Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79810 |
| ensemblid | ENSG00000049883.15 |
| hgncid | 25734 |
| symbol | PTCD2 |
| name | pentatricopeptide repeat domain 2 |
| refseq_nuc | NM_024754.5 |
| refseq_prot | NP_079030.3 |
| ensembl_nuc | ENST00000380639.10 |
| ensembl_prot | ENSP00000370013.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 72320373 |
| end | 72368395 |
| strand | + |
| ver | v1.2 |
| region | chr5:72320373-72368395 |
| region5000 | chr5:72315373-72373395 |
| regionname0 | PTCD2_chr5_72320373_72368395 |
| regionname5000 | PTCD2_chr5_72315373_72373395 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 388 | 325 | 82 | 60 | 131 | 14 | 38 | 101 | PTCD2_chr5_72315373_72373395 | PTCD2 | MVRDS others(383): Show |
chr5 | 72315373 | 72373395 |
| a0002 | 0/0 | 388 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | MVRDS others(383): Show |
chr5 | 72315373 | 72373395 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1164 | 324 | 82 | 60 | 130 | 14 | 38 | PTCD2_chr5_72315373_72373395 | PTCD2 | ATGGT others(1159): Show |
chr5 | 72315373 | 72373395 | ||
| a0001c0003 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | ATGGT others(1159): Show |
chr5 | 72315373 | 72373395 | ||
| a0002c0002 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | ATGGT others(1159): Show |
chr5 | 72315373 | 72373395 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11145 | 89 | 3 | 20 | 53 | 3 | 10 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0002 | 0/0 | 11145 | 49 | 0 | 6 | 39 | 0 | 4 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0003 | 0/0 | 11145 | 20 | 2 | 2 | 12 | 0 | 4 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0004 | 0/0 | 11145 | 16 | 2 | 5 | 4 | 2 | 3 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0005 | 0/0 | 11145 | 12 | 7 | 1 | 1 | 2 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0006 | 0/0 | 11145 | 10 | 0 | 5 | 0 | 2 | 3 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0007 | 0/0 | 11137 | 8 | 8 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11132): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0008 | 0/0 | 11145 | 8 | 1 | 3 | 0 | 1 | 3 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0009 | 0/0 | 11145 | 8 | 7 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0010 | 0/0 | 11145 | 6 | 6 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0011 | 0/0 | 11145 | 6 | 5 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0012 | 0/0 | 11145 | 5 | 0 | 0 | 5 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0013 | 0/0 | 11145 | 4 | 2 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0014 | 0/0 | 11145 | 4 | 1 | 2 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0015 | 0/0 | 11145 | 4 | 4 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0016 | 0/0 | 11145 | 3 | 0 | 2 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0017 | 0/0 | 11145 | 3 | 2 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0018 | 0/0 | 11145 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0019 | 0/0 | 11145 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0020 | 0/0 | 11145 | 3 | 2 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0021 | 0/0 | 11144 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11139): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0022 | 0/0 | 11145 | 2 | 0 | 0 | 0 | 0 | 2 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0023 | 0/0 | 11145 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0024 | 0/0 | 11145 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0025 | 0/0 | 11145 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0026 | 0/0 | 11145 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0027 | 0/0 | 11145 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0028 | 0/0 | 11145 | 2 | 0 | 0 | 0 | 0 | 2 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0029 | 0/0 | 11145 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0030 | 0/0 | 11145 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0031 | 0/0 | 11145 | 2 | 0 | 0 | 1 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0032 | 0/0 | 11144 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11139): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0033 | 0/0 | 11145 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0034 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0035 | 0/0 | 11136 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11131): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0036 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11132): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0037 | 0/0 | 11136 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11131): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0038 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0039 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0040 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0041 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0042 | 0/0 | 11145 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0043 | 0/0 | 11145 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0044 | 0/0 | 11145 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0045 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0046 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0047 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0048 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0049 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0050 | 0/0 | 11145 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0051 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0052 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0053 | 0/0 | 11145 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0054 | 0/0 | 11145 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0055 | 0/0 | 11145 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0056 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0057 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0058 | 0/0 | 11145 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0059 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0060 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0061 | 0/0 | 11144 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11139): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0062 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0063 | 0/0 | 11145 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0064 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0065 | 0/0 | 11145 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0066 | 0/0 | 11145 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0001t0067 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0001c0003t0002 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| a0002c0002t0002 | 0/0 | 11145 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | AGTAG others(11140): Show |
chr5 | 72315373 | 72373395 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 15 | 1 | 6 | 7 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0003 | 0/0 | 14 | 0 | 3 | 9 | 1 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0001 | 0/0 | 23 | 0 | 2 | 19 | 0 | 2 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0003g0004 | 0/0 | 6 | 1 | 1 | 3 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0004g0007 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0004g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0004g0013 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0006g0005 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0006g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0006g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0007g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0007g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0008g0005 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0008g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0008g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0008g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0009g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0009g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0011g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0011g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0012g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0012g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0012g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0012g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0013g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0013g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0013g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0014g0005 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0014g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0014g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0015g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0015g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0015g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0016g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0016g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0017g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0017g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0018g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0019g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0019g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0019g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0020g0011 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0021g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0022g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0023g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0023g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0024g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0024g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0025g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0026g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0026g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0027g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0028g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0028g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0029g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0029g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0030g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0030g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0031g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0031g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0032g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0032g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0033g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0033g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0034g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0035g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0036g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0037g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0038g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0039g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0040g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0041g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0042g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0043g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0044g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0045g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0046g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0047g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0048g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0049g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0050g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0051g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0052g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0053g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0054g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0055g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0056g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0057g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0058g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0059g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0060g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0061g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0062g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0063g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0064g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0065g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0066g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0001t0067g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0001c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0125 | EUR | GBR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00140 | hp1 | a0001 | c0001 | t0016 | g0004 | EUR | GBR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0007 | EUR | FIN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00621 | hp1 | a0001 | c0001 | t0012 | g0152 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0077 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0192 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00673 | hp2 | a0001 | c0001 | t0052 | g0172 | EAS | CHS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0016 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00741 | hp1 | a0001 | c0001 | t0009 | g0050 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01069 | hp2 | a0001 | c0001 | t0026 | g0121 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01071 | hp1 | a0001 | c0001 | t0026 | g0005 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01074 | hp2 | a0001 | c0001 | t0017 | g0039 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0016 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01099 | hp1 | a0001 | c0001 | t0055 | g0003 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0030 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01167 | hp1 | a0001 | c0001 | t0013 | g0094 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01168 | hp1 | a0001 | c0001 | t0016 | g0109 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0079 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01169 | hp1 | a0001 | c0001 | t0016 | g0004 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01192 | hp1 | a0001 | c0001 | t0065 | g0113 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0005 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01243 | hp1 | a0001 | c0001 | t0011 | g0066 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01243 | hp2 | a0001 | c0001 | t0013 | g0092 | AMR | PUR | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01261 | hp1 | a0001 | c0001 | t0033 | g0111 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01346 | hp1 | a0001 | c0001 | t0014 | g0030 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01358 | hp2 | a0001 | c0001 | t0043 | g0118 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01361 | hp1 | a0001 | c0001 | t0014 | g0015 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01433 | hp2 | a0001 | c0001 | t0063 | g0064 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0100 | EUR | IBS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0004 | EUR | IBS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0122 | EUR | IBS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0027 | EUR | IBS | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01884 | hp1 | a0001 | c0001 | t0011 | g0061 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01884 | hp2 | a0001 | c0001 | t0018 | g0020 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01891 | hp1 | a0001 | c0001 | t0066 | g0067 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01891 | hp2 | a0001 | c0001 | t0019 | g0151 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0016 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01978 | hp1 | a0001 | c0001 | t0053 | g0179 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01978 | hp2 | a0001 | c0001 | t0033 | g0029 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0057 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02074 | hp2 | a0001 | c0001 | t0031 | g0148 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02080 | hp2 | a0001 | c0001 | t0039 | g0080 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0063 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0082 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | CDX | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02257 | hp1 | a0001 | c0001 | t0023 | g0054 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02257 | hp2 | a0001 | c0001 | t0020 | g0011 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0062 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0055 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02280 | hp1 | a0001 | c0001 | t0032 | g0117 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02280 | hp2 | a0001 | c0001 | t0045 | g0007 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02451 | hp1 | a0001 | c0001 | t0023 | g0042 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0068 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02615 | hp2 | a0001 | c0001 | t0036 | g0120 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02622 | hp1 | a0001 | c0001 | t0015 | g0046 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0022 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0104 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0010 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02647 | hp2 | a0001 | c0001 | t0021 | g0014 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0124 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02698 | hp2 | a0001 | c0001 | t0058 | g0135 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02717 | hp1 | a0001 | c0001 | t0024 | g0130 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0127 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02723 | hp1 | a0001 | c0001 | t0035 | g0126 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02735 | hp2 | a0001 | c0001 | t0054 | g0002 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0108 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02738 | hp2 | a0001 | c0001 | t0028 | g0164 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02818 | hp2 | a0001 | c0001 | t0047 | g0022 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0044 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02886 | hp2 | a0001 | c0001 | t0020 | g0011 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02922 | hp1 | a0001 | c0001 | t0018 | g0020 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02922 | hp2 | a0001 | c0001 | t0021 | g0014 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0190 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02965 | hp2 | a0001 | c0001 | t0011 | g0059 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03041 | hp1 | a0001 | c0001 | t0015 | g0045 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03041 | hp2 | a0001 | c0001 | t0024 | g0131 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0133 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03130 | hp1 | a0001 | c0001 | t0015 | g0053 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0010 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03139 | hp2 | a0001 | c0001 | t0025 | g0032 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03195 | hp1 | a0001 | c0001 | t0025 | g0032 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0056 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03209 | hp1 | a0001 | c0001 | t0038 | g0114 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0049 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03225 | hp2 | a0001 | c0001 | t0048 | g0129 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0029 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03453 | hp2 | a0001 | c0001 | t0019 | g0146 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0123 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03516 | hp1 | a0001 | c0001 | t0015 | g0047 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0095 | AFR | ESN | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03540 | hp1 | a0001 | c0001 | t0037 | g0052 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03540 | hp2 | a0001 | c0001 | t0051 | g0018 | AFR | GWD | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0051 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03579 | hp2 | a0001 | c0001 | t0014 | g0005 | AFR | MSL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03654 | hp1 | a0001 | c0001 | t0050 | g0005 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0005 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0087 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03710 | hp1 | a0001 | c0001 | t0008 | g0015 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03710 | hp2 | a0001 | c0001 | t0022 | g0004 | SAS | PJL | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03831 | hp1 | a0001 | c0001 | t0042 | g0084 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03834 | hp1 | a0001 | c0001 | t0006 | g0128 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03927 | hp1 | a0001 | c0001 | t0044 | g0001 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03927 | hp2 | a0001 | c0001 | t0031 | g0006 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG03942 | hp2 | a0001 | c0001 | t0022 | g0004 | SAS | BEB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0005 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0013 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG04228 | hp1 | a0001 | c0001 | t0028 | g0002 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | STU | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0041 | AFR | YRI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18522 | hp2 | a0001 | c0001 | t0019 | g0018 | AFR | YRI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18906 | hp1 | a0001 | c0001 | t0017 | g0039 | AFR | YRI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18906 | hp2 | a0001 | c0001 | t0018 | g0020 | AFR | YRI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18943 | hp1 | a0001 | c0001 | t0041 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18952 | hp2 | a0001 | c0001 | t0030 | g0154 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18957 | hp1 | a0001 | c0001 | t0059 | g0165 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18967 | hp2 | a0001 | c0001 | t0046 | g0009 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18968 | hp1 | a0001 | c0001 | t0060 | g0037 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18982 | hp2 | a0001 | c0001 | t0040 | g0081 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18983 | hp1 | a0001 | c0001 | t0012 | g0006 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18989 | hp1 | a0001 | c0001 | t0029 | g0141 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18990 | hp1 | a0001 | c0001 | t0056 | g0037 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18991 | hp1 | a0001 | c0001 | t0034 | g0098 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19000 | hp2 | a0001 | c0001 | t0067 | g0138 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19006 | hp1 | a0001 | c0001 | t0057 | g0144 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19011 | hp1 | a0001 | c0001 | t0030 | g0178 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19011 | hp2 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | LWK | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | LWK | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19043 | hp1 | a0001 | c0001 | t0064 | g0115 | AFR | LWK | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19043 | hp2 | a0001 | c0001 | t0049 | g0069 | AFR | LWK | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19068 | hp1 | a0001 | c0001 | t0012 | g0006 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19080 | hp1 | a0001 | c0001 | t0012 | g0072 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19083 | hp2 | a0001 | c0001 | t0029 | g0181 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19091 | hp1 | a0001 | c0003 | t0002 | g0085 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19240 | hp1 | a0001 | c0001 | t0021 | g0014 | AFR | YRI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | YRI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA20129 | hp1 | a0001 | c0001 | t0061 | g0182 | AFR | ASW | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | ASW | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA20752 | hp1 | a0001 | c0001 | t0027 | g0003 | EUR | TSI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA20752 | hp2 | a0001 | c0001 | t0014 | g0005 | EUR | TSI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA20805 | hp1 | a0001 | c0001 | t0020 | g0011 | EUR | TSI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0005 | EUR | TSI | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | GIH | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | CLM | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02109 | hp2 | a0001 | c0001 | t0010 | g0043 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0099 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0132 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02559 | hp1 | a0001 | c0001 | t0032 | g0116 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG02559 | hp2 | a0001 | c0001 | t0062 | g0065 | AFR | ACB | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | USA | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | USA | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | USA | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | USA | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | LWK | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0093 | AFR | LWK | PTCD2_chr5_72315373_72373395 | PTCD2 | chr5 | 72315373 | 72373395 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:72331317 | T | C | 1 | a0002 | 1 | NA19068.hp2 | missense_variant | MODERATE | c.410T>C | p.Val137Ala | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/10 | 420/11145 | 410/1167 | 137/388 | chr5 | 72331317 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:72358361 | A | G | 1 | a0001c0003 | 1 | NA19091.hp1 | synonymous_variant | LOW | c.1101A>G | p.Leu367Leu | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1111/11145 | 1101/1167 | 367/388 | chr5 | 72358361 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:72358590 | G | T | 1 | a0001c0001t0067 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*163G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 163 | chr5 | 72358590 | ||||||
| chr5:72358592 | T | C | 1 | a0001c0001t0034 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*165T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 165 | chr5 | 72358592 | ||||||
| chr5:72358602 | C | A | 1 | a0001c0001t0035 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*175C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 175 | chr5 | 72358602 | ||||||
| chr5:72358670 | C | T | 1 | a0001c0001t0033 | 2 | HG01261.hp1 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*243C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 243 | chr5 | 72358670 | ||||||
| chr5:72358695 | G | T | 1 | a0001c0001t0066 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*268G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 268 | chr5 | 72358695 | ||||||
| chr5:72358755 | C | T | 1 | a0001c0001t0065 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*328C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 328 | chr5 | 72358755 | ||||||
| chr5:72358899 | A | C | 3 | a0001c0001t0021 a0001c0001t0032 a0001c0001t0064 |
6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*472A>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 472 | chr5 | 72358899 | ||||||
| chr5:72358931 | A | G | 5 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0062 others(2): Show |
12 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*504A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 504 | chr5 | 72358931 | ||||||
| chr5:72359028 | G | C | 48 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(45): Show |
205 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*601G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 601 | chr5 | 72359028 | ||||||
| chr5:72359110 | G | A | 5 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0062 others(2): Show |
12 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*683G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 683 | chr5 | 72359110 | ||||||
| chr5:72359200 | C | G | 1 | a0001c0001t0035 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*773C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 773 | chr5 | 72359200 | ||||||
| chr5:72359203 | T | C | 3 | a0001c0001t0007 a0001c0001t0036 a0001c0001t0037 |
10 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*776T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 776 | chr5 | 72359203 | ||||||
| chr5:72359356 | G | A | 21 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(18): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*929G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 929 | chr5 | 72359356 | ||||||
| chr5:72359423 | A | C | 3 | a0001c0001t0021 a0001c0001t0032 a0001c0001t0064 |
6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*996A>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 996 | chr5 | 72359423 | ||||||
| chr5:72359473 | G | T | 1 | a0001c0001t0022 | 2 | HG03710.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1046G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1046 | chr5 | 72359473 | ||||||
| chr5:72359529 | C | G | 1 | a0001c0001t0050 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1102C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1102 | chr5 | 72359529 | ||||||
| chr5:72360005 | T | C | 1 | a0001c0001t0022 | 2 | HG03710.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1578T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1578 | chr5 | 72360005 | ||||||
| chr5:72360016 | A | G | 3 | a0001c0001t0021 a0001c0001t0032 a0001c0001t0064 |
6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1589A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1589 | chr5 | 72360016 | ||||||
| chr5:72360209 | CA | C | 5 | a0001c0001t0021 a0001c0001t0032 a0001c0001t0035 others(2): Show |
8 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1798delA | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1798 | INFO_REALIGN_3_PRIME | chr5 | 72360209 | |||||
| chr5:72360346 | T | C | 1 | a0001c0001t0051 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1919T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1919 | chr5 | 72360346 | ||||||
| chr5:72360381 | G | A | 1 | a0001c0001t0062 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1954G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 1954 | chr5 | 72360381 | ||||||
| chr5:72360531 | G | A | 1 | a0001c0001t0017 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2104G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2104 | chr5 | 72360531 | ||||||
| chr5:72360735 | AGTGCAGT others(1): Show |
A | 4 | a0001c0001t0007 a0001c0001t0035 a0001c0001t0036 others(1): Show |
11 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2312_*2319delCAGT others(4): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2312 | INFO_REALIGN_3_PRIME | chr5 | 72360735 | |||||
| chr5:72360780 | G | A | 1 | a0001c0001t0012 | 5 | HG00621.hp1 NA18983.hp1 NA19011.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2353G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2353 | chr5 | 72360780 | ||||||
| chr5:72360795 | A | G | 1 | a0001c0001t0026 | 2 | HG01069.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2368A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2368 | chr5 | 72360795 | ||||||
| chr5:72360822 | A | G | 1 | a0001c0001t0050 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2395A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2395 | chr5 | 72360822 | ||||||
| chr5:72361065 | T | C | 1 | a0001c0001t0038 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2638T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2638 | chr5 | 72361065 | ||||||
| chr5:72361194 | T | G | 3 | a0001c0001t0007 a0001c0001t0036 a0001c0001t0037 |
10 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2767T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2767 | chr5 | 72361194 | ||||||
| chr5:72361367 | G | A | 1 | a0001c0001t0039 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2940G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 2940 | chr5 | 72361367 | ||||||
| chr5:72361488 | G | A | 3 | a0001c0001t0016 a0001c0001t0022 a0001c0001t0065 |
6 | HG00140.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3061G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3061 | chr5 | 72361488 | ||||||
| chr5:72361552 | A | G | 1 | a0001c0001t0060 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3125A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3125 | chr5 | 72361552 | ||||||
| chr5:72361587 | G | A | 5 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0014 others(2): Show |
25 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3160G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3160 | chr5 | 72361587 | ||||||
| chr5:72361609 | A | G | 1 | a0001c0001t0059 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3182A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3182 | chr5 | 72361609 | ||||||
| chr5:72361725 | G | A | 5 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0015 others(2): Show |
21 | HG00741.hp1 HG02055.hp1 HG02109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3298G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3298 | chr5 | 72361725 | ||||||
| chr5:72361833 | T | G | 1 | a0001c0001t0040 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3406T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3406 | chr5 | 72361833 | ||||||
| chr5:72362137 | T | C | 1 | a0001c0001t0048 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3710T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3710 | chr5 | 72362137 | ||||||
| chr5:72362278 | G | C | 5 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0062 others(2): Show |
12 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3851G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 3851 | chr5 | 72362278 | ||||||
| chr5:72362653 | A | G | 1 | a0001c0001t0058 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4226A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 4226 | chr5 | 72362653 | ||||||
| chr5:72362674 | T | C | 1 | a0001c0001t0015 | 4 | HG02622.hp1 HG03041.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4247T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 4247 | chr5 | 72362674 | ||||||
| chr5:72362705 | A | G | 1 | a0001c0001t0057 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4278A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 4278 | chr5 | 72362705 | ||||||
| chr5:72362760 | A | G | 1 | a0001c0001t0035 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4333A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 4333 | chr5 | 72362760 | ||||||
| chr5:72362823 | C | G | 2 | a0001c0001t0016 a0001c0001t0065 |
4 | HG00140.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4396C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 4396 | chr5 | 72362823 | ||||||
| chr5:72363007 | T | C | 5 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0015 others(2): Show |
21 | HG00741.hp1 HG02055.hp1 HG02109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4580T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 4580 | chr5 | 72363007 | ||||||
| chr5:72363103 | T | C | 3 | a0001c0001t0021 a0001c0001t0032 a0001c0001t0064 |
6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4676T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 4676 | chr5 | 72363103 | ||||||
| chr5:72363629 | C | T | 5 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0062 others(2): Show |
12 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5202C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 5202 | chr5 | 72363629 | ||||||
| chr5:72364262 | C | T | 1 | a0001c0001t0046 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5835C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 5835 | chr5 | 72364262 | ||||||
| chr5:72364279 | G | A | 5 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0015 others(2): Show |
21 | HG00741.hp1 HG02055.hp1 HG02109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5852G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 5852 | chr5 | 72364279 | ||||||
| chr5:72364404 | G | C | 2 | a0001c0001t0024 a0001c0001t0025 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5977G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 5977 | chr5 | 72364404 | ||||||
| chr5:72364538 | C | A | 1 | a0001c0001t0052 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6111C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6111 | chr5 | 72364538 | ||||||
| chr5:72364582 | T | A | 1 | a0001c0001t0041 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6155T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6155 | chr5 | 72364582 | ||||||
| chr5:72364619 | C | T | 1 | a0001c0001t0017 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6192C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6192 | chr5 | 72364619 | ||||||
| chr5:72364685 | A | T | 2 | a0001c0001t0024 a0001c0001t0025 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6258A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6258 | chr5 | 72364685 | ||||||
| chr5:72364923 | C | A | 1 | a0001c0001t0017 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6496C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6496 | chr5 | 72364923 | ||||||
| chr5:72364924 | G | T | 1 | a0001c0001t0017 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6497G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6497 | chr5 | 72364924 | ||||||
| chr5:72365012 | T | A | 15 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0013 others(12): Show |
82 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*6585T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6585 | chr5 | 72365012 | ||||||
| chr5:72365080 | G | T | 1 | a0001c0001t0066 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6653G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6653 | chr5 | 72365080 | ||||||
| chr5:72365304 | T | C | 1 | a0001c0001t0027 | 2 | NA20752.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6877T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 6877 | chr5 | 72365304 | ||||||
| chr5:72365568 | A | G | 1 | a0001c0001t0056 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7141A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7141 | chr5 | 72365568 | ||||||
| chr5:72365584 | G | A | 1 | a0001c0001t0042 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7157G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7157 | chr5 | 72365584 | ||||||
| chr5:72365688 | G | A | 1 | a0001c0001t0053 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7261G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7261 | chr5 | 72365688 | ||||||
| chr5:72365761 | A | G | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
123 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*7334A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7334 | chr5 | 72365761 | ||||||
| chr5:72365771 | A | G | 6 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0048 others(3): Show |
13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7344A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7344 | chr5 | 72365771 | ||||||
| chr5:72366000 | G | C | 6 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0048 others(3): Show |
13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7573G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7573 | chr5 | 72366000 | ||||||
| chr5:72366007 | G | A | 6 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0048 others(3): Show |
13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7580G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7580 | chr5 | 72366007 | ||||||
| chr5:72366066 | A | T | 2 | a0001c0001t0008 a0001c0001t0026 |
10 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7639A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7639 | chr5 | 72366066 | ||||||
| chr5:72366108 | C | T | 1 | a0001c0001t0023 | 2 | HG02257.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7681C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 7681 | chr5 | 72366108 | ||||||
| chr5:72366483 | A | G | 1 | a0001c0001t0036 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8056A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 8056 | chr5 | 72366483 | ||||||
| chr5:72366590 | G | A | 1 | a0001c0001t0043 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8163G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 8163 | chr5 | 72366590 | ||||||
| chr5:72366641 | T | A | 1 | a0001c0001t0028 | 2 | HG02738.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8214T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 8214 | chr5 | 72366641 | ||||||
| chr5:72366687 | A | G | 2 | a0001c0001t0036 a0001c0001t0048 |
2 | HG02615.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8260A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 8260 | chr5 | 72366687 | ||||||
| chr5:72367125 | C | A | 3 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0049 |
13 | HG01167.hp1 HG01243.hp2 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*8698C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 8698 | chr5 | 72367125 | ||||||
| chr5:72367172 | T | C | 1 | a0001c0001t0029 | 2 | NA18989.hp1 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8745T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 8745 | chr5 | 72367172 | ||||||
| chr5:72367355 | A | G | 1 | a0001c0001t0055 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8928A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 8928 | chr5 | 72367355 | ||||||
| chr5:72367522 | A | G | 1 | a0001c0001t0054 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9095A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 9095 | chr5 | 72367522 | ||||||
| chr5:72367569 | C | T | 2 | a0001c0001t0019 a0001c0001t0051 |
4 | HG01891.hp2 HG03453.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9142C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 9142 | chr5 | 72367569 | ||||||
| chr5:72367643 | T | G | 4 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0035 others(1): Show |
14 | HG01167.hp1 HG01243.hp2 HG02451.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*9216T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 9216 | chr5 | 72367643 | ||||||
| chr5:72367759 | G | A | 1 | a0001c0001t0044 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9332G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 9332 | chr5 | 72367759 | ||||||
| chr5:72367771 | G | A | 19 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(16): Show |
98 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*9344G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 9344 | chr5 | 72367771 | ||||||
| chr5:72368204 | G | A | 7 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0026 others(4): Show |
24 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*9777G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 9777 | chr5 | 72368204 | ||||||
| chr5:72368358 | C | T | 6 | a0001c0001t0009 a0001c0001t0018 a0001c0001t0025 others(3): Show |
16 | HG00741.hp1 HG01884.hp2 HG02615.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*9931C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 10/10 | 9931 | chr5 | 72368358 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:72320651 | G | A | 1 | a0001c0001t0003g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127+142G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72320651 | |||||||
| chr5:72320690 | C | T | 1 | a0001c0001t0008g0192 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.127+181C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72320690 | |||||||
| chr5:72320743 | T | C | 20 | a0001c0001t0009g0010 a0001c0001t0009g0044 a0001c0001t0009g0048 others(17): Show |
22 | HG00741.hp1 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.127+234T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72320743 | |||||||
| chr5:72320787 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.127+278C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72320787 | |||||||
| chr5:72320907 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.127+398G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72320907 | |||||||
| chr5:72320993 | G | A | 11 | a0001c0001t0005g0060 a0001c0001t0011g0059 a0001c0001t0011g0061 others(8): Show |
13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.127+484G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72320993 | |||||||
| chr5:72321428 | C | T | 2 | a0001c0001t0017g0039 a0001c0001t0017g0190 |
3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.128-744C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72321428 | |||||||
| chr5:72321472 | G | T | 1 | a0001c0001t0003g0189 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.128-700G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72321472 | |||||||
| chr5:72321735 | T | C | 144 | a0001c0001t0001g0110 a0001c0001t0002g0001 a0001c0001t0002g0009 others(141): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.128-437T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72321735 | |||||||
| chr5:72321833 | G | A | 1 | a0001c0001t0049g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-339G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72321833 | |||||||
| chr5:72321862 | G | A | 1 | a0001c0001t0010g0041 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.128-310G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72321862 | |||||||
| chr5:72322009 | T | G | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.128-163T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72322009 | |||||||
| chr5:72322082 | A | G | 4 | a0001c0001t0010g0041 a0001c0001t0010g0055 a0001c0001t0010g0056 others(1): Show |
4 | HG02055.hp1 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-90A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 1/9 | chr5 | 72322082 | |||||||
| chr5:72322449 | C | A | 75 | a0001c0001t0001g0110 a0001c0001t0002g0001 a0001c0001t0002g0009 others(72): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.220+185C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72322449 | |||||||
| chr5:72322640 | A | G | 2 | a0001c0001t0017g0039 a0001c0001t0017g0190 |
3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.220+376A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72322640 | |||||||
| chr5:72322728 | T | C | 1 | a0001c0001t0003g0070 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.220+464T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72322728 | |||||||
| chr5:72322857 | C | G | 1 | a0001c0001t0038g0114 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.220+593C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72322857 | |||||||
| chr5:72322946 | G | C | 4 | a0001c0001t0021g0014 a0001c0001t0032g0116 a0001c0001t0032g0117 others(1): Show |
6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+682G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72322946 | |||||||
| chr5:72323148 | T | C | 1 | a0001c0001t0058g0135 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.220+884T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72323148 | |||||||
| chr5:72323849 | G | C | 2 | a0001c0001t0017g0039 a0001c0001t0017g0190 |
3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.220+1585G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72323849 | |||||||
| chr5:72323892 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.220+1628C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72323892 | |||||||
| chr5:72323893 | G | A | 3 | a0001c0001t0002g0023 a0001c0001t0002g0071 a0001c0001t0012g0072 |
4 | NA18968.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+1629G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72323893 | |||||||
| chr5:72324170 | A | G | 1 | a0001c0001t0023g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.220+1906A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72324170 | |||||||
| chr5:72324418 | A | G | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(220): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.220+2154A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72324418 | |||||||
| chr5:72324695 | T | C | 1 | a0002c0002t0002g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.221-1917T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72324695 | |||||||
| chr5:72324926 | G | GT | 5 | a0001c0001t0007g0017 a0001c0001t0007g0132 a0001c0001t0007g0133 others(2): Show |
7 | HG02055.hp1 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-1674dupT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 72324926 | ||||||
| chr5:72325067 | C | T | 3 | a0001c0001t0024g0130 a0001c0001t0024g0131 a0001c0001t0025g0032 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-1545C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72325067 | |||||||
| chr5:72325549 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.221-1063C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72325549 | |||||||
| chr5:72325601 | G | A | 52 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0012 others(49): Show |
88 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.221-1011G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72325601 | |||||||
| chr5:72325838 | C | G | 3 | a0001c0001t0024g0130 a0001c0001t0024g0131 a0001c0001t0025g0032 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-774C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72325838 | |||||||
| chr5:72325862 | C | G | 3 | a0001c0001t0024g0130 a0001c0001t0024g0131 a0001c0001t0025g0032 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-750C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72325862 | |||||||
| chr5:72325916 | G | A | 2 | a0001c0001t0023g0042 a0001c0001t0023g0054 |
2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.221-696G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72325916 | |||||||
| chr5:72326067 | G | C | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0067g0138 |
3 | NA18948.hp2 NA19000.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.221-545G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72326067 | |||||||
| chr5:72326111 | A | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.221-501A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 2/9 | chr5 | 72326111 | |||||||
| chr5:72326817 | T | G | 1 | a0001c0001t0010g0043 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.350+76T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72326817 | |||||||
| chr5:72326949 | TA | T | 4 | a0001c0001t0021g0014 a0001c0001t0032g0116 a0001c0001t0032g0117 others(1): Show |
6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.350+210delA | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 72326949 | ||||||
| chr5:72327210 | C | T | 1 | a0001c0001t0049g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.350+469C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72327210 | |||||||
| chr5:72327313 | A | G | 1 | a0001c0001t0004g0100 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.350+572A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72327313 | |||||||
| chr5:72327353 | T | A | 3 | a0001c0001t0005g0060 a0001c0001t0011g0059 a0001c0001t0011g0061 |
3 | HG01884.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.350+612T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72327353 | |||||||
| chr5:72327472 | A | AT | 115 | a0001c0001t0001g0110 a0001c0001t0001g0134 a0001c0001t0001g0183 others(112): Show |
167 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.350+748dupT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 72327472 | ||||||
| chr5:72327472 | A | ATT | 4 | a0001c0001t0004g0013 a0001c0001t0032g0116 a0001c0001t0032g0117 others(1): Show |
6 | HG00741.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.350+747_350+748dup others(2): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 72327472 | ||||||
| chr5:72327679 | G | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0038 others(19): Show |
37 | HG00140.hp2 HG00621.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.350+938G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72327679 | |||||||
| chr5:72328386 | A | C | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.350+1645A>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72328386 | |||||||
| chr5:72328542 | A | G | 1 | a0001c0001t0005g0099 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.350+1801A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72328542 | |||||||
| chr5:72328847 | T | A | 1 | a0001c0001t0035g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.350+2106T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72328847 | |||||||
| chr5:72328869 | C | T | 2 | a0001c0001t0017g0039 a0001c0001t0017g0190 |
3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.350+2128C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72328869 | |||||||
| chr5:72328871 | C | T | 1 | a0001c0001t0059g0165 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.350+2130C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72328871 | |||||||
| chr5:72328872 | G | A | 1 | a0001c0001t0009g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350+2131G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72328872 | |||||||
| chr5:72329013 | C | T | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(220): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.351-2245C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329013 | |||||||
| chr5:72329085 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.351-2173T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329085 | |||||||
| chr5:72329168 | A | C | 20 | a0001c0001t0009g0010 a0001c0001t0009g0044 a0001c0001t0009g0048 others(17): Show |
22 | HG00741.hp1 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.351-2090A>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329168 | |||||||
| chr5:72329179 | C | A | 4 | a0001c0001t0021g0014 a0001c0001t0032g0116 a0001c0001t0032g0117 others(1): Show |
6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.351-2079C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329179 | |||||||
| chr5:72329314 | C | T | 1 | a0001c0001t0025g0032 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.351-1944C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329314 | |||||||
| chr5:72329438 | C | G | 4 | a0001c0001t0021g0014 a0001c0001t0032g0116 a0001c0001t0032g0117 others(1): Show |
6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.351-1820C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329438 | |||||||
| chr5:72329681 | GC | G | 73 | a0001c0001t0001g0110 a0001c0001t0002g0001 a0001c0001t0002g0009 others(70): Show |
117 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.351-1575delC | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 72329681 | ||||||
| chr5:72329712 | A | G | 1 | a0001c0001t0049g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.351-1546A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329712 | |||||||
| chr5:72329734 | T | C | 11 | a0001c0001t0005g0060 a0001c0001t0011g0059 a0001c0001t0011g0061 others(8): Show |
13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.351-1524T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72329734 | |||||||
| chr5:72329936 | C | CT | 80 | a0001c0001t0001g0110 a0001c0001t0001g0162 a0001c0001t0001g0163 others(77): Show |
124 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.351-1308dupT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 72329936 | ||||||
| chr5:72330038 | T | C | 2 | a0001c0001t0017g0039 a0001c0001t0017g0190 |
3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.351-1220T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330038 | |||||||
| chr5:72330081 | C | T | 11 | a0001c0001t0005g0060 a0001c0001t0011g0059 a0001c0001t0011g0061 others(8): Show |
13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.351-1177C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330081 | |||||||
| chr5:72330162 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0029g0141 |
3 | NA18942.hp1 NA18989.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.351-1096G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330162 | |||||||
| chr5:72330191 | C | T | 1 | a0001c0001t0002g0096 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.351-1067C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330191 | |||||||
| chr5:72330235 | C | T | 1 | a0001c0001t0053g0179 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.351-1023C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330235 | |||||||
| chr5:72330782 | G | C | 11 | a0001c0001t0005g0060 a0001c0001t0011g0059 a0001c0001t0011g0061 others(8): Show |
13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.351-476G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330782 | |||||||
| chr5:72330969 | C | T | 1 | a0001c0001t0030g0178 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.351-289C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330969 | |||||||
| chr5:72330975 | G | T | 1 | a0001c0001t0003g0112 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.351-283G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72330975 | |||||||
| chr5:72331098 | A | G | 1 | a0001c0001t0015g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.351-160A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 3/9 | chr5 | 72331098 | |||||||
| chr5:72331427 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.468+52T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72331427 | |||||||
| chr5:72331486 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.468+111G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72331486 | |||||||
| chr5:72331776 | C | T | 4 | a0001c0001t0013g0092 a0001c0001t0013g0093 a0001c0001t0013g0094 others(1): Show |
4 | HG01167.hp1 HG01243.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+401C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72331776 | |||||||
| chr5:72331921 | T | C | 1 | a0001c0001t0005g0077 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.468+546T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72331921 | |||||||
| chr5:72332025 | AC | A | 1 | a0001c0001t0002g0012 | 3 | HG00408.hp1 HG02074.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.468+651delC | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332025 | |||||||
| chr5:72332361 | T | A | 1 | a0001c0001t0001g0143 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.468+986T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332361 | |||||||
| chr5:72332449 | C | A | 1 | a0001c0001t0001g0143 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.468+1074C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332449 | |||||||
| chr5:72332473 | G | A | 2 | a0001c0001t0032g0116 a0001c0001t0032g0117 |
2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.468+1098G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332473 | |||||||
| chr5:72332528 | CTA | C | 15 | a0001c0001t0001g0161 a0001c0001t0006g0005 a0001c0001t0006g0016 others(12): Show |
22 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.468+1155_468+1156d others(4): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 72332528 | ||||||
| chr5:72332614 | AT | A | 3 | a0001c0001t0024g0130 a0001c0001t0024g0131 a0001c0001t0025g0032 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+1240delT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332614 | |||||||
| chr5:72332757 | G | A | 11 | a0001c0001t0005g0060 a0001c0001t0011g0059 a0001c0001t0011g0061 others(8): Show |
13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.468+1382G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332757 | |||||||
| chr5:72332931 | A | G | 7 | a0001c0001t0009g0010 a0001c0001t0009g0044 a0001c0001t0009g0048 others(4): Show |
9 | HG00741.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.468+1556A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332931 | |||||||
| chr5:72332944 | A | G | 2 | a0001c0001t0017g0039 a0001c0001t0017g0190 |
3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.468+1569A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72332944 | |||||||
| chr5:72333128 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA18983.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.468+1753C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72333128 | |||||||
| chr5:72333198 | G | A | 1 | a0001c0001t0013g0092 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.469-1820G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72333198 | |||||||
| chr5:72333329 | A | G | 1 | a0001c0001t0033g0111 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.469-1689A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72333329 | |||||||
| chr5:72333348 | C | T | 1 | a0001c0001t0004g0091 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.469-1670C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72333348 | |||||||
| chr5:72333529 | C | G | 2 | a0001c0001t0032g0116 a0001c0001t0032g0117 |
2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.469-1489C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72333529 | |||||||
| chr5:72333529 | C | T | 1 | a0001c0001t0049g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.469-1489C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72333529 | |||||||
| chr5:72333542 | A | G | 1 | a0001c0001t0011g0061 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.469-1476A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72333542 | |||||||
| chr5:72334042 | A | AT | 4 | a0001c0001t0021g0014 a0001c0001t0032g0116 a0001c0001t0032g0117 others(1): Show |
6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-968dupT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 72334042 | ||||||
| chr5:72334167 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.469-851A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72334167 | |||||||
| chr5:72334176 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.469-842A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72334176 | |||||||
| chr5:72334550 | CT | C | 144 | a0001c0001t0001g0033 a0001c0001t0001g0110 a0001c0001t0001g0161 others(141): Show |
205 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.469-455delT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 72334550 | ||||||
| chr5:72334621 | G | A | 2 | a0001c0001t0017g0039 a0001c0001t0017g0190 |
3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.469-397G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72334621 | |||||||
| chr5:72334755 | T | C | 1 | a0001c0001t0009g0048 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.469-263T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72334755 | |||||||
| chr5:72334941 | A | G | 1 | a0001c0001t0037g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.469-77A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72334941 | |||||||
| chr5:72334966 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.469-52C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 4/9 | chr5 | 72334966 | |||||||
| chr5:72335455 | C | CA | 108 | a0001c0001t0001g0110 a0001c0001t0001g0147 a0001c0001t0001g0149 others(105): Show |
138 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.548-320dupA | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 72335455 | ||||||
| chr5:72336710 | CA | C | 35 | a0001c0001t0001g0175 a0001c0001t0002g0026 a0001c0001t0002g0083 others(32): Show |
46 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.639+845delA | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 72336710 | ||||||
| chr5:72337758 | A | G | 1 | a0001c0001t0004g0082 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.640-864A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 6/9 | chr5 | 72337758 | |||||||
| chr5:72338014 | A | G | 1 | a0001c0001t0035g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.640-608A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 6/9 | chr5 | 72338014 | |||||||
| chr5:72338095 | G | T | 22 | a0001c0001t0001g0110 a0001c0001t0003g0004 a0001c0001t0003g0027 others(19): Show |
30 | HG00140.hp1 HG00558.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.640-527G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 6/9 | chr5 | 72338095 | |||||||
| chr5:72338304 | C | T | 1 | a0001c0001t0036g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.640-318C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 6/9 | chr5 | 72338304 | |||||||
| chr5:72338354 | C | G | 47 | a0001c0001t0005g0060 a0001c0001t0007g0017 a0001c0001t0007g0031 others(44): Show |
58 | HG00741.hp1 HG01074.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.640-268C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 6/9 | chr5 | 72338354 | |||||||
| chr5:72338373 | T | G | 1 | a0001c0001t0010g0055 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.640-249T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 6/9 | chr5 | 72338373 | |||||||
| chr5:72338786 | T | C | 3 | a0001c0001t0024g0130 a0001c0001t0024g0131 a0001c0001t0025g0032 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.753+51T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72338786 | |||||||
| chr5:72338797 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.753+62G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72338797 | |||||||
| chr5:72338880 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.753+145A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72338880 | |||||||
| chr5:72338885 | A | G | 22 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0038 others(19): Show |
37 | HG00140.hp2 HG00621.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.753+150A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72338885 | |||||||
| chr5:72339320 | G | C | 20 | a0001c0001t0009g0010 a0001c0001t0009g0044 a0001c0001t0009g0048 others(17): Show |
22 | HG00741.hp1 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.753+585G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72339320 | |||||||
| chr5:72339350 | A | T | 4 | a0001c0001t0001g0168 a0001c0001t0001g0174 a0001c0001t0001g0176 others(1): Show |
4 | NA18983.hp2 NA19003.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+615A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72339350 | |||||||
| chr5:72339419 | T | A | 6 | a0001c0001t0007g0017 a0001c0001t0007g0031 a0001c0001t0007g0127 others(3): Show |
9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.753+684T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72339419 | |||||||
| chr5:72339479 | G | A | 2 | a0001c0001t0023g0042 a0001c0001t0023g0054 |
2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.753+744G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72339479 | |||||||
| chr5:72339706 | T | TAGTTTTT others(304): Show |
9 | a0001c0001t0005g0060 a0001c0001t0011g0059 a0001c0001t0011g0062 others(6): Show |
11 | HG01433.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.753+982_753+983ins others(311): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 72339706 | ||||||
| chr5:72339706 | T | TAGTTTTT others(305): Show |
2 | a0001c0001t0011g0061 a0001c0001t0011g0066 |
2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.753+982_753+983ins others(312): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 72339706 | ||||||
| chr5:72339771 | C | T | 2 | a0001c0001t0032g0116 a0001c0001t0032g0117 |
2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.753+1036C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72339771 | |||||||
| chr5:72339986 | G | A | 143 | a0001c0001t0001g0110 a0001c0001t0002g0001 a0001c0001t0002g0009 others(140): Show |
205 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.753+1251G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72339986 | |||||||
| chr5:72340422 | G | C | 1 | a0001c0001t0001g0142 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.753+1687G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72340422 | |||||||
| chr5:72340492 | T | C | 1 | a0001c0001t0004g0078 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.753+1757T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72340492 | |||||||
| chr5:72340685 | T | G | 1 | a0001c0001t0004g0079 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.753+1950T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72340685 | |||||||
| chr5:72340751 | T | G | 48 | a0001c0001t0005g0060 a0001c0001t0007g0017 a0001c0001t0007g0031 others(45): Show |
59 | HG00741.hp1 HG01074.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.753+2016T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72340751 | |||||||
| chr5:72340841 | G | A | 18 | a0001c0001t0006g0005 a0001c0001t0006g0015 a0001c0001t0006g0016 others(15): Show |
25 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.753+2106G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72340841 | |||||||
| chr5:72340870 | C | T | 1 | a0001c0001t0018g0020 | 3 | HG01884.hp2 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.754-2092C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72340870 | |||||||
| chr5:72340969 | GT | G | 145 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0002g0001 others(142): Show |
207 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.754-1980delT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 72340969 | ||||||
| chr5:72341028 | G | A | 11 | a0001c0001t0005g0060 a0001c0001t0011g0059 a0001c0001t0011g0061 others(8): Show |
13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.754-1934G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341028 | |||||||
| chr5:72341033 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.754-1929C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341033 | |||||||
| chr5:72341143 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.754-1819C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341143 | |||||||
| chr5:72341161 | T | C | 11 | a0001c0001t0005g0060 a0001c0001t0011g0059 a0001c0001t0011g0061 others(8): Show |
13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.754-1801T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341161 | |||||||
| chr5:72341180 | A | G | 3 | a0001c0001t0024g0130 a0001c0001t0024g0131 a0001c0001t0025g0032 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-1782A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341180 | |||||||
| chr5:72341324 | G | A | 4 | a0001c0001t0021g0014 a0001c0001t0032g0116 a0001c0001t0032g0117 others(1): Show |
6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-1638G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341324 | |||||||
| chr5:72341516 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.754-1446T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341516 | |||||||
| chr5:72341812 | G | A | 3 | a0001c0001t0002g0097 a0001c0001t0039g0080 a0001c0001t0040g0081 |
3 | HG02080.hp2 NA18982.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.754-1150G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72341812 | |||||||
| chr5:72342016 | G | A | 1 | a0001c0001t0004g0079 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.754-946G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342016 | |||||||
| chr5:72342030 | G | A | 2 | a0001c0001t0011g0062 a0001c0001t0011g0063 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.754-932G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342030 | |||||||
| chr5:72342063 | TAAA | T | 6 | a0001c0001t0007g0017 a0001c0001t0007g0031 a0001c0001t0007g0127 others(3): Show |
9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.754-897_754-895del others(3): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 72342063 | ||||||
| chr5:72342227 | G | A | 1 | a0001c0001t0035g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.754-735G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342227 | |||||||
| chr5:72342399 | A | T | 3 | a0001c0001t0024g0130 a0001c0001t0024g0131 a0001c0001t0025g0032 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-563A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342399 | |||||||
| chr5:72342463 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.754-499T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342463 | |||||||
| chr5:72342620 | G | A | 3 | a0001c0001t0024g0130 a0001c0001t0024g0131 a0001c0001t0025g0032 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-342G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342620 | |||||||
| chr5:72342629 | A | C | 6 | a0001c0001t0007g0017 a0001c0001t0007g0031 a0001c0001t0007g0127 others(3): Show |
9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.754-333A>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342629 | |||||||
| chr5:72342629 | A | G | 1 | a0001c0001t0048g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.754-333A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342629 | |||||||
| chr5:72342798 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.754-164G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342798 | |||||||
| chr5:72342843 | T | C | 5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0142 others(2): Show |
7 | HG00408.hp2 HG00597.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.754-119T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 7/9 | chr5 | 72342843 | |||||||
| chr5:72343228 | C | G | 1 | a0001c0001t0036g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.828+192C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343228 | |||||||
| chr5:72343288 | AG | A | 2 | a0001c0001t0017g0039 a0001c0001t0017g0190 |
3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.828+253delG | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343288 | |||||||
| chr5:72343350 | G | C | 18 | a0001c0001t0006g0005 a0001c0001t0006g0015 a0001c0001t0006g0016 others(15): Show |
25 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.828+314G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343350 | |||||||
| chr5:72343416 | G | A | 1 | a0001c0001t0003g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.828+380G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343416 | |||||||
| chr5:72343428 | G | A | 2 | a0001c0001t0017g0039 a0001c0001t0017g0190 |
3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.828+392G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343428 | |||||||
| chr5:72343550 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0169 |
3 | NA18964.hp1 NA19000.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.828+514G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343550 | |||||||
| chr5:72343724 | C | T | 18 | a0001c0001t0006g0005 a0001c0001t0006g0015 a0001c0001t0006g0016 others(15): Show |
25 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.828+688C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343724 | |||||||
| chr5:72343768 | A | G | 1 | a0001c0001t0035g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.828+732A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343768 | |||||||
| chr5:72343817 | TTA | T | 11 | a0001c0001t0005g0060 a0001c0001t0011g0059 a0001c0001t0011g0061 others(8): Show |
13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.828+783_828+784del others(2): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 72343817 | ||||||
| chr5:72343874 | T | C | 1 | a0001c0001t0048g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.828+838T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343874 | |||||||
| chr5:72343950 | G | A | 18 | a0001c0001t0006g0005 a0001c0001t0006g0015 a0001c0001t0006g0016 others(15): Show |
25 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.828+914G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72343950 | |||||||
| chr5:72344005 | C | T | 1 | a0001c0001t0025g0032 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.828+969C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344005 | |||||||
| chr5:72344106 | C | T | 1 | a0001c0001t0005g0105 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.828+1070C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344106 | |||||||
| chr5:72344112 | C | T | 3 | a0001c0001t0005g0029 a0001c0001t0033g0029 a0001c0001t0033g0111 |
3 | HG01261.hp1 HG01978.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.828+1076C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344112 | |||||||
| chr5:72344242 | G | A | 1 | a0001c0001t0058g0135 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.828+1206G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344242 | |||||||
| chr5:72344654 | G | A | 36 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0012 others(33): Show |
65 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.828+1618G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344654 | |||||||
| chr5:72344730 | T | A | 1 | a0001c0001t0049g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.828+1694T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344730 | |||||||
| chr5:72344744 | C | T | 6 | a0001c0001t0007g0017 a0001c0001t0007g0031 a0001c0001t0007g0127 others(3): Show |
9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.828+1708C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344744 | |||||||
| chr5:72344749 | G | T | 3 | a0001c0001t0005g0029 a0001c0001t0033g0029 a0001c0001t0033g0111 |
3 | HG01261.hp1 HG01978.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.828+1713G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344749 | |||||||
| chr5:72344790 | C | G | 6 | a0001c0001t0007g0017 a0001c0001t0007g0031 a0001c0001t0007g0127 others(3): Show |
9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.828+1754C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344790 | |||||||
| chr5:72344830 | A | G | 1 | a0001c0001t0048g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.828+1794A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344830 | |||||||
| chr5:72344877 | A | G | 15 | a0001c0001t0005g0060 a0001c0001t0011g0059 a0001c0001t0011g0061 others(12): Show |
18 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.828+1841A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344877 | |||||||
| chr5:72344968 | G | A | 1 | a0001c0001t0002g0088 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.828+1932G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72344968 | |||||||
| chr5:72345015 | G | A | 1 | a0001c0001t0009g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.828+1979G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72345015 | |||||||
| chr5:72345024 | A | G | 1 | a0001c0001t0036g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.828+1988A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72345024 | |||||||
| chr5:72345293 | A | C | 48 | a0001c0001t0005g0060 a0001c0001t0007g0017 a0001c0001t0007g0031 others(45): Show |
59 | HG00741.hp1 HG01074.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.828+2257A>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72345293 | |||||||
| chr5:72345469 | C | T | 12 | a0001c0001t0005g0060 a0001c0001t0011g0059 a0001c0001t0011g0061 others(9): Show |
14 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.828+2433C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72345469 | |||||||
| chr5:72345493 | C | T | 3 | a0001c0001t0001g0158 a0001c0001t0056g0037 a0001c0001t0060g0037 |
3 | NA18968.hp1 NA18990.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.828+2457C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72345493 | |||||||
| chr5:72345664 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0162 a0001c0001t0001g0187 others(4): Show |
7 | HG01891.hp2 HG02622.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.828+2628G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72345664 | |||||||
| chr5:72345714 | G | T | 1 | a0001c0001t0049g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.828+2678G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72345714 | |||||||
| chr5:72346216 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.828+3180A>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72346216 | |||||||
| chr5:72346462 | C | T | 1 | a0001c0001t0015g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.828+3426C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72346462 | |||||||
| chr5:72346550 | C | T | 6 | a0001c0001t0007g0017 a0001c0001t0007g0031 a0001c0001t0007g0127 others(3): Show |
9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.828+3514C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72346550 | |||||||
| chr5:72347043 | A | G | 1 | a0001c0001t0038g0114 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.828+4007A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347043 | |||||||
| chr5:72347135 | A | G | 1 | a0001c0001t0002g0090 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.828+4099A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347135 | |||||||
| chr5:72347191 | G | A | 1 | a0001c0001t0048g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.828+4155G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347191 | |||||||
| chr5:72347198 | C | T | 11 | a0001c0001t0005g0060 a0001c0001t0011g0059 a0001c0001t0011g0061 others(8): Show |
13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.828+4162C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347198 | |||||||
| chr5:72347267 | C | T | 1 | a0001c0001t0064g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.828+4231C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347267 | |||||||
| chr5:72347359 | C | T | 1 | a0001c0001t0025g0032 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.828+4323C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347359 | |||||||
| chr5:72347374 | A | G | 1 | a0001c0001t0005g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.828+4338A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347374 | |||||||
| chr5:72347386 | T | C | 1 | a0001c0001t0011g0068 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.828+4350T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347386 | |||||||
| chr5:72347388 | C | T | 25 | a0001c0001t0005g0060 a0001c0001t0007g0017 a0001c0001t0007g0031 others(22): Show |
32 | HG01074.hp2 HG01243.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.828+4352C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347388 | |||||||
| chr5:72347413 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.828+4377C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347413 | |||||||
| chr5:72347866 | G | T | 1 | a0001c0001t0001g0156 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.829-4775G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72347866 | |||||||
| chr5:72348534 | A | G | 2 | a0001c0001t0017g0039 a0001c0001t0017g0190 |
3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.829-4107A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72348534 | |||||||
| chr5:72348924 | G | A | 1 | a0001c0001t0015g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.829-3717G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72348924 | |||||||
| chr5:72348974 | G | A | 21 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0028 others(18): Show |
29 | HG00140.hp1 HG00558.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.829-3667G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72348974 | |||||||
| chr5:72349384 | G | A | 3 | a0001c0001t0024g0130 a0001c0001t0024g0131 a0001c0001t0025g0032 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-3257G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72349384 | |||||||
| chr5:72349600 | G | T | 6 | a0001c0001t0007g0017 a0001c0001t0007g0031 a0001c0001t0007g0127 others(3): Show |
9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.829-3041G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72349600 | |||||||
| chr5:72349747 | C | T | 5 | a0001c0001t0007g0017 a0001c0001t0007g0031 a0001c0001t0007g0127 others(2): Show |
8 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.829-2894C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72349747 | |||||||
| chr5:72349826 | T | C | 6 | a0001c0001t0007g0017 a0001c0001t0007g0031 a0001c0001t0007g0127 others(3): Show |
9 | HG02451.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.829-2815T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72349826 | |||||||
| chr5:72350253 | C | T | 1 | a0001c0001t0007g0031 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.829-2388C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350253 | |||||||
| chr5:72350295 | AATTT | A | 18 | a0001c0001t0001g0147 a0001c0001t0006g0005 a0001c0001t0006g0015 others(15): Show |
25 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.829-2342_829-2339d others(6): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 72350295 | ||||||
| chr5:72350403 | G | C | 3 | a0001c0001t0005g0104 a0001c0001t0005g0105 a0001c0001t0038g0114 |
3 | HG02109.hp1 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.829-2238G>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350403 | |||||||
| chr5:72350516 | A | G | 4 | a0001c0001t0021g0014 a0001c0001t0032g0116 a0001c0001t0032g0117 others(1): Show |
6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.829-2125A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350516 | |||||||
| chr5:72350604 | G | T | 1 | a0001c0001t0005g0105 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.829-2037G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350604 | |||||||
| chr5:72350662 | T | C | 3 | a0001c0001t0020g0011 a0001c0001t0063g0064 a0001c0001t0066g0067 |
5 | HG01433.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.829-1979T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350662 | |||||||
| chr5:72350717 | A | G | 2 | a0001c0001t0021g0014 a0001c0001t0064g0115 |
4 | HG02647.hp2 HG02922.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.829-1924A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350717 | |||||||
| chr5:72350770 | G | T | 3 | a0001c0001t0024g0130 a0001c0001t0024g0131 a0001c0001t0025g0032 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-1871G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350770 | |||||||
| chr5:72350937 | A | G | 3 | a0001c0001t0024g0130 a0001c0001t0024g0131 a0001c0001t0025g0032 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-1704A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350937 | |||||||
| chr5:72350988 | G | A | 1 | a0001c0001t0008g0122 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.829-1653G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72350988 | |||||||
| chr5:72351274 | T | G | 6 | a0001c0001t0009g0010 a0001c0001t0009g0044 a0001c0001t0009g0048 others(3): Show |
8 | HG00741.hp1 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.829-1367T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351274 | |||||||
| chr5:72351296 | G | A | 1 | a0001c0001t0007g0132 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.829-1345G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351296 | |||||||
| chr5:72351331 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0157 a0001c0001t0058g0135 |
4 | HG01070.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-1310C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351331 | |||||||
| chr5:72351473 | G | A | 1 | a0001c0001t0038g0114 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.829-1168G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351473 | |||||||
| chr5:72351589 | A | G | 1 | a0001c0001t0008g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.829-1052A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351589 | |||||||
| chr5:72351793 | T | A | 3 | a0001c0001t0024g0130 a0001c0001t0024g0131 a0001c0001t0025g0032 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-848T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351793 | |||||||
| chr5:72351798 | C | G | 1 | a0001c0001t0013g0095 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.829-843C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351798 | |||||||
| chr5:72351920 | G | A | 4 | a0001c0001t0021g0014 a0001c0001t0032g0116 a0001c0001t0032g0117 others(1): Show |
6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.829-721G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351920 | |||||||
| chr5:72351988 | T | C | 1 | a0001c0001t0006g0123 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.829-653T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72351988 | |||||||
| chr5:72352208 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.829-433C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72352208 | |||||||
| chr5:72352229 | C | A | 1 | a0001c0001t0010g0043 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.829-412C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72352229 | |||||||
| chr5:72352308 | C | T | 1 | a0001c0001t0028g0164 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.829-333C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72352308 | |||||||
| chr5:72352394 | C | A | 2 | a0001c0001t0003g0101 a0001c0001t0003g0106 |
2 | NA19054.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.829-247C>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72352394 | |||||||
| chr5:72352405 | C | T | 2 | a0001c0001t0017g0039 a0001c0001t0017g0190 |
3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.829-236C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72352405 | |||||||
| chr5:72352471 | G | A | 2 | a0001c0001t0003g0107 a0001c0001t0003g0108 |
2 | HG02735.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.829-170G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72352471 | |||||||
| chr5:72352482 | T | C | 1 | a0001c0001t0012g0152 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.829-159T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 8/9 | chr5 | 72352482 | |||||||
| chr5:72352763 | G | A | 11 | a0001c0001t0005g0060 a0001c0001t0011g0059 a0001c0001t0011g0061 others(8): Show |
13 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.942+9G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72352763 | |||||||
| chr5:72353018 | T | C | 1 | a0001c0001t0003g0107 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.942+264T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72353018 | |||||||
| chr5:72353019 | T | C | 1 | a0001c0001t0052g0172 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.942+265T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72353019 | |||||||
| chr5:72353080 | C | T | 1 | a0001c0001t0004g0091 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.942+326C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72353080 | |||||||
| chr5:72353127 | A | G | 7 | a0001c0001t0007g0017 a0001c0001t0007g0031 a0001c0001t0007g0127 others(4): Show |
10 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.942+373A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72353127 | |||||||
| chr5:72353157 | A | G | 7 | a0001c0001t0007g0017 a0001c0001t0007g0031 a0001c0001t0007g0127 others(4): Show |
10 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.942+403A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72353157 | |||||||
| chr5:72353504 | CTT | C | 1 | a0001c0001t0018g0020 | 3 | HG01884.hp2 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.942+752_942+753del others(2): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 72353504 | ||||||
| chr5:72354133 | C | T | 1 | a0001c0001t0011g0068 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.942+1379C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72354133 | |||||||
| chr5:72354175 | G | A | 3 | a0001c0001t0024g0130 a0001c0001t0024g0131 a0001c0001t0025g0032 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.942+1421G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72354175 | |||||||
| chr5:72354382 | G | GA | 110 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0034 others(107): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.942+1654dupA | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 72354382 | ||||||
| chr5:72354382 | G | GAA | 48 | a0001c0001t0001g0021 a0001c0001t0001g0169 a0001c0001t0001g0188 others(45): Show |
59 | HG00642.hp2 HG00673.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.942+1653_942+1654d others(4): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 72354382 | ||||||
| chr5:72354382 | G | GAAA | 11 | a0001c0001t0005g0099 a0001c0001t0009g0048 a0001c0001t0009g0050 others(8): Show |
13 | HG00741.hp1 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.942+1652_942+1654d others(5): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 72354382 | ||||||
| chr5:72354428 | A | T | 4 | a0001c0001t0021g0014 a0001c0001t0032g0116 a0001c0001t0032g0117 others(1): Show |
6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.942+1674A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72354428 | |||||||
| chr5:72354443 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.942+1689A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72354443 | |||||||
| chr5:72354668 | G | A | 1 | a0001c0001t0004g0078 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.942+1914G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72354668 | |||||||
| chr5:72354901 | G | T | 1 | a0001c0001t0001g0019 | 3 | HG01167.hp2 HG01169.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.942+2147G>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72354901 | |||||||
| chr5:72354974 | A | T | 3 | a0001c0001t0024g0130 a0001c0001t0024g0131 a0001c0001t0025g0032 |
4 | HG02717.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.942+2220A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72354974 | |||||||
| chr5:72355234 | C | T | 1 | a0001c0001t0006g0123 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.942+2480C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72355234 | |||||||
| chr5:72355475 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0019g0018 a0001c0001t0019g0146 others(2): Show |
5 | HG01891.hp2 HG02622.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.942+2721C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72355475 | |||||||
| chr5:72355731 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.943-2472G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72355731 | |||||||
| chr5:72355793 | G | A | 1 | a0001c0001t0042g0084 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.943-2410G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72355793 | |||||||
| chr5:72355934 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0160 |
2 | NA18939.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.943-2269T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72355934 | |||||||
| chr5:72356171 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0019g0018 a0001c0001t0019g0146 others(2): Show |
5 | HG01891.hp2 HG02622.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.943-2032G>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72356171 | |||||||
| chr5:72356280 | T | C | 2 | a0001c0001t0017g0039 a0001c0001t0017g0190 |
3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.943-1923T>C | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72356280 | |||||||
| chr5:72356418 | A | T | 8 | a0001c0001t0007g0017 a0001c0001t0007g0031 a0001c0001t0007g0127 others(5): Show |
11 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.943-1785A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72356418 | |||||||
| chr5:72356513 | A | ATG | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(221): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.943-1690_943-1689i others(4): Show |
PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72356513 | |||||||
| chr5:72356626 | T | A | 1 | a0001c0001t0005g0102 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.943-1577T>A | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72356626 | |||||||
| chr5:72356835 | A | G | 1 | a0001c0001t0030g0154 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.943-1368A>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72356835 | |||||||
| chr5:72356927 | C | T | 1 | a0001c0001t0001g0019 | 3 | HG01167.hp2 HG01169.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.943-1276C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72356927 | |||||||
| chr5:72357077 | C | G | 1 | a0001c0001t0004g0082 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.943-1126C>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72357077 | |||||||
| chr5:72357363 | C | T | 3 | a0001c0001t0005g0029 a0001c0001t0033g0029 a0001c0001t0033g0111 |
3 | HG01261.hp1 HG01978.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.943-840C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72357363 | |||||||
| chr5:72357657 | A | T | 4 | a0001c0001t0021g0014 a0001c0001t0032g0116 a0001c0001t0032g0117 others(1): Show |
6 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-546A>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72357657 | |||||||
| chr5:72357847 | CT | C | 10 | a0001c0001t0011g0059 a0001c0001t0011g0061 a0001c0001t0011g0062 others(7): Show |
12 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.943-342delT | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 72357847 | ||||||
| chr5:72357860 | T | G | 10 | a0001c0001t0011g0059 a0001c0001t0011g0061 a0001c0001t0011g0062 others(7): Show |
12 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.943-343T>G | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72357860 | |||||||
| chr5:72358054 | C | T | 6 | a0001c0001t0009g0010 a0001c0001t0009g0044 a0001c0001t0009g0048 others(3): Show |
8 | HG00741.hp1 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.943-149C>T | PTCD2 | ENSG00000049883.15 | transcript | ENST00000380639.10 | protein_coding | 9/9 | chr5 | 72358054 |