c0001t0004g0162a0001c0001t0040g0205 | 3 | HG01109.hp2 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-160-13075_-160-13 others(323): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557749 | ||||||
| chr22:26557749
|
C | CAAAGAAG others(314): Show |
4 | a0001c0001t0004g0236a0001c0001t0004g0264a0001c0001t0005g0329others(1): Show | 4 | HG01168.hp1 HG01978.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-160-13075_-160-13 others(327): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557749 | ||||||
| chr22:26557749
|
C | CAAAGAAG others(315): Show |
68 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0128others(65): Show | 71 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.-160-13075_-160-13 others(328): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557749 | ||||||
| chr22:26557749
|
C | CAAAGAAG others(316): Show |
22 | a0001c0001t0001g0028a0001c0001t0001g0079a0001c0001t0001g0095others(19): Show | 22 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.-160-13075_-160-13 others(329): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557749 | ||||||
| chr22:26557749
|
C | CAAAGAAG others(314): Show |
1 | a0001c0001t0001g0231 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-160-13075_-160-13 others(327): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557749 | ||||||
| chr22:26557749
|
C | CAAAGAAG others(315): Show |
1 | a0001c0001t0001g0245 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-160-13075_-160-13 others(328): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557749 | ||||||
| chr22:26557749
|
C | CAAAGAAG others(315): Show |
1 | a0001c0001t0013g0378 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-160-13075_-160-13 others(328): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557749 | ||||||
| chr22:26557773
|
G | A | 21 | a0001c0004t0001g0043a0001c0004t0001g0049a0001c0004t0001g0076others(18): Show | 21 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-160-13098C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557773 | ||||||
| chr22:26557813
|
G | A | 2 | a0001c0018t0004g0078a0002c0013t0004g0029 | 2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-160-13138C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557813 | ||||||
| chr22:26557815
|
G | A | 1 | a0001c0001t0016g0377 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-160-13140C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557815 | ||||||
| chr22:26557908
|
G | A | 1 | a0001c0001t0004g0266 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-160-13233C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26557908 | ||||||
| chr22:26558073
|
T | TTA | 6 | a0001c0001t0008g0261a0001c0001t0008g0262a0001c0001t0008g0263others(3): Show | 6 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-160-13400_-160-13 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558073 | ||||||
| chr22:26558073
|
TTA | T | 23 | a0001c0001t0001g0317a0001c0001t0002g0316a0001c0001t0002g0319others(20): Show | 24 | HG00140.hp2 HG00423.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-160-13400_-160-13 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558073 | ||||||
| chr22:26558088
|
G | A | 295 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(292): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.-160-13413C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558088 | ||||||
| chr22:26558120
|
TAC | T | 3 | a0001c0001t0004g0382a0001c0001t0017g0138a0001c0001t0029g0124 | 3 | HG02615.hp2 HG02622.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-160-13447_-160-13 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558120 | ||||||
| chr22:26558120
|
TACAC | T | 4 | a0001c0001t0009g0146a0001c0001t0010g0183a0001c0001t0016g0148others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-160-13449_-160-13 others(10): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558120 | ||||||
| chr22:26558120
|
TACACAC | T | 13 | a0001c0001t0004g0098a0001c0001t0004g0348a0001c0001t0007g0083others(10): Show | 13 | HG00621.hp1 HG01993.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-160-13451_-160-13 others(12): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558120 | ||||||
| chr22:26558120
|
TACACACA others(1): Show |
T | 58 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0062others(55): Show | 58 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.-160-13453_-160-13 others(14): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558120 | ||||||
| chr22:26558120
|
TACACACA others(3): Show |
T | 23 | a0001c0001t0004g0059a0001c0001t0005g0074a0001c0001t0005g0090others(20): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.-160-13455_-160-13 others(16): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558120 | ||||||
| chr22:26558120
|
TACACACA others(5): Show |
T | 5 | a0001c0001t0004g0005a0001c0001t0004g0203a0001c0001t0037g0209others(2): Show | 6 | HG01256.hp1 HG01258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-160-13457_-160-13 others(18): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558120 | ||||||
| chr22:26558120
|
TACACACA others(7): Show |
T | 25 | a0001c0001t0001g0151a0001c0001t0003g0189a0001c0001t0003g0223others(22): Show | 25 | HG00438.hp1 HG00673.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-160-13459_-160-13 others(20): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558120 | ||||||
| chr22:26558120
|
TACACACA others(9): Show |
T | 105 | a0001c0001t0001g0050a0001c0001t0001g0156a0001c0001t0001g0233others(102): Show | 108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-160-13461_-160-13 others(22): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558120 | ||||||
| chr22:26558120
|
TACACACA others(11): Show |
T | 152 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.-160-13463_-160-13 others(24): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558120 | ||||||
| chr22:26558120
|
TACACACA others(15): Show |
T | 1 | a0001c0005t0002g0161 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-160-13467_-160-13 others(28): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558120 | ||||||
| chr22:26558164
|
C | T | 17 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(14): Show | 18 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160-13489G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558164 | ||||||
| chr22:26558166
|
C | T | 280 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(277): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.-160-13491G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558166 | ||||||
| chr22:26558241
|
T | TGC | 18 | a0001c0001t0001g0233a0001c0001t0003g0002a0001c0001t0003g0037others(15): Show | 19 | HG00438.hp1 HG01074.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.-160-13567_-160-13 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558241 | ||||||
| chr22:26558463
|
A | C | 1 | a0002c0002t0001g0092 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-160-13788T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558463 | ||||||
| chr22:26558612
|
T | C | 73 | a0001c0001t0001g0050a0001c0001t0001g0151a0001c0001t0001g0156others(70): Show | 75 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.-160-13937A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558612 | ||||||
| chr22:26558707
|
G | C | 221 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(218): Show | 228 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-160-14032C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558707 | ||||||
| chr22:26558759
|
G | A | 73 | a0001c0001t0001g0050a0001c0001t0001g0151a0001c0001t0001g0156others(70): Show | 75 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.-160-14084C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558759 | ||||||
| chr22:26558769
|
T | C | 1 | a0001c0001t0002g0353 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-160-14094A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558769 | ||||||
| chr22:26558834
|
C | T | 192 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(189): Show | 198 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-160-14159G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558834 | ||||||
| chr22:26558897
|
C | T | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-160-14222G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558897 | ||||||
| chr22:26558930
|
A | G | 9 | a0001c0001t0002g0153a0001c0001t0005g0001a0001c0001t0005g0283others(6): Show | 11 | HG00544.hp1 HG00597.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-160-14255T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26558930 | ||||||
| chr22:26559094
|
C | T | 1 | a0001c0001t0037g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-160-14419G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559094 | ||||||
| chr22:26559182
|
A | G | 2 | a0001c0001t0004g0382a0001c0001t0017g0138 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-160-14507T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559182 | ||||||
| chr22:26559192
|
C | T | 192 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(189): Show | 198 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-160-14517G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559192 | ||||||
| chr22:26559260
|
A | G | 192 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(189): Show | 198 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-160-14585T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559260 | ||||||
| chr22:26559312
|
G | A | 1 | a0001c0003t0043g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-160-14637C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559312 | ||||||
| chr22:26559320
|
T | C | 192 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(189): Show | 198 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-160-14645A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559320 | ||||||
| chr22:26559411
|
T | A | 73 | a0001c0001t0001g0050a0001c0001t0001g0151a0001c0001t0001g0156others(70): Show | 75 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.-160-14736A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559411 | ||||||
| chr22:26559468
|
CAG | C | 37 | a0001c0001t0001g0349a0001c0001t0002g0024a0001c0001t0002g0025others(34): Show | 37 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.-160-14795_-160-14 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559468 | ||||||
| chr22:26559554
|
C | T | 192 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(189): Show | 198 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-160-14879G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559554 | ||||||
| chr22:26559611
|
G | A | 3 | a0001c0004t0011g0137a0001c0004t0011g0265a0001c0004t0011g0384 | 3 | HG02809.hp1 HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-160-14936C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559611 | ||||||
| chr22:26559888
|
C | G | 73 | a0001c0001t0001g0050a0001c0001t0001g0151a0001c0001t0001g0156others(70): Show | 75 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.-160-15213G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559888 | ||||||
| chr22:26559894
|
A | T | 1 | a0002c0002t0015g0075 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-160-15219T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559894 | ||||||
| chr22:26559930
|
C | T | 198 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(195): Show | 204 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.-160-15255G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559930 | ||||||
| chr22:26559965
|
C | T | 17 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(14): Show | 18 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160-15290G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559965 | ||||||
| chr22:26559968
|
T | C | 65 | a0001c0001t0001g0317a0001c0001t0001g0349a0001c0001t0002g0024others(62): Show | 66 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.-160-15293A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26559968 | ||||||
| chr22:26560024
|
G | T | 59 | a0001c0001t0001g0317a0001c0001t0001g0349a0001c0001t0002g0024others(56): Show | 60 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.-160-15349C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560024 | ||||||
| chr22:26560034
|
T | C | 1 | a0001c0005t0001g0191 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-160-15359A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560034 | ||||||
| chr22:26560041
|
C | T | 1 | a0001c0001t0002g0309 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-160-15366G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560041 | ||||||
| chr22:26560104
|
C | T | 1 | a0001c0003t0043g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-160-15429G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560104 | ||||||
| chr22:26560155
|
G | A | 64 | a0001c0001t0001g0050a0001c0001t0001g0151a0001c0001t0001g0156others(61): Show | 66 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.-160-15480C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560155 | ||||||
| chr22:26560167
|
A | T | 2 | a0001c0001t0001g0050a0001c0017t0003g0275 | 2 | HG02083.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.-160-15492T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560167 | ||||||
| chr22:26560403
|
T | G | 1 | a0001c0001t0002g0097 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-160-15728A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560403 | ||||||
| chr22:26560426
|
T | C | 171 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(168): Show | 174 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.-160-15751A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560426 | ||||||
| chr22:26560463
|
G | A | 5 | a0001c0001t0003g0189a0001c0001t0003g0193a0001c0001t0003g0279others(2): Show | 5 | HG00673.hp1 NA18970.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.-160-15788C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560463 | ||||||
| chr22:26560466
|
G | A | 24 | a0001c0001t0002g0122a0001c0001t0004g0059a0001c0001t0005g0074others(21): Show | 25 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.-160-15791C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560466 | ||||||
| chr22:26560529
|
A | G | 177 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(174): Show | 180 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.-160-15854T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560529 | ||||||
| chr22:26560596
|
G | A | 44 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(41): Show | 44 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.-160-15921C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560596 | ||||||
| chr22:26560626
|
C | A | 1 | a0001c0001t0036g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-160-15951G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560626 | ||||||
| chr22:26560750
|
G | T | 1 | a0001c0001t0003g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-160-16075C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560750 | ||||||
| chr22:26560759
|
T | C | 1 | a0001c0001t0005g0144 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-160-16084A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560759 | ||||||
| chr22:26560845
|
C | T | 8 | a0001c0001t0002g0312a0001c0001t0002g0335a0001c0001t0003g0297others(5): Show | 8 | HG01255.hp2 HG01358.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.-160-16170G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26560845 | ||||||
| chr22:26561049
|
T | G | 3 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0003t0039g0022 | 3 | HG02717.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-160-16374A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561049 | ||||||
| chr22:26561104
|
T | C | 163 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(160): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-160-16429A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561104 | ||||||
| chr22:26561170
|
T | C | 9 | a0001c0001t0002g0122a0001c0001t0003g0023a0001c0001t0004g0059others(6): Show | 9 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-160-16495A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561170 | ||||||
| chr22:26561173
|
C | T | 2 | a0001c0006t0005g0042a0002c0002t0007g0041 | 2 | HG02735.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-160-16498G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561173 | ||||||
| chr22:26561282
|
T | C | 1 | a0001c0001t0003g0271 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-160-16607A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561282 | ||||||
| chr22:26561318
|
C | A | 129 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(126): Show | 132 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-160-16643G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561318 | ||||||
| chr22:26561341
|
G | T | 16 | a0001c0001t0001g0050a0001c0004t0001g0043a0001c0004t0001g0049others(13): Show | 16 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-160-16666C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561341 | ||||||
| chr22:26561420
|
G | A | 17 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(14): Show | 18 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160-16745C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561420 | ||||||
| chr22:26561421
|
G | A | 1 | a0001c0001t0004g0203 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-160-16746C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561421 | ||||||
| chr22:26561421
|
G | T | 2 | a0001c0001t0003g0279a0001c0001t0003g0311 | 2 | NA19057.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-160-16746C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561421 | ||||||
| chr22:26561505
|
C | T | 163 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(160): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-160-16830G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561505 | ||||||
| chr22:26561548
|
A | G | 163 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(160): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-160-16873T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561548 | ||||||
| chr22:26561549
|
A | AGTGTTTT others(5): Show |
163 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(160): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-160-16875_-160-16 others(18): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561549 | ||||||
| chr22:26561600
|
T | C | 2 | a0001c0003t0008g0135a0001c0003t0008g0136 | 2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-160-16925A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561600 | ||||||
| chr22:26561686
|
C | CATCATTA others(1): Show |
3 | a0001c0001t0002g0325a0001c0006t0005g0042a0002c0002t0007g0041 | 3 | HG02735.hp1 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-160-17019_-160-17 others(14): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561686 | ||||||
| chr22:26561765
|
C | A | 3 | a0001c0006t0005g0188a0001c0006t0005g0257a0001c0006t0005g0258 | 3 | NA18941.hp1 NA18972.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-160-17090G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561765 | ||||||
| chr22:26561808
|
T | C | 163 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(160): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-160-17133A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561808 | ||||||
| chr22:26561816
|
G | A | 127 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(124): Show | 130 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-160-17141C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561816 | ||||||
| chr22:26561865
|
C | T | 2 | a0001c0001t0002g0360a0001c0001t0002g0366 | 2 | HG01070.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.-160-17190G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561865 | ||||||
| chr22:26561895
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-160-17220A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561895 | ||||||
| chr22:26561941
|
T | G | 2 | a0001c0001t0008g0373a0001c0001t0008g0374 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-160-17266A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26561941 | ||||||
| chr22:26562032
|
GGCTGGTG others(8): Show |
G | 3 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0003t0039g0022 | 3 | HG02717.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-160-17372_-160-17 others(21): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562032 | ||||||
| chr22:26562138
|
A | G | 163 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(160): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-160-17463T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562138 | ||||||
| chr22:26562216
|
G | A | 163 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(160): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-160-17541C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562216 | ||||||
| chr22:26562352
|
C | T | 163 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(160): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-160-17677G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562352 | ||||||
| chr22:26562365
|
C | T | 127 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(124): Show | 130 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-160-17690G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562365 | ||||||
| chr22:26562375
|
C | T | 2 | a0001c0003t0022g0347a0001c0003t0022g0362 | 2 | HG01496.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-160-17700G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562375 | ||||||
| chr22:26562376
|
G | A | 163 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(160): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-160-17701C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562376 | ||||||
| chr22:26562427
|
T | C | 78 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0273others(75): Show | 80 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.-160-17752A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562427 | ||||||
| chr22:26562515
|
C | G | 68 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(65): Show | 68 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.-160-17840G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562515 | ||||||
| chr22:26562609
|
TTTTTC | T | 157 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(154): Show | 160 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-160-17939_-160-17 others(11): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562609 | ||||||
| chr22:26562625
|
TTTTC | T | 8 | a0001c0001t0010g0182a0001c0001t0010g0183a0001c0005t0001g0191others(5): Show | 8 | HG02647.hp2 HG02717.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-160-17954_-160-17 others(10): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562625 | ||||||
| chr22:26562629
|
C | CT | 126 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(123): Show | 129 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-160-17955dupA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562629 | ||||||
| chr22:26562629
|
C | CTT | 6 | a0001c0001t0008g0261a0001c0001t0008g0262a0001c0001t0008g0263others(3): Show | 6 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-160-17956_-160-17 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562629 | ||||||
| chr22:26562702
|
C | T | 163 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(160): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-160-18027G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562702 | ||||||
| chr22:26562718
|
G | A | 163 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(160): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-160-18043C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562718 | ||||||
| chr22:26562770
|
T | A | 1 | a0001c0001t0040g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-160-18095A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562770 | ||||||
| chr22:26562819
|
C | T | 2 | a0001c0003t0021g0270a0001c0003t0021g0387 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-160-18144G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562819 | ||||||
| chr22:26562835
|
C | T | 1 | a0001c0001t0018g0284 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-160-18160G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562835 | ||||||
| chr22:26562877
|
C | T | 14 | a0001c0001t0004g0149a0001c0001t0004g0162a0001c0001t0004g0348others(11): Show | 14 | HG01109.hp2 HG01496.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-160-18202G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562877 | ||||||
| chr22:26562927
|
G | A | 8 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(5): Show | 8 | NA18944.hp2 NA18948.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.-160-18252C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26562927 | ||||||
| chr22:26563016
|
A | G | 17 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(14): Show | 18 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160-18341T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26563016 | ||||||
| chr22:26563331
|
CT | C | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(150): Show | 156 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.-160-18657delA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26563331 | ||||||
| chr22:26563331
|
CTT | C | 7 | a0001c0001t0002g0168a0001c0001t0002g0170a0001c0001t0002g0171others(4): Show | 7 | HG00099.hp2 HG01081.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-160-18658_-160-18 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26563331 | ||||||
| chr22:26563415
|
G | A | 1 | a0001c0005t0001g0180 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-160-18740C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26563415 | ||||||
| chr22:26563490
|
G | A | 60 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(57): Show | 60 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-160-18815C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26563490 | ||||||
| chr22:26563531
|
G | A | 1 | a0001c0001t0004g0203 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-160-18856C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26563531 | ||||||
| chr22:26563625
|
G | A | 9 | a0001c0001t0004g0348a0001c0003t0008g0113a0001c0003t0008g0114others(6): Show | 9 | HG01496.hp2 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-160-18950C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26563625 | ||||||
| chr22:26563854
|
T | G | 1 | a0001c0004t0011g0216 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-160-19179A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26563854 | ||||||
| chr22:26563860
|
G | A | 90 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(87): Show | 92 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.-160-19185C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26563860 | ||||||
| chr22:26563893
|
G | A | 108 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(105): Show | 110 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-160-19218C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26563893 | ||||||
| chr22:26564218
|
G | T | 1 | a0001c0001t0014g0369 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-160-19543C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564218 | ||||||
| chr22:26564303
|
CAGCAAAG others(2): Show |
C | 9 | a0001c0001t0002g0153a0001c0001t0005g0001a0001c0001t0005g0283others(6): Show | 11 | HG00544.hp1 HG00597.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-160-19637_-160-19 others(15): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564303 | ||||||
| chr22:26564383
|
G | C | 106 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(103): Show | 108 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-160-19708C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564383 | ||||||
| chr22:26564415
|
G | A | 7 | a0001c0001t0001g0273a0001c0001t0001g0332a0001c0001t0002g0036others(4): Show | 7 | HG02074.hp1 NA18941.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.-160-19740C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564415 | ||||||
| chr22:26564436
|
C | T | 35 | a0001c0001t0001g0050a0001c0001t0004g0266a0001c0001t0004g0348others(32): Show | 35 | HG01255.hp1 HG01261.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.-160-19761G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564436 | ||||||
| chr22:26564473
|
G | A | 1 | a0001c0001t0003g0310 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-160-19798C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564473 | ||||||
| chr22:26564504
|
A | G | 106 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(103): Show | 108 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-160-19829T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564504 | ||||||
| chr22:26564506
|
G | A | 106 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(103): Show | 108 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-160-19831C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564506 | ||||||
| chr22:26564573
|
C | T | 9 | a0001c0001t0002g0153a0001c0001t0005g0001a0001c0001t0005g0283others(6): Show | 11 | HG00544.hp1 HG00597.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-160-19898G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564573 | ||||||
| chr22:26564682
|
C | A | 106 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(103): Show | 108 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-160-20007G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564682 | ||||||
| chr22:26564690
|
C | T | 4 | a0001c0001t0004g0285a0001c0001t0018g0277a0001c0001t0018g0284others(1): Show | 4 | HG01255.hp2 HG01358.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-160-20015G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564690 | ||||||
| chr22:26564723
|
T | C | 106 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(103): Show | 108 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-160-20048A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564723 | ||||||
| chr22:26564817
|
C | T | 17 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(14): Show | 18 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160-20142G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564817 | ||||||
| chr22:26564823
|
A | G | 106 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(103): Show | 108 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-160-20148T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564823 | ||||||
| chr22:26564914
|
T | C | 2 | a0001c0001t0024g0389a0001c0001t0024g0390 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-160-20239A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564914 | ||||||
| chr22:26564924
|
C | T | 23 | a0001c0001t0001g0050a0001c0001t0004g0266a0001c0004t0001g0043others(20): Show | 23 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-160-20249G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26564924 | ||||||
| chr22:26565500
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-160-20825C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26565500 | ||||||
| chr22:26565604
|
G | A | 2 | a0001c0009t0003g0276a0001c0009t0003g0313 | 2 | HG00140.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-160-20929C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26565604 | ||||||
| chr22:26565853
|
C | G | 7 | a0001c0001t0004g0266a0001c0004t0011g0137a0001c0004t0011g0216others(4): Show | 7 | HG02280.hp1 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-160-21178G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26565853 | ||||||
| chr22:26566067
|
T | C | 106 | a0001c0001t0001g0050a0001c0001t0001g0151a0001c0001t0001g0156others(103): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-160-21392A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26566067 | ||||||
| chr22:26566106
|
G | A | 1 | a0001c0004t0004g0046 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-160-21431C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26566106 | ||||||
| chr22:26566312
|
G | C | 4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG03669.hp1 HG03704.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-160-21637C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26566312 | ||||||
| chr22:26566512
|
C | G | 94 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(91): Show | 96 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.-160-21837G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26566512 | ||||||
| chr22:26566638
|
G | A | 4 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(1): Show | 4 | NA18968.hp1 NA18982.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160-21963C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26566638 | ||||||
| chr22:26566764
|
T | TAAAC | 4 | a0001c0001t0004g0149a0001c0001t0004g0162a0001c0001t0008g0261others(1): Show | 4 | HG01109.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-160-22093_-160-22 others(10): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26566764 | ||||||
| chr22:26566764
|
TAAAC | T | 67 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(64): Show | 67 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-160-22093_-160-22 others(10): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26566764 | ||||||
| chr22:26566849
|
C | T | 1 | a0001c0001t0036g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-160-22174G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26566849 | ||||||
| chr22:26567064
|
G | C | 106 | a0001c0001t0001g0050a0001c0001t0001g0151a0001c0001t0001g0156others(103): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-160-22389C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26567064 | ||||||
| chr22:26567099
|
C | T | 9 | a0001c0001t0002g0153a0001c0001t0005g0001a0001c0001t0005g0283others(6): Show | 11 | HG00544.hp1 HG00597.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-160-22424G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26567099 | ||||||
| chr22:26567109
|
G | A | 3 | a0001c0004t0011g0137a0001c0004t0011g0265a0001c0004t0011g0384 | 3 | HG02809.hp1 HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-160-22434C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26567109 | ||||||
| chr22:26567110
|
G | C | 1 | a0001c0001t0017g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-160-22435C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26567110 | ||||||
| chr22:26567288
|
C | T | 76 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(73): Show | 78 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.-160-22613G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26567288 | ||||||
| chr22:26567435
|
G | A | 2 | a0001c0005t0005g0158a0001c0005t0005g0159 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-161+22618C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26567435 | ||||||
| chr22:26567473
|
A | G | 317 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(314): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-161+22580T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26567473 | ||||||
| chr22:26567516
|
G | A | 1 | a0001c0001t0002g0342 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-161+22537C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26567516 | ||||||
| chr22:26567542
|
G | A | 16 | a0001c0001t0001g0050a0001c0004t0001g0043a0001c0004t0001g0049others(13): Show | 16 | HG01255.hp1 HG01261.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-161+22511C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26567542 | ||||||
| chr22:26567726
|
G | C | 1 | a0001c0006t0005g0318 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-161+22327C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26567726 | ||||||
| chr22:26567778
|
G | T | 20 | a0001c0001t0001g0317a0001c0001t0002g0316a0001c0001t0002g0319others(17): Show | 21 | HG00140.hp2 HG00423.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.-161+22275C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26567778 | ||||||
| chr22:26567840
|
C | T | 1 | a0002c0002t0007g0041 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-161+22213G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26567840 | ||||||
| chr22:26567861
|
T | C | 1 | a0001c0003t0039g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-161+22192A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26567861 | ||||||
| chr22:26568117
|
C | A | 2 | a0001c0003t0002g0202a0001c0003t0002g0365 | 2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-161+21936G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26568117 | ||||||
| chr22:26568304
|
C | T | 1 | a0001c0001t0004g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-161+21749G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26568304 | ||||||
| chr22:26568628
|
C | T | 1 | a0001c0008t0001g0167 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-161+21425G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26568628 | ||||||
| chr22:26568664
|
T | G | 1 | a0002c0002t0042g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-161+21389A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26568664 | ||||||
| chr22:26568864
|
C | CT | 22 | a0001c0001t0001g0063a0001c0001t0001g0109a0001c0001t0001g0332others(19): Show | 22 | HG01168.hp2 HG01243.hp2 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.-161+21188dupA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26568864 | ||||||
| chr22:26568890
|
A | AG | 390 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(387): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.-161+21162_-161+21 others(7): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26568890 | ||||||
| chr22:26568923
|
G | A | 3 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0003t0039g0022 | 3 | HG02717.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-161+21130C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26568923 | ||||||
| chr22:26568924
|
C | T | 3 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0003t0039g0022 | 3 | HG02717.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-161+21129G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26568924 | ||||||
| chr22:26568925
|
C | A | 3 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0003t0039g0022 | 3 | HG02717.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-161+21128G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26568925 | ||||||
| chr22:26568926
|
C | T | 3 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0003t0039g0022 | 3 | HG02717.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-161+21127G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26568926 | ||||||
| chr22:26568932
|
C | T | 39 | a0001c0001t0001g0317a0001c0001t0002g0316a0001c0001t0002g0319others(36): Show | 42 | HG00140.hp2 HG00423.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.-161+21121G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26568932 | ||||||
| chr22:26569023
|
T | C | 317 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(314): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-161+21030A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569023 | ||||||
| chr22:26569025
|
A | G | 101 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(98): Show | 101 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-161+21028T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569025 | ||||||
| chr22:26569085
|
G | A | 16 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(13): Show | 17 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(14): Show |
intron_variant | MODIFIER | c.-161+20968C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569085 | ||||||
| chr22:26569189
|
G | A | 1 | a0001c0001t0037g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-161+20864C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569189 | ||||||
| chr22:26569205
|
T | C | 1 | a0001c0001t0003g0282 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-161+20848A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569205 | ||||||
| chr22:26569218
|
C | T | 1 | a0001c0003t0004g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-161+20835G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569218 | ||||||
| chr22:26569245
|
T | C | 60 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(57): Show | 60 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-161+20808A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569245 | ||||||
| chr22:26569249
|
T | C | 1 | a0001c0007t0009g0331 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-161+20804A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569249 | ||||||
| chr22:26569304
|
C | T | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161+20749G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569304 | ||||||
| chr22:26569365
|
A | G | 1 | a0001c0005t0019g0190 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-161+20688T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569365 | ||||||
| chr22:26569396
|
T | G | 20 | a0001c0001t0002g0122a0001c0001t0003g0023a0001c0001t0004g0059others(17): Show | 20 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-161+20657A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569396 | ||||||
| chr22:26569566
|
TCAAGGCC others(46): Show |
T | 1 | a0001c0001t0001g0102 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-161+20434_-161+20 others(59): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569566 | ||||||
| chr22:26569773
|
A | C | 1 | a0001c0005t0002g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-161+20280T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569773 | ||||||
| chr22:26569949
|
C | CA | 14 | a0001c0001t0001g0058a0001c0001t0001g0099a0001c0001t0002g0330others(11): Show | 14 | HG01433.hp2 HG02630.hp1 HG03688.hp1 others(11): Show |
intron_variant | MODIFIER | c.-161+20103dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569949 | ||||||
| chr22:26569949
|
CA | C | 81 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(78): Show | 82 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.-161+20103delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569949 | ||||||
| chr22:26569980
|
GAAAAGAA others(3): Show |
G | 34 | a0001c0001t0001g0065a0001c0001t0001g0208a0001c0001t0001g0229others(31): Show | 35 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.-161+20063_-161+20 others(16): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569980 | ||||||
| chr22:26569980
|
GAAAAGAA others(4): Show |
G | 1 | a0002c0002t0023g0246 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-161+20062_-161+20 others(17): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569980 | ||||||
| chr22:26569981
|
AAAAGAAA others(7): Show |
A | 38 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0082others(35): Show | 39 | HG00140.hp2 HG00609.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-161+20058_-161+20 others(20): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569981 | ||||||
| chr22:26569981
|
AAAAGAAA others(11): Show |
A | 27 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(24): Show | 27 | HG00621.hp2 HG00738.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-161+20054_-161+20 others(24): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569981 | ||||||
| chr22:26569981
|
AAAAGAAA others(15): Show |
A | 17 | a0001c0001t0001g0050a0001c0001t0001g0099a0001c0001t0002g0274others(14): Show | 19 | HG00099.hp1 HG01099.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.-161+20050_-161+20 others(28): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569981 | ||||||
| chr22:26569981
|
AAAAGAAA others(19): Show |
A | 142 | a0001c0001t0001g0061a0001c0001t0001g0151a0001c0001t0001g0156others(139): Show | 147 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.-161+20046_-161+20 others(32): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569981 | ||||||
| chr22:26569981
|
AAAAGAAA others(23): Show |
A | 14 | a0001c0001t0001g0128a0001c0001t0002g0312a0001c0001t0003g0279others(11): Show | 14 | HG02015.hp2 HG02257.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-161+20042_-161+20 others(36): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569981 | ||||||
| chr22:26569981
|
AAAAGAAA others(27): Show |
A | 1 | a0001c0003t0039g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-161+20038_-161+20 others(40): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569981 | ||||||
| chr22:26569981
|
AAAAGAAA others(31): Show |
A | 1 | a0001c0001t0008g0373 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-161+20034_-161+20 others(44): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569981 | ||||||
| chr22:26569981
|
AAAAGAAA others(35): Show |
A | 1 | a0001c0001t0008g0374 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-161+20030_-161+20 others(48): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569981 | ||||||
| chr22:26569985
|
GAAAGAA | G | 46 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(43): Show | 46 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.-161+20062_-161+20 others(12): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569985 | ||||||
| chr22:26569989
|
GAA | G | 38 | a0001c0001t0001g0079a0001c0001t0001g0093a0001c0001t0001g0094others(35): Show | 38 | HG00544.hp2 HG00738.hp1 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.-161+20062_-161+20 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569989 | ||||||
| chr22:26569991
|
A | AAG | 19 | a0001c0001t0001g0091a0001c0001t0002g0153a0001c0001t0002g0342others(16): Show | 19 | HG00099.hp2 HG00735.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-161+20061_-161+20 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569991 | ||||||
| chr22:26569991
|
A | AAGAAAG | 8 | a0001c0001t0002g0111a0001c0001t0002g0168a0001c0001t0002g0171others(5): Show | 8 | HG00597.hp1 HG01070.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.-161+20061_-161+20 others(12): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569991 | ||||||
| chr22:26569991
|
A | AAGAAAGA others(3): Show |
1 | a0001c0001t0004g0084 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-161+20061_-161+20 others(16): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26569991 | ||||||
| chr22:26570029
|
A | G | 2 | a0001c0018t0004g0078a0002c0013t0004g0029 | 2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-161+20024T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570029 | ||||||
| chr22:26570037
|
A | C | 107 | a0001c0001t0001g0050a0001c0001t0001g0151a0001c0001t0001g0156others(104): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.-161+20016T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570037 | ||||||
| chr22:26570041
|
A | C | 124 | a0001c0001t0001g0050a0001c0001t0001g0151a0001c0001t0001g0156others(121): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.-161+20012T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570041 | ||||||
| chr22:26570041
|
A | G | 17 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(14): Show | 18 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(15): Show |
intron_variant | MODIFIER | c.-161+20012T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570041 | ||||||
| chr22:26570045
|
C | A | 18 | a0001c0001t0001g0243a0001c0001t0002g0342a0001c0001t0002g0366others(15): Show | 18 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-161+20008G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570045 | ||||||
| chr22:26570045
|
CAGAA | C | 55 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(52): Show | 56 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.-161+20004_-161+20 others(10): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570045 | ||||||
| chr22:26570049
|
A | C | 148 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(145): Show | 149 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.-161+20004T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570049 | ||||||
| chr22:26570053
|
A | C | 170 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(167): Show | 171 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.-161+20000T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570053 | ||||||
| chr22:26570057
|
A | C | 8 | a0001c0001t0002g0111a0001c0001t0002g0168a0001c0001t0002g0170others(5): Show | 8 | HG00099.hp2 HG01081.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.-161+19996T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570057 | ||||||
| chr22:26570062
|
A | G | 3 | a0001c0001t0001g0208a0001c0001t0001g0229a0001c0001t0001g0238 | 3 | HG00558.hp1 NA18960.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.-161+19991T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570062 | ||||||
| chr22:26570066
|
G | A | 3 | a0001c0001t0001g0208a0001c0001t0001g0229a0001c0001t0001g0238 | 3 | HG00558.hp1 NA18960.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.-161+19987C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570066 | ||||||
| chr22:26570096
|
GA | G | 10 | a0001c0001t0002g0122a0001c0001t0003g0023a0001c0001t0004g0059others(7): Show | 10 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.-161+19956delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570096 | ||||||
| chr22:26570193
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-161+19860A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570193 | ||||||
| chr22:26570276
|
C | T | 1 | a0001c0006t0005g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-161+19777G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570276 | ||||||
| chr22:26570446
|
C | G | 2 | a0001c0006t0005g0257a0001c0006t0005g0258 | 2 | NA18972.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-161+19607G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570446 | ||||||
| chr22:26570457
|
C | T | 1 | a0001c0001t0016g0377 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-161+19596G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570457 | ||||||
| chr22:26570490
|
T | G | 1 | a0001c0001t0001g0151 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-161+19563A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570490 | ||||||
| chr22:26570549
|
G | C | 3 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0003t0039g0022 | 3 | HG02717.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-161+19504C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570549 | ||||||
| chr22:26570553
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-161+19500G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570553 | ||||||
| chr22:26570589
|
C | T | 7 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0185others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-161+19464G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570589 | ||||||
| chr22:26570637
|
A | G | 356 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(353): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.-161+19416T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570637 | ||||||
| chr22:26570640
|
CA | C | 7 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0185others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-161+19412delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570640 | ||||||
| chr22:26570704
|
C | T | 7 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0002g0185others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-161+19349G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570704 | ||||||
| chr22:26570717
|
C | CCAGCATA others(22): Show |
6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161+19307_-161+19 others(35): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570717 | ||||||
| chr22:26570717
|
CCAGCATA others(22): Show |
C | 317 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(314): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-161+19307_-161+19 others(35): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570717 | ||||||
| chr22:26570801
|
A | G | 1 | a0001c0001t0002g0352 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-161+19252T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570801 | ||||||
| chr22:26570851
|
C | G | 20 | a0001c0001t0001g0317a0001c0001t0002g0316a0001c0001t0002g0319others(17): Show | 21 | HG00140.hp2 HG00423.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.-161+19202G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570851 | ||||||
| chr22:26570861
|
T | A | 2 | a0001c0001t0024g0389a0001c0001t0024g0390 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-161+19192A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570861 | ||||||
| chr22:26570861
|
T | G | 1 | a0001c0001t0017g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-161+19192A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26570861 | ||||||
| chr22:26571038
|
T | C | 18 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(15): Show | 19 | HG00597.hp1 HG03098.hp2 NA18950.hp2 others(16): Show |
intron_variant | MODIFIER | c.-161+19015A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26571038 | ||||||
| chr22:26571198
|
C | T | 75 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(72): Show | 76 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.-161+18855G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26571198 | ||||||
| chr22:26571199
|
G | A | 7 | a0001c0001t0003g0106a0001c0001t0004g0030a0001c0001t0004g0031others(4): Show | 7 | HG00438.hp2 NA18956.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.-161+18854C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26571199 | ||||||
| chr22:26571408
|
A | G | 215 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(212): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-161+18645T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26571408 | ||||||
| chr22:26571428
|
A | AT | 18 | a0001c0001t0002g0274a0001c0001t0003g0002a0001c0001t0003g0037others(15): Show | 19 | HG00438.hp1 HG01074.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.-161+18624dupA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26571428 | ||||||
| chr22:26571485
|
T | C | 1 | a0001c0001t0037g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-161+18568A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26571485 | ||||||
| chr22:26571534
|
T | C | 98 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(95): Show | 98 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.-161+18519A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26571534 | ||||||
| chr22:26571644
|
G | A | 1 | a0001c0001t0004g0382 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-161+18409C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26571644 | ||||||
| chr22:26571964
|
T | C | 3 | a0001c0004t0011g0216a0001c0004t0011g0217a0001c0004t0011g0218 | 3 | HG02280.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-161+18089A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26571964 | ||||||
| chr22:26572053
|
G | C | 11 | a0001c0001t0004g0149a0001c0001t0004g0162a0001c0001t0004g0348others(8): Show | 11 | HG01109.hp2 HG01496.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-161+18000C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26572053 | ||||||
| chr22:26572246
|
T | G | 215 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(212): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-161+17807A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26572246 | ||||||
| chr22:26572541
|
G | T | 226 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(223): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-161+17512C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26572541 | ||||||
| chr22:26572566
|
C | T | 1 | a0001c0001t0040g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-161+17487G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26572566 | ||||||
| chr22:26572783
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-161+17270G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26572783 | ||||||
| chr22:26572809
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-161+17244T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26572809 | ||||||
| chr22:26572914
|
G | A | 2 | a0001c0003t0021g0270a0001c0003t0021g0387 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-161+17139C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26572914 | ||||||
| chr22:26573096
|
A | C | 205 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(202): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.-161+16957T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573096 | ||||||
| chr22:26573097
|
G | A | 3 | a0001c0001t0004g0084a0001c0001t0004g0100a0002c0002t0001g0101 | 3 | NA18999.hp2 NA19012.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-161+16956C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573097 | ||||||
| chr22:26573139
|
T | C | 3 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0003t0039g0022 | 3 | HG02717.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-161+16914A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573139 | ||||||
| chr22:26573249
|
T | G | 16 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(13): Show | 17 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(14): Show |
intron_variant | MODIFIER | c.-161+16804A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573249 | ||||||
| chr22:26573285
|
C | T | 213 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(210): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-161+16768G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573285 | ||||||
| chr22:26573319
|
C | T | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0244 | 3 | HG00621.hp2 NA18944.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-161+16734G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573319 | ||||||
| chr22:26573366
|
A | G | 272 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(269): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-161+16687T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573366 | ||||||
| chr22:26573397
|
C | T | 1 | a0004c0020t0001g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-161+16656G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573397 | ||||||
| chr22:26573699
|
T | C | 2 | a0001c0006t0001g0195a0001c0006t0005g0104 | 2 | HG00140.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-161+16354A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573699 | ||||||
| chr22:26573702
|
T | C | 16 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(13): Show | 17 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(14): Show |
intron_variant | MODIFIER | c.-161+16351A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573702 | ||||||
| chr22:26573726
|
C | T | 1 | a0001c0001t0002g0352 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-161+16327G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573726 | ||||||
| chr22:26573837
|
C | T | 5 | a0001c0001t0006g0071a0001c0006t0001g0195a0001c0006t0005g0104others(2): Show | 5 | HG00140.hp2 HG00738.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161+16216G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573837 | ||||||
| chr22:26573850
|
A | G | 1 | a0001c0004t0003g0051 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-161+16203T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573850 | ||||||
| chr22:26573877
|
G | A | 1 | a0001c0003t0002g0185 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-161+16176C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573877 | ||||||
| chr22:26573892
|
T | C | 213 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(210): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-161+16161A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26573892 | ||||||
| chr22:26574051
|
T | C | 274 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(271): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.-161+16002A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26574051 | ||||||
| chr22:26574471
|
C | G | 1 | a0001c0001t0009g0146 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161+15582G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26574471 | ||||||
| chr22:26574472
|
C | T | 1 | a0001c0001t0009g0146 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161+15581G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26574472 | ||||||
| chr22:26574531
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-161+15522A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26574531 | ||||||
| chr22:26574574
|
A | G | 2 | a0001c0001t0037g0209a0001c0003t0010g0211 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-161+15479T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26574574 | ||||||
| chr22:26574611
|
C | T | 1 | a0001c0001t0008g0017 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-161+15442G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26574611 | ||||||
| chr22:26574643
|
C | A | 11 | a0001c0001t0004g0149a0001c0001t0004g0162a0001c0001t0004g0348others(8): Show | 11 | HG01109.hp2 HG01496.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-161+15410G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26574643 | ||||||
| chr22:26574643
|
C | T | 3 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0003t0039g0022 | 3 | HG02717.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-161+15410G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26574643 | ||||||
| chr22:26574691
|
C | T | 1 | a0001c0001t0005g0144 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-161+15362G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26574691 | ||||||
| chr22:26574749
|
T | A | 16 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(13): Show | 17 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(14): Show |
intron_variant | MODIFIER | c.-161+15304A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26574749 | ||||||
| chr22:26574822
|
G | A | 34 | a0001c0001t0004g0203a0001c0001t0006g0199a0001c0001t0006g0200others(31): Show | 35 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.-161+15231C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26574822 | ||||||
| chr22:26574881
|
C | T | 45 | a0001c0001t0001g0317a0001c0001t0002g0316a0001c0001t0002g0319others(42): Show | 48 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-161+15172G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26574881 | ||||||
| chr22:26574937
|
G | T | 45 | a0001c0001t0001g0317a0001c0001t0002g0316a0001c0001t0002g0319others(42): Show | 48 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-161+15116C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26574937 | ||||||
| chr22:26575023
|
C | G | 1 | a0001c0001t0004g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-161+15030G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575023 | ||||||
| chr22:26575097
|
G | A | 1 | a0001c0001t0002g0221 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-161+14956C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575097 | ||||||
| chr22:26575104
|
G | A | 3 | a0001c0001t0008g0373a0001c0001t0008g0374a0001c0003t0039g0022 | 3 | HG02717.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-161+14949C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575104 | ||||||
| chr22:26575190
|
T | G | 30 | a0001c0001t0001g0349a0001c0001t0002g0024a0001c0001t0002g0025others(27): Show | 30 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-161+14863A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575190 | ||||||
| chr22:26575246
|
C | T | 1 | a0001c0001t0017g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-161+14807G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575246 | ||||||
| chr22:26575463
|
TC | T | 33 | a0001c0001t0004g0203a0001c0001t0006g0199a0001c0001t0006g0200others(30): Show | 34 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.-161+14589delG | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575463 | ||||||
| chr22:26575555
|
G | A | 2 | a0001c0009t0003g0276a0001c0009t0003g0313 | 2 | HG00140.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-161+14498C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575555 | ||||||
| chr22:26575760
|
C | T | 2 | a0001c0001t0001g0050a0001c0004t0035g0250 | 2 | HG02083.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-161+14293G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575760 | ||||||
| chr22:26575770
|
C | T | 74 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0273others(71): Show | 78 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.-161+14283G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575770 | ||||||
| chr22:26575852
|
C | T | 1 | a0001c0001t0006g0038 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-161+14201G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575852 | ||||||
| chr22:26575864
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-161+14189A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575864 | ||||||
| chr22:26575911
|
G | A | 16 | a0001c0001t0001g0088a0001c0001t0004g0089a0001c0001t0006g0003others(13): Show | 17 | HG00597.hp1 NA18950.hp2 NA18956.hp2 others(14): Show |
intron_variant | MODIFIER | c.-161+14142C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575911 | ||||||
| chr22:26575951
|
GTGCCACC others(11): Show |
G | 1 | a0001c0001t0001g0147 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-161+14084_-161+14 others(24): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575951 | ||||||
| chr22:26575971
|
G | T | 1 | a0001c0001t0001g0147 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-161+14082C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575971 | ||||||
| chr22:26575987
|
C | T | 1 | a0001c0003t0043g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-161+14066G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26575987 | ||||||
| chr22:26576012
|
T | TA | 75 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0273others(72): Show | 79 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-161+14040dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26576012 | ||||||
| chr22:26576031
|
T | TA | 33 | a0001c0001t0004g0203a0001c0001t0006g0199a0001c0001t0006g0200others(30): Show | 34 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.-161+14021dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26576031 | ||||||
| chr22:26576212
|
T | C | 49 | a0001c0001t0001g0050a0001c0001t0001g0349a0001c0001t0002g0024others(46): Show | 49 | HG00423.hp2 HG00735.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.-161+13841A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26576212 | ||||||
| chr22:26576295
|
AAAGT | A | 33 | a0001c0001t0004g0203a0001c0001t0006g0199a0001c0001t0006g0200others(30): Show | 34 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.-161+13754_-161+13 others(10): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26576295 | ||||||
| chr22:26576301
|
A | G | 1 | a0001c0001t0003g0297 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-161+13752T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26576301 | ||||||
| chr22:26576376
|
T | C | 82 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(79): Show | 82 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.-161+13677A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26576376 | ||||||
| chr22:26576442
|
G | A | 1 | a0001c0001t0003g0223 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-161+13611C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26576442 | ||||||
| chr22:26576556
|
G | A | 1 | a0001c0001t0006g0085 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-161+13497C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26576556 | ||||||
| chr22:26576832
|
C | T | 1 | a0001c0005t0019g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-161+13221G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26576832 | ||||||
| chr22:26576843
|
T | C | 2 | a0001c0004t0003g0051a0002c0002t0004g0048 | 2 | HG02071.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-161+13210A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26576843 | ||||||
| chr22:26576849
|
T | C | 1 | a0001c0001t0004g0005 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-161+13204A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26576849 | ||||||
| chr22:26576863
|
G | A | 156 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(153): Show | 162 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-161+13190C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26576863 | ||||||
| chr22:26576868
|
G | A | 12 | a0001c0001t0008g0261a0001c0001t0008g0262a0001c0001t0008g0263others(9): Show | 12 | HG01243.hp1 HG02109.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.-161+13185C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26576868 | ||||||
| chr22:26576871
|
T | C | 1 | a0001c0001t0004g0005 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-161+13182A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26576871 | ||||||
| chr22:26577012
|
T | C | 1 | a0001c0001t0001g0239 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-161+13041A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577012 | ||||||
| chr22:26577074
|
C | T | 13 | a0001c0001t0004g0149a0001c0001t0004g0162a0001c0001t0004g0348others(10): Show | 13 | HG00323.hp1 HG01109.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.-161+12979G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577074 | ||||||
| chr22:26577095
|
C | CA | 51 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0001g0063others(48): Show | 51 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.-161+12957dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577095 | ||||||
| chr22:26577095
|
C | CAA | 46 | a0001c0001t0001g0317a0001c0001t0001g0320a0001c0001t0002g0192others(43): Show | 47 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.-161+12956_-161+12 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577095 | ||||||
| chr22:26577095
|
C | CAAA | 10 | a0001c0001t0002g0327a0001c0001t0002g0330a0001c0001t0003g0193others(7): Show | 11 | HG00423.hp1 HG00738.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.-161+12955_-161+12 others(9): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577095 | ||||||
| chr22:26577095
|
CA | C | 17 | a0001c0001t0004g0005a0001c0001t0004g0149a0001c0001t0004g0162others(14): Show | 18 | HG01109.hp2 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-161+12957delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577095 | ||||||
| chr22:26577134
|
G | A | 2 | a0001c0003t0021g0270a0001c0003t0021g0387 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-161+12919C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577134 | ||||||
| chr22:26577142
|
G | A | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161+12911C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577142 | ||||||
| chr22:26577172
|
G | T | 3 | a0001c0001t0004g0181a0001c0001t0004g0370a0001c0001t0004g0372 | 3 | HG01884.hp2 HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-161+12881C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577172 | ||||||
| chr22:26577265
|
T | TA | 154 | a0001c0001t0001g0028a0001c0001t0001g0050a0001c0001t0001g0151others(151): Show | 159 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.-161+12787dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577265 | ||||||
| chr22:26577265
|
TA | T | 25 | a0001c0001t0004g0033a0001c0001t0004g0149a0001c0001t0004g0162others(22): Show | 25 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.-161+12787delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577265 | ||||||
| chr22:26577266
|
A | T | 1 | a0002c0002t0007g0057 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-161+12787T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577266 | ||||||
| chr22:26577296
|
T | C | 40 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(37): Show | 40 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.-161+12757A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577296 | ||||||
| chr22:26577323
|
T | C | 1 | a0001c0001t0003g0223 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-161+12730A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577323 | ||||||
| chr22:26577328
|
T | C | 4 | a0001c0001t0007g0253a0001c0001t0007g0254a0001c0001t0007g0255others(1): Show | 4 | NA18950.hp1 NA18972.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-161+12725A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577328 | ||||||
| chr22:26577351
|
C | CT | 95 | a0001c0001t0001g0050a0001c0001t0001g0088a0001c0001t0001g0349others(92): Show | 97 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-161+12701dupA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577351 | ||||||
| chr22:26577438
|
A | G | 1 | a0001c0001t0003g0271 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-161+12615T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577438 | ||||||
| chr22:26577573
|
A | T | 1 | a0001c0001t0040g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-161+12480T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577573 | ||||||
| chr22:26577628
|
T | C | 2 | a0001c0001t0024g0389a0001c0001t0024g0390 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-161+12425A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577628 | ||||||
| chr22:26577645
|
G | A | 1 | a0001c0001t0002g0360 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-161+12408C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577645 | ||||||
| chr22:26577649
|
A | AT | 76 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0061others(73): Show | 76 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.-161+12403dupA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577649 | ||||||
| chr22:26577649
|
A | ATT | 5 | a0001c0001t0004g0067a0001c0001t0008g0110a0001c0001t0010g0004others(2): Show | 6 | HG02145.hp2 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161+12402_-161+12 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577649 | ||||||
| chr22:26577649
|
AT | A | 58 | a0001c0001t0001g0156a0001c0001t0001g0226a0001c0001t0001g0240others(55): Show | 58 | HG00140.hp1 HG00544.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.-161+12403delA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577649 | ||||||
| chr22:26577649
|
ATT | A | 134 | a0001c0001t0001g0050a0001c0001t0001g0107a0001c0001t0001g0108others(131): Show | 139 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.-161+12402_-161+12 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577649 | ||||||
| chr22:26577649
|
ATTTTT | A | 11 | a0001c0001t0008g0261a0001c0001t0008g0262a0001c0001t0008g0263others(8): Show | 11 | HG01243.hp1 HG01243.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-161+12399_-161+12 others(11): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577649 | ||||||
| chr22:26577806
|
G | C | 6 | a0001c0001t0001g0220a0001c0001t0001g0240a0001c0001t0001g0241others(3): Show | 6 | HG00609.hp1 HG00621.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161+12247C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577806 | ||||||
| chr22:26577808
|
G | A | 57 | a0001c0001t0001g0050a0001c0001t0001g0349a0001c0001t0002g0024others(54): Show | 58 | HG00423.hp2 HG00597.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.-161+12245C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577808 | ||||||
| chr22:26577842
|
A | C | 1 | a0001c0001t0016g0148 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-161+12211T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577842 | ||||||
| chr22:26577850
|
G | T | 1 | a0001c0001t0003g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-161+12203C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577850 | ||||||
| chr22:26577894
|
G | A | 10 | a0001c0001t0004g0348a0001c0001t0016g0346a0001c0003t0008g0113others(7): Show | 10 | HG01496.hp2 HG02486.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-161+12159C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577894 | ||||||
| chr22:26577953
|
C | A | 4 | a0001c0001t0004g0005a0001c0001t0004g0266a0001c0004t0011g0265others(1): Show | 5 | HG01256.hp1 HG01258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161+12100G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26577953 | ||||||
| chr22:26578205
|
T | C | 3 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0027g0150 | 3 | HG00323.hp1 HG02698.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-161+11848A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26578205 | ||||||
| chr22:26578207
|
C | G | 72 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0273others(69): Show | 76 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.-161+11846G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26578207 | ||||||
| chr22:26578284
|
G | A | 8 | a0001c0001t0004g0348a0001c0001t0016g0346a0001c0003t0008g0113others(5): Show | 8 | HG01496.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-161+11769C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26578284 | ||||||
| chr22:26578326
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-161+11727C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26578326 | ||||||
| chr22:26578441
|
G | A | 23 | a0001c0001t0001g0050a0001c0001t0003g0002a0001c0001t0003g0037others(20): Show | 24 | HG00597.hp1 HG01255.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.-161+11612C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26578441 | ||||||
| chr22:26578648
|
G | A | 10 | a0001c0001t0004g0348a0001c0001t0016g0346a0001c0003t0008g0113others(7): Show | 10 | HG01496.hp2 HG02486.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-161+11405C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26578648 | ||||||
| chr22:26578772
|
T | A | 10 | a0001c0001t0004g0348a0001c0001t0016g0346a0001c0003t0008g0113others(7): Show | 10 | HG01496.hp2 HG02486.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-161+11281A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26578772 | ||||||
| chr22:26578776
|
G | A | 102 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(99): Show | 103 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-161+11277C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26578776 | ||||||
| chr22:26578841
|
ATTTC | A | 4 | a0001c0001t0008g0017a0001c0001t0008g0018a0001c0001t0013g0019others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-161+11208_-161+11 others(10): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26578841 | ||||||
| chr22:26578875
|
G | A | 4 | a0001c0003t0001g0056a0001c0003t0001g0115a0001c0003t0004g0210others(1): Show | 4 | HG02109.hp1 HG02976.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-161+11178C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26578875 | ||||||
| chr22:26578912
|
C | A | 1 | a0001c0001t0004g0203 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-161+11141G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26578912 | ||||||
| chr22:26578922
|
G | T | 108 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(105): Show | 109 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.-161+11131C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26578922 | ||||||
| chr22:26578965
|
C | T | 2 | a0001c0001t0004g0363a0001c0001t0023g0341 | 2 | HG01069.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-161+11088G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26578965 | ||||||
| chr22:26579016
|
G | A | 1 | a0001c0001t0003g0165 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-161+11037C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26579016 | ||||||
| chr22:26579081
|
A | G | 1 | a0001c0001t0018g0277 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-161+10972T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26579081 | ||||||
| chr22:26579103
|
G | A | 31 | a0001c0001t0001g0147a0001c0001t0001g0208a0001c0001t0001g0220others(28): Show | 31 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.-161+10950C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26579103 | ||||||
| chr22:26579132
|
G | A | 98 | a0001c0001t0001g0050a0001c0001t0001g0147a0001c0001t0001g0208others(95): Show | 100 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.-161+10921C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26579132 | ||||||
| chr22:26579290
|
A | G | 1 | a0001c0009t0003g0276 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-161+10763T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26579290 | ||||||
| chr22:26579312
|
G | A | 5 | a0001c0001t0004g0370a0001c0001t0004g0371a0001c0001t0004g0372others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161+10741C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26579312 | ||||||
| chr22:26579326
|
G | A | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161+10727C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26579326 | ||||||
| chr22:26579394
|
G | C | 4 | a0001c0001t0004g0005a0001c0001t0004g0266a0001c0004t0011g0265others(1): Show | 5 | HG01256.hp1 HG01258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161+10659C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26579394 | ||||||
| chr22:26579426
|
G | A | 1 | a0001c0003t0022g0362 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-161+10627C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26579426 | ||||||
| chr22:26579552
|
A | G | 97 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0273others(94): Show | 102 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.-161+10501T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26579552 | ||||||
| chr22:26579692
|
G | A | 1 | a0001c0001t0002g0340 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-161+10361C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26579692 | ||||||
| chr22:26579720
|
G | A | 1 | a0001c0003t0021g0270 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-161+10333C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26579720 | ||||||
| chr22:26579726
|
G | A | 1 | a0001c0003t0004g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-161+10327C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26579726 | ||||||
| chr22:26580013
|
G | A | 14 | a0001c0001t0004g0005a0001c0001t0004g0149a0001c0001t0004g0266others(11): Show | 15 | HG01256.hp1 HG01258.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-161+10040C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26580013 | ||||||
| chr22:26580041
|
T | C | 19 | a0001c0001t0004g0008a0001c0001t0004g0181a0001c0001t0004g0264others(16): Show | 20 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.-161+10012A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26580041 | ||||||
| chr22:26580162
|
T | C | 7 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-161+9891A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26580162 | ||||||
| chr22:26580350
|
C | T | 5 | a0001c0001t0004g0370a0001c0001t0004g0371a0001c0001t0004g0372others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161+9703G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26580350 | ||||||
| chr22:26580404
|
C | T | 118 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-161+9649G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26580404 | ||||||
| chr22:26580502
|
A | G | 2 | a0001c0001t0008g0017a0001c0001t0008g0018 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-161+9551T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26580502 | ||||||
| chr22:26580580
|
C | T | 118 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-161+9473G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26580580 | ||||||
| chr22:26580675
|
C | T | 1 | a0002c0002t0002g0323 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-161+9378G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26580675 | ||||||
| chr22:26580806
|
G | A | 112 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(109): Show | 116 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-161+9247C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26580806 | ||||||
| chr22:26580871
|
G | A | 1 | a0001c0001t0003g0322 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-161+9182C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26580871 | ||||||
| chr22:26581015
|
TACATACA others(17): Show |
T | 10 | a0001c0001t0001g0332a0001c0001t0002g0325a0001c0001t0002g0366others(7): Show | 10 | HG01069.hp1 HG01070.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.-161+9014_-161+903 others(28): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581015 | ||||||
| chr22:26581015
|
TACATACA others(19): Show |
T | 108 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(105): Show | 112 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-161+9012_-161+903 others(30): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581015 | ||||||
| chr22:26581019
|
T | TAC | 6 | a0001c0001t0003g0165a0001c0001t0007g0120a0001c0001t0007g0166others(3): Show | 6 | HG00639.hp1 HG00735.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161+9032_-161+903 others(6): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581019 | ||||||
| chr22:26581019
|
TAC | T | 24 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0002g0122others(21): Show | 24 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.-161+9032_-161+903 others(6): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581019 | ||||||
| chr22:26581019
|
TACAC | T | 137 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(134): Show | 139 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.-161+9030_-161+903 others(8): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581019 | ||||||
| chr22:26581019
|
TACACAC | T | 11 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG02486.hp1 HG02602.hp2 HG03540.hp2 others(8): Show |
intron_variant | MODIFIER | c.-161+9028_-161+903 others(10): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581019 | ||||||
| chr22:26581019
|
TACACACA others(1): Show |
T | 66 | a0001c0001t0002g0192a0001c0001t0003g0189a0001c0001t0003g0193others(63): Show | 68 | HG00639.hp2 HG00673.hp1 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.-161+9026_-161+903 others(12): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581019 | ||||||
| chr22:26581019
|
TACACACA others(3): Show |
T | 16 | a0001c0001t0002g0221a0001c0001t0004g0005a0001c0001t0004g0264others(13): Show | 17 | HG01256.hp1 HG01258.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-161+9024_-161+903 others(14): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581019 | ||||||
| chr22:26581044
|
A | G | 3 | a0001c0001t0004g0181a0001c0001t0010g0182a0001c0001t0010g0183 | 3 | HG02647.hp2 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-161+9009T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581044 | ||||||
| chr22:26581046
|
ACACACAC others(1): Show |
A | 3 | a0001c0001t0004g0181a0001c0001t0010g0182a0001c0001t0010g0183 | 3 | HG02647.hp2 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-161+8999_-161+900 others(12): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581046 | ||||||
| chr22:26581050
|
A | G | 1 | a0001c0001t0006g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-161+9003T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581050 | ||||||
| chr22:26581054
|
G | A | 118 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-161+8999C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581054 | ||||||
| chr22:26581118
|
C | T | 1 | a0001c0001t0004g0059 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-161+8935G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581118 | ||||||
| chr22:26581249
|
T | C | 1 | a0002c0002t0004g0121 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-161+8804A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581249 | ||||||
| chr22:26581287
|
T | C | 119 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(116): Show | 123 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.-161+8766A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581287 | ||||||
| chr22:26581323
|
T | G | 1 | a0001c0001t0002g0122 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-161+8730A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581323 | ||||||
| chr22:26581415
|
T | C | 16 | a0001c0001t0002g0221a0001c0001t0004g0005a0001c0001t0004g0149others(13): Show | 17 | HG01256.hp1 HG01258.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-161+8638A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581415 | ||||||
| chr22:26581493
|
T | G | 1 | a0001c0001t0017g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-161+8560A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581493 | ||||||
| chr22:26581636
|
G | A | 15 | a0001c0001t0004g0005a0001c0001t0004g0149a0001c0001t0004g0264others(12): Show | 16 | HG01256.hp1 HG01258.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-161+8417C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581636 | ||||||
| chr22:26581790
|
C | T | 1 | a0001c0001t0001g0344 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-161+8263G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581790 | ||||||
| chr22:26581871
|
C | T | 38 | a0001c0001t0001g0147a0001c0001t0001g0208a0001c0001t0001g0220others(35): Show | 38 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.-161+8182G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26581871 | ||||||
| chr22:26582039
|
A | G | 1 | a0001c0001t0002g0274 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-161+8014T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582039 | ||||||
| chr22:26582148
|
C | G | 1 | a0001c0001t0017g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-161+7905G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582148 | ||||||
| chr22:26582157
|
T | G | 6 | a0001c0001t0008g0017a0001c0001t0008g0018a0001c0001t0013g0019others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161+7896A>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582157 | ||||||
| chr22:26582376
|
G | C | 113 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-161+7677C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582376 | ||||||
| chr22:26582412
|
A | G | 113 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-161+7641T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582412 | ||||||
| chr22:26582423
|
A | G | 113 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-161+7630T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582423 | ||||||
| chr22:26582472
|
T | C | 1 | a0001c0001t0017g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-161+7581A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582472 | ||||||
| chr22:26582566
|
G | A | 1 | a0001c0001t0004g0222 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-161+7487C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582566 | ||||||
| chr22:26582660
|
T | C | 1 | a0001c0001t0003g0326 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-161+7393A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582660 | ||||||
| chr22:26582678
|
C | T | 1 | a0001c0001t0017g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-161+7375G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582678 | ||||||
| chr22:26582814
|
C | T | 3 | a0001c0005t0001g0184a0001c0005t0005g0158a0001c0005t0005g0159 | 3 | HG01081.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-161+7239G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582814 | ||||||
| chr22:26582815
|
G | A | 1 | a0001c0001t0006g0123 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-161+7238C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582815 | ||||||
| chr22:26582857
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-161+7196C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582857 | ||||||
| chr22:26582883
|
G | A | 114 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(111): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-161+7170C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582883 | ||||||
| chr22:26582904
|
G | C | 5 | a0001c0001t0004g0370a0001c0001t0004g0371a0001c0001t0004g0372others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161+7149C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582904 | ||||||
| chr22:26582926
|
A | T | 1 | a0001c0006t0005g0178 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-161+7127T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26582926 | ||||||
| chr22:26583060
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-161+6993G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583060 | ||||||
| chr22:26583118
|
G | GA | 15 | a0001c0001t0003g0040a0001c0001t0004g0386a0001c0001t0006g0145others(12): Show | 15 | HG00741.hp1 HG01192.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.-161+6934dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583118 | ||||||
| chr22:26583118
|
GA | G | 92 | a0001c0001t0001g0317a0001c0001t0001g0320a0001c0001t0001g0332others(89): Show | 97 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-161+6934delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583118 | ||||||
| chr22:26583205
|
C | T | 113 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-161+6848G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583205 | ||||||
| chr22:26583361
|
G | A | 5 | a0001c0001t0004g0370a0001c0001t0004g0371a0001c0001t0004g0372others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161+6692C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583361 | ||||||
| chr22:26583428
|
C | T | 3 | a0001c0004t0007g0035a0001c0006t0005g0042a0002c0002t0007g0041 | 3 | HG02735.hp1 HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-161+6625G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583428 | ||||||
| chr22:26583436
|
C | CA | 42 | a0001c0001t0001g0050a0001c0001t0001g0247a0001c0001t0001g0248others(39): Show | 43 | HG00621.hp1 HG01255.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.-161+6616dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583436 | ||||||
| chr22:26583436
|
C | CAAAAA | 64 | a0001c0001t0001g0317a0001c0001t0001g0320a0001c0001t0002g0274others(61): Show | 68 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.-161+6612_-161+661 others(9): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583436 | ||||||
| chr22:26583436
|
C | CAAAAAA | 42 | a0001c0001t0001g0332a0001c0001t0001g0344a0001c0001t0001g0349others(39): Show | 42 | HG00423.hp1 HG00733.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.-161+6611_-161+661 others(10): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583436 | ||||||
| chr22:26583436
|
CA | C | 14 | a0001c0001t0001g0151a0001c0001t0001g0220a0001c0001t0002g0153others(11): Show | 14 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.-161+6616delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583436 | ||||||
| chr22:26583555
|
CA | C | 116 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(113): Show | 120 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-161+6497delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583555 | ||||||
| chr22:26583636
|
T | A | 109 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(106): Show | 110 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-161+6417A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583636 | ||||||
| chr22:26583769
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-161+6284C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583769 | ||||||
| chr22:26583784
|
G | A | 37 | a0001c0001t0001g0344a0001c0001t0001g0349a0001c0001t0002g0024others(34): Show | 37 | HG00735.hp2 HG01069.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.-161+6269C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583784 | ||||||
| chr22:26583840
|
C | CA | 11 | a0001c0001t0004g0005a0001c0001t0004g0149a0001c0001t0004g0266others(8): Show | 12 | HG01256.hp1 HG01258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-161+6212dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583840 | ||||||
| chr22:26583840
|
CA | C | 15 | a0001c0001t0004g0008a0001c0001t0004g0382a0001c0001t0004g0383others(12): Show | 16 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-161+6212delT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583840 | ||||||
| chr22:26583881
|
T | A | 1 | a0001c0001t0016g0148 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-161+6172A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26583881 | ||||||
| chr22:26584000
|
G | A | 1 | a0001c0001t0004g0337 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-161+6053C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26584000 | ||||||
| chr22:26584111
|
G | A | 383 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(380): Show | 392 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(389): Show |
intron_variant | MODIFIER | c.-161+5942C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26584111 | ||||||
| chr22:26584191
|
G | C | 7 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0002g0153others(4): Show | 7 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(4): Show |
intron_variant | MODIFIER | c.-161+5862C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26584191 | ||||||
| chr22:26584290
|
A | T | 1 | a0001c0001t0003g0271 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-161+5763T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26584290 | ||||||
| chr22:26584369
|
G | C | 6 | a0001c0001t0004g0370a0001c0001t0004g0371a0001c0001t0004g0372others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161+5684C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26584369 | ||||||
| chr22:26584374
|
G | A | 1 | a0001c0003t0039g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-161+5679C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26584374 | ||||||
| chr22:26584579
|
C | T | 113 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-161+5474G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26584579 | ||||||
| chr22:26584618
|
T | C | 75 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(72): Show | 79 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-161+5435A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26584618 | ||||||
| chr22:26584686
|
C | T | 1 | a0001c0006t0005g0178 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-161+5367G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26584686 | ||||||
| chr22:26584695
|
A | C | 1 | a0001c0001t0007g0166 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-161+5358T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26584695 | ||||||
| chr22:26585075
|
A | G | 114 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(111): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-161+4978T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26585075 | ||||||
| chr22:26585276
|
C | A | 133 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(130): Show | 138 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-161+4777G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26585276 | ||||||
| chr22:26585353
|
G | GC | 390 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(387): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.-161+4699dupG | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26585353 | ||||||
| chr22:26585475
|
C | T | 21 | a0001c0001t0001g0208a0001c0001t0004g0005a0001c0001t0004g0149others(18): Show | 22 | HG01256.hp1 HG01258.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.-161+4578G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26585475 | ||||||
| chr22:26585545
|
C | T | 1 | a0001c0001t0023g0341 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-161+4508G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26585545 | ||||||
| chr22:26585698
|
T | C | 113 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-161+4355A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26585698 | ||||||
| chr22:26585743
|
C | G | 2 | a0001c0006t0005g0257a0001c0006t0005g0258 | 2 | NA18972.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-161+4310G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26585743 | ||||||
| chr22:26585838
|
C | G | 113 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-161+4215G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26585838 | ||||||
| chr22:26585866
|
C | T | 2 | a0001c0001t0003g0164a0001c0001t0003g0165 | 2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-161+4187G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26585866 | ||||||
| chr22:26585915
|
T | C | 300 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(297): Show | 307 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.-161+4138A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26585915 | ||||||
| chr22:26585960
|
G | A | 1 | a0001c0001t0025g0129 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-161+4093C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26585960 | ||||||
| chr22:26585968
|
G | C | 3 | a0001c0001t0024g0389a0001c0001t0024g0390a0001c0019t0044g0391 | 3 | HG02257.hp2 HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-161+4085C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26585968 | ||||||
| chr22:26585977
|
A | G | 113 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-161+4076T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26585977 | ||||||
| chr22:26585983
|
G | C | 372 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(369): Show | 381 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(378): Show |
intron_variant | MODIFIER | c.-161+4070C>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26585983 | ||||||
| chr22:26586030
|
G | A | 2 | a0001c0001t0014g0368a0001c0001t0014g0369 | 2 | NA18987.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-161+4023C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586030 | ||||||
| chr22:26586045
|
A | AAAT | 5 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(2): Show | 5 | NA18968.hp1 NA18982.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161+4005_-161+400 others(7): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586045 | ||||||
| chr22:26586061
|
A | C | 11 | a0001c0001t0004g0162a0001c0001t0008g0017a0001c0001t0008g0018others(8): Show | 11 | HG00733.hp1 HG00738.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-161+3992T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586061 | ||||||
| chr22:26586102
|
C | T | 113 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-161+3951G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586102 | ||||||
| chr22:26586171
|
G | A | 1 | a0001c0001t0004g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-161+3882C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586171 | ||||||
| chr22:26586249
|
T | A | 7 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0002g0153others(4): Show | 7 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(4): Show |
intron_variant | MODIFIER | c.-161+3804A>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586249 | ||||||
| chr22:26586352
|
C | T | 1 | a0002c0002t0007g0157 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-161+3701G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586352 | ||||||
| chr22:26586353
|
G | A | 2 | a0001c0006t0005g0257a0001c0006t0005g0258 | 2 | NA18972.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-161+3700C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586353 | ||||||
| chr22:26586395
|
G | A | 113 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-161+3658C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586395 | ||||||
| chr22:26586531
|
T | C | 1 | a0001c0001t0017g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-161+3522A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586531 | ||||||
| chr22:26586663
|
CT | C | 37 | a0001c0001t0001g0344a0001c0001t0001g0349a0001c0001t0002g0024others(34): Show | 37 | HG00735.hp2 HG01069.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.-161+3389delA | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586663 | ||||||
| chr22:26586848
|
G | A | 1 | a0001c0006t0005g0259 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-161+3205C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586848 | ||||||
| chr22:26586942
|
T | C | 1 | a0002c0002t0042g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-161+3111A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586942 | ||||||
| chr22:26586961
|
T | C | 3 | a0001c0001t0008g0261a0001c0001t0008g0262a0001c0001t0008g0263 | 3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-161+3092A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586961 | ||||||
| chr22:26586980
|
G | A | 5 | a0001c0001t0006g0130a0001c0001t0006g0132a0001c0001t0006g0134others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161+3073C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26586980 | ||||||
| chr22:26587137
|
A | T | 3 | a0001c0001t0002g0340a0001c0010t0002g0338a0001c0010t0002g0339 | 3 | HG01346.hp2 HG02258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-161+2916T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26587137 | ||||||
| chr22:26587208
|
T | C | 4 | a0001c0001t0004g0005a0001c0001t0004g0264a0001c0001t0004g0266others(1): Show | 5 | HG01256.hp1 HG01258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161+2845A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26587208 | ||||||
| chr22:26587323
|
G | T | 113 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-161+2730C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26587323 | ||||||
| chr22:26587543
|
A | G | 114 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(111): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-161+2510T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26587543 | ||||||
| chr22:26587785
|
A | T | 1 | a0001c0001t0006g0269 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-161+2268T>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26587785 | ||||||
| chr22:26588026
|
TGA | T | 113 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-161+2025_-161+202 others(6): Show |
TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588026 | ||||||
| chr22:26588091
|
T | C | 1 | a0001c0004t0011g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-161+1962A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588091 | ||||||
| chr22:26588177
|
C | G | 1 | a0001c0001t0017g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-161+1876G>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588177 | ||||||
| chr22:26588199
|
T | TA | 334 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0061others(331): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-161+1853dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588199 | ||||||
| chr22:26588273
|
A | G | 1 | a0001c0001t0003g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-161+1780T>C | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588273 | ||||||
| chr22:26588287
|
C | A | 5 | a0001c0001t0004g0370a0001c0001t0004g0371a0001c0001t0004g0372others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161+1766G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588287 | ||||||
| chr22:26588397
|
T | C | 1 | a0001c0001t0017g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-161+1656A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588397 | ||||||
| chr22:26588454
|
T | TA | 3 | a0001c0003t0008g0135a0001c0003t0008g0136a0001c0004t0011g0137 | 3 | HG02809.hp2 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-161+1598dupT | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588454 | ||||||
| chr22:26588507
|
T | C | 76 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0320others(73): Show | 80 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.-161+1546A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588507 | ||||||
| chr22:26588534
|
C | T | 1 | a0001c0001t0017g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-161+1519G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588534 | ||||||
| chr22:26588672
|
C | A | 36 | a0001c0001t0001g0344a0001c0001t0001g0349a0001c0001t0002g0340others(33): Show | 36 | HG00735.hp2 HG01069.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.-161+1381G>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588672 | ||||||
| chr22:26588676
|
C | T | 6 | a0001c0001t0008g0017a0001c0001t0008g0018a0001c0001t0013g0019others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161+1377G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588676 | ||||||
| chr22:26588749
|
C | T | 3 | a0001c0001t0005g0144a0001c0001t0006g0145a0002c0002t0005g0143 | 3 | NA18942.hp2 NA18979.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-161+1304G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588749 | ||||||
| chr22:26588848
|
G | T | 1 | a0001c0005t0002g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-161+1205C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588848 | ||||||
| chr22:26588851
|
T | C | 5 | a0001c0001t0004g0370a0001c0001t0004g0371a0001c0001t0004g0372others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161+1202A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26588851 | ||||||
| chr22:26589047
|
G | T | 1 | a0001c0001t0017g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-161+1006C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26589047 | ||||||
| chr22:26589160
|
G | A | 15 | a0001c0001t0004g0008a0001c0001t0004g0382a0001c0001t0004g0383others(12): Show | 16 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-161+893C>T | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26589160 | ||||||
| chr22:26589249
|
C | T | 2 | a0001c0006t0005g0141a0001c0006t0026g0140 | 2 | HG02074.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-161+804G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26589249 | ||||||
| chr22:26589647
|
C | T | 1 | a0004c0020t0001g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-161+406G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26589647 | ||||||
| chr22:26589734
|
C | T | 1 | a0001c0001t0017g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-161+319G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26589734 | ||||||
| chr22:26589774
|
G | T | 126 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(123): Show | 128 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.-161+279C>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26589774 | ||||||
| chr22:26589953
|
A | C | 1 | a0001c0001t0003g0016 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-161+100T>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26589953 | ||||||
| chr22:26590011
|
T | C | 390 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0050others(387): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.-161+42A>G | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26590011 | ||||||
| chr22:26590019
|
C | T | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0013others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161+34G>A | TPST2 | ENSG00000128294.16 | transcript | ENST00000338754.9 | protein_coding | 1/6 | chr22 | 26590019 |