Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5782 |
|---|---|
| ensemblid | ENSG00000127947.16 |
| hgncid | 9645 |
| symbol | PTPN12 |
| name | protein tyrosine phosphatase non-receptor type 12 |
| refseq_nuc | NM_002835.4 |
| refseq_prot | NP_002826.3 |
| ensembl_nuc | ENST00000248594.11 |
| ensembl_prot | ENSP00000248594.6 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 77537295 |
| end | 77640069 |
| strand | + |
| ver | v1.2 |
| region | chr7:77537295-77640069 |
| region5000 | chr7:77532295-77645069 |
| regionname0 | PTPN12_chr7_77537295_77640069 |
| regionname5000 | PTPN12_chr7_77532295_77645069 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 780 | 124 | 53 | 14 | 41 | 7 | 8 | 30 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0002 | 0/0 | 780 | 112 | 21 | 24 | 51 | 3 | 13 | 42 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0003 | 1/0 | 780 | 66 | 12 | 17 | 18 | 5 | 13 | 14 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0004 | 0/0 | 780 | 6 | 0 | 3 | 0 | 1 | 2 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0005 | 0/0 | 780 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2343 | 123 | 52 | 14 | 41 | 7 | 8 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| c0002 | 0/0 | 2343 | 112 | 21 | 24 | 51 | 3 | 13 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| c0003 | 1/0 | 2343 | 65 | 12 | 16 | 18 | 5 | 13 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| c0004 | 0/0 | 2343 | 6 | 0 | 3 | 0 | 1 | 2 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| c0005 | 0/0 | 2343 | 2 | 0 | 2 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| c0006 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| c0007 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1043 | 304 | 83 | 59 | 110 | 16 | 35 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| t0002 | 0/0 | 1043 | 3 | 2 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| t0003 | 0/0 | 1043 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| t0004 | 0/0 | 1043 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| t0005 | 1/0 | 1042 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0218 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0269 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2343 | 123 | 52 | 14 | 41 | 7 | 8 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0001c0007 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0002c0002 | 0/0 | 2343 | 112 | 21 | 24 | 51 | 3 | 13 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0003c0003 | 1/0 | 2343 | 65 | 12 | 16 | 18 | 5 | 13 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0003c0006 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0004c0004 | 0/0 | 2343 | 6 | 0 | 3 | 0 | 1 | 2 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0005c0005 | 0/0 | 2343 | 2 | 0 | 2 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3385 | 122 | 51 | 14 | 41 | 7 | 8 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0001c0001t0003 | 0/0 | 3385 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0001c0007t0001 | 0/0 | 3385 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0002c0002t0001 | 0/0 | 3385 | 111 | 21 | 24 | 51 | 3 | 12 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0002c0002t0004 | 0/0 | 3385 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0003c0003t0001 | 0/0 | 3385 | 61 | 10 | 15 | 18 | 5 | 13 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0003c0003t0002 | 0/0 | 3385 | 3 | 2 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0003c0003t0005 | 1/0 | 3384 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0003c0006t0001 | 0/0 | 3385 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0004c0004t0001 | 0/0 | 3385 | 6 | 0 | 3 | 0 | 1 | 2 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| a0005c0005t0001 | 0/0 | 3385 | 2 | 0 | 2 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | copy fasta | chr7 | 77532295 | 77645069 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0269 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0007t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0005g0218 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0006t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0004c0004t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0004c0004t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0004c0004t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0004c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0004c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0004c0004t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0005c0005t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0005c0005t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0001 | g0199 | EUR | GBR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00099 | hp2 | a0004 | c0004 | t0001 | g0290 | EUR | GBR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0093 | EUR | GBR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0169 | EUR | GBR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0297 | EUR | FIN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00323 | hp1 | a0003 | c0003 | t0001 | g0196 | EUR | FIN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | FIN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00408 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00423 | hp2 | a0003 | c0003 | t0001 | g0187 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00438 | hp1 | a0003 | c0003 | t0001 | g0186 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00642 | hp1 | a0003 | c0003 | t0001 | g0205 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00642 | hp2 | a0004 | c0004 | t0001 | g0285 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0067 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00733 | hp2 | a0003 | c0003 | t0001 | g0210 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00735 | hp2 | a0003 | c0003 | t0001 | g0216 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00738 | hp1 | a0003 | c0003 | t0001 | g0214 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00738 | hp2 | a0005 | c0005 | t0001 | g0051 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00741 | hp1 | a0004 | c0004 | t0001 | g0286 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0220 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0103 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0304 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01074 | hp2 | a0003 | c0003 | t0001 | g0244 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0055 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0198 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0200 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0195 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0033 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0057 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01243 | hp1 | a0003 | c0003 | t0002 | g0153 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01255 | hp1 | a0003 | c0003 | t0001 | g0213 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0171 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0100 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01257 | hp1 | a0005 | c0005 | t0001 | g0048 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0102 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01261 | hp1 | a0003 | c0003 | t0001 | g0202 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0081 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01346 | hp2 | a0003 | c0006 | t0001 | g0201 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0203 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01361 | hp2 | a0003 | c0003 | t0001 | g0219 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0204 | EUR | IBS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0053 | EUR | IBS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | IBS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0054 | EUR | IBS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0086 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0098 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0063 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01993 | hp2 | a0004 | c0004 | t0001 | g0287 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02015 | hp2 | a0003 | c0003 | t0001 | g0179 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0178 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CDX | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | CDX | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02257 | hp1 | a0003 | c0003 | t0001 | g0212 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0104 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02451 | hp2 | a0003 | c0003 | t0001 | g0242 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02572 | hp1 | a0003 | c0003 | t0001 | g0108 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0306 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02683 | hp2 | a0004 | c0004 | t0001 | g0289 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0012 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0215 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02717 | hp1 | a0003 | c0003 | t0002 | g0151 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0194 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0043 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02738 | hp2 | a0003 | c0003 | t0001 | g0231 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0128 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0088 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0110 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0122 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0206 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03130 | hp1 | a0003 | c0003 | t0002 | g0152 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0090 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03195 | hp2 | a0001 | c0007 | t0001 | g0252 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0085 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0020 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0084 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03453 | hp2 | a0003 | c0003 | t0001 | g0223 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0111 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0089 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03654 | hp2 | a0004 | c0004 | t0001 | g0288 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0017 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | STU | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0299 | SAS | STU | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03704 | hp2 | a0003 | c0003 | t0001 | g0197 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03710 | hp1 | a0003 | c0003 | t0001 | g0230 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03710 | hp2 | a0002 | c0002 | t0004 | g0052 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0247 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03831 | hp2 | a0003 | c0003 | t0001 | g0184 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0222 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03942 | hp2 | a0003 | c0003 | t0001 | g0217 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0211 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0077 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0193 | SAS | STU | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0061 | SAS | STU | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0028 | SAS | STU | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | STU | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | CHB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18942 | hp2 | a0003 | c0003 | t0001 | g0172 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18957 | hp2 | a0003 | c0003 | t0001 | g0183 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18964 | hp2 | a0003 | c0003 | t0001 | g0190 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0207 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18984 | hp1 | a0003 | c0003 | t0001 | g0185 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18992 | hp2 | a0003 | c0003 | t0001 | g0188 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18993 | hp1 | a0003 | c0003 | t0001 | g0208 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19005 | hp2 | a0003 | c0003 | t0001 | g0191 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | LWK | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | LWK | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | LWK | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19054 | hp2 | a0003 | c0003 | t0001 | g0248 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19060 | hp1 | a0003 | c0003 | t0001 | g0189 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19064 | hp1 | a0003 | c0003 | t0001 | g0182 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19082 | hp2 | a0003 | c0003 | t0001 | g0192 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19090 | hp2 | a0003 | c0003 | t0001 | g0181 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19091 | hp2 | a0003 | c0003 | t0001 | g0180 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | YRI | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | YRI | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0101 | AFR | ASW | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | ASW | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | TSI | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | TSI | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20805 | hp2 | a0003 | c0003 | t0001 | g0170 | EUR | TSI | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0068 | SAS | GIH | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0209 | SAS | GIH | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0107 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | USA | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | USA | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | USA | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | USA | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0269 | REF | REF | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0005 | g0218 | REF | REF | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77618504
|
G | A | 4 | a0001a0002a0004others(1): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
missense_variant | MODERATE | c.964G>A | p.Val322Ile | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/18 | 1216/3384 | 964/2343 | 322/780 | chr7 | 77618504 | ||
| chr7:77627090
|
A | G | 1 | a0005 | 2 | HG00738.hp2 HG01257.hp1 |
missense_variant | MODERATE | c.1411A>G | p.Ile471Val | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/18 | 1663/3384 | 1411/2343 | 471/780 | chr7 | 77627090 | ||
| chr7:77627396
|
A | G | 2 | a0002a0005 | 114 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
missense_variant | MODERATE | c.1717A>G | p.Thr573Ala | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/18 | 1969/3384 | 1717/2343 | 573/780 | chr7 | 77627396 | ||
| chr7:77635823
|
G | A | 1 | a0004 | 6 | HG00099.hp2 HG00642.hp2 HG00741.hp1 others(3): Show |
missense_variant | MODERATE | c.2116G>A | p.Glu706Lys | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/18 | 2368/3384 | 2116/2343 | 706/780 | chr7 | 77635823 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77610785
|
T | C | 1 | a0003c0006 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.783T>C | p.Asn261Asn | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 10/18 | 1035/3384 | 783/2343 | 261/780 | chr7 | 77610785 | ||
| chr7:77627002
|
C | T | 1 | a0001c0007 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1323C>T | p.Val441Val | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/18 | 1575/3384 | 1323/2343 | 441/780 | chr7 | 77627002 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77537299
|
G | GC | 10 | a0001c0001t0001a0001c0001t0003a0001c0007t0001others(7): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
5_prime_UTR_variant | MODIFIER | c.-247dupC | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/18 | 246 | INFO_REALIGN_3_PRIME | chr7 | 77537299 | ||||
| chr7:77537386
|
G | C | 1 | a0001c0001t0003 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-161G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/18 | 161 | chr7 | 77537386 | |||||
| chr7:77639602
|
A | G | 1 | a0003c0003t0002 | 3 | HG01243.hp1 HG02717.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*322A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 18/18 | 322 | chr7 | 77639602 | |||||
| chr7:77639840
|
G | A | 1 | a0002c0002t0004 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*560G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 18/18 | 560 | chr7 | 77639840 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77537675
|
C | G | 2 | a0002c0002t0001g0309a0002c0002t0001g0310 | 2 | NA18983.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.99+30C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77537675 | ||||||
| chr7:77537706
|
C | A | 1 | a0003c0003t0001g0001 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.99+61C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77537706 | ||||||
| chr7:77537760
|
G | T | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.99+115G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77537760 | ||||||
| chr7:77537827
|
G | A | 1 | a0002c0002t0001g0002 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.99+182G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77537827 | ||||||
| chr7:77537899
|
C | G | 1 | a0002c0002t0001g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.99+254C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77537899 | ||||||
| chr7:77537958
|
T | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(122): Show | 125 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.99+313T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77537958 | ||||||
| chr7:77537978
|
C | CG | 60 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0249others(57): Show | 60 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.99+344dupG | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77537978 | |||||
| chr7:77537978
|
CG | C | 168 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.99+344delG | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77537978 | |||||
| chr7:77537983
|
G | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+338G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77537983 | ||||||
| chr7:77538054
|
C | T | 3 | a0003c0003t0001g0169a0003c0003t0001g0170a0003c0003t0001g0171 | 3 | HG00140.hp2 HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.99+409C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538054 | ||||||
| chr7:77538247
|
T | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.99+602T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538247 | ||||||
| chr7:77538269
|
C | G | 1 | a0002c0002t0001g0113 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.99+624C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538269 | ||||||
| chr7:77538323
|
A | G | 2 | a0003c0003t0001g0244a0003c0003t0001g0304 | 2 | HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.99+678A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538323 | ||||||
| chr7:77538477
|
G | T | 2 | a0001c0001t0001g0302a0001c0001t0001g0303 | 2 | NA18980.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.99+832G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538477 | ||||||
| chr7:77538691
|
A | G | 10 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+1046A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538691 | ||||||
| chr7:77538708
|
A | G | 1 | a0003c0003t0001g0244 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.99+1063A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538708 | ||||||
| chr7:77538709
|
C | A | 1 | a0003c0003t0001g0244 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.99+1064C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538709 | ||||||
| chr7:77538862
|
A | G | 3 | a0003c0003t0001g0169a0003c0003t0001g0170a0003c0003t0001g0171 | 3 | HG00140.hp2 HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.99+1217A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538862 | ||||||
| chr7:77538875
|
G | C | 1 | a0003c0003t0001g0172 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.99+1230G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538875 | ||||||
| chr7:77538924
|
A | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+1279A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538924 | ||||||
| chr7:77538960
|
A | G | 75 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0115others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.99+1315A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538960 | ||||||
| chr7:77539040
|
A | C | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG02132.hp1 HG02523.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.99+1395A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539040 | ||||||
| chr7:77539068
|
G | A | 174 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.99+1423G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539068 | ||||||
| chr7:77539218
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+1573C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539218 | ||||||
| chr7:77539231
|
G | C | 3 | a0003c0003t0001g0169a0003c0003t0001g0170a0003c0003t0001g0171 | 3 | HG00140.hp2 HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.99+1586G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539231 | ||||||
| chr7:77539243
|
C | T | 1 | a0003c0003t0001g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.99+1598C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539243 | ||||||
| chr7:77539301
|
G | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(111): Show | 114 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.99+1656G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539301 | ||||||
| chr7:77539347
|
T | C | 1 | a0001c0001t0001g0249 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.99+1702T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539347 | ||||||
| chr7:77539576
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+1931G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539576 | ||||||
| chr7:77539609
|
T | TTTGG | 3 | a0003c0003t0001g0169a0003c0003t0001g0170a0003c0003t0001g0171 | 3 | HG00140.hp2 HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.99+1983_99+1986dup others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77539609 | |||||
| chr7:77539629
|
G | GT | 6 | a0001c0001t0001g0105a0002c0002t0001g0106a0002c0002t0001g0126others(3): Show | 6 | HG02135.hp1 HG02451.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+1994dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77539629 | |||||
| chr7:77539805
|
G | C | 3 | a0003c0003t0001g0169a0003c0003t0001g0170a0003c0003t0001g0171 | 3 | HG00140.hp2 HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.99+2160G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539805 | ||||||
| chr7:77540197
|
A | G | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+2552A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540197 | ||||||
| chr7:77540219
|
A | ATTTC | 3 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0111 | 3 | HG02559.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.99+2598_99+2601dup others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77540219 | |||||
| chr7:77540239
|
C | CT | 47 | a0001c0001t0001g0109a0001c0001t0001g0129a0001c0001t0001g0130others(44): Show | 47 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.99+2597dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77540239 | |||||
| chr7:77540243
|
C | T | 250 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(247): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.99+2598C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540243 | ||||||
| chr7:77540465
|
C | G | 158 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0027others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.99+2820C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540465 | ||||||
| chr7:77540490
|
C | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG00609.hp1 NA19003.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.99+2845C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540490 | ||||||
| chr7:77540537
|
A | G | 1 | a0002c0002t0001g0126 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99+2892A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540537 | ||||||
| chr7:77540538
|
G | T | 1 | a0002c0002t0001g0126 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99+2893G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540538 | ||||||
| chr7:77540539
|
T | G | 1 | a0002c0002t0001g0126 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99+2894T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540539 | ||||||
| chr7:77540609
|
A | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+2964A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540609 | ||||||
| chr7:77540647
|
CT | C | 38 | a0001c0001t0001g0003a0001c0001t0001g0109a0001c0001t0001g0133others(35): Show | 38 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.99+3015delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77540647 | |||||
| chr7:77540933
|
A | G | 1 | a0003c0003t0001g0223 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.99+3288A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540933 | ||||||
| chr7:77541015
|
G | A | 4 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+3370G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541015 | ||||||
| chr7:77541080
|
G | C | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+3435G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541080 | ||||||
| chr7:77541280
|
C | T | 112 | a0001c0001t0001g0027a0002c0002t0001g0002a0002c0002t0001g0004others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.99+3635C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541280 | ||||||
| chr7:77541385
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+3740C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541385 | ||||||
| chr7:77541422
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+3777T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541422 | ||||||
| chr7:77541465
|
G | C | 3 | a0002c0002t0001g0021a0002c0002t0001g0022a0002c0002t0001g0023 | 3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.99+3820G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541465 | ||||||
| chr7:77541556
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.99+3911C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541556 | ||||||
| chr7:77541566
|
C | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG00609.hp1 NA19003.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.99+3921C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541566 | ||||||
| chr7:77541603
|
C | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+3958C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541603 | ||||||
| chr7:77541686
|
G | C | 1 | a0003c0003t0001g0178 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+4041G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541686 | ||||||
| chr7:77541745
|
A | G | 6 | a0002c0002t0001g0018a0002c0002t0001g0100a0002c0002t0001g0101others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+4100A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541745 | ||||||
| chr7:77542013
|
TA | T | 259 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.99+4370delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77542013 | |||||
| chr7:77542030
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+4385C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542030 | ||||||
| chr7:77542155
|
T | G | 7 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+4510T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542155 | ||||||
| chr7:77542300
|
T | C | 259 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.99+4655T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542300 | ||||||
| chr7:77542318
|
G | A | 7 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+4673G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542318 | ||||||
| chr7:77542417
|
T | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+4772T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542417 | ||||||
| chr7:77542497
|
G | A | 1 | a0003c0003t0001g0178 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+4852G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542497 | ||||||
| chr7:77542612
|
G | A | 1 | a0002c0002t0001g0024 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+4967G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542612 | ||||||
| chr7:77542637
|
G | A | 268 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(265): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.99+4992G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542637 | ||||||
| chr7:77542646
|
C | T | 1 | a0002c0002t0001g0017 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.99+5001C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542646 | ||||||
| chr7:77542660
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+5015C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542660 | ||||||
| chr7:77542692
|
A | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG01891.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+5047A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542692 | ||||||
| chr7:77542818
|
G | C | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+5173G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542818 | ||||||
| chr7:77542823
|
A | C | 1 | a0001c0001t0001g0228 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.99+5178A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542823 | ||||||
| chr7:77542959
|
G | C | 3 | a0003c0003t0001g0193a0003c0003t0001g0231a0003c0003t0001g0299 | 3 | HG02738.hp2 HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.99+5314G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542959 | ||||||
| chr7:77542987
|
A | C | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+5342A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542987 | ||||||
| chr7:77543039
|
C | G | 6 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0111others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+5394C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543039 | ||||||
| chr7:77543078
|
A | G | 6 | a0002c0002t0001g0095a0002c0002t0001g0096a0002c0002t0001g0097others(3): Show | 6 | HG01952.hp1 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+5433A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543078 | ||||||
| chr7:77543133
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+5488G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543133 | ||||||
| chr7:77543266
|
A | AT | 237 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(234): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.99+5629dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77543266 | |||||
| chr7:77543344
|
CT | C | 152 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0129others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.99+5715delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77543344 | |||||
| chr7:77543344
|
CTT | C | 88 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.99+5714_99+5715del others(2): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77543344 | |||||
| chr7:77543360
|
T | A | 1 | a0003c0003t0001g0194 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.99+5715T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543360 | ||||||
| chr7:77543482
|
C | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.99+5837C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543482 | ||||||
| chr7:77543557
|
T | G | 1 | a0002c0002t0001g0028 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.99+5912T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543557 | ||||||
| chr7:77543566
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+5921G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543566 | ||||||
| chr7:77543650
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+6005C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543650 | ||||||
| chr7:77543698
|
C | T | 1 | a0002c0002t0001g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.99+6053C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543698 | ||||||
| chr7:77543885
|
G | A | 42 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(39): Show | 42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.99+6240G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543885 | ||||||
| chr7:77543889
|
C | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+6244C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543889 | ||||||
| chr7:77543956
|
G | A | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.99+6311G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543956 | ||||||
| chr7:77543966
|
G | A | 253 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(250): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.99+6321G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543966 | ||||||
| chr7:77544149
|
G | C | 237 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(234): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.99+6504G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77544149 | ||||||
| chr7:77544392
|
C | T | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG00609.hp1 HG00735.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+6747C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77544392 | ||||||
| chr7:77544633
|
G | T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+6988G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77544633 | ||||||
| chr7:77544804
|
G | A | 156 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(153): Show | 156 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.99+7159G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77544804 | ||||||
| chr7:77544819
|
A | T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+7174A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77544819 | ||||||
| chr7:77544928
|
T | C | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+7283T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77544928 | ||||||
| chr7:77545031
|
T | C | 46 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(43): Show | 46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.99+7386T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77545031 | ||||||
| chr7:77545102
|
T | C | 2 | a0002c0002t0001g0029a0002c0002t0001g0030 | 2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.99+7457T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77545102 | ||||||
| chr7:77545180
|
T | G | 46 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(43): Show | 46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.99+7535T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77545180 | ||||||
| chr7:77545498
|
TATG | T | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+7856_99+7858del others(3): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77545498 | |||||
| chr7:77545564
|
A | AT | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+7921dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77545564 | |||||
| chr7:77545580
|
C | G | 1 | a0003c0003t0001g0220 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.99+7935C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77545580 | ||||||
| chr7:77545632
|
T | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+7987T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77545632 | ||||||
| chr7:77545967
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.99+8322T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77545967 | ||||||
| chr7:77545988
|
G | A | 3 | a0003c0003t0002g0151a0003c0003t0002g0152a0003c0003t0002g0153 | 3 | HG01243.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.99+8343G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77545988 | ||||||
| chr7:77546017
|
C | T | 1 | a0002c0002t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.99+8372C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546017 | ||||||
| chr7:77546030
|
C | G | 1 | a0001c0001t0001g0156 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.99+8385C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546030 | ||||||
| chr7:77546049
|
G | A | 1 | a0002c0002t0001g0123 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.99+8404G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546049 | ||||||
| chr7:77546235
|
A | G | 1 | a0002c0002t0001g0092 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.99+8590A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546235 | ||||||
| chr7:77546251
|
A | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+8606A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546251 | ||||||
| chr7:77546257
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+8612C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546257 | ||||||
| chr7:77546487
|
A | C | 1 | a0002c0002t0001g0016 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.99+8842A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546487 | ||||||
| chr7:77546575
|
G | T | 1 | a0003c0003t0001g0171 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.99+8930G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546575 | ||||||
| chr7:77546577
|
A | G | 1 | a0003c0003t0001g0171 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.99+8932A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546577 | ||||||
| chr7:77546662
|
G | A | 111 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(108): Show | 111 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.99+9017G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546662 | ||||||
| chr7:77546693
|
C | T | 1 | a0003c0003t0001g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.99+9048C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546693 | ||||||
| chr7:77546770
|
T | TA | 9 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0254others(6): Show | 9 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+9126dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77546770 | |||||
| chr7:77546904
|
T | C | 247 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.99+9259T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546904 | ||||||
| chr7:77547015
|
G | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+9370G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77547015 | ||||||
| chr7:77547073
|
A | G | 82 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 82 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.99+9428A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77547073 | ||||||
| chr7:77547128
|
TGTCTCTG others(13): Show |
T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+9510_99+9529del others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77547128 | |||||
| chr7:77547269
|
T | C | 6 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(3): Show | 6 | NA18946.hp1 NA18981.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+9624T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77547269 | ||||||
| chr7:77547558
|
T | C | 2 | a0002c0002t0001g0300a0002c0002t0001g0301 | 2 | HG00423.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.99+9913T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77547558 | ||||||
| chr7:77547573
|
C | A | 309 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(306): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.99+9928C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77547573 | ||||||
| chr7:77548056
|
A | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+10411A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77548056 | ||||||
| chr7:77548706
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+11061T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77548706 | ||||||
| chr7:77548939
|
A | G | 1 | a0002c0002t0001g0113 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.99+11294A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77548939 | ||||||
| chr7:77549199
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+11554G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77549199 | ||||||
| chr7:77549586
|
T | G | 17 | a0001c0001t0001g0112a0001c0001t0001g0140a0001c0001t0001g0174others(14): Show | 17 | HG00639.hp1 HG01243.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+11941T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77549586 | ||||||
| chr7:77549590
|
T | G | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0003g0176others(1): Show | 4 | HG02572.hp2 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+11945T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77549590 | ||||||
| chr7:77549704
|
G | C | 7 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+12059G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77549704 | ||||||
| chr7:77549806
|
C | T | 1 | a0002c0002t0001g0106 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.99+12161C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77549806 | ||||||
| chr7:77549817
|
G | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+12172G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77549817 | ||||||
| chr7:77549871
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+12226T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77549871 | ||||||
| chr7:77550203
|
T | G | 5 | a0001c0001t0001g0105a0001c0001t0001g0154a0001c0001t0001g0155others(2): Show | 5 | HG00280.hp1 HG00323.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+12558T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77550203 | ||||||
| chr7:77550398
|
C | T | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.99+12753C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77550398 | ||||||
| chr7:77550598
|
C | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0177 | 3 | NA19056.hp1 NA19079.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.99+12953C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77550598 | ||||||
| chr7:77550683
|
A | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+13038A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77550683 | ||||||
| chr7:77550718
|
G | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+13073G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77550718 | ||||||
| chr7:77550808
|
T | A | 8 | a0003c0003t0001g0196a0003c0003t0001g0197a0003c0003t0001g0198others(5): Show | 8 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+13163T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77550808 | ||||||
| chr7:77550935
|
G | GTC | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+13290_99+13291i others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77550935 | ||||||
| chr7:77551105
|
G | T | 3 | a0002c0002t0001g0088a0002c0002t0001g0089a0002c0002t0001g0090 | 3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.99+13460G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551105 | ||||||
| chr7:77551221
|
C | A | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.99+13576C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551221 | ||||||
| chr7:77551289
|
T | G | 247 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.99+13644T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551289 | ||||||
| chr7:77551308
|
G | A | 76 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(73): Show | 76 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.99+13663G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551308 | ||||||
| chr7:77551328
|
T | A | 1 | a0002c0002t0001g0106 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.99+13683T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551328 | ||||||
| chr7:77551373
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+13728C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551373 | ||||||
| chr7:77551415
|
C | T | 246 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.99+13770C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551415 | ||||||
| chr7:77551551
|
A | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+13906A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551551 | ||||||
| chr7:77551601
|
A | C | 1 | a0002c0002t0001g0087 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.99+13956A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551601 | ||||||
| chr7:77551835
|
T | C | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+14190T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551835 | ||||||
| chr7:77552009
|
T | C | 112 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.99+14364T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552009 | ||||||
| chr7:77552037
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0243 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.99+14392C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552037 | ||||||
| chr7:77552074
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.99+14429A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552074 | ||||||
| chr7:77552210
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.99+14565G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552210 | ||||||
| chr7:77552280
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.99+14635G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552280 | ||||||
| chr7:77552300
|
GT | G | 101 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(98): Show | 101 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.99+14668delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77552300 | |||||
| chr7:77552355
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.99+14710C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552355 | ||||||
| chr7:77552878
|
T | A | 1 | a0001c0001t0001g0232 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.99+15233T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552878 | ||||||
| chr7:77552972
|
G | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+15327G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552972 | ||||||
| chr7:77553266
|
G | A | 5 | a0001c0001t0001g0105a0001c0001t0001g0154a0001c0001t0001g0155others(2): Show | 5 | HG00280.hp1 HG00323.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+15621G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77553266 | ||||||
| chr7:77553289
|
G | T | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+15644G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77553289 | ||||||
| chr7:77553480
|
A | T | 1 | a0002c0002t0001g0099 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.99+15835A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77553480 | ||||||
| chr7:77553534
|
A | C | 1 | a0001c0001t0003g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.99+15889A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77553534 | ||||||
| chr7:77553534
|
A | T | 160 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(157): Show | 160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.99+15889A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77553534 | ||||||
| chr7:77553763
|
C | G | 1 | a0001c0001t0001g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.99+16118C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77553763 | ||||||
| chr7:77553807
|
A | C | 1 | a0001c0001t0001g0133 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.99+16162A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77553807 | ||||||
| chr7:77553851
|
A | AT | 125 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.99+16217dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77553851 | |||||
| chr7:77553851
|
A | ATT | 112 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.99+16216_99+16217d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77553851 | |||||
| chr7:77553908
|
CAT | C | 74 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(71): Show | 74 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.99+16266_99+16267d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77553908 | |||||
| chr7:77553945
|
CT | C | 247 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.99+16311delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77553945 | |||||
| chr7:77554085
|
C | T | 161 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(158): Show | 161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.99+16440C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77554085 | ||||||
| chr7:77554250
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+16605C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77554250 | ||||||
| chr7:77554326
|
C | G | 1 | a0002c0002t0001g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.99+16681C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77554326 | ||||||
| chr7:77554691
|
T | C | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-16387T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77554691 | ||||||
| chr7:77554699
|
A | G | 160 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(157): Show | 160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.100-16379A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77554699 | ||||||
| chr7:77554713
|
T | G | 1 | a0002c0002t0001g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.100-16365T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77554713 | ||||||
| chr7:77554848
|
T | G | 1 | a0002c0002t0001g0087 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.100-16230T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77554848 | ||||||
| chr7:77555083
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-15995C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555083 | ||||||
| chr7:77555193
|
C | T | 111 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(108): Show | 111 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.100-15885C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555193 | ||||||
| chr7:77555206
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-15872C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555206 | ||||||
| chr7:77555218
|
CT | C | 11 | a0001c0001t0001g0105a0001c0001t0001g0163a0001c0001t0001g0305others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-15846delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77555218 | |||||
| chr7:77555434
|
C | A | 1 | a0002c0002t0001g0087 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.100-15644C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555434 | ||||||
| chr7:77555452
|
C | T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-15626C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555452 | ||||||
| chr7:77555598
|
T | C | 1 | a0001c0001t0003g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100-15480T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555598 | ||||||
| chr7:77555609
|
T | A | 2 | a0002c0002t0001g0031a0002c0002t0001g0124 | 2 | HG00609.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.100-15469T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555609 | ||||||
| chr7:77555832
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.100-15246G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555832 | ||||||
| chr7:77556048
|
GGTGTTTG others(5): Show |
G | 1 | a0001c0001t0001g0294 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.100-15029_100-1501 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77556048 | ||||||
| chr7:77556049
|
G | GTGTT | 5 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(2): Show | 5 | HG00140.hp2 HG01256.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-15005_100-1500 others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77556049 | |||||
| chr7:77556049
|
GTGTTTGT others(5): Show |
G | 241 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(238): Show | 241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.100-15013_100-1500 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77556049 | |||||
| chr7:77556146
|
C | T | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-14932C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77556146 | ||||||
| chr7:77556338
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-14740C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77556338 | ||||||
| chr7:77556602
|
C | T | 1 | a0003c0003t0001g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.100-14476C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77556602 | ||||||
| chr7:77556634
|
G | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-14444G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77556634 | ||||||
| chr7:77556952
|
TTTTG | T | 160 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(157): Show | 160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.100-14110_100-1410 others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77556952 | |||||
| chr7:77556978
|
GT | G | 73 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(70): Show | 73 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.100-14090delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77556978 | |||||
| chr7:77557000
|
G | A | 1 | a0001c0007t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.100-14078G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557000 | ||||||
| chr7:77557213
|
C | T | 2 | a0002c0002t0001g0008a0002c0002t0001g0015 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.100-13865C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557213 | ||||||
| chr7:77557266
|
C | G | 1 | a0001c0001t0001g0239 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.100-13812C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557266 | ||||||
| chr7:77557392
|
C | T | 1 | a0002c0002t0001g0083 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.100-13686C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557392 | ||||||
| chr7:77557563
|
T | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.100-13515T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557563 | ||||||
| chr7:77557626
|
A | C | 1 | a0002c0002t0001g0123 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.100-13452A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557626 | ||||||
| chr7:77557675
|
C | G | 1 | a0001c0001t0001g0121 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.100-13403C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557675 | ||||||
| chr7:77557797
|
CA | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0003g0176 | 3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-13280delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557797 | ||||||
| chr7:77557945
|
T | C | 7 | a0002c0002t0001g0018a0002c0002t0001g0084a0002c0002t0001g0085others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-13133T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557945 | ||||||
| chr7:77557990
|
C | T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-13088C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557990 | ||||||
| chr7:77558210
|
CA | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.100-12851delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77558210 | |||||
| chr7:77558210
|
CAA | C | 12 | a0001c0001t0001g0120a0001c0001t0001g0130a0001c0001t0001g0167others(9): Show | 12 | HG01243.hp1 HG02055.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.100-12852_100-1285 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77558210 | |||||
| chr7:77558283
|
C | A | 2 | a0002c0002t0001g0032a0002c0002t0001g0033 | 2 | HG01169.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.100-12795C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77558283 | ||||||
| chr7:77558535
|
A | C | 9 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0254others(6): Show | 9 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-12543A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77558535 | ||||||
| chr7:77558574
|
C | T | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-12504C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77558574 | ||||||
| chr7:77558741
|
A | G | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.100-12337A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77558741 | ||||||
| chr7:77558847
|
A | C | 1 | a0002c0002t0001g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.100-12231A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77558847 | ||||||
| chr7:77559003
|
GA | G | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-12074delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559003 | ||||||
| chr7:77559004
|
A | ACT | 5 | a0002c0002t0001g0008a0002c0002t0001g0010a0002c0002t0001g0011others(2): Show | 5 | HG02257.hp2 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-12065_100-1206 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77559004 | |||||
| chr7:77559040
|
G | C | 1 | a0002c0002t0001g0034 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.100-12038G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559040 | ||||||
| chr7:77559155
|
C | T | 2 | a0002c0002t0001g0004a0002c0002t0001g0082 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.100-11923C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559155 | ||||||
| chr7:77559216
|
G | A | 3 | a0002c0002t0001g0021a0002c0002t0001g0022a0002c0002t0001g0023 | 3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.100-11862G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559216 | ||||||
| chr7:77559321
|
T | C | 248 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.100-11757T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559321 | ||||||
| chr7:77559581
|
CT | C | 36 | a0001c0001t0001g0109a0001c0001t0001g0133a0001c0001t0001g0134others(33): Show | 36 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.100-11495delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77559581 | |||||
| chr7:77559584
|
C | T | 74 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(71): Show | 74 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.100-11494C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559584 | ||||||
| chr7:77559604
|
A | G | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.100-11474A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559604 | ||||||
| chr7:77559766
|
A | AT | 112 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.100-11310dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77559766 | |||||
| chr7:77559830
|
G | A | 1 | a0002c0002t0001g0125 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.100-11248G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559830 | ||||||
| chr7:77560077
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0167 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.100-11001A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560077 | ||||||
| chr7:77560098
|
A | G | 1 | a0002c0002t0001g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.100-10980A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560098 | ||||||
| chr7:77560279
|
C | T | 1 | a0002c0002t0001g0016 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.100-10799C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560279 | ||||||
| chr7:77560284
|
G | A | 161 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(158): Show | 161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.100-10794G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560284 | ||||||
| chr7:77560478
|
A | G | 4 | a0002c0002t0001g0008a0002c0002t0001g0010a0002c0002t0001g0011others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-10600A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560478 | ||||||
| chr7:77560527
|
AACC | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-10547_100-1054 others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77560527 | |||||
| chr7:77560592
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-10486C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560592 | ||||||
| chr7:77560623
|
G | A | 1 | a0003c0003t0001g0220 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.100-10455G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560623 | ||||||
| chr7:77560753
|
T | C | 80 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(77): Show | 80 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.100-10325T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560753 | ||||||
| chr7:77560834
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-10244A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560834 | ||||||
| chr7:77560971
|
C | T | 1 | a0002c0002t0001g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.100-10107C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560971 | ||||||
| chr7:77561057
|
T | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100-10021T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561057 | ||||||
| chr7:77561128
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.100-9950C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561128 | ||||||
| chr7:77561232
|
G | T | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100-9846G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561232 | ||||||
| chr7:77561549
|
C | T | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.100-9529C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561549 | ||||||
| chr7:77561602
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.100-9476A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561602 | ||||||
| chr7:77561614
|
G | A | 2 | a0002c0002t0001g0002a0002c0002t0001g0035 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.100-9464G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561614 | ||||||
| chr7:77561681
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-9397G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561681 | ||||||
| chr7:77561759
|
TTTAA | T | 254 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(251): Show | 254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.100-9296_100-9293d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77561759 | |||||
| chr7:77561768
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-9310T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561768 | ||||||
| chr7:77561782
|
A | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-9296A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561782 | ||||||
| chr7:77561783
|
A | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-9295A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561783 | ||||||
| chr7:77561784
|
T | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-9294T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561784 | ||||||
| chr7:77561855
|
G | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-9223G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561855 | ||||||
| chr7:77561860
|
C | G | 3 | a0002c0002t0001g0018a0002c0002t0001g0103a0002c0002t0001g0104 | 3 | HG01070.hp2 HG01071.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.100-9218C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561860 | ||||||
| chr7:77561946
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | NA18998.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.100-9132C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561946 | ||||||
| chr7:77561994
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-9084G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561994 | ||||||
| chr7:77562065
|
A | G | 9 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0254others(6): Show | 9 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-9013A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562065 | ||||||
| chr7:77562217
|
C | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-8861C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562217 | ||||||
| chr7:77562656
|
G | T | 1 | a0002c0002t0001g0081 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.100-8422G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562656 | ||||||
| chr7:77562688
|
G | T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-8390G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562688 | ||||||
| chr7:77562797
|
A | G | 5 | a0002c0002t0001g0018a0002c0002t0001g0103a0002c0002t0001g0104others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-8281A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562797 | ||||||
| chr7:77562854
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-8224T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562854 | ||||||
| chr7:77562885
|
A | G | 1 | a0002c0002t0001g0296 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.100-8193A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562885 | ||||||
| chr7:77562949
|
T | C | 2 | a0003c0003t0001g0107a0003c0003t0001g0111 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.100-8129T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562949 | ||||||
| chr7:77562958
|
C | CA | 7 | a0001c0001t0001g0307a0001c0001t0001g0308a0003c0003t0001g0020others(4): Show | 7 | HG00140.hp2 HG01256.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-8107dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77562958 | |||||
| chr7:77562958
|
C | CAA | 56 | a0001c0001t0001g0109a0001c0001t0001g0127a0001c0001t0001g0129others(53): Show | 56 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.100-8108_100-8107d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77562958 | |||||
| chr7:77562958
|
C | CAAA | 112 | a0001c0001t0001g0105a0001c0001t0001g0157a0002c0002t0001g0002others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.100-8109_100-8107d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77562958 | |||||
| chr7:77562958
|
C | CAAAA | 81 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(78): Show | 81 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.100-8110_100-8107d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77562958 | |||||
| chr7:77563103
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-7975T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77563103 | ||||||
| chr7:77563254
|
G | A | 1 | a0001c0001t0001g0269 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.100-7824G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77563254 | ||||||
| chr7:77563481
|
G | T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-7597G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77563481 | ||||||
| chr7:77563538
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.100-7540G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77563538 | ||||||
| chr7:77564149
|
G | A | 1 | a0003c0003t0001g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.100-6929G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564149 | ||||||
| chr7:77564176
|
G | A | 2 | a0002c0002t0001g0029a0002c0002t0001g0030 | 2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100-6902G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564176 | ||||||
| chr7:77564215
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.100-6863T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564215 | ||||||
| chr7:77564249
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100-6829G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564249 | ||||||
| chr7:77564656
|
T | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-6422T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564656 | ||||||
| chr7:77564746
|
G | GT | 14 | a0001c0001t0003g0176a0003c0003t0001g0107a0003c0003t0001g0128others(11): Show | 14 | HG01167.hp1 HG01261.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-6302dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTGTTTTT others(2): Show |
6 | a0002c0002t0001g0025a0002c0002t0001g0036a0002c0002t0001g0037others(3): Show | 6 | NA18939.hp1 NA18946.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-6331_100-6330i others(11): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTGTTTTT others(3): Show |
1 | a0002c0002t0001g0039 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.100-6331_100-6330i others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTT | 10 | a0001c0001t0001g0174a0001c0001t0001g0175a0003c0003t0001g0108others(7): Show | 10 | HG00735.hp2 HG00738.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-6303_100-6302d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTGTTT others(3): Show |
1 | a0002c0002t0001g0040 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.100-6329_100-6328i others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTT | 20 | a0001c0001t0001g0019a0001c0001t0001g0112a0001c0001t0001g0114others(17): Show | 20 | HG00438.hp2 HG02015.hp1 HG02523.hp1 others(17): Show |
intron_variant | MODIFIER | c.100-6305_100-6302d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTT | 13 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0119others(10): Show | 13 | HG01243.hp1 HG02132.hp1 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-6306_100-6302d others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTT | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0027others(17): Show | 20 | HG00673.hp1 HG01074.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-6307_100-6302d others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTTT | 31 | a0001c0001t0001g0118a0001c0001t0001g0121a0001c0001t0001g0239others(28): Show | 31 | HG00423.hp1 HG00738.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.100-6308_100-6302d others(9): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTTT others(1): Show |
34 | a0001c0001t0001g0245a0001c0001t0001g0262a0001c0001t0001g0263others(31): Show | 34 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.100-6309_100-6302d others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTTT others(2): Show |
17 | a0001c0001t0001g0258a0002c0002t0001g0014a0002c0002t0001g0015others(14): Show | 17 | HG00140.hp1 HG00733.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-6310_100-6302d others(11): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTTT others(3): Show |
17 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0154others(14): Show | 17 | HG00673.hp2 HG01243.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-6311_100-6302d others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTTT others(4): Show |
7 | a0001c0001t0001g0131a0001c0001t0001g0264a0002c0002t0001g0022others(4): Show | 7 | HG02109.hp2 HG03486.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-6312_100-6302d others(13): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTTT others(5): Show |
2 | a0001c0001t0001g0132a0002c0002t0001g0086 | 2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.100-6313_100-6302d others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTTT others(6): Show |
2 | a0001c0001t0001g0297a0004c0004t0001g0290 | 2 | HG00099.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.100-6314_100-6302d others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTTT others(7): Show |
1 | a0001c0001t0001g0250 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.100-6315_100-6302d others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTTT others(8): Show |
5 | a0002c0002t0001g0031a0002c0002t0001g0079a0002c0002t0001g0082others(2): Show | 5 | HG00408.hp2 HG00609.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-6316_100-6302d others(17): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTTT others(9): Show |
4 | a0001c0001t0001g0105a0002c0002t0001g0018a0002c0002t0001g0080others(1): Show | 4 | HG01070.hp2 HG02135.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-6317_100-6302d others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTTT others(10): Show |
1 | a0002c0002t0001g0103 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.100-6318_100-6302d others(19): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTTT others(11): Show |
1 | a0002c0002t0001g0247 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.100-6319_100-6302d others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTTT others(14): Show |
3 | a0002c0002t0001g0004a0002c0002t0001g0090a0002c0002t0001g0104 | 3 | HG02293.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.100-6322_100-6302d others(23): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
G | GTTTTTTT others(15): Show |
1 | a0002c0002t0001g0222 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.100-6323_100-6302d others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
GTTTTTTT others(3): Show |
G | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-6311_100-6302d others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.100-6314_100-6302d others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564746
|
GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0001g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.100-6315_100-6302d others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | |||||
| chr7:77564748
|
T | TTTTTTG | 11 | a0001c0001t0001g0109a0001c0001t0001g0139a0001c0001t0001g0141others(8): Show | 11 | HG00609.hp1 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-6325_100-6324i others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564748 | |||||
| chr7:77564749
|
T | TTTTTG | 22 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(19): Show | 22 | HG00280.hp2 HG00735.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.100-6325_100-6324i others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564749 | |||||
| chr7:77564761
|
T | G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-6317T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564761 | ||||||
| chr7:77564762
|
T | G | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-6316T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564762 | ||||||
| chr7:77564795
|
T | G | 249 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(246): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.100-6283T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564795 | ||||||
| chr7:77564796
|
G | T | 249 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(246): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.100-6282G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564796 | ||||||
| chr7:77564820
|
C | T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-6258C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564820 | ||||||
| chr7:77564886
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-6192T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564886 | ||||||
| chr7:77564960
|
G | T | 2 | a0002c0002t0001g0070a0002c0002t0001g0071 | 2 | HG01099.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.100-6118G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564960 | ||||||
| chr7:77564979
|
A | ATCTCCTG others(86): Show |
4 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-6097_100-6005d others(95): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564979 | |||||
| chr7:77565182
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-5896G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77565182 | ||||||
| chr7:77565462
|
T | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-5616T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77565462 | ||||||
| chr7:77565477
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-5601G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77565477 | ||||||
| chr7:77565494
|
C | G | 1 | a0002c0002t0001g0078 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.100-5584C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77565494 | ||||||
| chr7:77565544
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.100-5534T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77565544 | ||||||
| chr7:77566082
|
A | G | 1 | a0004c0004t0001g0289 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.100-4996A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566082 | ||||||
| chr7:77566113
|
A | G | 249 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(246): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.100-4965A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566113 | ||||||
| chr7:77566138
|
G | A | 46 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(43): Show | 46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.100-4940G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566138 | ||||||
| chr7:77566178
|
A | G | 256 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(253): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.100-4900A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566178 | ||||||
| chr7:77566222
|
A | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-4856A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566222 | ||||||
| chr7:77566361
|
T | C | 1 | a0003c0003t0001g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.100-4717T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566361 | ||||||
| chr7:77566596
|
A | G | 1 | a0002c0002t0001g0056 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.100-4482A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566596 | ||||||
| chr7:77566599
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100-4479G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566599 | ||||||
| chr7:77566705
|
CAG | C | 74 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(71): Show | 74 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.100-4370_100-4369d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77566705 | |||||
| chr7:77566823
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.100-4255G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566823 | ||||||
| chr7:77566886
|
A | G | 3 | a0002c0002t0001g0100a0002c0002t0001g0101a0002c0002t0001g0102 | 3 | HG01256.hp2 HG01258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.100-4192A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566886 | ||||||
| chr7:77567115
|
A | G | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-3963A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567115 | ||||||
| chr7:77567195
|
T | TA | 45 | a0001c0001t0001g0117a0001c0001t0001g0232a0001c0001t0001g0302others(42): Show | 45 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.100-3868dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77567195 | |||||
| chr7:77567195
|
TA | T | 7 | a0001c0001t0001g0168a0002c0002t0001g0046a0002c0002t0001g0053others(4): Show | 7 | HG01081.hp1 HG01358.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-3868delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77567195 | |||||
| chr7:77567214
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0003g0176 | 3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-3864G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567214 | ||||||
| chr7:77567253
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.100-3825G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567253 | ||||||
| chr7:77567269
|
T | G | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0003g0176 | 3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-3809T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567269 | ||||||
| chr7:77567456
|
G | A | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100-3622G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567456 | ||||||
| chr7:77567573
|
A | G | 5 | a0002c0002t0001g0095a0002c0002t0001g0096a0002c0002t0001g0097others(2): Show | 5 | HG01952.hp1 HG01975.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-3505A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567573 | ||||||
| chr7:77567614
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-3464C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567614 | ||||||
| chr7:77567632
|
A | ATG | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG00280.hp2 HG01358.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3443_100-3442d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77567632 | |||||
| chr7:77567900
|
G | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-3178G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567900 | ||||||
| chr7:77567986
|
T | C | 278 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.100-3092T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567986 | ||||||
| chr7:77568236
|
G | T | 1 | a0003c0003t0001g0191 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.100-2842G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568236 | ||||||
| chr7:77568250
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.100-2828C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568250 | ||||||
| chr7:77568315
|
T | C | 247 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.100-2763T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568315 | ||||||
| chr7:77568316
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-2762G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568316 | ||||||
| chr7:77568373
|
C | T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-2705C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568373 | ||||||
| chr7:77568392
|
T | C | 1 | a0002c0002t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.100-2686T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568392 | ||||||
| chr7:77568455
|
A | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-2623A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568455 | ||||||
| chr7:77568638
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100-2440G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568638 | ||||||
| chr7:77568847
|
A | AT | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-2231_100-2230i others(3): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568847 | ||||||
| chr7:77568850
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-2228A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568850 | ||||||
| chr7:77568899
|
C | G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-2179C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568899 | ||||||
| chr7:77569396
|
A | T | 5 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 5 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-1682A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77569396 | ||||||
| chr7:77569433
|
T | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100-1645T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77569433 | ||||||
| chr7:77569671
|
T | C | 1 | a0002c0002t0001g0082 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.100-1407T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77569671 | ||||||
| chr7:77569678
|
C | T | 1 | a0002c0002t0001g0043 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.100-1400C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77569678 | ||||||
| chr7:77569718
|
C | T | 2 | a0003c0003t0001g0244a0003c0003t0001g0304 | 2 | HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.100-1360C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77569718 | ||||||
| chr7:77569725
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.100-1353C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77569725 | ||||||
| chr7:77570012
|
A | G | 1 | a0002c0002t0001g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.100-1066A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77570012 | ||||||
| chr7:77570162
|
C | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-916C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77570162 | ||||||
| chr7:77570349
|
T | C | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.100-729T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77570349 | ||||||
| chr7:77570351
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.100-727A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77570351 | ||||||
| chr7:77570647
|
T | C | 6 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(3): Show | 6 | NA18946.hp1 NA18981.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-431T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77570647 | ||||||
| chr7:77570828
|
A | G | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.100-250A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77570828 | ||||||
| chr7:77571035
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.100-43C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77571035 | ||||||
| chr7:77571043
|
C | G | 4 | a0003c0003t0001g0005a0003c0003t0001g0188a0003c0003t0001g0189others(1): Show | 4 | HG00408.hp1 NA18964.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-35C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77571043 | ||||||
| chr7:77571075
|
A | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(78): Show | 81 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
splice_region_variant&intron_variant | LOW | c.100-3A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77571075 | ||||||
| chr7:77571320
|
A | T | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(5): Show | 8 | HG02080.hp2 HG02132.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+134A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571320 | ||||||
| chr7:77571508
|
C | G | 1 | a0002c0002t0001g0096 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.208+322C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571508 | ||||||
| chr7:77571572
|
A | G | 112 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.208+386A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571572 | ||||||
| chr7:77571608
|
A | G | 1 | a0002c0002t0004g0052 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.208+422A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571608 | ||||||
| chr7:77571628
|
T | G | 1 | a0001c0001t0001g0273 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.208+442T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571628 | ||||||
| chr7:77571695
|
TTTTA | T | 171 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(168): Show | 171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.208+533_208+536del others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77571695 | |||||
| chr7:77571695
|
TTTTATTT others(1): Show |
T | 80 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(77): Show | 80 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.208+529_208+536del others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77571695 | |||||
| chr7:77571695
|
TTTTATTT others(5): Show |
T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+525_208+536del others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77571695 | |||||
| chr7:77571719
|
A | ATTTG | 3 | a0003c0003t0001g0206a0003c0003t0001g0212a0003c0003t0001g0223 | 3 | HG02257.hp1 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.208+549_208+552dup others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77571719 | |||||
| chr7:77571719
|
A | G | 9 | a0002c0002t0001g0009a0002c0002t0001g0013a0002c0002t0001g0016others(6): Show | 9 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.208+533A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571719 | ||||||
| chr7:77571795
|
C | T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.208+609C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571795 | ||||||
| chr7:77571952
|
G | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.208+766G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571952 | ||||||
| chr7:77571993
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208+807C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571993 | ||||||
| chr7:77572098
|
CT | C | 11 | a0001c0001t0001g0147a0001c0001t0001g0307a0001c0001t0001g0308others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.208+928delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77572098 | |||||
| chr7:77572098
|
CTT | C | 246 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.208+927_208+928del others(2): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77572098 | |||||
| chr7:77572342
|
G | C | 8 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(5): Show | 8 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+1156G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77572342 | ||||||
| chr7:77572541
|
TTTG | T | 80 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(77): Show | 80 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.208+1361_208+1363d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77572541 | |||||
| chr7:77572678
|
A | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+1492A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77572678 | ||||||
| chr7:77572851
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+1665G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77572851 | ||||||
| chr7:77572919
|
T | C | 249 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(246): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.208+1733T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77572919 | ||||||
| chr7:77572968
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+1782A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77572968 | ||||||
| chr7:77573032
|
G | A | 108 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(105): Show | 108 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.208+1846G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573032 | ||||||
| chr7:77573039
|
C | T | 111 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(108): Show | 111 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.208+1853C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573039 | ||||||
| chr7:77573082
|
C | CAAAAAAA others(5): Show |
1 | a0002c0002t0001g0047 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.208+1899_208+1910d others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573082 | |||||
| chr7:77573082
|
C | CAAAAAAA others(6): Show |
2 | a0002c0002t0001g0002a0002c0002t0001g0035 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.208+1898_208+1910d others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573082 | |||||
| chr7:77573082
|
C | CAAAAAAA others(9): Show |
1 | a0002c0002t0001g0057 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.208+1910_208+1911i others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573082 | |||||
| chr7:77573082
|
C | CAAAAAAA others(14): Show |
1 | a0002c0002t0001g0024 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.208+1910_208+1911i others(23): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573082 | |||||
| chr7:77573082
|
C | CAAAAAAA others(36): Show |
1 | a0002c0002t0001g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.208+1910_208+1911i others(45): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573082 | |||||
| chr7:77573090
|
AAAAAAAC others(8): Show |
A | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0003g0176others(1): Show | 4 | HG02572.hp2 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+1911_208+1925d others(17): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573090 | |||||
| chr7:77573091
|
AAAAAAC | A | 12 | a0001c0001t0001g0105a0001c0001t0001g0127a0001c0001t0001g0129others(9): Show | 12 | HG00280.hp1 HG02109.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.208+1911_208+1916d others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573091 | |||||
| chr7:77573092
|
AAAAAC | A | 7 | a0001c0001t0001g0147a0001c0001t0001g0236a0001c0001t0001g0269others(4): Show | 7 | HG01884.hp2 HG01993.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+1911_208+1915d others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573092 | |||||
| chr7:77573093
|
AAAAC | A | 87 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0019others(84): Show | 87 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.208+1911_208+1914d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573093 | |||||
| chr7:77573094
|
AAAC | A | 27 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0133others(24): Show | 27 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.208+1911_208+1913d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573094 | |||||
| chr7:77573096
|
AC | A | 6 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0111others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+1911delC | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573096 | ||||||
| chr7:77573097
|
C | A | 106 | a0001c0001t0001g0307a0001c0001t0001g0308a0002c0002t0001g0002others(103): Show | 106 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.208+1911C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573097 | ||||||
| chr7:77573100
|
A | AAAAAAAA others(7): Show |
4 | a0002c0002t0001g0058a0002c0002t0001g0089a0002c0002t0001g0102others(1): Show | 4 | HG01258.hp1 HG02683.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+1918_208+1919i others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573100 | |||||
| chr7:77573100
|
A | AAAAAAAA others(6): Show |
34 | a0002c0002t0001g0008a0002c0002t0001g0013a0002c0002t0001g0014others(31): Show | 34 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.208+1918_208+1919i others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573100 | |||||
| chr7:77573100
|
A | AAAAAAAA others(5): Show |
47 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0010others(44): Show | 47 | HG00639.hp2 HG00673.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.208+1918_208+1919i others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573100 | |||||
| chr7:77573100
|
A | AAAAAAAA others(4): Show |
5 | a0002c0002t0001g0021a0002c0002t0001g0023a0002c0002t0001g0045others(2): Show | 5 | HG01074.hp1 HG01243.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+1918_208+1919i others(13): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573100 | |||||
| chr7:77573100
|
A | AAACAAAA others(5): Show |
1 | a0002c0002t0001g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.208+1916_208+1917i others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573100 | |||||
| chr7:77573100
|
A | AACAAAAA others(4): Show |
1 | a0002c0002t0001g0082 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.208+1915_208+1916i others(13): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573100 | |||||
| chr7:77573101
|
A | AAAAAAAA others(5): Show |
1 | a0002c0002t0001g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.208+1918_208+1919i others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573101 | |||||
| chr7:77573105
|
C | A | 242 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(239): Show | 242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.208+1919C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573105 | ||||||
| chr7:77573112
|
A | C | 1 | a0002c0002t0001g0104 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.208+1926A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573112 | ||||||
| chr7:77573130
|
A | G | 4 | a0003c0003t0001g0005a0003c0003t0001g0188a0003c0003t0001g0189others(1): Show | 4 | HG00408.hp1 NA18964.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+1944A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573130 | ||||||
| chr7:77573202
|
T | C | 2 | a0002c0002t0001g0004a0002c0002t0001g0082 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.208+2016T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573202 | ||||||
| chr7:77573377
|
G | C | 35 | a0001c0001t0001g0109a0001c0001t0001g0133a0001c0001t0001g0134others(32): Show | 35 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.208+2191G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573377 | ||||||
| chr7:77573415
|
G | A | 27 | a0001c0001t0001g0027a0001c0001t0001g0234a0001c0001t0001g0235others(24): Show | 27 | HG00423.hp1 HG00438.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.208+2229G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573415 | ||||||
| chr7:77573475
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+2289G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573475 | ||||||
| chr7:77573498
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02132.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.208+2312A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573498 | ||||||
| chr7:77573755
|
T | C | 1 | a0002c0002t0001g0086 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208+2569T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573755 | ||||||
| chr7:77573802
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+2616C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573802 | ||||||
| chr7:77573830
|
C | T | 1 | a0003c0003t0001g0171 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.208+2644C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573830 | ||||||
| chr7:77574003
|
C | T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.208+2817C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574003 | ||||||
| chr7:77574037
|
CT | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+2853delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77574037 | |||||
| chr7:77574196
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+3010C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574196 | ||||||
| chr7:77574213
|
G | C | 1 | a0002c0002t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.208+3027G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574213 | ||||||
| chr7:77574241
|
C | T | 2 | a0002c0002t0001g0004a0002c0002t0001g0082 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.208+3055C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574241 | ||||||
| chr7:77574390
|
G | A | 1 | a0002c0002t0001g0034 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.208+3204G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574390 | ||||||
| chr7:77574555
|
C | A | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+3369C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574555 | ||||||
| chr7:77574566
|
T | C | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.208+3380T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574566 | ||||||
| chr7:77574768
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+3582C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574768 | ||||||
| chr7:77574848
|
T | G | 1 | a0001c0001t0003g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.208+3662T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574848 | ||||||
| chr7:77574942
|
G | T | 2 | a0002c0002t0001g0004a0002c0002t0001g0082 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.208+3756G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574942 | ||||||
| chr7:77574980
|
T | C | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.208+3794T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574980 | ||||||
| chr7:77575019
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+3833A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77575019 | ||||||
| chr7:77575026
|
G | A | 1 | a0002c0002t0001g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.208+3840G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77575026 | ||||||
| chr7:77575038
|
C | T | 242 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(239): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.208+3852C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77575038 | ||||||
| chr7:77575325
|
ACACG | A | 74 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(71): Show | 74 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.208+4155_208+4158d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77575325 | |||||
| chr7:77575434
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0003g0176 | 3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.208+4248G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77575434 | ||||||
| chr7:77575849
|
C | G | 3 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0111 | 3 | HG02559.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.208+4663C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77575849 | ||||||
| chr7:77575859
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+4673A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77575859 | ||||||
| chr7:77576019
|
T | C | 2 | a0003c0003t0001g0107a0003c0003t0001g0111 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.208+4833T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576019 | ||||||
| chr7:77576182
|
C | G | 1 | a0001c0001t0001g0027 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.208+4996C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576182 | ||||||
| chr7:77576197
|
A | G | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(72): Show | 75 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.208+5011A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576197 | ||||||
| chr7:77576278
|
A | G | 2 | a0002c0002t0001g0061a0002c0002t0001g0077 | 2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.208+5092A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576278 | ||||||
| chr7:77576342
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.209-5085C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576342 | ||||||
| chr7:77576604
|
C | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-4823C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576604 | ||||||
| chr7:77576605
|
G | A | 2 | a0002c0002t0001g0061a0002c0002t0001g0077 | 2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.209-4822G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576605 | ||||||
| chr7:77576665
|
C | G | 1 | a0001c0001t0003g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.209-4762C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576665 | ||||||
| chr7:77576731
|
C | T | 1 | a0003c0003t0001g0178 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.209-4696C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576731 | ||||||
| chr7:77577160
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.209-4267G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77577160 | ||||||
| chr7:77577204
|
A | G | 1 | a0002c0002t0001g0063 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.209-4223A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77577204 | ||||||
| chr7:77577285
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.209-4142G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77577285 | ||||||
| chr7:77577328
|
A | G | 1 | a0003c0003t0001g0210 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.209-4099A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77577328 | ||||||
| chr7:77577432
|
A | G | 112 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.209-3995A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77577432 | ||||||
| chr7:77577691
|
G | A | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.209-3736G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77577691 | ||||||
| chr7:77578273
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.209-3154C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77578273 | ||||||
| chr7:77578356
|
C | T | 2 | a0002c0002t0001g0070a0002c0002t0001g0071 | 2 | HG01099.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.209-3071C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77578356 | ||||||
| chr7:77578466
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.209-2961T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77578466 | ||||||
| chr7:77578530
|
A | C | 1 | a0002c0002t0001g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.209-2897A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77578530 | ||||||
| chr7:77578850
|
G | A | 1 | a0003c0003t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.209-2577G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77578850 | ||||||
| chr7:77578868
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.209-2559A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77578868 | ||||||
| chr7:77579207
|
C | T | 1 | a0002c0002t0001g0078 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.209-2220C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77579207 | ||||||
| chr7:77579360
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-2067T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77579360 | ||||||
| chr7:77579591
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.209-1836A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77579591 | ||||||
| chr7:77579645
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-1782T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77579645 | ||||||
| chr7:77579656
|
A | T | 1 | a0002c0002t0001g0296 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.209-1771A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77579656 | ||||||
| chr7:77579972
|
T | C | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-1455T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77579972 | ||||||
| chr7:77580184
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.209-1243G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77580184 | ||||||
| chr7:77580249
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-1178T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77580249 | ||||||
| chr7:77580465
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.209-962A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77580465 | ||||||
| chr7:77580707
|
T | C | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.209-720T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77580707 | ||||||
| chr7:77580815
|
A | G | 2 | a0002c0002t0001g0067a0002c0002t0001g0068 | 2 | HG00733.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.209-612A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77580815 | ||||||
| chr7:77581038
|
TTTTTG | T | 4 | a0003c0003t0001g0206a0003c0003t0001g0212a0003c0003t0001g0223others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-364_209-360del others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77581038 | |||||
| chr7:77581038
|
TTTTTGTT others(8): Show |
T | 112 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.209-374_209-360del others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77581038 | |||||
| chr7:77581075
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.209-352T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77581075 | ||||||
| chr7:77581172
|
T | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-255T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77581172 | ||||||
| chr7:77581399
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-28A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77581399 | ||||||
| chr7:77581816
|
A | G | 1 | a0003c0003t0001g0178 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.285+313A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77581816 | ||||||
| chr7:77581954
|
C | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+451C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77581954 | ||||||
| chr7:77582084
|
C | CT | 15 | a0001c0001t0001g0003a0001c0001t0001g0175a0001c0001t0001g0226others(12): Show | 15 | HG00140.hp2 HG01175.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.285+609dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582084
|
C | CTTTTTT | 9 | a0001c0001t0001g0019a0001c0001t0001g0228a0001c0001t0001g0259others(6): Show | 9 | HG01952.hp2 HG02015.hp1 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.285+604_285+609dup others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582084
|
C | CTTTTTTT | 9 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0274others(6): Show | 9 | HG02004.hp2 HG02922.hp2 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.285+603_285+609dup others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582084
|
C | CTTTTTTT others(1): Show |
10 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0249others(7): Show | 10 | HG00423.hp1 HG01981.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+602_285+609dup others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582084
|
C | CTTTTTTT others(2): Show |
25 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0115others(22): Show | 25 | HG00099.hp2 HG00438.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.285+601_285+609dup others(9): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582084
|
C | CTTTTTTT others(3): Show |
11 | a0001c0001t0001g0006a0001c0001t0001g0114a0001c0001t0001g0117others(8): Show | 11 | HG00741.hp1 HG01258.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.285+600_285+609dup others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582084
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0267others(1): Show | 4 | HG00639.hp1 HG00673.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+599_285+609dup others(11): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582084
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0001g0109a0001c0001t0001g0120a0001c0001t0001g0269others(1): Show | 4 | HG02523.hp1 HG06807.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+598_285+609dup others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582084
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0119 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.285+597_285+609dup others(13): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582084
|
C | CTTTTTTT others(10): Show |
1 | a0004c0004t0001g0287 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.285+593_285+609dup others(17): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582084
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.285+588_285+609dup others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582084
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0001g0121 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.285+582_285+609dup others(28): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582084
|
CT | C | 74 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0136others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.285+609delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582084
|
CTT | C | 116 | a0001c0001t0001g0105a0001c0001t0001g0127a0001c0001t0001g0129others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.285+608_285+609del others(2): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582084
|
CTTTTTTT others(8): Show |
C | 1 | a0002c0002t0001g0099 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.285+595_285+609del others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | |||||
| chr7:77582126
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.285+623G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582126 | ||||||
| chr7:77582193
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+690C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582193 | ||||||
| chr7:77582196
|
G | A | 1 | a0002c0002t0001g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.285+693G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582196 | ||||||
| chr7:77582312
|
G | T | 305 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.285+809G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582312 | ||||||
| chr7:77582381
|
C | G | 5 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 5 | HG02280.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+878C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582381 | ||||||
| chr7:77582386
|
A | T | 246 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.285+883A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582386 | ||||||
| chr7:77582506
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.285+1003G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582506 | ||||||
| chr7:77582526
|
G | A | 2 | a0002c0002t0001g0067a0002c0002t0001g0068 | 2 | HG00733.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.285+1023G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582526 | ||||||
| chr7:77582745
|
A | G | 1 | a0002c0002t0001g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.286-810A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582745 | ||||||
| chr7:77582748
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.286-807C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582748 | ||||||
| chr7:77582762
|
T | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.286-793T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582762 | ||||||
| chr7:77582783
|
C | CA | 100 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.286-756dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582783 | |||||
| chr7:77582947
|
A | G | 2 | a0002c0002t0001g0086a0002c0002t0001g0229 | 2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.286-608A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582947 | ||||||
| chr7:77583119
|
T | C | 1 | a0002c0002t0001g0076 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.286-436T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77583119 | ||||||
| chr7:77583133
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-422G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77583133 | ||||||
| chr7:77583265
|
T | C | 1 | a0003c0003t0001g0192 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.286-290T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77583265 | ||||||
| chr7:77583275
|
T | C | 112 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.286-280T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77583275 | ||||||
| chr7:77583324
|
C | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-231C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77583324 | ||||||
| chr7:77583429
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.286-126A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77583429 | ||||||
| chr7:77583740
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.381+90A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77583740 | ||||||
| chr7:77583928
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.381+278G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77583928 | ||||||
| chr7:77583992
|
TCTC | T | 3 | a0003c0003t0002g0151a0003c0003t0002g0152a0003c0003t0002g0153 | 3 | HG01243.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.381+343_381+345del others(3): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77583992 | ||||||
| chr7:77584023
|
T | A | 1 | a0001c0001t0001g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.381+373T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584023 | ||||||
| chr7:77584046
|
A | G | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.381+396A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584046 | ||||||
| chr7:77584142
|
A | ATTAG | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+493_381+496dup others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 77584142 | |||||
| chr7:77584155
|
G | A | 97 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0009others(94): Show | 97 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.381+505G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584155 | ||||||
| chr7:77584249
|
A | T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.381+599A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584249 | ||||||
| chr7:77584311
|
G | C | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.381+661G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584311 | ||||||
| chr7:77584601
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.382-942C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584601 | ||||||
| chr7:77584669
|
A | T | 1 | a0001c0001t0001g0234 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.382-874A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584669 | ||||||
| chr7:77584674
|
G | A | 242 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(239): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.382-869G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584674 | ||||||
| chr7:77584731
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-812G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584731 | ||||||
| chr7:77584745
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-798C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584745 | ||||||
| chr7:77584766
|
A | G | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0305 | 3 | HG01109.hp2 HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.382-777A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584766 | ||||||
| chr7:77584794
|
G | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0297 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.382-749G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584794 | ||||||
| chr7:77584834
|
G | A | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-709G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584834 | ||||||
| chr7:77584876
|
C | CA | 23 | a0001c0001t0001g0109a0001c0001t0001g0174a0001c0001t0001g0175others(20): Show | 23 | HG00438.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.382-650dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 77584876 | |||||
| chr7:77584876
|
C | CAA | 6 | a0001c0001t0001g0307a0001c0001t0001g0308a0003c0003t0001g0020others(3): Show | 6 | HG00140.hp2 HG01256.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-651_382-650dup others(2): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 77584876 | |||||
| chr7:77585165
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-378G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77585165 | ||||||
| chr7:77585257
|
T | C | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.382-286T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77585257 | ||||||
| chr7:77585266
|
T | C | 1 | a0002c0002t0001g0070 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.382-277T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77585266 | ||||||
| chr7:77585307
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-236C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77585307 | ||||||
| chr7:77585315
|
A | G | 1 | a0003c0003t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.382-228A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77585315 | ||||||
| chr7:77585642
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+61A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77585642 | ||||||
| chr7:77585680
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.420+99T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77585680 | ||||||
| chr7:77585726
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.420+145A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77585726 | ||||||
| chr7:77585838
|
C | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | HG00639.hp1 HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.420+257C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77585838 | ||||||
| chr7:77586123
|
T | C | 1 | a0003c0003t0001g0178 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.420+542T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77586123 | ||||||
| chr7:77586126
|
G | A | 242 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(239): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.420+545G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77586126 | ||||||
| chr7:77586164
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.420+583G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77586164 | ||||||
| chr7:77586294
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.420+713G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77586294 | ||||||
| chr7:77586439
|
ACCAGGAA others(20): Show |
A | 1 | a0005c0005t0001g0048 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.420+863_420+889del others(27): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 77586439 | |||||
| chr7:77586481
|
G | A | 46 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(43): Show | 46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.420+900G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77586481 | ||||||
| chr7:77586524
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.420+943C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77586524 | ||||||
| chr7:77586657
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0278 | 2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.420+1076A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77586657 | ||||||
| chr7:77587098
|
C | T | 74 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(71): Show | 74 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.420+1517C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587098 | ||||||
| chr7:77587163
|
T | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.420+1582T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587163 | ||||||
| chr7:77587245
|
A | T | 1 | a0002c0002t0001g0036 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.420+1664A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587245 | ||||||
| chr7:77587385
|
A | AT | 81 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(78): Show | 81 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.420+1813dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 77587385 | |||||
| chr7:77587468
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.420+1887T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587468 | ||||||
| chr7:77587479
|
A | G | 1 | a0003c0003t0001g0210 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.420+1898A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587479 | ||||||
| chr7:77587557
|
A | G | 1 | a0002c0002t0001g0056 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.420+1976A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587557 | ||||||
| chr7:77587686
|
C | A | 61 | a0002c0002t0001g0009a0002c0002t0001g0012a0002c0002t0001g0013others(58): Show | 61 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.420+2105C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587686 | ||||||
| chr7:77587686
|
C | G | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(72): Show | 75 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.420+2105C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587686 | ||||||
| chr7:77587722
|
C | T | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.420+2141C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587722 | ||||||
| chr7:77587787
|
T | C | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.420+2206T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587787 | ||||||
| chr7:77587829
|
A | C | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.420+2248A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587829 | ||||||
| chr7:77587851
|
T | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+2270T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587851 | ||||||
| chr7:77587961
|
G | T | 1 | a0003c0003t0001g0180 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.420+2380G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587961 | ||||||
| chr7:77588157
|
T | A | 35 | a0001c0001t0001g0109a0001c0001t0001g0133a0001c0001t0001g0134others(32): Show | 35 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.420+2576T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588157 | ||||||
| chr7:77588167
|
G | T | 61 | a0002c0002t0001g0009a0002c0002t0001g0012a0002c0002t0001g0013others(58): Show | 61 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.420+2586G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588167 | ||||||
| chr7:77588184
|
A | G | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.420+2603A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588184 | ||||||
| chr7:77588202
|
C | G | 11 | a0001c0001t0001g0105a0001c0001t0001g0127a0001c0001t0001g0129others(8): Show | 11 | HG00280.hp1 HG00323.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.420+2621C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588202 | ||||||
| chr7:77588328
|
C | T | 1 | a0002c0002t0001g0063 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.420+2747C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588328 | ||||||
| chr7:77588507
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.420+2926T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588507 | ||||||
| chr7:77588625
|
A | G | 114 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(111): Show | 114 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.420+3044A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588625 | ||||||
| chr7:77588698
|
A | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.420+3117A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588698 | ||||||
| chr7:77588725
|
A | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+3144A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588725 | ||||||
| chr7:77588737
|
C | G | 1 | a0002c0002t0001g0079 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.420+3156C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588737 | ||||||
| chr7:77588944
|
C | T | 1 | a0002c0002t0001g0221 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.421-3241C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588944 | ||||||
| chr7:77589017
|
C | T | 73 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(70): Show | 73 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.421-3168C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77589017 | ||||||
| chr7:77589203
|
CTGTT | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-2977_421-2974d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 77589203 | |||||
| chr7:77589221
|
G | C | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421-2964G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77589221 | ||||||
| chr7:77589360
|
G | C | 1 | a0001c0001t0001g0245 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.421-2825G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77589360 | ||||||
| chr7:77589462
|
C | A | 3 | a0002c0002t0001g0021a0002c0002t0001g0022a0002c0002t0001g0023 | 3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.421-2723C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77589462 | ||||||
| chr7:77589643
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.421-2542A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77589643 | ||||||
| chr7:77589922
|
T | G | 79 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(76): Show | 79 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.421-2263T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77589922 | ||||||
| chr7:77590030
|
T | C | 1 | a0002c0002t0001g0037 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.421-2155T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590030 | ||||||
| chr7:77590180
|
T | G | 1 | a0001c0001t0001g0308 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.421-2005T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590180 | ||||||
| chr7:77590243
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.421-1942T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590243 | ||||||
| chr7:77590299
|
A | G | 1 | a0003c0003t0001g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.421-1886A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590299 | ||||||
| chr7:77590346
|
A | C | 1 | a0001c0001t0001g0129 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.421-1839A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590346 | ||||||
| chr7:77590559
|
C | CT | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(72): Show | 75 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.421-1612dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 77590559 | |||||
| chr7:77590559
|
C | CTT | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.421-1613_421-1612d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 77590559 | |||||
| chr7:77590562
|
T | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.421-1623T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590562 | ||||||
| chr7:77590618
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.421-1567T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590618 | ||||||
| chr7:77590843
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.421-1342C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590843 | ||||||
| chr7:77590873
|
T | TA | 6 | a0002c0002t0001g0069a0003c0003t0001g0020a0003c0003t0001g0169others(3): Show | 6 | HG00140.hp2 HG01256.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-1298dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 77590873 | |||||
| chr7:77590985
|
C | T | 157 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(154): Show | 157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.421-1200C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590985 | ||||||
| chr7:77591051
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.421-1134A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591051 | ||||||
| chr7:77591077
|
A | G | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.421-1108A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591077 | ||||||
| chr7:77591178
|
C | T | 1 | a0003c0003t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.421-1007C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591178 | ||||||
| chr7:77591189
|
A | G | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.421-996A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591189 | ||||||
| chr7:77591231
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.421-954G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591231 | ||||||
| chr7:77591403
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-782C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591403 | ||||||
| chr7:77591468
|
T | G | 1 | a0001c0001t0001g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.421-717T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591468 | ||||||
| chr7:77591585
|
C | G | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.421-600C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591585 | ||||||
| chr7:77591717
|
C | T | 3 | a0002c0002t0001g0088a0002c0002t0001g0089a0002c0002t0001g0090 | 3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.421-468C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591717 | ||||||
| chr7:77592164
|
A | AT | 46 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(43): Show | 46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.421-10dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 77592164 | |||||
| chr7:77592348
|
T | A | 2 | a0002c0002t0001g0004a0002c0002t0001g0082 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.492+92T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77592348 | ||||||
| chr7:77592393
|
T | C | 1 | a0001c0001t0001g0293 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.492+137T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77592393 | ||||||
| chr7:77592855
|
A | G | 5 | a0002c0002t0001g0002a0002c0002t0001g0029a0002c0002t0001g0030others(2): Show | 5 | HG01175.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.492+599A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77592855 | ||||||
| chr7:77592914
|
A | T | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.492+658A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77592914 | ||||||
| chr7:77592979
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.492+723A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77592979 | ||||||
| chr7:77593039
|
C | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+783C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593039 | ||||||
| chr7:77593254
|
G | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+998G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593254 | ||||||
| chr7:77593269
|
CA | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.492+1029delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 77593269 | |||||
| chr7:77593269
|
CAA | C | 161 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(158): Show | 161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.492+1028_492+1029d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 77593269 | |||||
| chr7:77593482
|
T | G | 1 | a0002c0002t0001g0104 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.492+1226T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593482 | ||||||
| chr7:77593536
|
T | A | 1 | a0002c0002t0001g0043 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.492+1280T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593536 | ||||||
| chr7:77593551
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.492+1295G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593551 | ||||||
| chr7:77593568
|
C | T | 1 | a0002c0002t0001g0081 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.492+1312C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593568 | ||||||
| chr7:77593569
|
A | G | 167 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.492+1313A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593569 | ||||||
| chr7:77593583
|
A | C | 1 | a0002c0002t0001g0092 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.492+1327A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593583 | ||||||
| chr7:77593621
|
C | A | 79 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(76): Show | 79 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.492+1365C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593621 | ||||||
| chr7:77593831
|
C | G | 113 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(110): Show | 113 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.492+1575C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593831 | ||||||
| chr7:77593894
|
G | A | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | HG00639.hp1 HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.492+1638G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593894 | ||||||
| chr7:77593948
|
T | C | 113 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(110): Show | 113 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.492+1692T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593948 | ||||||
| chr7:77594027
|
T | A | 247 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.492+1771T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77594027 | ||||||
| chr7:77594118
|
G | T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.492+1862G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77594118 | ||||||
| chr7:77594141
|
T | A | 1 | a0002c0002t0001g0086 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.492+1885T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77594141 | ||||||
| chr7:77594303
|
A | AAAAACGT others(24): Show |
1 | a0002c0002t0001g0106 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.492+2048_492+2078d others(33): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 77594303 | |||||
| chr7:77594304
|
A | G | 73 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(70): Show | 73 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.492+2048A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77594304 | ||||||
| chr7:77594377
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+2121T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77594377 | ||||||
| chr7:77594431
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.492+2175T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77594431 | ||||||
| chr7:77595162
|
G | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.493-2680G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77595162 | ||||||
| chr7:77595555
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0305 | 3 | HG01109.hp2 HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.493-2287G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77595555 | ||||||
| chr7:77595682
|
A | C | 1 | a0004c0004t0001g0290 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.493-2160A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77595682 | ||||||
| chr7:77595736
|
T | A | 1 | a0002c0002t0001g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.493-2106T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77595736 | ||||||
| chr7:77595805
|
T | A | 1 | a0003c0003t0001g0186 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.493-2037T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77595805 | ||||||
| chr7:77595811
|
T | A | 1 | a0001c0001t0001g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.493-2031T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77595811 | ||||||
| chr7:77596122
|
G | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.493-1720G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596122 | ||||||
| chr7:77596213
|
CA | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-1626delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 77596213 | |||||
| chr7:77596282
|
A | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.493-1560A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596282 | ||||||
| chr7:77596392
|
A | T | 1 | a0002c0002t0001g0037 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.493-1450A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596392 | ||||||
| chr7:77596527
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.493-1315C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596527 | ||||||
| chr7:77596548
|
G | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.493-1294G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596548 | ||||||
| chr7:77596752
|
A | T | 1 | a0002c0002t0001g0083 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.493-1090A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596752 | ||||||
| chr7:77596896
|
C | T | 2 | a0002c0002t0001g0045a0002c0002t0001g0046 | 2 | HG01074.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.493-946C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596896 | ||||||
| chr7:77596983
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.493-859A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596983 | ||||||
| chr7:77596988
|
G | GAATAGTG others(9): Show |
119 | a0001c0001t0001g0307a0001c0001t0001g0308a0002c0002t0001g0002others(116): Show | 119 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.493-846_493-845ins others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 77596988 | |||||
| chr7:77597147
|
G | A | 56 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(53): Show | 56 | HG00099.hp2 HG00438.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.493-695G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77597147 | ||||||
| chr7:77597162
|
C | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-680C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77597162 | ||||||
| chr7:77597342
|
C | T | 1 | a0003c0003t0001g0210 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.493-500C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77597342 | ||||||
| chr7:77597416
|
C | T | 1 | a0002c0002t0001g0024 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.493-426C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77597416 | ||||||
| chr7:77597432
|
T | C | 1 | a0002c0002t0001g0067 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.493-410T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77597432 | ||||||
| chr7:77597924
|
C | T | 79 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(76): Show | 79 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.552+23C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77597924 | ||||||
| chr7:77598265
|
C | G | 113 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(110): Show | 113 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.552+364C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598265 | ||||||
| chr7:77598433
|
A | G | 3 | a0002c0002t0001g0113a0002c0002t0001g0300a0002c0002t0001g0301 | 3 | HG00423.hp1 HG00673.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.552+532A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598433 | ||||||
| chr7:77598502
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+601C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598502 | ||||||
| chr7:77598572
|
A | G | 1 | a0002c0002t0001g0092 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.552+671A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598572 | ||||||
| chr7:77598678
|
G | C | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+777G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598678 | ||||||
| chr7:77598790
|
T | G | 1 | a0001c0001t0001g0150 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.552+889T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598790 | ||||||
| chr7:77598935
|
T | A | 1 | a0002c0002t0001g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.552+1034T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598935 | ||||||
| chr7:77598993
|
T | G | 1 | a0001c0001t0001g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.552+1092T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598993 | ||||||
| chr7:77598997
|
A | G | 73 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(70): Show | 73 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.552+1096A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598997 | ||||||
| chr7:77599143
|
C | G | 4 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+1242C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599143 | ||||||
| chr7:77599158
|
A | G | 1 | a0002c0002t0001g0016 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.552+1257A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599158 | ||||||
| chr7:77599253
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.552+1352A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599253 | ||||||
| chr7:77599279
|
T | C | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.552+1378T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599279 | ||||||
| chr7:77599317
|
C | CT | 13 | a0001c0001t0001g0162a0001c0001t0001g0174a0001c0001t0001g0175others(10): Show | 13 | HG00140.hp2 HG00438.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.553-1329dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 77599317 | |||||
| chr7:77599317
|
C | CTT | 181 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.553-1330_553-1329d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 77599317 | |||||
| chr7:77599317
|
C | CTTT | 10 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | HG00423.hp1 HG00673.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.553-1331_553-1329d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 77599317 | |||||
| chr7:77599320
|
T | A | 2 | a0003c0003t0001g0244a0003c0003t0001g0304 | 2 | HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.553-1344T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599320 | ||||||
| chr7:77599408
|
A | G | 1 | a0002c0002t0001g0043 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.553-1256A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599408 | ||||||
| chr7:77599617
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-1047G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599617 | ||||||
| chr7:77599932
|
G | A | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.553-732G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599932 | ||||||
| chr7:77600036
|
A | G | 242 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(239): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.553-628A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600036 | ||||||
| chr7:77600092
|
T | A | 2 | a0003c0003t0001g0107a0003c0003t0001g0111 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.553-572T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600092 | ||||||
| chr7:77600226
|
A | G | 309 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(306): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.553-438A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600226 | ||||||
| chr7:77600318
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.553-346T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600318 | ||||||
| chr7:77600324
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-340C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600324 | ||||||
| chr7:77600468
|
T | A | 6 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0111others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.553-196T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600468 | ||||||
| chr7:77600544
|
T | C | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.553-120T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600544 | ||||||
| chr7:77600660
|
G | A | 1 | a0002c0002t0001g0101 | 1 | NA20129.hp1 | splice_region_variant&intron_variant | LOW | c.553-4G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600660 | ||||||
| chr7:77600927
|
G | A | 1 | a0002c0002t0001g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.695+121G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77600927 | ||||||
| chr7:77601011
|
A | G | 1 | a0001c0001t0003g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.695+205A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601011 | ||||||
| chr7:77601022
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0177 | 3 | NA19056.hp1 NA19079.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.695+216G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601022 | ||||||
| chr7:77601253
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0003g0176 | 3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.695+447C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601253 | ||||||
| chr7:77601378
|
T | A | 8 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(5): Show | 8 | HG00140.hp2 HG01256.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.695+572T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601378 | ||||||
| chr7:77601680
|
T | C | 1 | a0002c0002t0001g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.695+874T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601680 | ||||||
| chr7:77601728
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.695+922A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601728 | ||||||
| chr7:77601827
|
A | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.695+1021A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601827 | ||||||
| chr7:77601949
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.695+1143A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601949 | ||||||
| chr7:77601993
|
A | C | 5 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.695+1187A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601993 | ||||||
| chr7:77602066
|
T | A | 4 | a0001c0001t0001g0112a0001c0001t0001g0265a0001c0001t0001g0266others(1): Show | 4 | HG00639.hp1 HG02486.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.695+1260T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602066 | ||||||
| chr7:77602168
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+1362A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602168 | ||||||
| chr7:77602193
|
G | A | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.695+1387G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602193 | ||||||
| chr7:77602212
|
T | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+1406T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602212 | ||||||
| chr7:77602257
|
A | G | 1 | a0002c0002t0004g0052 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.695+1451A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602257 | ||||||
| chr7:77602488
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+1682A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602488 | ||||||
| chr7:77602605
|
G | A | 1 | a0002c0002t0001g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.695+1799G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602605 | ||||||
| chr7:77602620
|
T | TA | 10 | a0002c0002t0001g0173a0003c0003t0001g0020a0003c0003t0001g0108others(7): Show | 10 | HG00140.hp2 HG00639.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.695+1827dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77602620 | |||||
| chr7:77602621
|
A | T | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.695+1815A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602621 | ||||||
| chr7:77603192
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+2386A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77603192 | ||||||
| chr7:77603313
|
T | A | 2 | a0003c0003t0001g0107a0003c0003t0001g0111 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.695+2507T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77603313 | ||||||
| chr7:77603375
|
A | G | 1 | a0003c0003t0001g0220 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.695+2569A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77603375 | ||||||
| chr7:77603379
|
A | G | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.695+2573A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77603379 | ||||||
| chr7:77603507
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.695+2701C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77603507 | ||||||
| chr7:77603883
|
C | CT | 57 | a0001c0001t0001g0003a0001c0001t0001g0121a0001c0001t0001g0157others(54): Show | 57 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.695+3100dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77603883 | |||||
| chr7:77603883
|
C | CTT | 45 | a0001c0001t0001g0109a0001c0001t0001g0127a0001c0001t0001g0129others(42): Show | 45 | HG00280.hp1 HG00280.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.695+3099_695+3100d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77603883 | |||||
| chr7:77603883
|
CT | C | 8 | a0001c0001t0001g0274a0001c0001t0001g0278a0001c0001t0001g0307others(5): Show | 8 | HG01167.hp1 HG01891.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.695+3100delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77603883 | |||||
| chr7:77604209
|
C | CATTTTT | 3 | a0003c0003t0001g0020a0003c0003t0001g0170a0003c0003t0001g0171 | 3 | HG01256.hp1 HG03239.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.696-3026_696-3025i others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604209 | ||||||
| chr7:77604209
|
C | CT | 111 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0027others(108): Show | 111 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.696-3002dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77604209 | |||||
| chr7:77604209
|
C | CTT | 102 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0109others(99): Show | 102 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.696-3003_696-3002d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77604209 | |||||
| chr7:77604209
|
C | CTTT | 25 | a0001c0001t0001g0105a0001c0001t0001g0127a0001c0001t0001g0129others(22): Show | 25 | HG00140.hp1 HG00639.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.696-3004_696-3002d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77604209 | |||||
| chr7:77604209
|
C | CTTTT | 9 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(6): Show | 9 | HG00423.hp1 HG00735.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-3005_696-3002d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77604209 | |||||
| chr7:77604209
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0150 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.696-3014_696-3002d others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77604209 | |||||
| chr7:77604209
|
CT | C | 6 | a0003c0003t0001g0108a0003c0003t0001g0110a0003c0003t0001g0178others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-3002delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77604209 | |||||
| chr7:77604209
|
CTTTTTTT others(5): Show |
C | 17 | a0003c0003t0001g0005a0003c0003t0001g0172a0003c0003t0001g0179others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(14): Show |
intron_variant | MODIFIER | c.696-3013_696-3002d others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77604209 | |||||
| chr7:77604239
|
G | A | 1 | a0002c0002t0001g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.696-2996G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604239 | ||||||
| chr7:77604272
|
A | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.696-2963A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604272 | ||||||
| chr7:77604475
|
A | G | 1 | a0003c0003t0001g0178 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.696-2760A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604475 | ||||||
| chr7:77604501
|
A | G | 1 | a0003c0003t0001g0184 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.696-2734A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604501 | ||||||
| chr7:77604510
|
A | G | 247 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.696-2725A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604510 | ||||||
| chr7:77604807
|
A | T | 2 | a0003c0003t0001g0107a0003c0003t0001g0111 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.696-2428A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604807 | ||||||
| chr7:77604809
|
T | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.696-2426T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604809 | ||||||
| chr7:77604836
|
A | G | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0003g0176 | 3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.696-2399A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604836 | ||||||
| chr7:77605058
|
C | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-2177C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605058 | ||||||
| chr7:77605206
|
G | C | 1 | a0002c0002t0001g0037 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.696-2029G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605206 | ||||||
| chr7:77605282
|
T | G | 49 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(46): Show | 49 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.696-1953T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605282 | ||||||
| chr7:77605323
|
T | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(76): Show | 79 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.696-1912T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605323 | ||||||
| chr7:77605409
|
G | GGTTT | 4 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(1): Show | 4 | HG02717.hp2 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1826_696-1825i others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | ||||||
| chr7:77605409
|
G | GGTTTTTT | 4 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0255others(1): Show | 4 | HG02015.hp1 HG02897.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.696-1826_696-1825i others(9): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | ||||||
| chr7:77605409
|
G | GGTTTTTT others(1): Show |
11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0175others(8): Show | 11 | HG00673.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.696-1826_696-1825i others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | ||||||
| chr7:77605409
|
G | GGTTTTTT others(2): Show |
25 | a0001c0001t0001g0027a0001c0001t0001g0112a0001c0001t0001g0121others(22): Show | 25 | HG00438.hp2 HG00642.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.696-1826_696-1825i others(11): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | ||||||
| chr7:77605409
|
G | GGTTTTTT others(3): Show |
19 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0120others(16): Show | 19 | HG00639.hp1 HG01952.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.696-1826_696-1825i others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | ||||||
| chr7:77605409
|
G | GGTTTTTT others(4): Show |
7 | a0001c0001t0001g0119a0001c0001t0001g0239a0001c0001t0001g0240others(4): Show | 7 | HG00741.hp1 HG01884.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.696-1826_696-1825i others(13): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | ||||||
| chr7:77605409
|
G | GGTTTTTT others(5): Show |
3 | a0001c0001t0001g0117a0001c0001t0001g0298a0004c0004t0001g0290 | 3 | HG00099.hp2 HG02080.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.696-1826_696-1825i others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | ||||||
| chr7:77605409
|
G | GGTTTTTT others(6): Show |
2 | a0001c0001t0001g0114a0001c0001t0001g0271 | 2 | NA18949.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.696-1826_696-1825i others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | ||||||
| chr7:77605409
|
G | GGTTTTTT others(8): Show |
1 | a0001c0001t0001g0118 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.696-1826_696-1825i others(17): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | ||||||
| chr7:77605409
|
G | GT | 11 | a0003c0003t0001g0184a0003c0003t0001g0191a0003c0003t0001g0203others(8): Show | 11 | HG00733.hp2 HG00735.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.696-1798dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | |||||
| chr7:77605409
|
G | GTTTGTTT others(7): Show |
1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.696-1823_696-1822i others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | |||||
| chr7:77605409
|
G | GTTTTTTT others(3): Show |
3 | a0003c0003t0001g0178a0003c0003t0001g0242a0003c0003t0002g0152 | 3 | HG02055.hp1 HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.696-1807_696-1798d others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | |||||
| chr7:77605409
|
G | GTTTTTTT others(4): Show |
2 | a0003c0003t0001g0108a0003c0003t0002g0153 | 2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.696-1808_696-1798d others(13): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | |||||
| chr7:77605409
|
G | GTTTTTTT others(5): Show |
1 | a0003c0003t0001g0107 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.696-1809_696-1798d others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | |||||
| chr7:77605409
|
G | GTTTTTTT others(8): Show |
2 | a0003c0003t0001g0111a0003c0003t0002g0151 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.696-1812_696-1798d others(17): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | |||||
| chr7:77605409
|
GT | G | 18 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0131others(15): Show | 18 | HG00280.hp2 HG00323.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.696-1798delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | |||||
| chr7:77605409
|
GTT | G | 38 | a0001c0001t0001g0109a0001c0001t0001g0135a0001c0001t0001g0136others(35): Show | 38 | HG00609.hp1 HG00735.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.696-1799_696-1798d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | |||||
| chr7:77605409
|
GTTT | G | 89 | a0001c0001t0001g0160a0001c0007t0001g0252a0002c0002t0001g0002others(86): Show | 89 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.696-1800_696-1798d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | |||||
| chr7:77605409
|
GTTTT | G | 13 | a0002c0002t0001g0004a0002c0002t0001g0014a0002c0002t0001g0021others(10): Show | 13 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.696-1801_696-1798d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | |||||
| chr7:77605409
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.696-1807_696-1798d others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | |||||
| chr7:77605410
|
T | G | 6 | a0001c0001t0001g0105a0001c0001t0001g0130a0001c0001t0001g0154others(3): Show | 6 | HG00280.hp1 HG00323.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-1825T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605410 | ||||||
| chr7:77605411
|
T | G | 15 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0131others(12): Show | 15 | HG00280.hp2 HG01358.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.696-1824T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605411 | ||||||
| chr7:77605412
|
T | G | 38 | a0001c0001t0001g0109a0001c0001t0001g0135a0001c0001t0001g0136others(35): Show | 38 | HG00609.hp1 HG00735.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.696-1823T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605412 | ||||||
| chr7:77605413
|
T | G | 89 | a0001c0001t0001g0160a0001c0007t0001g0252a0002c0002t0001g0002others(86): Show | 89 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.696-1822T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605413 | ||||||
| chr7:77605414
|
T | G | 13 | a0002c0002t0001g0004a0002c0002t0001g0014a0002c0002t0001g0021others(10): Show | 13 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.696-1821T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605414 | ||||||
| chr7:77605416
|
T | G | 1 | a0001c0001t0001g0293 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.696-1819T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605416 | ||||||
| chr7:77605418
|
T | G | 1 | a0001c0001t0001g0241 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.696-1817T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605418 | ||||||
| chr7:77605420
|
T | G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.696-1815T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605420 | ||||||
| chr7:77605442
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-1793C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605442 | ||||||
| chr7:77605580
|
C | T | 1 | a0002c0002t0001g0078 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.696-1655C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605580 | ||||||
| chr7:77605586
|
AT | A | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.696-1637delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605586 | |||||
| chr7:77605725
|
A | G | 1 | a0003c0003t0001g0001 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.696-1510A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605725 | ||||||
| chr7:77605744
|
C | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1491C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605744 | ||||||
| chr7:77605872
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1363C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605872 | ||||||
| chr7:77605888
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.696-1347C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605888 | ||||||
| chr7:77605945
|
C | CT | 64 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(61): Show | 64 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.696-1264dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605945 | |||||
| chr7:77605945
|
C | CTT | 27 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0130others(24): Show | 27 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.696-1265_696-1264d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605945 | |||||
| chr7:77605945
|
C | CTTT | 22 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0138others(19): Show | 22 | HG00642.hp2 HG01109.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.696-1266_696-1264d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605945 | |||||
| chr7:77605945
|
C | CTTTT | 9 | a0001c0001t0001g0109a0001c0001t0001g0127a0001c0001t0001g0136others(6): Show | 9 | HG00735.hp1 HG02486.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-1267_696-1264d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605945 | |||||
| chr7:77605945
|
CT | C | 120 | a0001c0001t0001g0307a0001c0001t0001g0308a0002c0002t0001g0002others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.696-1264delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605945 | |||||
| chr7:77605945
|
CTT | C | 11 | a0002c0002t0001g0095a0002c0002t0001g0096a0002c0002t0001g0097others(8): Show | 11 | HG00323.hp1 HG01952.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.696-1265_696-1264d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605945 | |||||
| chr7:77605948
|
T | C | 5 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-1287T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605948 | ||||||
| chr7:77605949
|
T | C | 3 | a0003c0003t0002g0151a0003c0003t0002g0152a0003c0003t0002g0153 | 3 | HG01243.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.696-1286T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605949 | ||||||
| chr7:77605989
|
T | C | 242 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(239): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.696-1246T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605989 | ||||||
| chr7:77606108
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1127G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77606108 | ||||||
| chr7:77606200
|
G | T | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.696-1035G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77606200 | ||||||
| chr7:77606470
|
T | G | 1 | a0002c0002t0001g0099 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.696-765T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77606470 | ||||||
| chr7:77606565
|
TAA | T | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.696-666_696-665del others(2): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77606565 | |||||
| chr7:77606831
|
T | C | 242 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(239): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.696-404T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77606831 | ||||||
| chr7:77606880
|
C | T | 1 | a0002c0002t0001g0059 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.696-355C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77606880 | ||||||
| chr7:77607169
|
A | T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.696-66A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77607169 | ||||||
| chr7:77607186
|
A | C | 3 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0111 | 3 | HG02559.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.696-49A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77607186 | ||||||
| chr7:77607659
|
G | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.762+358G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607659 | ||||||
| chr7:77607664
|
A | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.762+363A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607664 | ||||||
| chr7:77607695
|
G | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.762+394G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607695 | ||||||
| chr7:77607746
|
C | CT | 7 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.762+458dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77607746 | |||||
| chr7:77607858
|
A | G | 2 | a0002c0002t0001g0085a0003c0003t0001g0110 | 2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.762+557A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607858 | ||||||
| chr7:77607934
|
T | C | 5 | a0001c0001t0001g0278a0003c0003t0001g0020a0003c0003t0001g0169others(2): Show | 5 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.762+633T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607934 | ||||||
| chr7:77607936
|
G | T | 5 | a0001c0001t0001g0278a0003c0003t0001g0020a0003c0003t0001g0169others(2): Show | 5 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.762+635G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607936 | ||||||
| chr7:77607945
|
G | A | 5 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0238others(2): Show | 5 | HG00438.hp2 HG00673.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.762+644G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607945 | ||||||
| chr7:77607975
|
G | A | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.762+674G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607975 | ||||||
| chr7:77608073
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.762+772C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608073 | ||||||
| chr7:77608424
|
C | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.762+1123C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608424 | ||||||
| chr7:77608592
|
T | C | 1 | a0002c0002t0001g0173 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.762+1291T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608592 | ||||||
| chr7:77608740
|
C | G | 9 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0254others(6): Show | 9 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.762+1439C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608740 | ||||||
| chr7:77608763
|
C | T | 1 | a0002c0002t0004g0052 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.762+1462C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608763 | ||||||
| chr7:77608827
|
C | T | 107 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(104): Show | 107 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.762+1526C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608827 | ||||||
| chr7:77608867
|
A | G | 85 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 85 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.762+1566A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608867 | ||||||
| chr7:77608883
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.762+1582A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608883 | ||||||
| chr7:77608912
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+1611T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608912 | ||||||
| chr7:77608978
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+1677T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608978 | ||||||
| chr7:77609033
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.762+1732A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609033 | ||||||
| chr7:77609214
|
C | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.763-1551C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609214 | ||||||
| chr7:77609215
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0177 | 3 | NA19056.hp1 NA19079.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.763-1550G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609215 | ||||||
| chr7:77609261
|
T | TTC | 3 | a0001c0001t0001g0238a0001c0001t0001g0257a0001c0001t0001g0266 | 3 | HG02723.hp2 HG02895.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.763-1492_763-1491d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77609261 | |||||
| chr7:77609273
|
C | CT | 163 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.763-1476dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77609273 | |||||
| chr7:77609273
|
C | CTCT | 71 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(68): Show | 71 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.763-1491_763-1490i others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77609273 | |||||
| chr7:77609273
|
C | CTCTT | 6 | a0001c0001t0001g0259a0001c0001t0001g0261a0001c0001t0001g0262others(3): Show | 6 | HG03471.hp2 NA18946.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.763-1491_763-1490i others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77609273 | |||||
| chr7:77609273
|
C | CTT | 10 | a0001c0001t0001g0156a0002c0002t0001g0012a0003c0003t0001g0107others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.763-1477_763-1476d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77609273 | |||||
| chr7:77609274
|
T | TC | 3 | a0002c0002t0001g0021a0002c0002t0001g0022a0002c0002t0001g0023 | 3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.763-1491_763-1490i others(3): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609274 | ||||||
| chr7:77609275
|
T | C | 1 | a0003c0003t0001g0196 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.763-1490T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609275 | ||||||
| chr7:77609325
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.763-1440G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609325 | ||||||
| chr7:77609361
|
T | A | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(72): Show | 75 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.763-1404T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609361 | ||||||
| chr7:77609651
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.763-1114C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609651 | ||||||
| chr7:77609724
|
T | TA | 46 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(43): Show | 46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.763-1033dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77609724 | |||||
| chr7:77609888
|
A | C | 4 | a0001c0001t0001g0307a0001c0001t0001g0308a0002c0002t0001g0078others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.763-877A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609888 | ||||||
| chr7:77609894
|
C | CA | 106 | a0001c0001t0001g0175a0001c0001t0001g0307a0001c0001t0001g0308others(103): Show | 106 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.763-861dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77609894 | |||||
| chr7:77609896
|
A | AC | 3 | a0002c0002t0001g0017a0002c0002t0001g0040a0002c0002t0001g0091 | 3 | HG03669.hp2 NA19043.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.763-869_763-868ins others(1): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609896 | ||||||
| chr7:77609905
|
C | A | 251 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(248): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.763-860C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609905 | ||||||
| chr7:77610037
|
C | T | 7 | a0002c0002t0001g0018a0002c0002t0001g0084a0002c0002t0001g0085others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.763-728C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610037 | ||||||
| chr7:77610139
|
T | G | 35 | a0001c0001t0001g0109a0001c0001t0001g0133a0001c0001t0001g0134others(32): Show | 35 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.763-626T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610139 | ||||||
| chr7:77610148
|
A | C | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.763-617A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610148 | ||||||
| chr7:77610149
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.763-616C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610149 | ||||||
| chr7:77610163
|
A | G | 1 | a0003c0003t0001g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.763-602A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610163 | ||||||
| chr7:77610353
|
C | T | 3 | a0002c0002t0001g0021a0002c0002t0001g0022a0002c0002t0001g0023 | 3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.763-412C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610353 | ||||||
| chr7:77610418
|
T | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0233others(10): Show | 13 | HG00099.hp2 HG00642.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.763-347T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610418 | ||||||
| chr7:77610584
|
A | G | 1 | a0002c0002t0001g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.763-181A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610584 | ||||||
| chr7:77610638
|
T | G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.763-127T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610638 | ||||||
| chr7:77610752
|
T | C | 62 | a0002c0002t0001g0009a0002c0002t0001g0012a0002c0002t0001g0013others(59): Show | 62 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.763-13T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610752 | ||||||
| chr7:77611123
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+77G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611123 | ||||||
| chr7:77611295
|
T | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+249T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611295 | ||||||
| chr7:77611427
|
T | C | 244 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.939+381T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611427 | ||||||
| chr7:77611435
|
A | G | 1 | a0003c0003t0001g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.939+389A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611435 | ||||||
| chr7:77611458
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+412T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611458 | ||||||
| chr7:77611495
|
A | T | 78 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(75): Show | 78 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.939+449A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611495 | ||||||
| chr7:77611576
|
C | A | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | HG00639.hp1 HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.939+530C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611576 | ||||||
| chr7:77611691
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG00280.hp2 HG01358.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.939+645C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611691 | ||||||
| chr7:77611969
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.939+923G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611969 | ||||||
| chr7:77611981
|
A | AT | 109 | a0001c0001t0001g0132a0001c0001t0001g0174a0001c0001t0001g0175others(106): Show | 109 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+951dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77611981 | |||||
| chr7:77612117
|
G | C | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.939+1071G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612117 | ||||||
| chr7:77612236
|
A | T | 3 | a0003c0003t0002g0151a0003c0003t0002g0152a0003c0003t0002g0153 | 3 | HG01243.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.939+1190A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612236 | ||||||
| chr7:77612243
|
C | T | 1 | a0002c0002t0001g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.939+1197C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612243 | ||||||
| chr7:77612244
|
A | C | 1 | a0002c0002t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.939+1198A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612244 | ||||||
| chr7:77612472
|
A | G | 1 | a0002c0002t0001g0036 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.939+1426A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612472 | ||||||
| chr7:77612524
|
C | T | 1 | a0002c0002t0001g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.939+1478C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612524 | ||||||
| chr7:77612542
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.939+1496G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612542 | ||||||
| chr7:77612665
|
C | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0159 | 2 | NA19003.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.939+1619C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612665 | ||||||
| chr7:77612727
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.939+1681G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612727 | ||||||
| chr7:77612757
|
T | C | 117 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0003g0176others(114): Show | 117 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.939+1711T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612757 | ||||||
| chr7:77612770
|
G | GT | 8 | a0003c0003t0001g0196a0003c0003t0001g0197a0003c0003t0001g0198others(5): Show | 8 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.939+1732dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77612770 | |||||
| chr7:77612770
|
G | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0275a0001c0001t0001g0305 | 3 | HG01109.hp2 HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.939+1724G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612770 | ||||||
| chr7:77612790
|
T | G | 166 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(163): Show | 166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.939+1744T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612790 | ||||||
| chr7:77612794
|
G | GT | 7 | a0001c0001t0001g0307a0001c0001t0001g0308a0002c0002t0001g0032others(4): Show | 7 | HG01169.hp1 HG01175.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.939+1758dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77612794 | |||||
| chr7:77612821
|
T | C | 244 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.939+1775T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612821 | ||||||
| chr7:77612864
|
C | T | 1 | a0002c0002t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.939+1818C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612864 | ||||||
| chr7:77612874
|
C | T | 1 | a0002c0002t0001g0056 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.939+1828C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612874 | ||||||
| chr7:77613023
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.939+1977A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613023 | ||||||
| chr7:77613167
|
G | GT | 12 | a0001c0001t0001g0131a0001c0001t0001g0154a0002c0002t0001g0061others(9): Show | 12 | HG00642.hp1 HG01109.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.939+2146dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77613167 | |||||
| chr7:77613167
|
GT | G | 108 | a0001c0001t0001g0148a0001c0001t0001g0159a0001c0001t0001g0163others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.939+2146delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77613167 | |||||
| chr7:77613167
|
GTT | G | 108 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(105): Show | 108 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.939+2145_939+2146d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77613167 | |||||
| chr7:77613167
|
GTTT | G | 6 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 6 | HG01109.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.939+2144_939+2146d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77613167 | |||||
| chr7:77613173
|
T | G | 4 | a0001c0001t0001g0284a0001c0001t0001g0291a0001c0001t0001g0303others(1): Show | 4 | HG01981.hp2 HG02683.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.939+2127T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613173 | ||||||
| chr7:77613174
|
T | G | 67 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(64): Show | 67 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.939+2128T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613174 | ||||||
| chr7:77613175
|
T | G | 1 | a0001c0001t0001g0259 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.939+2129T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613175 | ||||||
| chr7:77613180
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.939+2134T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613180 | ||||||
| chr7:77613189
|
T | A | 1 | a0002c0002t0001g0221 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.939+2143T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613189 | ||||||
| chr7:77613222
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.939+2176T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613222 | ||||||
| chr7:77613272
|
T | C | 119 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0307others(116): Show | 119 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.939+2226T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613272 | ||||||
| chr7:77613340
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.939+2294A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613340 | ||||||
| chr7:77613468
|
C | T | 12 | a0001c0001t0001g0027a0001c0001t0001g0240a0001c0001t0001g0259others(9): Show | 12 | HG01952.hp2 HG01975.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.939+2422C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613468 | ||||||
| chr7:77613620
|
G | A | 1 | a0002c0002t0001g0013 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.939+2574G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613620 | ||||||
| chr7:77613728
|
G | A | 46 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(43): Show | 46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.939+2682G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613728 | ||||||
| chr7:77613778
|
G | A | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.939+2732G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613778 | ||||||
| chr7:77613783
|
G | T | 1 | a0002c0002t0001g0037 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.939+2737G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613783 | ||||||
| chr7:77613807
|
G | C | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.939+2761G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613807 | ||||||
| chr7:77613853
|
T | C | 1 | a0002c0002t0001g0058 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.939+2807T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613853 | ||||||
| chr7:77613859
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+2813A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613859 | ||||||
| chr7:77613879
|
T | G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.939+2833T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613879 | ||||||
| chr7:77613956
|
A | G | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.939+2910A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613956 | ||||||
| chr7:77613984
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.939+2938C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613984 | ||||||
| chr7:77614028
|
A | C | 1 | a0005c0005t0001g0051 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.939+2982A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614028 | ||||||
| chr7:77614068
|
A | T | 76 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(73): Show | 76 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.939+3022A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614068 | ||||||
| chr7:77614075
|
T | TTTGTAGA others(4): Show |
251 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(248): Show | 251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.939+3033_939+3043d others(13): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77614075 | |||||
| chr7:77614075
|
T | TTTTGTAG others(5): Show |
2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.939+3031_939+3032i others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77614075 | |||||
| chr7:77614087
|
T | TTGTCTCA others(5): Show |
4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+3043_939+3044i others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77614087 | |||||
| chr7:77614094
|
G | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02486.hp1 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.939+3048G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614094 | ||||||
| chr7:77614274
|
A | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+3228A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614274 | ||||||
| chr7:77614405
|
G | A | 1 | a0002c0002t0001g0092 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.939+3359G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614405 | ||||||
| chr7:77614611
|
C | G | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.939+3565C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614611 | ||||||
| chr7:77614696
|
G | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG02135.hp1 NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.939+3650G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614696 | ||||||
| chr7:77614746
|
A | G | 1 | a0002c0002t0001g0106 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.939+3700A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614746 | ||||||
| chr7:77615014
|
C | G | 46 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(43): Show | 46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.940-3466C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77615014 | ||||||
| chr7:77615158
|
G | A | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.940-3322G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77615158 | ||||||
| chr7:77615448
|
CAA | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-3031_940-3030d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77615448 | ||||||
| chr7:77615673
|
C | T | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.940-2807C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77615673 | ||||||
| chr7:77615780
|
A | G | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.940-2700A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77615780 | ||||||
| chr7:77615837
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-2643G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77615837 | ||||||
| chr7:77616316
|
G | A | 5 | a0002c0002t0001g0018a0002c0002t0001g0103a0002c0002t0001g0104others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-2164G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77616316 | ||||||
| chr7:77616336
|
G | A | 3 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0111 | 3 | HG02559.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.940-2144G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77616336 | ||||||
| chr7:77616657
|
G | T | 72 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(69): Show | 72 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.940-1823G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77616657 | ||||||
| chr7:77616806
|
G | A | 52 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(49): Show | 52 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.940-1674G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77616806 | ||||||
| chr7:77616874
|
T | C | 257 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.940-1606T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77616874 | ||||||
| chr7:77616939
|
C | T | 78 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(75): Show | 78 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.940-1541C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77616939 | ||||||
| chr7:77617088
|
G | A | 12 | a0001c0001t0001g0027a0001c0001t0001g0240a0001c0001t0001g0259others(9): Show | 12 | HG01952.hp2 HG01975.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.940-1392G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77617088 | ||||||
| chr7:77617099
|
G | A | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.940-1381G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77617099 | ||||||
| chr7:77617517
|
G | A | 1 | a0003c0003t0001g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.940-963G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77617517 | ||||||
| chr7:77617784
|
A | AGTCCTAA others(7): Show |
4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-693_940-680dup others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77617784 | |||||
| chr7:77617796
|
A | T | 1 | a0002c0002t0001g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.940-684A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77617796 | ||||||
| chr7:77618126
|
A | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-354A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77618126 | ||||||
| chr7:77618266
|
T | C | 3 | a0003c0003t0002g0151a0003c0003t0002g0152a0003c0003t0002g0153 | 3 | HG01243.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.940-214T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77618266 | ||||||
| chr7:77618278
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.940-202G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77618278 | ||||||
| chr7:77618606
|
G | T | 1 | a0002c0002t0001g0125 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1025+41G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77618606 | ||||||
| chr7:77618666
|
CT | C | 8 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(5): Show | 8 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1025+105delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77618666 | |||||
| chr7:77619247
|
T | C | 2 | a0002c0002t0001g0004a0002c0002t0001g0082 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1025+682T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77619247 | ||||||
| chr7:77619267
|
G | A | 3 | a0002c0002t0001g0088a0002c0002t0001g0089a0002c0002t0001g0090 | 3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1025+702G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77619267 | ||||||
| chr7:77619302
|
A | G | 12 | a0001c0001t0001g0027a0001c0001t0001g0240a0001c0001t0001g0259others(9): Show | 12 | HG01952.hp2 HG01975.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1025+737A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77619302 | ||||||
| chr7:77619399
|
A | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | HG01884.hp2 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+834A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77619399 | ||||||
| chr7:77619551
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1025+986G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77619551 | ||||||
| chr7:77619740
|
T | A | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | HG00639.hp1 HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1025+1175T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77619740 | ||||||
| chr7:77620034
|
A | T | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+1469A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620034 | ||||||
| chr7:77620135
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+1570A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620135 | ||||||
| chr7:77620212
|
CTCT | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0003g0176 | 3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1025+1652_1025+165 others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77620212 | |||||
| chr7:77620374
|
T | C | 1 | a0003c0003t0001g0190 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1025+1809T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620374 | ||||||
| chr7:77620385
|
A | T | 1 | a0001c0001t0001g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1025+1820A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620385 | ||||||
| chr7:77620602
|
A | G | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0003g0176 | 3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1025+2037A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620602 | ||||||
| chr7:77620619
|
A | T | 2 | a0003c0003t0001g0207a0003c0003t0001g0208 | 2 | NA18971.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1025+2054A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620619 | ||||||
| chr7:77620773
|
C | T | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+2208C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620773 | ||||||
| chr7:77620961
|
C | G | 44 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(41): Show | 44 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1025+2396C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620961 | ||||||
| chr7:77621046
|
G | A | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+2481G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621046 | ||||||
| chr7:77621051
|
C | CAT | 4 | a0001c0001t0001g0019a0001c0001t0001g0276a0001c0001t0001g0307others(1): Show | 4 | HG01891.hp1 HG02015.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2504_1025+250 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77621051 | |||||
| chr7:77621051
|
CAT | C | 90 | a0001c0001t0001g0003a0001c0001t0001g0109a0001c0001t0001g0133others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1025+2504_1025+250 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77621051 | |||||
| chr7:77621069
|
T | A | 1 | a0002c0002t0001g0031 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1025+2504T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621069 | ||||||
| chr7:77621071
|
A | T | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1025+2506A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621071 | ||||||
| chr7:77621098
|
T | TTTTA | 7 | a0001c0001t0001g0305a0003c0003t0001g0107a0003c0003t0001g0108others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1025+2554_1025+255 others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77621098 | |||||
| chr7:77621098
|
T | TTTTATTT others(1): Show |
4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2550_1025+255 others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77621098 | |||||
| chr7:77621098
|
TTTTA | T | 8 | a0002c0002t0001g0025a0002c0002t0001g0036a0002c0002t0001g0038others(5): Show | 8 | NA18946.hp2 NA18949.hp1 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.1025+2554_1025+255 others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77621098 | |||||
| chr7:77621242
|
C | CAG | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2677_1025+267 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621242 | ||||||
| chr7:77621439
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2874T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621439 | ||||||
| chr7:77621573
|
G | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG02135.hp1 NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1025+3008G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621573 | ||||||
| chr7:77621616
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1025+3051C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621616 | ||||||
| chr7:77621670
|
C | CA | 52 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(49): Show | 52 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1025+3115dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77621670 | |||||
| chr7:77621763
|
A | G | 40 | a0001c0001t0001g0109a0001c0001t0001g0133a0001c0001t0001g0134others(37): Show | 40 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1025+3198A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621763 | ||||||
| chr7:77621773
|
G | A | 9 | a0003c0003t0001g0194a0003c0003t0001g0204a0003c0003t0001g0205others(6): Show | 9 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1025+3208G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621773 | ||||||
| chr7:77621906
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0243 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1025+3341A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621906 | ||||||
| chr7:77621909
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+3344G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621909 | ||||||
| chr7:77622047
|
C | T | 1 | a0002c0002t0001g0014 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1025+3482C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77622047 | ||||||
| chr7:77622095
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+3530T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77622095 | ||||||
| chr7:77622206
|
T | C | 5 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025+3641T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77622206 | ||||||
| chr7:77622654
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-4051C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77622654 | ||||||
| chr7:77622671
|
T | TACTCAG | 114 | a0001c0001t0001g0307a0001c0001t0001g0308a0002c0002t0001g0002others(111): Show | 114 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1026-4034_1026-403 others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77622671 | ||||||
| chr7:77622849
|
T | TTTCCAAT others(33): Show |
4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-3844_1026-384 others(44): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77622849 | |||||
| chr7:77623012
|
C | CA | 48 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(45): Show | 48 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.1026-3681dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77623012 | |||||
| chr7:77623137
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1026-3568T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77623137 | ||||||
| chr7:77623267
|
G | A | 1 | a0002c0002t0001g0037 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1026-3438G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77623267 | ||||||
| chr7:77623389
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1026-3316G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77623389 | ||||||
| chr7:77623713
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1026-2992C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77623713 | ||||||
| chr7:77623934
|
G | A | 8 | a0003c0003t0001g0196a0003c0003t0001g0197a0003c0003t0001g0198others(5): Show | 8 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-2771G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77623934 | ||||||
| chr7:77624156
|
G | A | 280 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1026-2549G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77624156 | ||||||
| chr7:77624773
|
C | T | 1 | a0002c0002t0001g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1026-1932C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77624773 | ||||||
| chr7:77624901
|
G | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1026-1804G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77624901 | ||||||
| chr7:77625067
|
A | G | 5 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-1638A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625067 | ||||||
| chr7:77625230
|
A | G | 23 | a0003c0003t0001g0128a0003c0003t0001g0194a0003c0003t0001g0195others(20): Show | 23 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1026-1475A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625230 | ||||||
| chr7:77625253
|
G | GT | 15 | a0001c0001t0001g0121a0001c0001t0001g0142a0001c0001t0001g0144others(12): Show | 15 | HG00140.hp2 HG00438.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1026-1437dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625253 | |||||
| chr7:77625413
|
A | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1292A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625413 | ||||||
| chr7:77625453
|
C | T | 280 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1026-1252C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625453 | ||||||
| chr7:77625468
|
G | GCGCCCTC others(11): Show |
1 | a0001c0001t0001g0141 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1026-1236_1026-123 others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | |||||
| chr7:77625468
|
G | GCGCCCTC others(13): Show |
1 | a0001c0001t0001g0177 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1026-1236_1026-123 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | |||||
| chr7:77625468
|
G | GCGCCTCT others(12): Show |
1 | a0001c0001t0001g0142 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1026-1236_1026-123 others(23): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | |||||
| chr7:77625468
|
G | GCGCGCGC others(25): Show |
1 | a0001c0001t0001g0159 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1026-1236_1026-123 others(36): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | |||||
| chr7:77625468
|
G | GCGCTCTC others(9): Show |
2 | a0001c0001t0001g0134a0001c0001t0001g0246 | 2 | HG00280.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1026-1236_1026-123 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | |||||
| chr7:77625468
|
G | GCGCTCTC others(15): Show |
1 | a0001c0001t0001g0109 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1026-1236_1026-123 others(26): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | |||||
| chr7:77625468
|
G | GCTCTCTC others(11): Show |
2 | a0001c0001t0001g0161a0001c0001t0001g0243 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1026-1234_1026-123 others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | |||||
| chr7:77625468
|
G | GCTCTCTC others(13): Show |
3 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0167 | 3 | HG02486.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1026-1234_1026-123 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | |||||
| chr7:77625468
|
G | GCTCTCTC others(21): Show |
2 | a0001c0001t0001g0164a0001c0001t0001g0166 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1026-1234_1026-123 others(32): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | |||||
| chr7:77625468
|
G | GCTCTCTC others(25): Show |
1 | a0001c0001t0001g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1026-1234_1026-123 others(36): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | |||||
| chr7:77625468
|
G | GCTCTCTC others(37): Show |
1 | a0001c0001t0001g0168 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1026-1234_1026-123 others(48): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | |||||
| chr7:77625468
|
GCTCGCTC others(7): Show |
G | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1026-1233_1026-122 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | |||||
| chr7:77625470
|
T | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG00609.hp1 HG01358.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1026-1235T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625470 | ||||||
| chr7:77625470
|
T | TCGCTCG | 6 | a0002c0002t0001g0031a0002c0002t0001g0047a0002c0002t0001g0061others(3): Show | 6 | HG00609.hp2 HG00738.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625470 | |||||
| chr7:77625470
|
T | TCGCTCGC others(3): Show |
6 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0264others(3): Show | 6 | HG00438.hp2 HG01255.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625470 | |||||
| chr7:77625470
|
TCG | T | 3 | a0001c0001t0001g0156a0003c0003t0001g0215a0003c0003t0001g0223 | 3 | HG02280.hp1 HG02698.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1026-1233_1026-123 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625470 | |||||
| chr7:77625472
|
G | GCT | 6 | a0003c0003t0001g0188a0003c0003t0001g0190a0003c0003t0001g0193others(3): Show | 6 | HG00733.hp2 HG01516.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1183_1026-118 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(7): Show |
1 | a0002c0002t0001g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(9): Show |
1 | a0004c0004t0001g0290 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(19): Show |
1 | a0001c0001t0001g0241 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(30): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(5): Show |
6 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0270others(3): Show | 6 | HG00741.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(7): Show |
8 | a0001c0001t0001g0027a0001c0001t0001g0239a0001c0001t0001g0251others(5): Show | 8 | HG01952.hp2 HG01975.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(9): Show |
3 | a0001c0001t0001g0257a0001c0001t0001g0266a0001c0001t0001g0293 | 3 | HG02723.hp2 HG02895.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(11): Show |
3 | a0001c0001t0001g0228a0001c0001t0001g0255a0001c0001t0001g0268 | 3 | HG02897.hp2 NA19030.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(13): Show |
8 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0249others(5): Show | 8 | HG01884.hp2 HG02165.hp1 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(15): Show |
1 | a0001c0001t0001g0224 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(26): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(17): Show |
4 | a0001c0001t0001g0114a0001c0001t0001g0121a0001c0001t0001g0227others(1): Show | 4 | HG02486.hp2 HG03209.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(28): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(19): Show |
4 | a0001c0001t0001g0112a0001c0001t0001g0118a0001c0001t0001g0225others(1): Show | 4 | HG02647.hp1 HG02818.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(30): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(21): Show |
4 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0120others(1): Show | 4 | HG02080.hp2 HG02132.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(32): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(23): Show |
1 | a0001c0001t0001g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(34): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(3): Show |
2 | a0002c0002t0001g0004a0002c0002t0001g0173 | 2 | HG00639.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(5): Show |
2 | a0001c0001t0001g0174a0002c0002t0001g0075 | 2 | HG02572.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(9): Show |
2 | a0002c0002t0001g0022a0002c0002t0001g0091 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(11): Show |
1 | a0002c0002t0001g0082 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(13): Show |
3 | a0001c0001t0001g0175a0002c0002t0001g0014a0002c0002t0001g0101 | 3 | HG02165.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(15): Show |
1 | a0002c0002t0001g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(26): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(17): Show |
1 | a0002c0002t0001g0049 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(28): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(19): Show |
1 | a0002c0002t0001g0090 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(30): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(23): Show |
2 | a0002c0002t0001g0088a0002c0002t0001g0089 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(34): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(25): Show |
4 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(36): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(27): Show |
1 | a0001c0001t0001g0245 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(38): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(31): Show |
1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(42): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(37): Show |
1 | a0001c0001t0001g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(48): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(1): Show |
6 | a0002c0002t0001g0026a0002c0002t0001g0053a0002c0002t0001g0054others(3): Show | 6 | HG01516.hp2 HG01517.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(3): Show |
8 | a0002c0002t0001g0012a0002c0002t0001g0029a0002c0002t0001g0038others(5): Show | 8 | HG02698.hp1 HG03195.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(5): Show |
9 | a0001c0001t0001g0250a0001c0001t0001g0297a0002c0002t0001g0028others(6): Show | 9 | HG00280.hp1 HG00323.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(7): Show |
11 | a0002c0002t0001g0017a0002c0002t0001g0024a0002c0002t0001g0025others(8): Show | 11 | HG00140.hp1 HG00673.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(9): Show |
6 | a0002c0002t0001g0018a0002c0002t0001g0073a0002c0002t0001g0076others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(11): Show |
8 | a0002c0002t0001g0036a0002c0002t0001g0040a0002c0002t0001g0042others(5): Show | 8 | HG00408.hp2 HG00733.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(13): Show |
7 | a0002c0002t0001g0056a0002c0002t0001g0057a0002c0002t0001g0072others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(15): Show |
3 | a0002c0002t0001g0106a0002c0002t0001g0125a0002c0002t0004g0052 | 3 | HG03710.hp2 NA18964.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(26): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(17): Show |
2 | a0002c0002t0001g0063a0002c0002t0001g0086 | 2 | HG01891.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(28): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(19): Show |
1 | a0002c0002t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(30): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(21): Show |
1 | a0002c0002t0001g0002 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(32): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCGC others(23): Show |
1 | a0002c0002t0001g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(34): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCTC others(13): Show |
1 | a0001c0001t0001g0145 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCGCTC others(19): Show |
1 | a0003c0006t0001g0201 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(30): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCT | 5 | a0003c0003t0001g0179a0003c0003t0001g0182a0003c0003t0001g0191others(2): Show | 5 | HG02015.hp2 NA18993.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026-1185_1026-118 others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCTCT | 4 | a0003c0003t0001g0005a0003c0003t0001g0192a0003c0003t0001g0197others(1): Show | 4 | HG00408.hp1 HG03704.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-1187_1026-118 others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCTCTC others(1): Show |
4 | a0003c0003t0001g0181a0003c0003t0001g0183a0003c0003t0001g0186others(1): Show | 4 | HG00438.hp1 HG01255.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1189_1026-118 others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCTCTC others(3): Show |
3 | a0001c0001t0001g0148a0003c0003t0001g0189a0003c0003t0001g0202 | 3 | HG01261.hp1 NA19060.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1026-1191_1026-118 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCTCTC others(7): Show |
1 | a0003c0003t0001g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1026-1195_1026-118 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCTCTC others(11): Show |
3 | a0001c0001t0001g0150a0003c0003t0001g0196a0003c0003t0001g0200 | 3 | HG00323.hp1 HG01109.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1026-1199_1026-118 others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCTCTC others(13): Show |
1 | a0003c0003t0001g0172 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1026-1201_1026-118 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCTCTC others(15): Show |
1 | a0003c0003t0001g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1026-1203_1026-118 others(26): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCTCTC others(19): Show |
1 | a0003c0003t0001g0205 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1026-1207_1026-118 others(30): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCTCTC others(27): Show |
2 | a0001c0001t0001g0143a0001c0001t0001g0146 | 2 | HG00735.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1026-1215_1026-118 others(38): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCTCTC others(29): Show |
2 | a0001c0001t0001g0144a0001c0001t0001g0147 | 2 | HG01169.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1026-1217_1026-118 others(40): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTCTCTC others(31): Show |
1 | a0003c0003t0001g0203 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1026-1219_1026-118 others(42): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTTGCGC others(3): Show |
1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1026-1231_1026-123 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTTGCGC others(5): Show |
2 | a0003c0003t0001g0107a0003c0003t0001g0111 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1026-1231_1026-123 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTTGCGC others(7): Show |
1 | a0003c0003t0001g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1026-1231_1026-123 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | GCTTGCGC others(13): Show |
1 | a0003c0003t0001g0178 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1026-1231_1026-123 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
G | T | 23 | a0001c0001t0001g0109a0001c0001t0001g0133a0001c0001t0001g0134others(20): Show | 23 | HG00280.hp2 HG01243.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.1026-1233G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625472 | ||||||
| chr7:77625472
|
GCT | G | 8 | a0001c0001t0001g0105a0001c0001t0001g0136a0001c0001t0001g0137others(5): Show | 8 | HG02135.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-1183_1026-118 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
GCTCTCT | G | 4 | a0003c0003t0001g0001a0003c0003t0001g0195a0003c0003t0001g0220others(1): Show | 4 | HG01070.hp1 HG01074.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-1187_1026-118 others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
GCTCTCTC others(3): Show |
G | 2 | a0003c0003t0001g0128a0003c0003t0001g0304 | 2 | HG01071.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1026-1191_1026-118 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
GCTCTCTC others(5): Show |
G | 1 | a0003c0003t0001g0299 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1026-1193_1026-118 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625472
|
GCTCTCTC others(7): Show |
G | 1 | a0003c0003t0001g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1026-1195_1026-118 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | |||||
| chr7:77625474
|
T | TCG | 4 | a0002c0002t0001g0069a0002c0002t0001g0083a0002c0002t0001g0085others(1): Show | 4 | HG01975.hp2 HG03225.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625474 | |||||
| chr7:77625474
|
T | TCGCG | 14 | a0001c0001t0001g0236a0001c0001t0001g0256a0001c0001t0001g0258others(11): Show | 14 | HG00639.hp1 HG01099.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625474 | |||||
| chr7:77625474
|
T | TCGCGCG | 6 | a0001c0001t0001g0253a0001c0001t0001g0260a0001c0001t0001g0263others(3): Show | 6 | HG03130.hp2 HG03139.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625474 | |||||
| chr7:77625474
|
T | TCGCGCGC others(1): Show |
17 | a0001c0001t0001g0019a0001c0001t0001g0233a0001c0001t0001g0237others(14): Show | 17 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625474 | |||||
| chr7:77625476
|
T | G | 46 | a0001c0001t0001g0236a0001c0001t0001g0253a0001c0001t0001g0254others(43): Show | 46 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.1026-1229T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625476 | ||||||
| chr7:77625478
|
T | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1026-1227T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625478 | ||||||
| chr7:77625478
|
T | G | 41 | a0001c0001t0001g0105a0001c0001t0001g0154a0001c0001t0001g0155others(38): Show | 41 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1026-1227T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625478 | ||||||
| chr7:77625480
|
T | G | 14 | a0001c0001t0001g0105a0001c0001t0001g0154a0001c0001t0001g0155others(11): Show | 14 | HG00140.hp2 HG01256.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1026-1225T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625480 | ||||||
| chr7:77625481
|
C | CTCTCTCT others(9): Show |
1 | a0001c0001t0001g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1026-1209_1026-120 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625481 | |||||
| chr7:77625482
|
T | G | 6 | a0001c0001t0001g0254a0001c0001t0001g0279a0003c0003t0001g0020others(3): Show | 6 | HG00140.hp2 HG01256.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026-1223T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625482 | ||||||
| chr7:77625504
|
T | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1201T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625504 | ||||||
| chr7:77625504
|
TCTCTCTC others(19): Show |
T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1026-1195_1026-117 others(30): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625504 | |||||
| chr7:77625506
|
TCTCTCTC others(17): Show |
T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1193_1026-117 others(28): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625506 | |||||
| chr7:77625508
|
TCTCTCTC others(9): Show |
T | 2 | a0002c0002t0001g0032a0002c0002t0001g0033 | 2 | HG01169.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1026-1191_1026-117 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625508 | |||||
| chr7:77625510
|
T | A | 10 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(7): Show | 10 | HG00280.hp1 HG00323.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1026-1195T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625510 | ||||||
| chr7:77625510
|
TCTCTCTC others(7): Show |
T | 1 | a0002c0002t0001g0043 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1026-1189_1026-117 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625510 | |||||
| chr7:77625511
|
C | G | 1 | a0002c0002t0001g0309 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1026-1194C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625511 | ||||||
| chr7:77625512
|
TCTCTCTC others(5): Show |
T | 4 | a0001c0001t0001g0307a0001c0001t0001g0308a0002c0002t0001g0009others(1): Show | 4 | HG01891.hp1 HG02922.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1187_1026-117 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625512 | |||||
| chr7:77625516
|
TCTCTCTC others(7): Show |
T | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1026-1183_1026-117 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625516 | |||||
| chr7:77625518
|
T | A | 1 | a0003c0003t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1026-1187T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625518 | ||||||
| chr7:77625518
|
TCTCTCA | T | 3 | a0002c0002t0001g0060a0002c0002t0001g0064a0002c0002t0001g0126 | 3 | NA18987.hp1 NA18992.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1026-1171_1026-116 others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625518 | |||||
| chr7:77625520
|
T | A | 9 | a0001c0001t0001g0109a0001c0001t0001g0133a0001c0001t0001g0134others(6): Show | 9 | HG00280.hp2 HG01358.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-1185T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625520 | ||||||
| chr7:77625520
|
T | TCTCTCTC others(9): Show |
2 | a0001c0001t0001g0158a0003c0003t0002g0153 | 2 | HG00609.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1026-1182_1026-118 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625520 | |||||
| chr7:77625520
|
T | TCTCTCTC others(11): Show |
2 | a0001c0001t0001g0139a0003c0003t0002g0152 | 2 | HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1026-1182_1026-118 others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625520 | |||||
| chr7:77625520
|
T | TCTCTCTC others(15): Show |
2 | a0001c0001t0001g0138a0001c0001t0001g0140 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1026-1182_1026-118 others(26): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625520 | |||||
| chr7:77625520
|
T | TCTCTCTC others(17): Show |
1 | a0003c0003t0002g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1026-1182_1026-118 others(28): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625520 | |||||
| chr7:77625520
|
T | TCTCTCTC others(21): Show |
1 | a0001c0001t0001g0157 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1026-1182_1026-118 others(32): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625520 | |||||
| chr7:77625522
|
T | A | 21 | a0001c0001t0001g0019a0001c0001t0001g0233a0001c0001t0001g0236others(18): Show | 21 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1026-1183T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625522 | ||||||
| chr7:77625522
|
TCA | T | 3 | a0001c0001t0003g0176a0002c0002t0001g0034a0002c0002t0001g0059 | 3 | HG02293.hp2 HG03471.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1026-1181_1026-118 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625522 | |||||
| chr7:77625524
|
A | ACT | 53 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0027others(50): Show | 53 | HG00099.hp2 HG00438.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1026-1177_1026-117 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625524 | |||||
| chr7:77625524
|
A | T | 135 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0143others(132): Show | 135 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1026-1181A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625524 | ||||||
| chr7:77625526
|
T | A | 1 | a0002c0002t0001g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1026-1179T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625526 | ||||||
| chr7:77625530
|
A | G | 36 | a0001c0001t0001g0109a0001c0001t0001g0133a0001c0001t0001g0134others(33): Show | 36 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1026-1175A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625530 | ||||||
| chr7:77625530
|
A | T | 7 | a0001c0001t0001g0149a0002c0002t0001g0014a0002c0002t0001g0053others(4): Show | 7 | HG01081.hp1 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.1026-1175A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625530 | ||||||
| chr7:77625532
|
T | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1026-1173T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625532 | ||||||
| chr7:77625536
|
A | G | 5 | a0001c0001t0001g0305a0003c0003t0001g0020a0003c0003t0001g0169others(2): Show | 5 | HG00140.hp2 HG01109.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-1169A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625536 | ||||||
| chr7:77625540
|
G | T | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1026-1165G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625540 | ||||||
| chr7:77625542
|
G | A | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1026-1163G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625542 | ||||||
| chr7:77625548
|
T | A | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1026-1157T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625548 | ||||||
| chr7:77625550
|
T | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1155T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625550 | ||||||
| chr7:77625552
|
T | G | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1026-1153T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625552 | ||||||
| chr7:77625554
|
G | A | 36 | a0001c0001t0001g0109a0001c0001t0001g0133a0001c0001t0001g0134others(33): Show | 36 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1026-1151G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625554 | ||||||
| chr7:77625554
|
G | T | 1 | a0001c0001t0001g0241 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1026-1151G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625554 | ||||||
| chr7:77625554
|
GCT | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1140_1026-113 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625554 | |||||
| chr7:77625556
|
T | G | 1 | a0001c0001t0001g0241 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1026-1149T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625556 | ||||||
| chr7:77625558
|
T | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1147T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625558 | ||||||
| chr7:77625563
|
C | CT | 50 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0112others(47): Show | 50 | HG00438.hp2 HG00639.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1026-1141dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | |||||
| chr7:77625563
|
C | CTT | 88 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0116others(85): Show | 88 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | |||||
| chr7:77625563
|
C | CTTT | 36 | a0001c0001t0001g0006a0001c0001t0001g0143a0001c0001t0001g0145others(33): Show | 36 | HG00609.hp2 HG00673.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | |||||
| chr7:77625563
|
C | CTTTT | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0002c0002t0001g0033others(1): Show | 4 | HG01175.hp1 HG02055.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | |||||
| chr7:77625563
|
C | CTTTTT | 8 | a0001c0001t0001g0144a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01169.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(9): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | |||||
| chr7:77625563
|
C | CTTTTTTT | 4 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(11): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | |||||
| chr7:77625563
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0157a0001c0001t0001g0246 | 2 | HG01517.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | |||||
| chr7:77625563
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0133a0001c0001t0001g0159 | 2 | HG01358.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | |||||
| chr7:77625563
|
C | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0003c0003t0001g0178 | 3 | HG00280.hp2 HG02055.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1026-1142C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625563 | ||||||
| chr7:77625563
|
CTCTTTTT | C | 10 | a0001c0001t0001g0105a0001c0001t0001g0129a0001c0001t0001g0130others(7): Show | 10 | HG00280.hp1 HG00323.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1026-1140_1026-113 others(11): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | |||||
| chr7:77625563
|
CTCTTTTT others(3): Show |
C | 1 | a0002c0002t0001g0040 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1026-1140_1026-113 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | |||||
| chr7:77625563
|
CTCTTTTT others(4): Show |
C | 2 | a0002c0002t0001g0071a0002c0002t0001g0078 | 2 | HG02004.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1026-1140_1026-113 others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | |||||
| chr7:77625563
|
CTCTTTTT others(5): Show |
C | 5 | a0001c0001t0001g0109a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02258.hp2 NA18970.hp2 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-1140_1026-112 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | |||||
| chr7:77625563
|
CTCTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1026-1140_1026-112 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | |||||
| chr7:77625565
|
C | CT | 10 | a0001c0001t0001g0277a0003c0003t0001g0001a0003c0003t0001g0184others(7): Show | 10 | HG00735.hp2 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1026-1117dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625565 | |||||
| chr7:77625565
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0158 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1026-1126_1026-111 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625565 | |||||
| chr7:77625565
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1026-1127_1026-111 others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625565 | |||||
| chr7:77625565
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1026-1128_1026-111 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625565 | |||||
| chr7:77625565
|
C | T | 216 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1026-1140C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625565 | ||||||
| chr7:77625594
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1026-1111C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625594 | ||||||
| chr7:77625640
|
A | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026-1065A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625640 | ||||||
| chr7:77626060
|
G | A | 2 | a0002c0002t0001g0061a0002c0002t0001g0077 | 2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1026-645G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626060 | ||||||
| chr7:77626228
|
A | G | 5 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-477A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626228 | ||||||
| chr7:77626238
|
A | T | 98 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0009others(95): Show | 98 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1026-467A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626238 | ||||||
| chr7:77626313
|
T | C | 1 | a0002c0002t0001g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1026-392T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626313 | ||||||
| chr7:77626362
|
G | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0257 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1026-343G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626362 | ||||||
| chr7:77626489
|
G | A | 1 | a0002c0002t0001g0036 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1026-216G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626489 | ||||||
| chr7:77626505
|
C | A | 255 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(252): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1026-200C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626505 | ||||||
| chr7:77626547
|
C | A | 72 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(69): Show | 72 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1026-158C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626547 | ||||||
| chr7:77626624
|
T | C | 74 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(71): Show | 74 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1026-81T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626624 | ||||||
| chr7:77627859
|
A | G | 1 | a0002c0002t0001g0123 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1996+184A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77627859 | ||||||
| chr7:77627923
|
TTTTTCTT others(5): Show |
T | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1996+251_1996+262d others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 77627923 | |||||
| chr7:77627975
|
C | G | 4 | a0002c0002t0001g0008a0002c0002t0001g0010a0002c0002t0001g0011others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1996+300C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77627975 | ||||||
| chr7:77627977
|
G | T | 1 | a0001c0001t0001g0116 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1996+302G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77627977 | ||||||
| chr7:77627994
|
TAA | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1996+320_1996+321d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77627994 | ||||||
| chr7:77627998
|
T | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1996+323T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77627998 | ||||||
| chr7:77628338
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1996+663A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77628338 | ||||||
| chr7:77628560
|
A | AT | 117 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0291others(114): Show | 117 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1996+900dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 77628560 | |||||
| chr7:77628560
|
A | ATT | 6 | a0002c0002t0001g0009a0002c0002t0001g0013a0002c0002t0001g0016others(3): Show | 6 | HG02004.hp1 NA18953.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1996+899_1996+900d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 77628560 | |||||
| chr7:77628582
|
T | C | 1 | a0003c0003t0001g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1996+907T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77628582 | ||||||
| chr7:77628650
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1996+975G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77628650 | ||||||
| chr7:77628682
|
C | T | 78 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(75): Show | 78 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.1996+1007C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77628682 | ||||||
| chr7:77628798
|
A | G | 1 | a0002c0002t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1996+1123A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77628798 | ||||||
| chr7:77629011
|
G | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1996+1336G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629011 | ||||||
| chr7:77629030
|
A | C | 5 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1996+1355A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629030 | ||||||
| chr7:77629240
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1996+1565C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629240 | ||||||
| chr7:77629243
|
C | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1996+1568C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629243 | ||||||
| chr7:77629500
|
T | C | 1 | a0002c0002t0001g0222 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1996+1825T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629500 | ||||||
| chr7:77629564
|
T | A | 12 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0254others(9): Show | 12 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.1996+1889T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629564 | ||||||
| chr7:77629696
|
T | C | 255 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(252): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1996+2021T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629696 | ||||||
| chr7:77629714
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1996+2039G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629714 | ||||||
| chr7:77629758
|
A | T | 1 | a0002c0002t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1996+2083A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629758 | ||||||
| chr7:77629798
|
G | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1996+2123G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629798 | ||||||
| chr7:77629939
|
C | CA | 82 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0019others(79): Show | 82 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1996+2283dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 77629939 | |||||
| chr7:77629939
|
CA | C | 22 | a0002c0002t0001g0004a0002c0002t0001g0025a0002c0002t0001g0036others(19): Show | 22 | HG00140.hp2 HG01099.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1996+2283delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 77629939 | |||||
| chr7:77629966
|
A | C | 242 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(239): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1996+2291A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629966 | ||||||
| chr7:77630202
|
C | T | 2 | a0002c0002t0001g0086a0002c0002t0001g0229 | 2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1997-2146C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77630202 | ||||||
| chr7:77630252
|
A | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1997-2096A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77630252 | ||||||
| chr7:77630518
|
C | G | 248 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1997-1830C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77630518 | ||||||
| chr7:77631101
|
A | G | 5 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1997-1247A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631101 | ||||||
| chr7:77631152
|
A | G | 5 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1997-1196A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631152 | ||||||
| chr7:77631285
|
A | G | 2 | a0002c0002t0001g0222a0002c0002t0001g0247 | 2 | HG03831.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1997-1063A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631285 | ||||||
| chr7:77631331
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1997-1017A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631331 | ||||||
| chr7:77631584
|
A | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1997-764A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631584 | ||||||
| chr7:77631639
|
C | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1997-709C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631639 | ||||||
| chr7:77631767
|
T | A | 4 | a0002c0002t0001g0008a0002c0002t0001g0010a0002c0002t0001g0011others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1997-581T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631767 | ||||||
| chr7:77631824
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1997-524A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631824 | ||||||
| chr7:77631825
|
T | C | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1997-523T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631825 | ||||||
| chr7:77631980
|
T | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1997-368T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631980 | ||||||
| chr7:77632033
|
T | A | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1997-315T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77632033 | ||||||
| chr7:77632082
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1997-266G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77632082 | ||||||
| chr7:77632282
|
A | G | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1997-66A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77632282 | ||||||
| chr7:77632301
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1997-47T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77632301 | ||||||
| chr7:77632331
|
T | G | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1997-17T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77632331 | ||||||
| chr7:77632503
|
T | G | 117 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0003g0176others(114): Show | 117 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.2074+78T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632503 | ||||||
| chr7:77632745
|
T | C | 72 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(69): Show | 72 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.2074+320T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632745 | ||||||
| chr7:77632746
|
C | T | 72 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(69): Show | 72 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.2074+321C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632746 | ||||||
| chr7:77632762
|
G | A | 3 | a0002c0002t0001g0021a0002c0002t0001g0022a0002c0002t0001g0023 | 3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2074+337G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632762 | ||||||
| chr7:77632913
|
C | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | NA18998.hp1 NA19066.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2074+488C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632913 | ||||||
| chr7:77632936
|
G | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2074+511G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632936 | ||||||
| chr7:77632951
|
G | A | 1 | a0002c0002t0001g0025 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2074+526G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632951 | ||||||
| chr7:77632965
|
A | G | 35 | a0001c0001t0001g0109a0001c0001t0001g0133a0001c0001t0001g0134others(32): Show | 35 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2074+540A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632965 | ||||||
| chr7:77633100
|
G | A | 1 | a0003c0003t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2074+675G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633100 | ||||||
| chr7:77633192
|
C | T | 2 | a0002c0002t0001g0056a0002c0002t0001g0123 | 2 | HG02135.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2074+767C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633192 | ||||||
| chr7:77633270
|
T | TA | 163 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0127others(160): Show | 163 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.2074+855dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 77633270 | |||||
| chr7:77633363
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2074+938A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633363 | ||||||
| chr7:77633375
|
C | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2074+950C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633375 | ||||||
| chr7:77633534
|
C | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2074+1109C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633534 | ||||||
| chr7:77633658
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2074+1233T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633658 | ||||||
| chr7:77633793
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2074+1368C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633793 | ||||||
| chr7:77633820
|
T | A | 242 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(239): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.2074+1395T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633820 | ||||||
| chr7:77633876
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2074+1451G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633876 | ||||||
| chr7:77633979
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2074+1554C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633979 | ||||||
| chr7:77634180
|
C | CAG | 255 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(252): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.2075-1601_2075-160 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 77634180 | |||||
| chr7:77634205
|
A | G | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2075-1577A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634205 | ||||||
| chr7:77634249
|
T | C | 4 | a0002c0002t0001g0008a0002c0002t0001g0010a0002c0002t0001g0011others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2075-1533T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634249 | ||||||
| chr7:77634369
|
T | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2075-1413T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634369 | ||||||
| chr7:77634409
|
T | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2075-1373T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634409 | ||||||
| chr7:77634457
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2075-1325T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634457 | ||||||
| chr7:77634472
|
T | C | 255 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(252): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.2075-1310T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634472 | ||||||
| chr7:77634499
|
G | A | 1 | a0002c0002t0001g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2075-1283G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634499 | ||||||
| chr7:77634542
|
C | T | 72 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(69): Show | 72 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.2075-1240C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634542 | ||||||
| chr7:77634636
|
G | A | 33 | a0001c0001t0001g0109a0001c0001t0001g0133a0001c0001t0001g0134others(30): Show | 33 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.2075-1146G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634636 | ||||||
| chr7:77634772
|
G | T | 1 | a0001c0001t0001g0249 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2075-1010G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634772 | ||||||
| chr7:77634855
|
G | A | 1 | a0003c0003t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2075-927G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634855 | ||||||
| chr7:77634976
|
G | C | 1 | a0002c0002t0001g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2075-806G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634976 | ||||||
| chr7:77635188
|
A | T | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2075-594A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77635188 | ||||||
| chr7:77635189
|
C | T | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2075-593C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77635189 | ||||||
| chr7:77635341
|
A | G | 2 | a0002c0002t0001g0029a0002c0002t0001g0030 | 2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2075-441A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77635341 | ||||||
| chr7:77635394
|
A | C | 1 | a0002c0002t0001g0059 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2075-388A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77635394 | ||||||
| chr7:77635536
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2075-246T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77635536 | ||||||
| chr7:77635585
|
CAG | C | 3 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0111 | 3 | HG02559.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2075-195_2075-194d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 77635585 | |||||
| chr7:77635615
|
AT | A | 15 | a0001c0001t0001g0105a0001c0001t0001g0127a0001c0001t0001g0129others(12): Show | 15 | HG00280.hp1 HG00323.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.2075-155delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 77635615 | |||||
| chr7:77635660
|
A | G | 1 | a0002c0002t0001g0028 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2075-122A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77635660 | ||||||
| chr7:77635889
|
T | A | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2142+40T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77635889 | ||||||
| chr7:77636164
|
A | C | 3 | a0002c0002t0001g0021a0002c0002t0001g0022a0002c0002t0001g0023 | 3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2142+315A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636164 | ||||||
| chr7:77636202
|
A | G | 2 | a0002c0002t0001g0004a0002c0002t0001g0082 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2142+353A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636202 | ||||||
| chr7:77636270
|
G | A | 8 | a0003c0003t0001g0196a0003c0003t0001g0197a0003c0003t0001g0198others(5): Show | 8 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.2142+421G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636270 | ||||||
| chr7:77636341
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2142+492G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636341 | ||||||
| chr7:77636355
|
A | G | 8 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2142+506A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636355 | ||||||
| chr7:77636390
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2142+541T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636390 | ||||||
| chr7:77636391
|
G | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2142+542G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636391 | ||||||
| chr7:77636408
|
C | G | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0003g0176 | 3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2142+559C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636408 | ||||||
| chr7:77636436
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2143-582G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636436 | ||||||
| chr7:77636441
|
G | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2143-577G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636441 | ||||||
| chr7:77636507
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2143-511C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636507 | ||||||
| chr7:77636636
|
T | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2143-382T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636636 | ||||||
| chr7:77636680
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2143-338A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636680 | ||||||
| chr7:77636761
|
GCAAAA | G | 3 | a0002c0002t0001g0021a0002c0002t0001g0022a0002c0002t0001g0023 | 3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2143-254_2143-250d others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 77636761 | |||||
| chr7:77636816
|
C | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2143-202C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636816 | ||||||
| chr7:77636870
|
A | G | 1 | a0003c0003t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2143-148A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636870 | ||||||
| chr7:77636907
|
A | G | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2143-111A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636907 | ||||||
| chr7:77636996
|
G | T | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2143-22G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636996 | ||||||
| chr7:77637252
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2173+204A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637252 | ||||||
| chr7:77637310
|
T | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2173+262T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637310 | ||||||
| chr7:77637422
|
AG | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173+375delG | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637422 | ||||||
| chr7:77637541
|
T | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173+493T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637541 | ||||||
| chr7:77637571
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0169a0003c0003t0001g0170others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173+523A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637571 | ||||||
| chr7:77637814
|
G | A | 3 | a0003c0003t0002g0151a0003c0003t0002g0152a0003c0003t0002g0153 | 3 | HG01243.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2173+766G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637814 | ||||||
| chr7:77637852
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2174-772C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637852 | ||||||
| chr7:77637857
|
C | CA | 30 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0136others(27): Show | 30 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.2174-748dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 77637857 | |||||
| chr7:77637857
|
C | CAA | 17 | a0001c0001t0001g0105a0001c0001t0001g0127a0001c0001t0001g0130others(14): Show | 17 | HG00280.hp1 HG00323.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.2174-749_2174-748d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 77637857 | |||||
| chr7:77637857
|
C | CAAA | 103 | a0001c0001t0001g0109a0001c0001t0001g0129a0001c0001t0001g0131others(100): Show | 103 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.2174-750_2174-748d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 77637857 | |||||
| chr7:77637857
|
C | CAAAA | 36 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0143others(33): Show | 36 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.2174-751_2174-748d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 77637857 | |||||
| chr7:77637941
|
TA | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0130others(15): Show | 18 | HG00280.hp1 HG00323.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.2174-679delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 77637941 | |||||
| chr7:77637943
|
A | ATTT | 4 | a0002c0002t0001g0018a0002c0002t0001g0103a0002c0002t0001g0104others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2174-681_2174-680i others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637943 | ||||||
| chr7:77637944
|
A | AT | 51 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0146others(48): Show | 51 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.2174-680_2174-679i others(3): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | ||||||
| chr7:77637944
|
A | ATT | 46 | a0001c0001t0001g0133a0001c0001t0001g0143a0001c0001t0001g0144others(43): Show | 46 | HG00408.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.2174-680_2174-679i others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | ||||||
| chr7:77637944
|
A | ATTT | 28 | a0001c0001t0001g0109a0001c0001t0001g0141a0001c0001t0001g0142others(25): Show | 28 | HG00423.hp1 HG00609.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2174-680_2174-679i others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | ||||||
| chr7:77637944
|
A | ATTTTT | 3 | a0002c0002t0001g0004a0002c0002t0001g0076a0003c0003t0001g0110 | 3 | HG02976.hp2 HG03579.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.2174-680_2174-679i others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | ||||||
| chr7:77637944
|
A | T | 5 | a0002c0002t0001g0018a0002c0002t0001g0103a0002c0002t0001g0104others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.2174-680A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | ||||||
| chr7:77637944
|
AAT | A | 19 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(16): Show | 19 | HG00140.hp2 HG00438.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.2174-679_2174-678d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | ||||||
| chr7:77637944
|
AATT | A | 51 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0027others(48): Show | 51 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.2174-679_2174-677d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | ||||||
| chr7:77637944
|
AATTT | A | 3 | a0001c0001t0001g0259a0003c0003t0001g0242a0004c0004t0001g0287 | 3 | HG01993.hp2 HG02451.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.2174-679_2174-676d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | ||||||
| chr7:77637944
|
AATTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0156 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2174-679_2174-670d others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | ||||||
| chr7:77637944
|
AATTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2174-679_2174-668d others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | ||||||
| chr7:77637945
|
A | AT | 27 | a0001c0001t0001g0137a0003c0003t0001g0005a0003c0003t0001g0181others(24): Show | 27 | HG00408.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.2174-650dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 77637945 | |||||
| chr7:77637945
|
A | T | 162 | a0001c0001t0001g0019a0001c0001t0001g0105a0001c0001t0001g0109others(159): Show | 162 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.2174-679A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637945 | ||||||
| chr7:77638139
|
T | C | 1 | a0002c0002t0001g0078 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2174-485T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77638139 | ||||||
| chr7:77638196
|
G | T | 1 | a0001c0001t0001g0241 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2174-428G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77638196 | ||||||
| chr7:77638815
|
C | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0281 | 3 | HG01255.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2281+84C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 17/17 | chr7 | 77638815 | ||||||
| chr7:77638885
|
C | A | 67 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(64): Show | 67 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.2281+154C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 17/17 | chr7 | 77638885 | ||||||
| chr7:77639121
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02132.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.2282-98T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 17/17 | chr7 | 77639121 |