Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 80380 |
|---|---|
| ensemblid | ENSG00000197646.8 |
| hgncid | 18731 |
| symbol | PDCD1LG2 |
| name | programmed cell death 1 ligand 2 |
| refseq_nuc | NM_025239.4 |
| refseq_prot | NP_079515.2 |
| ensembl_nuc | ENST00000397747.5 |
| ensembl_prot | ENSP00000380855.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 5510531 |
| end | 5571282 |
| strand | + |
| ver | v1.2 |
| region | chr9:5510531-5571282 |
| region5000 | chr9:5505531-5576282 |
| regionname0 | PDCD1LG2_chr9_5510531_5571282 |
| regionname5000 | PDCD1LG2_chr9_5505531_5576282 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 273 | 286 | 28 | 56 | 160 | 10 | 31 | 123 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002 | 0/0 | 273 | 108 | 57 | 10 | 30 | 0 | 11 | 22 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0003 | 0/0 | 273 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0004 | 0/0 | 273 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0005 | 0/0 | 273 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0006 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0007 | 1/0 | 273 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0008 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0009 | 0/0 | 273 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0010 | 0/0 | 273 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 822 | 286 | 28 | 56 | 160 | 10 | 31 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| c0002 | 0/0 | 822 | 104 | 53 | 10 | 30 | 0 | 11 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| c0003 | 0/0 | 822 | 5 | 5 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| c0004 | 0/0 | 822 | 4 | 4 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| c0005 | 0/0 | 822 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| c0006 | 0/0 | 822 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| c0007 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| c0008 | 0/0 | 822 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| c0009 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| c0010 | 1/0 | 822 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| c0011 | 0/0 | 822 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1611 | 215 | 46 | 30 | 106 | 4 | 27 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0002 | 0/0 | 1611 | 92 | 9 | 27 | 38 | 4 | 14 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0003 | 0/0 | 1611 | 33 | 6 | 2 | 21 | 1 | 3 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0004 | 0/0 | 1611 | 18 | 0 | 2 | 16 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0005 | 0/0 | 1611 | 6 | 4 | 2 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0006 | 0/0 | 1611 | 6 | 6 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0007 | 0/0 | 1611 | 6 | 6 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0008 | 0/0 | 1611 | 5 | 0 | 0 | 5 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0009 | 0/0 | 1611 | 4 | 4 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0010 | 0/0 | 1611 | 4 | 0 | 0 | 4 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0011 | 0/0 | 1611 | 3 | 2 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0012 | 0/0 | 1611 | 2 | 1 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0013 | 0/0 | 1611 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0014 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0015 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0016 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0017 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0018 | 0/0 | 1611 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0019 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0020 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0021 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0022 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| t0023 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 822 | 286 | 28 | 56 | 160 | 10 | 31 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002 | 0/0 | 822 | 104 | 53 | 10 | 30 | 0 | 11 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0004 | 0/0 | 822 | 4 | 4 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0003c0003 | 0/0 | 822 | 5 | 5 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0004c0006 | 0/0 | 822 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0005c0011 | 0/0 | 822 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0006c0007 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0007c0010 | 1/0 | 822 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0008c0009 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0009c0008 | 0/0 | 822 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0010c0005 | 0/0 | 822 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2432 | 162 | 23 | 28 | 86 | 4 | 20 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0001c0001t0002 | 0/0 | 2432 | 69 | 1 | 25 | 31 | 4 | 8 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0001c0001t0003 | 0/0 | 2432 | 23 | 2 | 1 | 16 | 1 | 3 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0001c0001t0004 | 0/0 | 2432 | 18 | 0 | 2 | 16 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0001c0001t0007 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0001c0001t0008 | 0/0 | 2432 | 5 | 0 | 0 | 5 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0001c0001t0010 | 0/0 | 2432 | 4 | 0 | 0 | 4 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0001c0001t0012 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0001c0001t0016 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0001c0001t0017 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0001c0001t0018 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0001 | 0/0 | 2432 | 48 | 22 | 2 | 19 | 0 | 5 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0002 | 0/0 | 2432 | 23 | 8 | 2 | 7 | 0 | 6 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0003 | 0/0 | 2432 | 6 | 1 | 1 | 4 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0005 | 0/0 | 2432 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0006 | 0/0 | 2432 | 6 | 6 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0007 | 0/0 | 2432 | 4 | 4 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0009 | 0/0 | 2432 | 3 | 3 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0011 | 0/0 | 2432 | 3 | 2 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0012 | 0/0 | 2432 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0013 | 0/0 | 2432 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0014 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0015 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0020 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0021 | 0/0 | 2432 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0022 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0002t0023 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0002c0004t0005 | 0/0 | 2432 | 4 | 4 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0003c0003t0001 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0003c0003t0003 | 0/0 | 2432 | 3 | 3 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0003c0003t0009 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0004c0006t0019 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0005c0011t0001 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0006c0007t0003 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0007c0010t0001 | 1/0 | 2432 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0008c0009t0001 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0009c0008t0001 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| a0010c0005t0007 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | copy fasta | chr9 | 5505531 | 5576282 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0008g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0008g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0008g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0008g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0008g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0010g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0010g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0010g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0010g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0012g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0016g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0017g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0018g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0003g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0003g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0003g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0005g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0007g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0009g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0009g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0009g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0011g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0011g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0012g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0013g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0014g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0015g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0020g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0021g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0022g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0023g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0004t0005g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0004t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0004t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0003c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0003c0003t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0003c0003t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0003c0003t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0003c0003t0009g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0004c0006t0019g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0005c0011t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0006c0007t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0007c0010t0001g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0008c0009t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0009c0008t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0010c0005t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0018 | g0321 | EUR | GBR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0351 | EUR | GBR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | FIN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00408 | hp2 | a0001 | c0001 | t0010 | g0085 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00423 | hp1 | a0006 | c0007 | t0003 | g0365 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0367 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0361 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00735 | hp1 | a0002 | c0002 | t0003 | g0384 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00741 | hp2 | a0002 | c0002 | t0005 | g0160 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0328 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0055 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01109 | hp1 | a0002 | c0002 | t0012 | g0330 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0326 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0327 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01192 | hp1 | a0002 | c0002 | t0011 | g0107 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01243 | hp1 | a0002 | c0002 | t0005 | g0234 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0269 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0305 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0342 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0143 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0282 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0319 | EUR | IBS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0316 | EUR | IBS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01884 | hp2 | a0002 | c0002 | t0009 | g0332 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01978 | hp1 | a0002 | c0002 | t0021 | g0374 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0078 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0371 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02027 | hp2 | a0001 | c0001 | t0010 | g0039 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0270 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02055 | hp2 | a0002 | c0002 | t0006 | g0024 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02129 | hp2 | a0001 | c0001 | t0008 | g0364 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0353 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0349 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0379 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0329 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CDX | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02155 | hp2 | a0001 | c0001 | t0008 | g0368 | EAS | CDX | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | CDX | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CDX | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02257 | hp2 | a0002 | c0004 | t0005 | g0229 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0131 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02523 | hp1 | a0002 | c0002 | t0003 | g0373 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02572 | hp1 | a0002 | c0004 | t0005 | g0231 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0097 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02615 | hp1 | a0002 | c0002 | t0014 | g0339 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02615 | hp2 | a0002 | c0002 | t0006 | g0105 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02622 | hp2 | a0002 | c0002 | t0006 | g0071 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02630 | hp1 | a0002 | c0002 | t0006 | g0068 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0138 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0251 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02647 | hp2 | a0003 | c0003 | t0003 | g0248 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0360 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02717 | hp1 | a0004 | c0006 | t0019 | g0104 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02717 | hp2 | a0001 | c0001 | t0012 | g0247 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0266 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0090 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02809 | hp1 | a0002 | c0002 | t0007 | g0001 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02809 | hp2 | a0002 | c0002 | t0006 | g0072 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0230 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0341 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0252 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02922 | hp2 | a0010 | c0005 | t0007 | g0117 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0331 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02970 | hp1 | a0003 | c0003 | t0003 | g0250 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02976 | hp1 | a0002 | c0004 | t0005 | g0006 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02976 | hp2 | a0002 | c0002 | t0006 | g0232 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0163 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03041 | hp1 | a0002 | c0002 | t0020 | g0110 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0228 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0267 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0119 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03139 | hp1 | a0002 | c0002 | t0011 | g0043 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03139 | hp2 | a0003 | c0003 | t0009 | g0324 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03195 | hp1 | a0002 | c0002 | t0015 | g0145 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03209 | hp1 | a0002 | c0004 | t0005 | g0006 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03209 | hp2 | a0002 | c0002 | t0009 | g0335 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0074 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03453 | hp1 | a0003 | c0003 | t0001 | g0029 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0381 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0347 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0318 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0317 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0375 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0348 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0333 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0350 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0380 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0242 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0187 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03927 | hp2 | a0009 | c0008 | t0001 | g0245 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04115 | hp2 | a0005 | c0011 | t0001 | g0190 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0205 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18522 | hp1 | a0002 | c0002 | t0007 | g0116 | AFR | YRI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18522 | hp2 | a0002 | c0002 | t0013 | g0015 | AFR | YRI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | CHB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | CHB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CHB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18906 | hp1 | a0002 | c0002 | t0007 | g0001 | AFR | YRI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0271 | AFR | YRI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18952 | hp2 | a0002 | c0002 | t0003 | g0340 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0359 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18959 | hp2 | a0001 | c0001 | t0008 | g0352 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0362 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0372 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18969 | hp1 | a0001 | c0001 | t0010 | g0150 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18977 | hp1 | a0001 | c0001 | t0016 | g0222 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18981 | hp1 | a0002 | c0002 | t0003 | g0377 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0366 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18992 | hp1 | a0001 | c0001 | t0008 | g0378 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18992 | hp2 | a0002 | c0002 | t0003 | g0358 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18994 | hp2 | a0001 | c0001 | t0008 | g0370 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0383 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0382 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19004 | hp2 | a0001 | c0001 | t0010 | g0246 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0369 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19030 | hp1 | a0003 | c0003 | t0003 | g0249 | AFR | LWK | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | LWK | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0108 | AFR | LWK | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0273 | AFR | LWK | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19057 | hp2 | a0001 | c0001 | t0017 | g0309 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19077 | hp1 | a0008 | c0009 | t0001 | g0274 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0363 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0376 | AFR | YRI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | YRI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ASW | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20129 | hp2 | a0002 | c0002 | t0007 | g0001 | AFR | ASW | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0276 | EUR | TSI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0106 | EUR | TSI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | GIH | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0320 | SAS | GIH | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0272 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02559 | hp2 | a0002 | c0002 | t0011 | g0086 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03471 | hp1 | a0002 | c0002 | t0009 | g0334 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | USA | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG06807 | hp2 | a0002 | c0002 | t0013 | g0015 | AFR | USA | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0323 | AFR | USA | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20300 | hp2 | a0002 | c0002 | t0023 | g0118 | AFR | USA | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA21309 | hp2 | a0002 | c0002 | t0022 | g0355 | AFR | LWK | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0188 | REF | REF | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| homoSapiens_grch38 | hp1 | a0007 | c0010 | t0001 | g0149 | REF | REF | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:5534862
|
G | C | 2 | a0003a0010 | 6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
missense_variant | MODERATE | c.173G>C | p.Ser58Thr | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/7 | 460/2432 | 173/822 | 58/273 | chr9 | 5534862 | ||
| chr9:5549451
|
G | A | 1 | a0010 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.478G>A | p.Val160Ile | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/7 | 765/2432 | 478/822 | 160/273 | chr9 | 5549451 | ||
| chr9:5549507
|
T | A | 1 | a0004 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.534T>A | p.Ser178Arg | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/7 | 821/2432 | 534/822 | 178/273 | chr9 | 5549507 | ||
| chr9:5549514
|
C | T | 1 | a0005 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.541C>T | p.Arg181Cys | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/7 | 828/2432 | 541/822 | 181/273 | chr9 | 5549514 | ||
| chr9:5549568
|
G | A | 1 | a0006 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.595G>A | p.Val199Met | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/7 | 882/2432 | 595/822 | 199/273 | chr9 | 5549568 | ||
| chr9:5549574
|
G | A | 1 | a0009 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.601G>A | p.Glu201Lys | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/7 | 888/2432 | 601/822 | 201/273 | chr9 | 5549574 | ||
| chr9:5557672
|
T | C | 9 | a0001a0002a0003others(6): Show | 405 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(402): Show |
missense_variant | MODERATE | c.686T>C | p.Phe229Ser | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/7 | 973/2432 | 686/822 | 229/273 | chr9 | 5557672 | ||
| chr9:5557708
|
T | C | 5 | a0002a0003a0004others(2): Show | 116 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(113): Show |
missense_variant | MODERATE | c.722T>C | p.Ile241Thr | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/7 | 1009/2432 | 722/822 | 241/273 | chr9 | 5557708 | ||
| chr9:5557716
|
A | G | 1 | a0008 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.730A>G | p.Arg244Gly | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/7 | 1017/2432 | 730/822 | 244/273 | chr9 | 5557716 | ||
| chr9:5557717
|
G | A | 1 | a0008 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.731G>A | p.Arg244Lys | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/7 | 1018/2432 | 731/822 | 244/273 | chr9 | 5557717 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:5549540
|
C | T | 1 | a0002c0004 | 4 | HG02257.hp2 HG02572.hp1 HG02976.hp1 others(1): Show |
synonymous_variant | LOW | c.567C>T | p.Asn189Asn | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/7 | 854/2432 | 567/822 | 189/273 | chr9 | 5549540 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:5510544
|
G | A | 1 | a0002c0002t0014 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-274G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/7 | 12003 | chr9 | 5510544 | |||||
| chr9:5510601
|
A | G | 7 | a0001c0001t0007a0001c0001t0012a0002c0002t0007others(4): Show | 11 | HG01109.hp1 HG02717.hp2 HG02809.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-217A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/7 | 11946 | chr9 | 5510601 | |||||
| chr9:5510631
|
A | G | 7 | a0001c0001t0003a0001c0001t0008a0002c0002t0003others(4): Show | 40 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-187A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/7 | 11916 | chr9 | 5510631 | |||||
| chr9:5510644
|
A | G | 11 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(8): Show | 109 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(106): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-174A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/7 | chr9 | 5510644 | ||||||
| chr9:5510679
|
T | C | 2 | a0001c0001t0012a0002c0002t0012 | 2 | HG01109.hp1 HG02717.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-139T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/7 | chr9 | 5510679 | ||||||
| chr9:5510742
|
A | G | 4 | a0002c0002t0009a0002c0002t0011a0002c0002t0020others(1): Show | 8 | HG01192.hp1 HG01884.hp2 HG02559.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-76A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/7 | 11805 | chr9 | 5510742 | |||||
| chr9:5570463
|
T | C | 2 | a0002c0002t0015a0002c0002t0021 | 2 | HG01978.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*504T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 504 | chr9 | 5570463 | |||||
| chr9:5570584
|
T | C | 1 | a0001c0001t0016 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*625T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 625 | chr9 | 5570584 | |||||
| chr9:5570777
|
A | C | 3 | a0001c0001t0004a0001c0001t0008a0001c0001t0010 | 27 | HG00408.hp2 HG01261.hp1 HG01496.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*818A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 818 | chr9 | 5570777 | |||||
| chr9:5570824
|
C | T | 4 | a0002c0002t0006a0002c0002t0020a0002c0002t0022others(1): Show | 9 | HG02055.hp2 HG02615.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*865C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 865 | chr9 | 5570824 | |||||
| chr9:5570887
|
C | T | 1 | a0002c0002t0013 | 2 | HG06807.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*928C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 928 | chr9 | 5570887 | |||||
| chr9:5570940
|
A | C | 1 | a0001c0001t0017 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*981A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 981 | chr9 | 5570940 | |||||
| chr9:5570944
|
C | T | 3 | a0002c0002t0005a0002c0002t0023a0002c0004t0005 | 7 | HG00741.hp2 HG01243.hp1 HG02257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*985C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 985 | chr9 | 5570944 | |||||
| chr9:5571105
|
A | G | 1 | a0001c0001t0018 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1146A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 1146 | chr9 | 5571105 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:5510837
|
T | TG | 143 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0253others(140): Show | 148 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.-15+34_-15+35insG | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5510837 | ||||||
| chr9:5510838
|
A | T | 143 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0253others(140): Show | 148 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.-15+35A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5510838 | ||||||
| chr9:5510948
|
C | T | 1 | a0002c0002t0003g0384 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-15+145C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5510948 | ||||||
| chr9:5511111
|
G | A | 1 | a0001c0001t0012g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-15+308G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511111 | ||||||
| chr9:5511143
|
T | C | 3 | a0003c0003t0003g0248a0003c0003t0003g0249a0003c0003t0003g0250 | 3 | HG02647.hp2 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-15+340T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511143 | ||||||
| chr9:5511190
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0002t0001g0251others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+387T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511190 | ||||||
| chr9:5511203
|
C | G | 1 | a0001c0001t0010g0246 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-15+400C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511203 | ||||||
| chr9:5511373
|
G | A | 3 | a0003c0003t0003g0248a0003c0003t0003g0249a0003c0003t0003g0250 | 3 | HG02647.hp2 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-15+570G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511373 | ||||||
| chr9:5511625
|
A | G | 2 | a0001c0001t0001g0382a0002c0002t0001g0383 | 2 | NA18998.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-15+822A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511625 | ||||||
| chr9:5511646
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-15+843G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511646 | ||||||
| chr9:5511723
|
G | A | 1 | a0001c0001t0003g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-15+920G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511723 | ||||||
| chr9:5511824
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0002t0001g0251others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+1021T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511824 | ||||||
| chr9:5511865
|
C | A | 1 | a0001c0001t0001g0258 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-15+1062C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511865 | ||||||
| chr9:5511921
|
C | T | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-15+1118C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511921 | ||||||
| chr9:5511940
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG00558.hp2 NA18945.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.-15+1137G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511940 | ||||||
| chr9:5511986
|
A | G | 2 | a0001c0001t0012g0247a0002c0002t0001g0381 | 2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+1183A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511986 | ||||||
| chr9:5512089
|
C | T | 1 | a0001c0001t0001g0380 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-15+1286C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512089 | ||||||
| chr9:5512129
|
C | A | 1 | a0002c0002t0006g0024 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-15+1326C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512129 | ||||||
| chr9:5512203
|
C | G | 5 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0002t0001g0251others(2): Show | 6 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+1400C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512203 | ||||||
| chr9:5512204
|
G | A | 1 | a0001c0001t0012g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-15+1401G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512204 | ||||||
| chr9:5512270
|
C | G | 35 | a0001c0001t0003g0020a0001c0001t0003g0257a0001c0001t0003g0349others(32): Show | 36 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-15+1467C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512270 | ||||||
| chr9:5512369
|
G | C | 1 | a0001c0001t0001g0025 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-15+1566G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512369 | ||||||
| chr9:5512459
|
T | C | 72 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0258others(69): Show | 75 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-15+1656T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512459 | ||||||
| chr9:5512484
|
G | A | 1 | a0002c0002t0002g0027 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-15+1681G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512484 | ||||||
| chr9:5512486
|
G | A | 105 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(102): Show | 109 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.-15+1683G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512486 | ||||||
| chr9:5512505
|
C | A | 2 | a0001c0001t0012g0247a0002c0002t0001g0381 | 2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+1702C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512505 | ||||||
| chr9:5512507
|
A | G | 6 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0002t0001g0251others(3): Show | 7 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+1704A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512507 | ||||||
| chr9:5512522
|
T | G | 148 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(145): Show | 154 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.-15+1719T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512522 | ||||||
| chr9:5512534
|
C | G | 1 | a0002c0002t0001g0348 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-15+1731C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512534 | ||||||
| chr9:5512655
|
A | G | 1 | a0009c0008t0001g0245 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-15+1852A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512655 | ||||||
| chr9:5512656
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-15+1853T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512656 | ||||||
| chr9:5512731
|
A | G | 1 | a0002c0002t0001g0323 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+1928A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512731 | ||||||
| chr9:5512786
|
C | A | 104 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(101): Show | 108 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.-15+1983C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512786 | ||||||
| chr9:5512818
|
C | T | 102 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(99): Show | 106 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.-15+2015C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512818 | ||||||
| chr9:5512849
|
G | C | 5 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0002t0001g0251others(2): Show | 6 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+2046G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512849 | ||||||
| chr9:5513057
|
C | T | 3 | a0002c0002t0001g0347a0003c0003t0003g0249a0003c0003t0003g0250 | 3 | HG02970.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-15+2254C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513057 | ||||||
| chr9:5513080
|
A | T | 2 | a0001c0001t0002g0112a0001c0001t0002g0113 | 2 | HG01928.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-15+2277A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513080 | ||||||
| chr9:5513290
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG00558.hp2 NA18945.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.-15+2487G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513290 | ||||||
| chr9:5513529
|
A | G | 5 | a0001c0001t0001g0343a0001c0001t0001g0344a0001c0001t0001g0345others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+2726A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513529 | ||||||
| chr9:5513545
|
T | C | 7 | a0001c0001t0007g0119a0001c0001t0012g0247a0002c0002t0001g0381others(4): Show | 9 | HG02717.hp2 HG02809.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+2742T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513545 | ||||||
| chr9:5513546
|
G | A | 2 | a0001c0001t0012g0247a0002c0002t0001g0381 | 2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+2743G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513546 | ||||||
| chr9:5513563
|
T | A | 1 | a0002c0002t0009g0332 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-15+2760T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513563 | ||||||
| chr9:5513578
|
T | C | 1 | a0002c0002t0001g0381 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-15+2775T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513578 | ||||||
| chr9:5513619
|
A | C | 1 | a0001c0001t0003g0379 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-15+2816A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513619 | ||||||
| chr9:5513671
|
G | T | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | NA18945.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.-15+2868G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513671 | ||||||
| chr9:5513897
|
T | C | 1 | a0002c0002t0002g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-15+3094T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513897 | ||||||
| chr9:5513988
|
T | C | 1 | a0001c0001t0001g0380 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-15+3185T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513988 | ||||||
| chr9:5513992
|
T | C | 2 | a0001c0001t0001g0120a0002c0002t0001g0333 | 2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-15+3189T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513992 | ||||||
| chr9:5514167
|
A | C | 1 | a0001c0001t0001g0258 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-15+3364A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514167 | ||||||
| chr9:5514199
|
G | A | 3 | a0001c0001t0002g0031a0001c0001t0002g0032a0002c0002t0002g0033 | 3 | NA18612.hp2 NA18964.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-15+3396G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514199 | ||||||
| chr9:5514331
|
T | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0002t0001g0251others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+3528T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514331 | ||||||
| chr9:5514351
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0002t0001g0251others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+3548T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514351 | ||||||
| chr9:5514372
|
A | C | 120 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(117): Show | 125 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.-15+3569A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514372 | ||||||
| chr9:5514375
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-15+3572G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514375 | ||||||
| chr9:5514575
|
T | A | 1 | a0001c0001t0001g0025 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-15+3772T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514575 | ||||||
| chr9:5514772
|
G | GA | 16 | a0001c0001t0001g0034a0001c0001t0001g0122a0001c0001t0001g0123others(13): Show | 16 | HG01106.hp2 HG01358.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+3991dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5514772 | |||||
| chr9:5514772
|
GA | G | 28 | a0001c0001t0001g0115a0001c0001t0001g0121a0001c0001t0001g0227others(25): Show | 29 | HG00597.hp2 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-15+3991delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5514772 | |||||
| chr9:5514772
|
GAAA | G | 35 | a0001c0001t0003g0020a0001c0001t0003g0257a0001c0001t0003g0350others(32): Show | 36 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-15+3989_-15+3991d others(5): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5514772 | |||||
| chr9:5514839
|
T | C | 261 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0034others(258): Show | 273 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.-15+4036T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514839 | ||||||
| chr9:5514841
|
G | A | 2 | a0001c0001t0004g0260a0002c0002t0001g0261 | 2 | NA18612.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-15+4038G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514841 | ||||||
| chr9:5514869
|
G | A | 1 | a0003c0003t0009g0324 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+4066G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514869 | ||||||
| chr9:5514882
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0002t0001g0251others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+4079T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514882 | ||||||
| chr9:5514919
|
T | C | 121 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(118): Show | 126 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-15+4116T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514919 | ||||||
| chr9:5515054
|
C | T | 1 | a0002c0002t0014g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-15+4251C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515054 | ||||||
| chr9:5515111
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-15+4308G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515111 | ||||||
| chr9:5515177
|
T | C | 1 | a0002c0002t0001g0347 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-15+4374T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515177 | ||||||
| chr9:5515207
|
A | C | 121 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(118): Show | 126 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-15+4404A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515207 | ||||||
| chr9:5515247
|
C | G | 1 | a0002c0002t0002g0109 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-15+4444C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515247 | ||||||
| chr9:5515251
|
A | G | 121 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(118): Show | 126 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-15+4448A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515251 | ||||||
| chr9:5515640
|
A | G | 1 | a0002c0002t0002g0341 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-15+4837A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515640 | ||||||
| chr9:5515710
|
G | T | 1 | a0001c0001t0001g0322 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-15+4907G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515710 | ||||||
| chr9:5515816
|
A | G | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-15+5013A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515816 | ||||||
| chr9:5515922
|
C | CA | 28 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0120others(25): Show | 32 | HG00438.hp2 HG00733.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-15+5146dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | |||||
| chr9:5515922
|
C | CAA | 68 | a0001c0001t0001g0034a0001c0001t0001g0067a0001c0001t0001g0069others(65): Show | 70 | HG00140.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-15+5145_-15+5146d others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | |||||
| chr9:5515922
|
C | CAAA | 42 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0049others(39): Show | 44 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.-15+5144_-15+5146d others(5): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | |||||
| chr9:5515922
|
C | CAAAA | 9 | a0001c0001t0001g0322a0001c0001t0002g0022a0001c0001t0002g0036others(6): Show | 10 | HG00544.hp1 HG01109.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+5143_-15+5146d others(6): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | |||||
| chr9:5515922
|
CA | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0223a0001c0001t0001g0224others(6): Show | 10 | HG02735.hp1 HG03225.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+5146delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | |||||
| chr9:5515922
|
CAA | C | 34 | a0001c0001t0001g0115a0001c0001t0001g0121a0001c0001t0001g0233others(31): Show | 35 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.-15+5145_-15+5146d others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | |||||
| chr9:5515922
|
CAAA | C | 55 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0258others(52): Show | 57 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-15+5144_-15+5146d others(5): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | |||||
| chr9:5515922
|
CAAAA | C | 5 | a0001c0001t0001g0225a0001c0001t0001g0314a0001c0001t0001g0315others(2): Show | 6 | HG01993.hp1 NA18939.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+5143_-15+5146d others(6): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | |||||
| chr9:5515922
|
CAAAAAAA | C | 35 | a0001c0001t0003g0020a0001c0001t0003g0257a0001c0001t0003g0349others(32): Show | 36 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-15+5140_-15+5146d others(9): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | |||||
| chr9:5515941
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-15+5138A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515941 | ||||||
| chr9:5515944
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-15+5141A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515944 | ||||||
| chr9:5515990
|
G | C | 154 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(151): Show | 160 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.-15+5187G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515990 | ||||||
| chr9:5516007
|
G | C | 15 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG02027.hp1 HG02055.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.-15+5204G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516007 | ||||||
| chr9:5516067
|
T | C | 120 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(117): Show | 125 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.-15+5264T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516067 | ||||||
| chr9:5516084
|
C | G | 1 | a0002c0002t0001g0348 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-15+5281C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516084 | ||||||
| chr9:5516145
|
G | A | 5 | a0002c0002t0002g0019a0002c0002t0002g0329a0002c0002t0002g0331others(2): Show | 6 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+5342G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516145 | ||||||
| chr9:5516176
|
C | T | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-15+5373C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516176 | ||||||
| chr9:5516182
|
G | C | 31 | a0001c0001t0003g0020a0001c0001t0003g0257a0001c0001t0003g0350others(28): Show | 32 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.-15+5379G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516182 | ||||||
| chr9:5516197
|
A | G | 155 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(152): Show | 161 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.-15+5394A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516197 | ||||||
| chr9:5516208
|
C | T | 1 | a0002c0002t0002g0064 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-15+5405C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516208 | ||||||
| chr9:5516265
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-15+5462C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516265 | ||||||
| chr9:5516268
|
G | A | 2 | a0001c0001t0003g0349a0002c0002t0003g0377 | 2 | HG02135.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.-15+5465G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516268 | ||||||
| chr9:5516349
|
C | G | 1 | a0001c0001t0001g0221 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-15+5546C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516349 | ||||||
| chr9:5516395
|
A | G | 1 | a0001c0001t0002g0005 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-15+5592A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516395 | ||||||
| chr9:5516461
|
A | G | 2 | a0001c0001t0012g0247a0002c0002t0001g0381 | 2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+5658A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516461 | ||||||
| chr9:5516463
|
T | C | 3 | a0002c0002t0001g0348a0002c0002t0013g0015a0002c0002t0014g0339 | 4 | HG02615.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5660T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516463 | ||||||
| chr9:5516559
|
C | T | 1 | a0002c0002t0001g0220 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-15+5756C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516559 | ||||||
| chr9:5516612
|
C | A | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-15+5809C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516612 | ||||||
| chr9:5516703
|
C | T | 2 | a0002c0002t0002g0019a0002c0002t0002g0331 | 3 | HG02258.hp1 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-14-5830C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516703 | ||||||
| chr9:5516779
|
C | G | 1 | a0001c0001t0001g0311 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-14-5754C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516779 | ||||||
| chr9:5516866
|
G | T | 1 | a0001c0001t0002g0063 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-14-5667G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516866 | ||||||
| chr9:5516956
|
G | A | 20 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(17): Show | 20 | HG00140.hp2 HG00735.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.-14-5577G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516956 | ||||||
| chr9:5516980
|
C | T | 26 | a0001c0001t0001g0115a0001c0001t0001g0227a0001c0001t0001g0233others(23): Show | 28 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14-5553C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516980 | ||||||
| chr9:5517046
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-14-5487C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517046 | ||||||
| chr9:5517090
|
C | T | 1 | a0002c0002t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-14-5443C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517090 | ||||||
| chr9:5517265
|
G | A | 82 | a0001c0001t0001g0016a0001c0001t0001g0115a0001c0001t0001g0148others(79): Show | 84 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-14-5268G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517265 | ||||||
| chr9:5517559
|
C | T | 163 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0041others(160): Show | 170 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.-14-4974C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517559 | ||||||
| chr9:5517568
|
C | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0225a0001c0001t0004g0014 | 4 | NA18991.hp1 NA18998.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-4965C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517568 | ||||||
| chr9:5517582
|
A | C | 383 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(380): Show | 405 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(402): Show |
intron_variant | MODIFIER | c.-14-4951A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517582 | ||||||
| chr9:5517589
|
G | A | 1 | a0003c0003t0009g0324 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14-4944G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517589 | ||||||
| chr9:5517662
|
C | T | 3 | a0002c0002t0001g0131a0002c0002t0001g0146a0002c0002t0015g0145 | 3 | HG02258.hp2 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-14-4871C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517662 | ||||||
| chr9:5517719
|
G | A | 27 | a0001c0001t0003g0020a0001c0001t0003g0353a0001c0001t0003g0354others(24): Show | 28 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.-14-4814G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517719 | ||||||
| chr9:5517880
|
G | A | 1 | a0001c0001t0010g0150 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-14-4653G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517880 | ||||||
| chr9:5518008
|
A | G | 9 | a0001c0001t0001g0115a0001c0001t0001g0227a0001c0001t0001g0233others(6): Show | 10 | HG01243.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-4525A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518008 | ||||||
| chr9:5518169
|
G | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0151others(6): Show | 11 | HG01123.hp1 HG01255.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-4364G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518169 | ||||||
| chr9:5518211
|
C | T | 1 | a0001c0001t0002g0061 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-14-4322C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518211 | ||||||
| chr9:5518260
|
C | T | 69 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(66): Show | 70 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-14-4273C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518260 | ||||||
| chr9:5518265
|
G | A | 1 | a0002c0002t0001g0348 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-4268G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518265 | ||||||
| chr9:5518500
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-14-4033G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518500 | ||||||
| chr9:5518553
|
G | C | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-14-3980G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518553 | ||||||
| chr9:5518633
|
C | G | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-14-3900C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518633 | ||||||
| chr9:5518718
|
C | A | 1 | a0001c0001t0002g0106 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-14-3815C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518718 | ||||||
| chr9:5518780
|
C | T | 31 | a0001c0001t0003g0020a0001c0001t0003g0353a0001c0001t0003g0354others(28): Show | 32 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.-14-3753C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518780 | ||||||
| chr9:5518989
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-14-3544G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518989 | ||||||
| chr9:5519076
|
A | C | 1 | a0001c0001t0002g0026 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-14-3457A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519076 | ||||||
| chr9:5519100
|
G | C | 32 | a0001c0001t0003g0020a0001c0001t0003g0353a0001c0001t0003g0354others(29): Show | 33 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.-14-3433G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519100 | ||||||
| chr9:5519201
|
AG | A | 27 | a0001c0001t0003g0020a0001c0001t0003g0353a0001c0001t0003g0354others(24): Show | 28 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.-14-3328delG | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5519201 | |||||
| chr9:5519238
|
G | A | 4 | a0001c0001t0003g0376a0001c0001t0003g0379a0002c0002t0003g0375others(1): Show | 4 | HG01978.hp1 HG02145.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-3295G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519238 | ||||||
| chr9:5519257
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-14-3276A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519257 | ||||||
| chr9:5519343
|
C | G | 2 | a0002c0002t0001g0348a0002c0002t0014g0339 | 2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-14-3190C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519343 | ||||||
| chr9:5519369
|
T | C | 1 | a0001c0001t0012g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-14-3164T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519369 | ||||||
| chr9:5519370
|
T | C | 2 | a0001c0001t0002g0326a0001c0001t0002g0327 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-14-3163T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519370 | ||||||
| chr9:5519594
|
A | G | 14 | a0001c0001t0001g0115a0001c0001t0001g0121a0001c0001t0001g0227others(11): Show | 15 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-14-2939A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519594 | ||||||
| chr9:5519626
|
A | G | 1 | a0002c0002t0006g0072 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-14-2907A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519626 | ||||||
| chr9:5519707
|
C | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0317a0001c0001t0002g0318 | 4 | HG01106.hp1 HG02602.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-2826C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519707 | ||||||
| chr9:5519716
|
C | G | 1 | a0001c0001t0001g0336 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-14-2817C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519716 | ||||||
| chr9:5519738
|
T | C | 57 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(54): Show | 58 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.-14-2795T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519738 | ||||||
| chr9:5519786
|
C | T | 51 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(48): Show | 52 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.-14-2747C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519786 | ||||||
| chr9:5519944
|
C | T | 51 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(48): Show | 52 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.-14-2589C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519944 | ||||||
| chr9:5520215
|
G | A | 50 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(47): Show | 51 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.-14-2318G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520215 | ||||||
| chr9:5520317
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0158 | 5 | NA18955.hp2 NA18968.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-2216G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520317 | ||||||
| chr9:5520404
|
T | G | 2 | a0001c0001t0012g0247a0002c0002t0001g0381 | 2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-2129T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520404 | ||||||
| chr9:5520415
|
T | C | 2 | a0001c0001t0012g0247a0002c0002t0001g0381 | 2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-2118T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520415 | ||||||
| chr9:5520427
|
G | T | 31 | a0001c0001t0003g0020a0001c0001t0003g0353a0001c0001t0003g0354others(28): Show | 32 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.-14-2106G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520427 | ||||||
| chr9:5520761
|
A | C | 1 | a0002c0002t0001g0381 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-14-1772A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520761 | ||||||
| chr9:5520800
|
G | C | 1 | a0002c0002t0001g0333 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-14-1733G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520800 | ||||||
| chr9:5520876
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0158 | 5 | NA18955.hp2 NA18968.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-1657G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520876 | ||||||
| chr9:5520921
|
A | C | 1 | a0001c0001t0002g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-14-1612A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520921 | ||||||
| chr9:5520929
|
T | A | 11 | a0001c0001t0007g0119a0001c0001t0012g0247a0002c0002t0001g0381others(8): Show | 13 | HG02647.hp2 HG02717.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-1604T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520929 | ||||||
| chr9:5521094
|
G | A | 101 | a0001c0001t0001g0016a0001c0001t0001g0148a0001c0001t0001g0253others(98): Show | 104 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.-14-1439G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521094 | ||||||
| chr9:5521109
|
C | A | 101 | a0001c0001t0001g0016a0001c0001t0001g0148a0001c0001t0001g0253others(98): Show | 104 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.-14-1424C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521109 | ||||||
| chr9:5521367
|
T | G | 17 | a0001c0001t0001g0268a0001c0001t0007g0119a0002c0002t0001g0269others(14): Show | 19 | HG01099.hp2 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14-1166T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521367 | ||||||
| chr9:5521407
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-14-1126G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521407 | ||||||
| chr9:5521435
|
T | C | 1 | a0002c0004t0005g0229 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-14-1098T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521435 | ||||||
| chr9:5521655
|
G | T | 106 | a0001c0001t0001g0016a0001c0001t0001g0148a0001c0001t0001g0253others(103): Show | 109 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-14-878G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521655 | ||||||
| chr9:5521736
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0002t0001g0251others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-797T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521736 | ||||||
| chr9:5521740
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-14-793T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521740 | ||||||
| chr9:5521974
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02027.hp1 HG02056.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-559C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521974 | ||||||
| chr9:5522039
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-14-494C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5522039 | ||||||
| chr9:5522167
|
T | C | 36 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(33): Show | 37 | HG00140.hp2 HG00735.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.-14-366T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5522167 | ||||||
| chr9:5522173
|
G | C | 1 | a0001c0001t0001g0159 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-14-360G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5522173 | ||||||
| chr9:5522173
|
GACAA | G | 69 | a0001c0001t0001g0016a0001c0001t0001g0148a0001c0001t0001g0259others(66): Show | 71 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-14-354_-14-351del others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5522173 | |||||
| chr9:5522290
|
C | T | 1 | a0002c0002t0006g0024 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-14-243C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5522290 | ||||||
| chr9:5522617
|
G | C | 1 | a0001c0001t0017g0309 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.55+16G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5522617 | ||||||
| chr9:5522630
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.55+29G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5522630 | ||||||
| chr9:5522654
|
T | C | 1 | a0002c0002t0005g0160 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.55+53T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5522654 | ||||||
| chr9:5522711
|
C | T | 3 | a0001c0001t0001g0255a0001c0001t0001g0256a0002c0002t0001g0347 | 3 | HG02451.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.55+110C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5522711 | ||||||
| chr9:5522712
|
G | A | 4 | a0001c0001t0003g0376a0001c0001t0003g0379a0002c0002t0003g0375others(1): Show | 4 | HG01978.hp1 HG02145.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+111G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5522712 | ||||||
| chr9:5522741
|
C | CA | 42 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(39): Show | 44 | HG00140.hp2 HG00609.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.55+151dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5522741 | |||||
| chr9:5522909
|
G | A | 5 | a0001c0001t0007g0119a0002c0002t0007g0001a0002c0002t0007g0116others(2): Show | 7 | HG02809.hp1 HG02922.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+308G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5522909 | ||||||
| chr9:5522943
|
C | T | 50 | a0001c0001t0001g0016a0001c0001t0001g0148a0001c0001t0001g0259others(47): Show | 51 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.55+342C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5522943 | ||||||
| chr9:5523085
|
G | A | 1 | a0001c0001t0004g0313 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.55+484G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523085 | ||||||
| chr9:5523239
|
C | G | 2 | a0001c0001t0001g0216a0001c0001t0001g0224 | 2 | NA19062.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.55+638C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523239 | ||||||
| chr9:5523308
|
C | G | 29 | a0001c0001t0001g0258a0001c0001t0003g0020a0001c0001t0003g0337others(26): Show | 30 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.55+707C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523308 | ||||||
| chr9:5523469
|
G | T | 6 | a0002c0002t0002g0019a0002c0002t0002g0329a0002c0002t0002g0331others(3): Show | 7 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+868G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523469 | ||||||
| chr9:5523512
|
T | C | 4 | a0001c0001t0001g0161a0001c0001t0001g0236a0002c0002t0001g0011others(1): Show | 5 | HG00609.hp2 NA18945.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+911T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523512 | ||||||
| chr9:5523722
|
T | C | 1 | a0001c0001t0008g0352 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.55+1121T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523722 | ||||||
| chr9:5523773
|
C | T | 34 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(31): Show | 34 | HG00140.hp2 HG00735.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.55+1172C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523773 | ||||||
| chr9:5523850
|
C | T | 28 | a0001c0001t0001g0258a0001c0001t0003g0020a0001c0001t0003g0353others(25): Show | 29 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.55+1249C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523850 | ||||||
| chr9:5523951
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.55+1350C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523951 | ||||||
| chr9:5524037
|
T | C | 1 | a0001c0001t0017g0309 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.55+1436T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524037 | ||||||
| chr9:5524353
|
C | T | 6 | a0001c0001t0001g0255a0001c0001t0001g0256a0003c0003t0001g0029others(3): Show | 6 | HG02451.hp2 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+1752C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524353 | ||||||
| chr9:5524389
|
A | G | 10 | a0002c0002t0001g0070a0002c0002t0001g0266a0002c0002t0001g0267others(7): Show | 11 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.55+1788A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524389 | ||||||
| chr9:5524447
|
C | T | 1 | a0002c0002t0002g0064 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.55+1846C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524447 | ||||||
| chr9:5524571
|
T | A | 18 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0042others(15): Show | 18 | HG00140.hp2 HG00735.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+1970T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524571 | ||||||
| chr9:5524682
|
T | C | 1 | a0002c0002t0001g0252 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.55+2081T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524682 | ||||||
| chr9:5524749
|
C | T | 1 | a0004c0006t0019g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.55+2148C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524749 | ||||||
| chr9:5524812
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.55+2211A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524812 | ||||||
| chr9:5524904
|
A | G | 2 | a0001c0001t0002g0004a0001c0001t0002g0059 | 3 | NA18965.hp2 NA18969.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.55+2303A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524904 | ||||||
| chr9:5524915
|
A | G | 83 | a0001c0001t0001g0016a0001c0001t0001g0125a0001c0001t0001g0148others(80): Show | 86 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.55+2314A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524915 | ||||||
| chr9:5524967
|
T | C | 3 | a0002c0002t0001g0266a0002c0002t0001g0267a0002c0002t0001g0323 | 3 | HG02723.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.55+2366T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524967 | ||||||
| chr9:5524993
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.55+2392T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524993 | ||||||
| chr9:5525031
|
T | C | 4 | a0002c0002t0007g0001a0002c0002t0007g0116a0002c0002t0023g0118others(1): Show | 6 | HG02809.hp1 HG02922.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2430T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525031 | ||||||
| chr9:5525034
|
T | C | 3 | a0002c0002t0001g0266a0002c0002t0001g0267a0002c0002t0001g0323 | 3 | HG02723.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.55+2433T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525034 | ||||||
| chr9:5525073
|
C | T | 6 | a0001c0001t0001g0255a0001c0001t0001g0256a0003c0003t0001g0029others(3): Show | 6 | HG02451.hp2 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2472C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525073 | ||||||
| chr9:5525192
|
G | C | 6 | a0002c0002t0002g0019a0002c0002t0002g0329a0002c0002t0002g0331others(3): Show | 7 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+2591G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525192 | ||||||
| chr9:5525292
|
C | A | 1 | a0002c0002t0003g0377 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.55+2691C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525292 | ||||||
| chr9:5525343
|
TA | T | 273 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(270): Show | 288 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(285): Show |
intron_variant | MODIFIER | c.55+2757delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5525343 | |||||
| chr9:5525351
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.55+2750A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525351 | ||||||
| chr9:5525355
|
A | G | 6 | a0002c0002t0002g0019a0002c0002t0002g0329a0002c0002t0002g0331others(3): Show | 7 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+2754A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525355 | ||||||
| chr9:5525358
|
A | G | 1 | a0002c0002t0003g0377 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.55+2757A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525358 | ||||||
| chr9:5525359
|
G | A | 1 | a0002c0002t0003g0377 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.55+2758G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525359 | ||||||
| chr9:5525363
|
A | G | 2 | a0001c0001t0001g0338a0002c0002t0001g0347 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.55+2762A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525363 | ||||||
| chr9:5525370
|
A | T | 4 | a0002c0002t0001g0266a0002c0002t0001g0267a0002c0002t0001g0323others(1): Show | 4 | HG01884.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+2769A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525370 | ||||||
| chr9:5525388
|
A | G | 1 | a0001c0001t0001g0308 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.55+2787A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525388 | ||||||
| chr9:5525608
|
A | T | 26 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0115others(23): Show | 26 | HG01081.hp1 HG01109.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.55+3007A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525608 | ||||||
| chr9:5525733
|
T | C | 8 | a0002c0002t0001g0251a0002c0002t0001g0252a0003c0003t0001g0029others(5): Show | 8 | HG02647.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.55+3132T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525733 | ||||||
| chr9:5525744
|
T | C | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0268others(2): Show | 5 | HG01099.hp2 HG01192.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+3143T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525744 | ||||||
| chr9:5525768
|
G | A | 1 | a0001c0001t0001g0336 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.55+3167G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525768 | ||||||
| chr9:5525771
|
G | A | 3 | a0001c0001t0002g0075a0001c0001t0004g0260a0002c0002t0001g0261 | 3 | NA18612.hp1 NA18979.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.55+3170G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525771 | ||||||
| chr9:5525774
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.55+3173C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525774 | ||||||
| chr9:5525775
|
A | G | 117 | a0001c0001t0001g0008a0001c0001t0001g0041a0001c0001t0001g0042others(114): Show | 122 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.55+3174A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525775 | ||||||
| chr9:5525776
|
T | C | 15 | a0001c0001t0001g0212a0001c0001t0001g0217a0001c0001t0001g0225others(12): Show | 16 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.55+3175T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525776 | ||||||
| chr9:5525781
|
G | T | 1 | a0001c0001t0002g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.55+3180G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525781 | ||||||
| chr9:5525787
|
G | A | 1 | a0002c0002t0001g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.55+3186G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525787 | ||||||
| chr9:5525819
|
T | C | 1 | a0002c0002t0001g0252 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.55+3218T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525819 | ||||||
| chr9:5525823
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.55+3222C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525823 | ||||||
| chr9:5525828
|
C | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(54): Show | 62 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.55+3227C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525828 | ||||||
| chr9:5525831
|
G | A | 187 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(184): Show | 197 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.55+3230G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525831 | ||||||
| chr9:5525852
|
G | T | 176 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(173): Show | 186 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.55+3251G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525852 | ||||||
| chr9:5525859
|
C | T | 8 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0216others(5): Show | 8 | HG01081.hp1 HG02027.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.55+3258C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525859 | ||||||
| chr9:5525860
|
C | A | 8 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0216others(5): Show | 8 | HG01081.hp1 HG02027.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.55+3259C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525860 | ||||||
| chr9:5525861
|
G | A | 13 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0216others(10): Show | 15 | HG01081.hp1 HG02027.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.55+3260G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525861 | ||||||
| chr9:5525864
|
T | C | 4 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0002g0325others(1): Show | 4 | HG01081.hp1 HG02083.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+3263T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525864 | ||||||
| chr9:5525874
|
T | C | 28 | a0001c0001t0001g0133a0001c0001t0001g0164a0001c0001t0001g0165others(25): Show | 28 | HG00741.hp1 HG00741.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.55+3273T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525874 | ||||||
| chr9:5525884
|
A | T | 5 | a0001c0001t0001g0115a0002c0002t0001g0220a0002c0002t0001g0381others(2): Show | 6 | HG03139.hp2 HG03453.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+3283A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525884 | ||||||
| chr9:5525901
|
G | A | 1 | a0002c0002t0001g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.55+3300G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525901 | ||||||
| chr9:5525907
|
C | T | 2 | a0001c0001t0002g0103a0002c0002t0002g0097 | 2 | HG01981.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.55+3306C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525907 | ||||||
| chr9:5525908
|
A | G | 2 | a0001c0001t0002g0103a0002c0002t0002g0097 | 2 | HG01981.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.55+3307A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525908 | ||||||
| chr9:5525941
|
G | A | 17 | a0001c0001t0001g0069a0001c0001t0001g0115a0001c0001t0001g0157others(14): Show | 18 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+3340G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525941 | ||||||
| chr9:5526004
|
G | A | 1 | a0001c0001t0004g0304 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.55+3403G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526004 | ||||||
| chr9:5526041
|
C | T | 6 | a0001c0001t0001g0147a0003c0003t0001g0029a0003c0003t0003g0248others(3): Show | 6 | HG01109.hp2 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+3440C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526041 | ||||||
| chr9:5526046
|
C | CA | 77 | a0001c0001t0001g0115a0001c0001t0001g0134a0001c0001t0001g0147others(74): Show | 81 | HG00408.hp2 HG00609.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.55+3462dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5526046 | |||||
| chr9:5526046
|
C | CAA | 215 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(212): Show | 223 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.55+3461_55+3462dup others(2): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5526046 | |||||
| chr9:5526077
|
T | C | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0016others(141): Show | 150 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.55+3476T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526077 | ||||||
| chr9:5526087
|
G | A | 1 | a0001c0001t0001g0382 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.55+3486G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526087 | ||||||
| chr9:5526124
|
C | T | 306 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(303): Show | 319 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(316): Show |
intron_variant | MODIFIER | c.55+3523C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526124 | ||||||
| chr9:5526165
|
A | T | 2 | a0002c0002t0007g0001a0002c0002t0007g0116 | 4 | HG02809.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+3564A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526165 | ||||||
| chr9:5526211
|
T | G | 7 | a0001c0001t0002g0111a0001c0001t0004g0140a0001c0001t0004g0191others(4): Show | 7 | NA18942.hp1 NA18944.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+3610T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526211 | ||||||
| chr9:5526434
|
T | A | 52 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0157others(49): Show | 54 | HG00423.hp1 HG00597.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.55+3833T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526434 | ||||||
| chr9:5526473
|
T | C | 1 | a0002c0002t0001g0333 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.55+3872T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526473 | ||||||
| chr9:5526502
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.55+3901A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526502 | ||||||
| chr9:5526516
|
C | G | 1 | a0002c0002t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.55+3915C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526516 | ||||||
| chr9:5526667
|
G | A | 1 | a0002c0002t0002g0090 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.55+4066G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526667 | ||||||
| chr9:5526880
|
T | C | 2 | a0001c0001t0001g0159a0001c0001t0018g0321 | 2 | HG00140.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.55+4279T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526880 | ||||||
| chr9:5527014
|
A | G | 1 | a0002c0002t0002g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.55+4413A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527014 | ||||||
| chr9:5527351
|
A | G | 16 | a0001c0001t0001g0067a0001c0001t0001g0157a0001c0001t0001g0255others(13): Show | 16 | HG00140.hp2 HG00733.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.55+4750A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527351 | ||||||
| chr9:5527429
|
G | C | 1 | a0002c0004t0005g0229 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.55+4828G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527429 | ||||||
| chr9:5527525
|
T | C | 8 | a0001c0001t0001g0212a0001c0001t0002g0089a0001c0001t0004g0304others(5): Show | 8 | HG00408.hp2 HG00621.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.55+4924T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527525 | ||||||
| chr9:5527837
|
C | CTT | 12 | a0001c0001t0001g0122a0001c0001t0001g0227a0001c0001t0002g0018others(9): Show | 13 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.55+5244_55+5245dup others(2): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5527837 | |||||
| chr9:5527878
|
A | G | 33 | a0001c0001t0001g0069a0001c0001t0001g0194a0001c0001t0001g0198others(30): Show | 36 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.55+5277A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527878 | ||||||
| chr9:5527888
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.55+5287C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527888 | ||||||
| chr9:5527922
|
G | A | 5 | a0003c0003t0001g0029a0003c0003t0003g0248a0003c0003t0003g0249others(2): Show | 5 | HG02647.hp2 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+5321G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527922 | ||||||
| chr9:5527945
|
C | T | 2 | a0001c0001t0002g0112a0001c0001t0002g0113 | 2 | HG01928.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.55+5344C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527945 | ||||||
| chr9:5528045
|
G | T | 1 | a0001c0001t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.55+5444G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528045 | ||||||
| chr9:5528061
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.55+5460C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528061 | ||||||
| chr9:5528121
|
C | T | 1 | a0002c0002t0002g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.55+5520C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528121 | ||||||
| chr9:5528152
|
G | C | 1 | a0001c0001t0004g0260 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.55+5551G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528152 | ||||||
| chr9:5528155
|
G | A | 5 | a0002c0002t0006g0024a0002c0002t0006g0068a0002c0002t0006g0071others(2): Show | 5 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+5554G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528155 | ||||||
| chr9:5528198
|
T | C | 21 | a0001c0001t0001g0194a0001c0001t0001g0198a0001c0001t0001g0207others(18): Show | 22 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.55+5597T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528198 | ||||||
| chr9:5528276
|
T | TTA | 7 | a0002c0002t0001g0270a0002c0002t0001g0271a0002c0002t0001g0272others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+5686_55+5687dup others(2): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5528276 | |||||
| chr9:5528289
|
C | T | 86 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(83): Show | 88 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.55+5688C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528289 | ||||||
| chr9:5528440
|
T | C | 1 | a0001c0001t0004g0304 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.55+5839T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528440 | ||||||
| chr9:5528595
|
G | A | 5 | a0001c0001t0001g0069a0001c0001t0001g0253a0001c0001t0001g0254others(2): Show | 7 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+5994G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528595 | ||||||
| chr9:5528599
|
C | T | 7 | a0001c0001t0001g0233a0002c0002t0001g0230a0002c0002t0005g0234others(4): Show | 8 | HG01243.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.55+5998C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528599 | ||||||
| chr9:5528658
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(81): Show | 86 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.55+6057A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528658 | ||||||
| chr9:5528796
|
C | T | 1 | a0002c0002t0001g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.56-5949C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528796 | ||||||
| chr9:5528818
|
C | A | 2 | a0001c0001t0001g0115a0002c0002t0013g0015 | 3 | HG03453.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.56-5927C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528818 | ||||||
| chr9:5528832
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0264a0001c0001t0003g0354others(1): Show | 4 | NA18957.hp1 NA18978.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-5913C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528832 | ||||||
| chr9:5528882
|
A | T | 1 | a0001c0001t0001g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.56-5863A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528882 | ||||||
| chr9:5528899
|
T | A | 7 | a0001c0001t0001g0233a0002c0002t0001g0230a0002c0002t0005g0234others(4): Show | 8 | HG01243.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.56-5846T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528899 | ||||||
| chr9:5528908
|
T | G | 1 | a0001c0001t0002g0103 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.56-5837T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528908 | ||||||
| chr9:5528912
|
T | C | 22 | a0001c0001t0001g0194a0001c0001t0001g0198a0001c0001t0001g0207others(19): Show | 23 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.56-5833T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528912 | ||||||
| chr9:5528915
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.56-5830A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528915 | ||||||
| chr9:5528923
|
T | A | 9 | a0001c0001t0001g0122a0001c0001t0001g0227a0001c0001t0002g0018others(6): Show | 10 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-5822T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528923 | ||||||
| chr9:5528957
|
G | C | 8 | a0001c0001t0002g0103a0002c0002t0002g0045a0003c0003t0001g0029others(5): Show | 8 | HG01981.hp1 HG02647.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.56-5788G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528957 | ||||||
| chr9:5528966
|
T | A | 1 | a0001c0001t0001g0345 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.56-5779T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528966 | ||||||
| chr9:5529023
|
C | T | 2 | a0001c0001t0002g0106a0002c0002t0002g0329 | 2 | HG02145.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.56-5722C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529023 | ||||||
| chr9:5529027
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.56-5718C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529027 | ||||||
| chr9:5529126
|
G | A | 1 | a0001c0001t0001g0382 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.56-5619G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529126 | ||||||
| chr9:5529138
|
G | A | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.56-5607G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529138 | ||||||
| chr9:5529158
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0124 | 2 | NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.56-5587G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529158 | ||||||
| chr9:5529219
|
T | C | 1 | a0002c0002t0002g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.56-5526T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529219 | ||||||
| chr9:5529225
|
C | G | 1 | a0001c0001t0001g0380 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-5520C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529225 | ||||||
| chr9:5529294
|
T | C | 9 | a0001c0001t0001g0122a0001c0001t0001g0227a0001c0001t0002g0018others(6): Show | 10 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-5451T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529294 | ||||||
| chr9:5529324
|
T | C | 1 | a0002c0002t0014g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.56-5421T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529324 | ||||||
| chr9:5529650
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0308 | 2 | HG03239.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.56-5095A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529650 | ||||||
| chr9:5529705
|
A | C | 1 | a0002c0002t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.56-5040A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529705 | ||||||
| chr9:5529737
|
G | T | 7 | a0001c0001t0002g0103a0003c0003t0001g0029a0003c0003t0003g0248others(4): Show | 7 | HG01981.hp1 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-5008G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529737 | ||||||
| chr9:5529843
|
G | C | 3 | a0002c0002t0001g0251a0002c0002t0001g0252a0004c0006t0019g0104 | 3 | HG02647.hp1 HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.56-4902G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529843 | ||||||
| chr9:5529973
|
G | T | 1 | a0001c0001t0004g0293 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.56-4772G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529973 | ||||||
| chr9:5529982
|
C | G | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.56-4763C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529982 | ||||||
| chr9:5530017
|
A | G | 183 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(180): Show | 192 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.56-4728A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530017 | ||||||
| chr9:5530082
|
A | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01074.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.56-4663A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530082 | ||||||
| chr9:5530248
|
A | G | 35 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0194others(32): Show | 38 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.56-4497A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530248 | ||||||
| chr9:5530264
|
C | T | 1 | a0002c0002t0022g0355 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.56-4481C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530264 | ||||||
| chr9:5530473
|
C | CA | 14 | a0001c0001t0001g0144a0001c0001t0001g0177a0001c0001t0001g0277others(11): Show | 14 | HG00544.hp1 HG00642.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.56-4256dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5530473 | |||||
| chr9:5530473
|
CA | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0123a0001c0001t0001g0132others(7): Show | 11 | HG00609.hp1 HG01167.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.56-4256delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5530473 | |||||
| chr9:5530487
|
A | AC | 30 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0194others(27): Show | 33 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.56-4258_56-4257ins others(1): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530487 | ||||||
| chr9:5530487
|
A | C | 5 | a0002c0002t0001g0270a0002c0002t0001g0271a0002c0002t0001g0272others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-4258A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530487 | ||||||
| chr9:5530500
|
G | A | 6 | a0001c0001t0001g0227a0002c0002t0001g0065a0002c0002t0001g0251others(3): Show | 6 | HG02615.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-4245G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530500 | ||||||
| chr9:5530716
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0276 | 2 | NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.56-4029G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530716 | ||||||
| chr9:5530840
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02056.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.56-3905T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530840 | ||||||
| chr9:5530983
|
G | A | 6 | a0001c0001t0001g0227a0002c0002t0001g0065a0002c0002t0001g0251others(3): Show | 6 | HG02615.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-3762G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530983 | ||||||
| chr9:5531068
|
T | C | 10 | a0001c0001t0001g0192a0001c0001t0001g0206a0001c0001t0003g0376others(7): Show | 11 | HG01109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.56-3677T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531068 | ||||||
| chr9:5531293
|
T | C | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.56-3452T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531293 | ||||||
| chr9:5531311
|
A | G | 6 | a0002c0002t0001g0270a0002c0002t0001g0271a0002c0002t0001g0272others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-3434A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531311 | ||||||
| chr9:5531311
|
A | T | 1 | a0003c0003t0003g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.56-3434A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531311 | ||||||
| chr9:5531328
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.56-3417A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531328 | ||||||
| chr9:5531499
|
A | T | 1 | a0002c0002t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.56-3246A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531499 | ||||||
| chr9:5531647
|
T | C | 1 | a0002c0002t0001g0238 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.56-3098T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531647 | ||||||
| chr9:5531754
|
A | G | 2 | a0002c0002t0001g0163a0002c0002t0001g0333 | 2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.56-2991A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531754 | ||||||
| chr9:5531763
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.56-2982G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531763 | ||||||
| chr9:5531841
|
C | A | 1 | a0002c0002t0003g0384 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.56-2904C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531841 | ||||||
| chr9:5531861
|
A | T | 12 | a0001c0001t0001g0122a0001c0001t0001g0227a0001c0001t0002g0018others(9): Show | 13 | HG01106.hp1 HG01516.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.56-2884A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531861 | ||||||
| chr9:5531878
|
A | G | 1 | a0002c0002t0002g0320 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.56-2867A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531878 | ||||||
| chr9:5532122
|
A | C | 2 | a0001c0001t0001g0115a0002c0002t0013g0015 | 3 | HG03453.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.56-2623A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532122 | ||||||
| chr9:5532212
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.56-2533C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532212 | ||||||
| chr9:5532593
|
C | T | 5 | a0002c0002t0006g0024a0002c0002t0006g0068a0002c0002t0006g0071others(2): Show | 5 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-2152C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532593 | ||||||
| chr9:5532633
|
T | G | 2 | a0001c0001t0001g0115a0002c0002t0013g0015 | 3 | HG03453.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.56-2112T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532633 | ||||||
| chr9:5532694
|
G | A | 1 | a0002c0002t0007g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.56-2051G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532694 | ||||||
| chr9:5532821
|
C | T | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.56-1924C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532821 | ||||||
| chr9:5532871
|
T | C | 131 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(128): Show | 136 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.56-1874T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532871 | ||||||
| chr9:5532964
|
C | T | 8 | a0001c0001t0002g0031a0001c0001t0003g0362a0001c0001t0003g0363others(5): Show | 8 | NA18961.hp2 NA18962.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.56-1781C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532964 | ||||||
| chr9:5533280
|
A | G | 174 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(171): Show | 183 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.56-1465A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533280 | ||||||
| chr9:5533310
|
C | G | 1 | a0002c0002t0001g0200 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.56-1435C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533310 | ||||||
| chr9:5533325
|
C | T | 1 | a0002c0002t0001g0187 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.56-1420C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533325 | ||||||
| chr9:5533450
|
A | G | 48 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0157others(45): Show | 51 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.56-1295A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533450 | ||||||
| chr9:5533511
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.56-1234C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533511 | ||||||
| chr9:5533698
|
C | T | 1 | a0002c0002t0001g0348 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.56-1047C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533698 | ||||||
| chr9:5533831
|
T | C | 48 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0157others(45): Show | 51 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.56-914T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533831 | ||||||
| chr9:5533935
|
C | T | 6 | a0002c0002t0001g0270a0002c0002t0001g0271a0002c0002t0001g0272others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-810C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533935 | ||||||
| chr9:5534068
|
A | C | 2 | a0001c0001t0001g0115a0002c0002t0013g0015 | 3 | HG03453.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.56-677A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534068 | ||||||
| chr9:5534087
|
T | G | 53 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0130others(50): Show | 56 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.56-658T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534087 | ||||||
| chr9:5534243
|
C | T | 118 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(115): Show | 124 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.56-502C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534243 | ||||||
| chr9:5534301
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.56-444A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534301 | ||||||
| chr9:5534424
|
T | C | 24 | a0001c0001t0001g0067a0001c0001t0001g0194a0001c0001t0001g0198others(21): Show | 25 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.56-321T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534424 | ||||||
| chr9:5534432
|
G | T | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.56-313G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534432 | ||||||
| chr9:5534590
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.56-155G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534590 | ||||||
| chr9:5534608
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.56-137G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534608 | ||||||
| chr9:5534727
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0315 | 3 | NA18962.hp2 NA19066.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.56-18A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534727 | ||||||
| chr9:5535123
|
T | C | 36 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0194others(33): Show | 39 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.361+73T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535123 | ||||||
| chr9:5535236
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.361+186G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535236 | ||||||
| chr9:5535274
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.361+224A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535274 | ||||||
| chr9:5535535
|
G | C | 24 | a0001c0001t0001g0067a0001c0001t0001g0194a0001c0001t0001g0198others(21): Show | 25 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.361+485G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535535 | ||||||
| chr9:5535599
|
C | T | 5 | a0001c0001t0001g0069a0001c0001t0001g0253a0001c0001t0001g0254others(2): Show | 7 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.361+549C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535599 | ||||||
| chr9:5535825
|
T | G | 5 | a0003c0003t0001g0029a0003c0003t0003g0248a0003c0003t0003g0249others(2): Show | 5 | HG02647.hp2 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.361+775T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535825 | ||||||
| chr9:5535884
|
T | C | 6 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0103others(3): Show | 6 | HG00741.hp2 HG01981.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+834T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535884 | ||||||
| chr9:5535939
|
T | C | 1 | a0002c0002t0001g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.361+889T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535939 | ||||||
| chr9:5535946
|
C | A | 1 | a0001c0001t0004g0304 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.361+896C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535946 | ||||||
| chr9:5536058
|
G | T | 14 | a0001c0001t0001g0126a0001c0001t0001g0300a0001c0001t0001g0314others(11): Show | 15 | HG01993.hp1 HG02004.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.361+1008G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536058 | ||||||
| chr9:5536161
|
G | A | 1 | a0002c0002t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.361+1111G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536161 | ||||||
| chr9:5536167
|
A | G | 35 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0194others(32): Show | 38 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.361+1117A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536167 | ||||||
| chr9:5536288
|
A | G | 5 | a0001c0001t0001g0069a0001c0001t0001g0253a0001c0001t0001g0254others(2): Show | 7 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.361+1238A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536288 | ||||||
| chr9:5536307
|
G | A | 1 | a0008c0009t0001g0274 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.361+1257G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536307 | ||||||
| chr9:5536361
|
G | A | 1 | a0001c0001t0004g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.361+1311G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536361 | ||||||
| chr9:5536385
|
C | G | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.361+1335C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536385 | ||||||
| chr9:5536494
|
T | C | 1 | a0001c0001t0002g0022 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.361+1444T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536494 | ||||||
| chr9:5536780
|
T | C | 1 | a0002c0002t0002g0095 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.361+1730T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536780 | ||||||
| chr9:5536846
|
C | T | 1 | a0002c0002t0001g0347 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.361+1796C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536846 | ||||||
| chr9:5536849
|
G | A | 1 | a0001c0001t0002g0037 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.361+1799G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536849 | ||||||
| chr9:5536904
|
C | T | 2 | a0002c0002t0001g0131a0002c0002t0001g0146 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.361+1854C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536904 | ||||||
| chr9:5537066
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0123a0001c0001t0001g0141 | 4 | HG01167.hp1 HG01192.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+2016G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537066 | ||||||
| chr9:5537071
|
T | A | 35 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0194others(32): Show | 38 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.361+2021T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537071 | ||||||
| chr9:5537099
|
G | A | 1 | a0001c0001t0003g0372 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.361+2049G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537099 | ||||||
| chr9:5537326
|
G | C | 168 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(165): Show | 177 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.361+2276G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537326 | ||||||
| chr9:5537344
|
T | A | 1 | a0001c0001t0002g0044 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.361+2294T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537344 | ||||||
| chr9:5537493
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.361+2443C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537493 | ||||||
| chr9:5537530
|
C | T | 4 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(1): Show | 4 | HG01074.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.361+2480C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537530 | ||||||
| chr9:5537575
|
C | T | 169 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(166): Show | 178 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.361+2525C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537575 | ||||||
| chr9:5537581
|
G | C | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.361+2531G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537581 | ||||||
| chr9:5537646
|
G | A | 35 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0115others(32): Show | 39 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.361+2596G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537646 | ||||||
| chr9:5537688
|
A | G | 36 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0194others(33): Show | 39 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.361+2638A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537688 | ||||||
| chr9:5537761
|
G | T | 3 | a0001c0001t0001g0147a0001c0001t0002g0101a0001c0001t0002g0106 | 3 | HG01109.hp2 HG01123.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.361+2711G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537761 | ||||||
| chr9:5537871
|
C | G | 173 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(170): Show | 182 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.361+2821C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537871 | ||||||
| chr9:5537901
|
A | G | 5 | a0001c0001t0001g0130a0001c0001t0001g0188a0001c0001t0001g0276others(2): Show | 5 | HG01081.hp1 HG01358.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.361+2851A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537901 | ||||||
| chr9:5537930
|
G | A | 1 | a0002c0002t0006g0024 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.361+2880G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537930 | ||||||
| chr9:5537952
|
T | A | 1 | a0001c0001t0010g0085 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.361+2902T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537952 | ||||||
| chr9:5537973
|
G | C | 7 | a0001c0001t0001g0233a0002c0002t0001g0230a0002c0002t0005g0234others(4): Show | 8 | HG01243.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.361+2923G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537973 | ||||||
| chr9:5538298
|
G | T | 1 | a0001c0001t0002g0102 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.361+3248G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538298 | ||||||
| chr9:5538354
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.361+3304G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538354 | ||||||
| chr9:5538407
|
C | T | 115 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(112): Show | 119 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.361+3357C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538407 | ||||||
| chr9:5538411
|
C | T | 30 | a0001c0001t0001g0067a0001c0001t0001g0194a0001c0001t0001g0198others(27): Show | 31 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.361+3361C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538411 | ||||||
| chr9:5538428
|
G | A | 1 | a0001c0001t0001g0346 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.361+3378G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538428 | ||||||
| chr9:5538440
|
C | T | 120 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(117): Show | 126 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.361+3390C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538440 | ||||||
| chr9:5538501
|
T | A | 1 | a0001c0001t0001g0310 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.361+3451T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538501 | ||||||
| chr9:5538512
|
T | C | 35 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0194others(32): Show | 38 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.361+3462T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538512 | ||||||
| chr9:5538545
|
G | A | 1 | a0002c0002t0020g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.361+3495G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538545 | ||||||
| chr9:5538607
|
T | G | 33 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0115others(30): Show | 37 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.361+3557T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538607 | ||||||
| chr9:5538610
|
G | C | 33 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0115others(30): Show | 37 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.361+3560G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538610 | ||||||
| chr9:5538628
|
T | C | 2 | a0001c0001t0001g0115a0002c0002t0013g0015 | 3 | HG03453.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.361+3578T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538628 | ||||||
| chr9:5538637
|
G | A | 32 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0194others(29): Show | 35 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.361+3587G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538637 | ||||||
| chr9:5538667
|
G | A | 77 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(74): Show | 79 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.361+3617G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538667 | ||||||
| chr9:5538775
|
A | T | 3 | a0001c0001t0001g0227a0002c0002t0001g0065a0002c0002t0014g0339 | 3 | HG02615.hp1 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.361+3725A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538775 | ||||||
| chr9:5538793
|
G | A | 22 | a0001c0001t0001g0067a0001c0001t0001g0194a0001c0001t0001g0198others(19): Show | 23 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.361+3743G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538793 | ||||||
| chr9:5538879
|
A | G | 175 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(172): Show | 184 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.361+3829A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538879 | ||||||
| chr9:5538998
|
G | T | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.361+3948G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538998 | ||||||
| chr9:5539033
|
A | G | 6 | a0001c0001t0001g0227a0002c0002t0001g0065a0002c0002t0001g0251others(3): Show | 6 | HG02615.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+3983A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539033 | ||||||
| chr9:5539057
|
T | C | 2 | a0001c0001t0003g0362a0001c0001t0003g0363 | 2 | NA18961.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.361+4007T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539057 | ||||||
| chr9:5539151
|
T | G | 94 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(91): Show | 97 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.361+4101T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539151 | ||||||
| chr9:5539175
|
T | G | 1 | a0001c0001t0001g0201 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.361+4125T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539175 | ||||||
| chr9:5539247
|
G | C | 94 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(91): Show | 97 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.361+4197G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539247 | ||||||
| chr9:5539256
|
A | G | 1 | a0002c0002t0001g0230 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.361+4206A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539256 | ||||||
| chr9:5539451
|
G | A | 6 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(3): Show | 6 | HG00733.hp2 HG01496.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+4401G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539451 | ||||||
| chr9:5539536
|
C | T | 1 | a0001c0001t0001g0289 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.361+4486C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539536 | ||||||
| chr9:5539537
|
G | A | 6 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(3): Show | 6 | HG00733.hp2 HG01496.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+4487G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539537 | ||||||
| chr9:5539627
|
G | C | 2 | a0002c0002t0001g0131a0002c0002t0001g0146 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.361+4577G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539627 | ||||||
| chr9:5539866
|
T | A | 22 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0194others(19): Show | 24 | HG00741.hp1 HG00741.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.361+4816T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539866 | ||||||
| chr9:5539929
|
C | T | 92 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(89): Show | 94 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.361+4879C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539929 | ||||||
| chr9:5539988
|
T | C | 1 | a0002c0002t0002g0108 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.361+4938T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539988 | ||||||
| chr9:5540154
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.361+5104T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540154 | ||||||
| chr9:5540167
|
T | G | 53 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0157others(50): Show | 57 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.361+5117T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540167 | ||||||
| chr9:5540183
|
C | T | 10 | a0001c0001t0001g0067a0001c0001t0001g0194a0001c0001t0001g0198others(7): Show | 10 | HG00741.hp1 HG00741.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.361+5133C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540183 | ||||||
| chr9:5540202
|
C | T | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.361+5152C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540202 | ||||||
| chr9:5540215
|
C | G | 93 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(90): Show | 95 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.361+5165C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540215 | ||||||
| chr9:5540249
|
C | G | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.361+5199C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540249 | ||||||
| chr9:5540252
|
T | A | 3 | a0002c0002t0001g0066a0002c0002t0009g0334a0002c0002t0009g0335 | 3 | HG02257.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.361+5202T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540252 | ||||||
| chr9:5540326
|
C | A | 93 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(90): Show | 95 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.361+5276C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540326 | ||||||
| chr9:5540350
|
C | T | 46 | a0001c0001t0001g0025a0001c0001t0001g0041a0001c0001t0001g0042others(43): Show | 48 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.361+5300C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540350 | ||||||
| chr9:5540364
|
A | G | 1 | a0002c0002t0002g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.361+5314A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540364 | ||||||
| chr9:5540528
|
G | C | 1 | a0002c0002t0002g0108 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.361+5478G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540528 | ||||||
| chr9:5540600
|
A | C | 1 | a0002c0002t0005g0160 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.361+5550A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540600 | ||||||
| chr9:5540651
|
C | CTA | 95 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(92): Show | 97 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.361+5601_361+5602i others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540651 | ||||||
| chr9:5540697
|
G | C | 2 | a0001c0001t0001g0256a0002c0002t0011g0107 | 2 | HG01192.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.361+5647G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540697 | ||||||
| chr9:5540782
|
A | T | 3 | a0002c0002t0001g0251a0002c0002t0001g0252a0004c0006t0019g0104 | 3 | HG02647.hp1 HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.361+5732A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540782 | ||||||
| chr9:5540838
|
A | C | 1 | a0001c0001t0001g0195 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.361+5788A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540838 | ||||||
| chr9:5540891
|
C | A | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.361+5841C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540891 | ||||||
| chr9:5540893
|
A | C | 13 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(10): Show | 16 | HG00438.hp1 NA18939.hp2 NA18943.hp1 others(13): Show |
intron_variant | MODIFIER | c.361+5843A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540893 | ||||||
| chr9:5541255
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.361+6205T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541255 | ||||||
| chr9:5541461
|
G | T | 2 | a0001c0001t0001g0227a0002c0002t0014g0339 | 2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.361+6411G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541461 | ||||||
| chr9:5541526
|
T | C | 6 | a0001c0001t0001g0069a0001c0001t0001g0253a0001c0001t0001g0254others(3): Show | 8 | HG01981.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.361+6476T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541526 | ||||||
| chr9:5541539
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.361+6489G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541539 | ||||||
| chr9:5541558
|
A | G | 1 | a0002c0002t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.361+6508A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541558 | ||||||
| chr9:5541603
|
T | C | 1 | a0002c0002t0006g0072 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.361+6553T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541603 | ||||||
| chr9:5541607
|
T | C | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.361+6557T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541607 | ||||||
| chr9:5541797
|
C | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 6 | HG01074.hp2 HG01168.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+6747C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541797 | ||||||
| chr9:5541877
|
G | A | 91 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(88): Show | 93 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.361+6827G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541877 | ||||||
| chr9:5541931
|
C | G | 30 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0194others(27): Show | 34 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.361+6881C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541931 | ||||||
| chr9:5541984
|
C | G | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | NA18984.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.361+6934C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541984 | ||||||
| chr9:5542030
|
A | G | 47 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0157others(44): Show | 50 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.361+6980A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542030 | ||||||
| chr9:5542032
|
A | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0171a0001c0001t0003g0350 | 4 | HG00642.hp1 HG01928.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.361+6982A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542032 | ||||||
| chr9:5542119
|
T | C | 1 | a0002c0002t0001g0205 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.361+7069T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542119 | ||||||
| chr9:5542339
|
A | T | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.362-6996A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542339 | ||||||
| chr9:5542364
|
C | G | 1 | a0002c0002t0002g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.362-6971C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542364 | ||||||
| chr9:5542367
|
AG | A | 91 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(88): Show | 93 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.362-6967delG | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542367 | ||||||
| chr9:5542369
|
C | A | 91 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(88): Show | 93 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.362-6966C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542369 | ||||||
| chr9:5542535
|
T | C | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.362-6800T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542535 | ||||||
| chr9:5542552
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.362-6783G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542552 | ||||||
| chr9:5542570
|
A | T | 1 | a0001c0001t0002g0037 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.362-6765A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542570 | ||||||
| chr9:5542636
|
G | A | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.362-6699G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542636 | ||||||
| chr9:5542749
|
C | T | 1 | a0001c0001t0002g0088 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.362-6586C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542749 | ||||||
| chr9:5542813
|
C | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 6 | HG01074.hp2 HG01168.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-6522C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542813 | ||||||
| chr9:5542848
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.362-6487A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542848 | ||||||
| chr9:5542859
|
C | CA | 89 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(86): Show | 91 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.362-6468dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5542859 | |||||
| chr9:5542881
|
G | A | 10 | a0001c0001t0001g0255a0001c0001t0001g0256a0002c0002t0006g0024others(7): Show | 10 | HG01192.hp1 HG02055.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.362-6454G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542881 | ||||||
| chr9:5542987
|
CAT | C | 16 | a0001c0001t0001g0017a0001c0001t0001g0155a0001c0001t0001g0203others(13): Show | 19 | HG00642.hp2 HG00735.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.362-6339_362-6338d others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5542987 | |||||
| chr9:5543028
|
A | G | 6 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(3): Show | 6 | HG00733.hp2 HG01496.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.362-6307A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543028 | ||||||
| chr9:5543087
|
A | G | 1 | a0001c0001t0004g0293 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.362-6248A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543087 | ||||||
| chr9:5543142
|
C | T | 10 | a0001c0001t0001g0227a0002c0002t0001g0065a0002c0002t0001g0251others(7): Show | 13 | HG02145.hp2 HG02615.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.362-6193C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543142 | ||||||
| chr9:5543241
|
A | G | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.362-6094A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543241 | ||||||
| chr9:5543271
|
T | G | 3 | a0001c0001t0001g0147a0001c0001t0002g0101a0001c0001t0002g0106 | 3 | HG01109.hp2 HG01123.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.362-6064T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543271 | ||||||
| chr9:5543310
|
T | C | 1 | a0002c0002t0011g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.362-6025T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543310 | ||||||
| chr9:5543311
|
G | T | 1 | a0002c0002t0011g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.362-6024G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543311 | ||||||
| chr9:5543315
|
A | G | 1 | a0002c0002t0011g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.362-6020A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543315 | ||||||
| chr9:5543330
|
G | A | 46 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0115others(43): Show | 50 | HG00741.hp1 HG00741.hp2 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.362-6005G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543330 | ||||||
| chr9:5543336
|
A | G | 1 | a0002c0002t0011g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.362-5999A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543336 | ||||||
| chr9:5543340
|
T | C | 2 | a0002c0002t0002g0329a0002c0002t0011g0043 | 2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.362-5995T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543340 | ||||||
| chr9:5543346
|
T | C | 1 | a0001c0001t0002g0319 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.362-5989T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543346 | ||||||
| chr9:5543367
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.362-5968G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543367 | ||||||
| chr9:5543395
|
C | T | 7 | a0001c0001t0001g0209a0001c0001t0004g0140a0001c0001t0004g0191others(4): Show | 7 | NA18942.hp1 NA18944.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.362-5940C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543395 | ||||||
| chr9:5543400
|
G | T | 1 | a0001c0001t0010g0085 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.362-5935G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543400 | ||||||
| chr9:5543434
|
G | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG00558.hp2 NA18945.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.362-5901G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543434 | ||||||
| chr9:5543534
|
G | C | 16 | a0001c0001t0001g0130a0001c0001t0001g0188a0001c0001t0001g0189others(13): Show | 16 | HG01081.hp1 HG01358.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.362-5801G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543534 | ||||||
| chr9:5543538
|
C | CA | 134 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0083others(131): Show | 139 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.362-5775dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5543538 | |||||
| chr9:5543538
|
C | CAA | 15 | a0001c0001t0001g0049a0001c0001t0001g0132a0001c0001t0001g0165others(12): Show | 15 | HG01074.hp2 HG01192.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.362-5776_362-5775d others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5543538 | |||||
| chr9:5543538
|
CA | C | 21 | a0001c0001t0001g0067a0001c0001t0001g0161a0001c0001t0001g0194others(18): Show | 23 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.362-5775delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5543538 | |||||
| chr9:5543616
|
A | T | 11 | a0001c0001t0001g0067a0001c0001t0001g0194a0001c0001t0001g0198others(8): Show | 11 | HG00741.hp1 HG00741.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-5719A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543616 | ||||||
| chr9:5543690
|
G | T | 2 | a0001c0001t0001g0227a0002c0002t0014g0339 | 2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.362-5645G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543690 | ||||||
| chr9:5544027
|
A | C | 33 | a0001c0001t0001g0067a0001c0001t0001g0115a0001c0001t0001g0194others(30): Show | 35 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.362-5308A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544027 | ||||||
| chr9:5544191
|
G | A | 1 | a0002c0002t0002g0108 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.362-5144G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544191 | ||||||
| chr9:5544235
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.362-5100G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544235 | ||||||
| chr9:5544405
|
A | G | 155 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0069others(152): Show | 162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.362-4930A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544405 | ||||||
| chr9:5544437
|
G | C | 2 | a0003c0003t0001g0029a0003c0003t0003g0249 | 2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.362-4898G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544437 | ||||||
| chr9:5544502
|
C | T | 1 | a0002c0002t0009g0332 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.362-4833C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544502 | ||||||
| chr9:5544740
|
G | GT | 145 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0069others(142): Show | 152 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.362-4595_362-4594i others(3): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544740 | ||||||
| chr9:5544742
|
C | T | 145 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0069others(142): Show | 152 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.362-4593C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544742 | ||||||
| chr9:5544744
|
C | G | 145 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0069others(142): Show | 152 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.362-4591C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544744 | ||||||
| chr9:5544769
|
G | A | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.362-4566G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544769 | ||||||
| chr9:5544976
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.362-4359A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544976 | ||||||
| chr9:5544992
|
G | A | 87 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(84): Show | 89 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.362-4343G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544992 | ||||||
| chr9:5545117
|
C | A | 6 | a0001c0001t0001g0069a0001c0001t0001g0253a0001c0001t0001g0254others(3): Show | 8 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.362-4218C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545117 | ||||||
| chr9:5545163
|
A | G | 1 | a0002c0002t0001g0181 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.362-4172A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545163 | ||||||
| chr9:5545183
|
G | C | 88 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(85): Show | 91 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.362-4152G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545183 | ||||||
| chr9:5545198
|
T | C | 145 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0069others(142): Show | 152 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.362-4137T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545198 | ||||||
| chr9:5545273
|
G | T | 2 | a0002c0002t0006g0072a0002c0002t0022g0355 | 2 | HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.362-4062G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545273 | ||||||
| chr9:5545430
|
G | T | 2 | a0001c0001t0001g0179a0002c0002t0001g0180 | 2 | NA18975.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.362-3905G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545430 | ||||||
| chr9:5545431
|
C | A | 1 | a0001c0001t0003g0360 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.362-3904C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545431 | ||||||
| chr9:5545849
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.362-3486T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545849 | ||||||
| chr9:5545911
|
G | A | 1 | a0005c0011t0001g0190 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.362-3424G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545911 | ||||||
| chr9:5545922
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.362-3413T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545922 | ||||||
| chr9:5546030
|
T | C | 180 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(177): Show | 189 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.362-3305T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546030 | ||||||
| chr9:5546496
|
A | C | 91 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(88): Show | 93 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.362-2839A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546496 | ||||||
| chr9:5546571
|
T | C | 183 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(180): Show | 192 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.362-2764T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546571 | ||||||
| chr9:5546599
|
T | G | 3 | a0001c0001t0001g0189a0002c0002t0001g0172a0002c0002t0001g0187 | 3 | HG03491.hp1 HG03927.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.362-2736T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546599 | ||||||
| chr9:5546602
|
G | T | 1 | a0001c0001t0001g0158 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.362-2733G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546602 | ||||||
| chr9:5546616
|
C | T | 1 | a0002c0002t0002g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.362-2719C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546616 | ||||||
| chr9:5546664
|
C | G | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.362-2671C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546664 | ||||||
| chr9:5546775
|
C | T | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.362-2560C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546775 | ||||||
| chr9:5546857
|
G | A | 156 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(153): Show | 165 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.362-2478G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546857 | ||||||
| chr9:5546882
|
C | T | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.362-2453C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546882 | ||||||
| chr9:5546993
|
G | T | 1 | a0001c0001t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.362-2342G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546993 | ||||||
| chr9:5547148
|
A | G | 2 | a0002c0002t0007g0001a0002c0002t0007g0116 | 4 | HG02809.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.362-2187A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547148 | ||||||
| chr9:5547288
|
C | T | 24 | a0001c0001t0001g0067a0001c0001t0001g0194a0001c0001t0001g0198others(21): Show | 25 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.362-2047C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547288 | ||||||
| chr9:5547408
|
C | T | 25 | a0001c0001t0001g0126a0001c0001t0001g0157a0001c0001t0001g0215others(22): Show | 27 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.362-1927C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547408 | ||||||
| chr9:5547421
|
T | G | 4 | a0002c0002t0002g0329a0002c0002t0009g0332a0002c0002t0009g0334others(1): Show | 4 | HG01884.hp2 HG02145.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-1914T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547421 | ||||||
| chr9:5547659
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.362-1676G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547659 | ||||||
| chr9:5547688
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.362-1647G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547688 | ||||||
| chr9:5547927
|
ACT | A | 21 | a0001c0001t0001g0067a0001c0001t0001g0194a0001c0001t0001g0198others(18): Show | 22 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.362-1405_362-1404d others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5547927 | |||||
| chr9:5547936
|
C | CA | 20 | a0001c0001t0001g0008a0001c0001t0001g0142a0001c0001t0001g0152others(17): Show | 22 | HG01074.hp1 HG01169.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.362-1378dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5547936 | |||||
| chr9:5547936
|
CA | C | 35 | a0001c0001t0001g0067a0001c0001t0001g0130a0001c0001t0001g0194others(32): Show | 36 | HG00735.hp1 HG00741.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.362-1378delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5547936 | |||||
| chr9:5547950
|
A | G | 1 | a0002c0002t0001g0282 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.362-1385A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547950 | ||||||
| chr9:5547960
|
A | T | 1 | a0002c0002t0001g0282 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.362-1375A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547960 | ||||||
| chr9:5548121
|
C | T | 1 | a0002c0002t0015g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.362-1214C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5548121 | ||||||
| chr9:5548484
|
A | G | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.362-851A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5548484 | ||||||
| chr9:5548542
|
T | C | 24 | a0001c0001t0001g0067a0001c0001t0001g0194a0001c0001t0001g0198others(21): Show | 25 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.362-793T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5548542 | ||||||
| chr9:5549063
|
T | C | 6 | a0002c0002t0001g0270a0002c0002t0001g0271a0002c0002t0001g0272others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-272T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5549063 | ||||||
| chr9:5549080
|
T | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0144others(17): Show | 23 | HG00438.hp2 HG00673.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.362-255T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5549080 | ||||||
| chr9:5549099
|
G | A | 130 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0069others(127): Show | 137 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.362-236G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5549099 | ||||||
| chr9:5549743
|
G | C | 14 | a0001c0001t0001g0067a0001c0001t0001g0194a0001c0001t0001g0198others(11): Show | 14 | HG00741.hp1 HG00741.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.631+139G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5549743 | ||||||
| chr9:5549884
|
C | G | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.631+280C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5549884 | ||||||
| chr9:5549952
|
T | A | 2 | a0001c0001t0003g0020a0001c0001t0004g0218 | 3 | NA18951.hp2 NA18961.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.631+348T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5549952 | ||||||
| chr9:5550135
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.631+531A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550135 | ||||||
| chr9:5550288
|
A | G | 2 | a0002c0002t0007g0001a0002c0002t0007g0116 | 4 | HG02809.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+684A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550288 | ||||||
| chr9:5550320
|
T | C | 1 | a0010c0005t0007g0117 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.631+716T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550320 | ||||||
| chr9:5550351
|
T | G | 1 | a0001c0001t0001g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.631+747T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550351 | ||||||
| chr9:5550430
|
T | G | 1 | a0002c0002t0001g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.631+826T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550430 | ||||||
| chr9:5550534
|
T | A | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.631+930T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550534 | ||||||
| chr9:5550685
|
ATC | A | 15 | a0001c0001t0001g0067a0001c0001t0001g0194a0001c0001t0001g0198others(12): Show | 16 | HG00741.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.631+1095_631+1096d others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 5550685 | |||||
| chr9:5550698
|
TC | T | 6 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0103others(3): Show | 6 | HG00741.hp2 HG01981.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+1095delC | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550698 | ||||||
| chr9:5550699
|
C | CT | 28 | a0001c0001t0001g0126a0001c0001t0001g0157a0001c0001t0001g0215others(25): Show | 30 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.631+1107dupT | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 5550699 | |||||
| chr9:5550699
|
CT | C | 88 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(85): Show | 90 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.631+1107delT | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 5550699 | |||||
| chr9:5550762
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.631+1158C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550762 | ||||||
| chr9:5550763
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.631+1159G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550763 | ||||||
| chr9:5550786
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.631+1182C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550786 | ||||||
| chr9:5550882
|
T | C | 131 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(128): Show | 136 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.631+1278T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550882 | ||||||
| chr9:5550973
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1369G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550973 | ||||||
| chr9:5551037
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.631+1433A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551037 | ||||||
| chr9:5551261
|
C | T | 151 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(148): Show | 159 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.631+1657C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551261 | ||||||
| chr9:5551380
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.631+1776C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551380 | ||||||
| chr9:5551385
|
G | A | 21 | a0001c0001t0001g0067a0001c0001t0001g0194a0001c0001t0001g0198others(18): Show | 22 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.631+1781G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551385 | ||||||
| chr9:5551413
|
T | G | 1 | a0001c0001t0001g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.631+1809T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551413 | ||||||
| chr9:5551451
|
A | T | 130 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0069others(127): Show | 137 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.631+1847A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551451 | ||||||
| chr9:5551529
|
T | G | 1 | a0001c0001t0001g0312 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.631+1925T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551529 | ||||||
| chr9:5551602
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.631+1998G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551602 | ||||||
| chr9:5551795
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.631+2191G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551795 | ||||||
| chr9:5551864
|
C | A | 21 | a0001c0001t0001g0067a0001c0001t0001g0194a0001c0001t0001g0198others(18): Show | 22 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.631+2260C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551864 | ||||||
| chr9:5551945
|
G | A | 130 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0069others(127): Show | 137 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.631+2341G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551945 | ||||||
| chr9:5552030
|
G | A | 1 | a0001c0001t0002g0093 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.631+2426G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552030 | ||||||
| chr9:5552152
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.631+2548G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552152 | ||||||
| chr9:5552166
|
T | C | 6 | a0002c0002t0001g0270a0002c0002t0001g0271a0002c0002t0001g0272others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+2562T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552166 | ||||||
| chr9:5552514
|
G | A | 5 | a0001c0001t0001g0069a0001c0001t0001g0253a0001c0001t0001g0254others(2): Show | 7 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.631+2910G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552514 | ||||||
| chr9:5552588
|
T | C | 1 | a0001c0001t0002g0079 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.631+2984T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552588 | ||||||
| chr9:5552753
|
T | G | 1 | a0004c0006t0019g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.631+3149T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552753 | ||||||
| chr9:5552786
|
A | G | 2 | a0001c0001t0001g0115a0002c0002t0002g0045 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.631+3182A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552786 | ||||||
| chr9:5552884
|
C | T | 1 | a0001c0001t0017g0309 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.631+3280C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552884 | ||||||
| chr9:5552900
|
T | G | 1 | a0002c0002t0001g0347 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.631+3296T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552900 | ||||||
| chr9:5552910
|
G | A | 1 | a0002c0002t0001g0383 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.631+3306G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552910 | ||||||
| chr9:5553068
|
T | C | 1 | a0001c0001t0012g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.631+3464T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553068 | ||||||
| chr9:5553162
|
A | C | 1 | a0002c0002t0001g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.631+3558A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553162 | ||||||
| chr9:5553191
|
A | C | 2 | a0002c0002t0006g0024a0002c0002t0006g0232 | 2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.631+3587A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553191 | ||||||
| chr9:5553237
|
A | C | 8 | a0001c0001t0001g0115a0002c0002t0001g0270a0002c0002t0001g0271others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.631+3633A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553237 | ||||||
| chr9:5553251
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.631+3647C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553251 | ||||||
| chr9:5553441
|
A | G | 1 | a0002c0002t0006g0072 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.631+3837A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553441 | ||||||
| chr9:5553703
|
C | A | 2 | a0001c0001t0001g0308a0002c0002t0001g0381 | 2 | HG03486.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.632-3915C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553703 | ||||||
| chr9:5553710
|
G | A | 1 | a0002c0002t0002g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.632-3908G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553710 | ||||||
| chr9:5553765
|
T | A | 69 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0122others(66): Show | 76 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.632-3853T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553765 | ||||||
| chr9:5553843
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.632-3775C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553843 | ||||||
| chr9:5553957
|
G | A | 6 | a0001c0001t0001g0227a0001c0001t0001g0343a0001c0001t0001g0344others(3): Show | 6 | HG02615.hp1 HG03225.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.632-3661G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553957 | ||||||
| chr9:5553991
|
C | T | 25 | a0001c0001t0001g0067a0001c0001t0001g0182a0001c0001t0001g0194others(22): Show | 26 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.632-3627C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553991 | ||||||
| chr9:5554035
|
T | C | 139 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0069others(136): Show | 147 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.632-3583T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554035 | ||||||
| chr9:5554095
|
C | A | 1 | a0001c0001t0001g0158 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.632-3523C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554095 | ||||||
| chr9:5554109
|
T | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0164a0001c0001t0001g0165others(3): Show | 7 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.632-3509T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554109 | ||||||
| chr9:5554219
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.632-3399A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554219 | ||||||
| chr9:5554274
|
C | T | 1 | a0001c0001t0010g0150 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.632-3344C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554274 | ||||||
| chr9:5554275
|
G | A | 2 | a0001c0001t0001g0256a0002c0002t0011g0107 | 2 | HG01192.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.632-3343G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554275 | ||||||
| chr9:5554401
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.632-3217C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554401 | ||||||
| chr9:5554430
|
A | G | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.632-3188A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554430 | ||||||
| chr9:5554770
|
C | T | 88 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(85): Show | 90 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.632-2848C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554770 | ||||||
| chr9:5554773
|
G | A | 137 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0069others(134): Show | 145 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.632-2845G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554773 | ||||||
| chr9:5554977
|
G | A | 5 | a0003c0003t0001g0029a0003c0003t0003g0248a0003c0003t0003g0249others(2): Show | 5 | HG02647.hp2 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.632-2641G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554977 | ||||||
| chr9:5555007
|
TA | T | 94 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(91): Show | 96 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.632-2602delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 5555007 | |||||
| chr9:5555023
|
A | C | 142 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0069others(139): Show | 150 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.632-2595A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555023 | ||||||
| chr9:5555130
|
A | T | 1 | a0001c0001t0017g0309 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.632-2488A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555130 | ||||||
| chr9:5555160
|
A | C | 72 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0122others(69): Show | 79 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.632-2458A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555160 | ||||||
| chr9:5555200
|
A | T | 5 | a0003c0003t0001g0029a0003c0003t0003g0248a0003c0003t0003g0249others(2): Show | 5 | HG02647.hp2 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.632-2418A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555200 | ||||||
| chr9:5555304
|
C | A | 87 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(84): Show | 89 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.632-2314C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555304 | ||||||
| chr9:5555348
|
C | T | 92 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(89): Show | 94 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.632-2270C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555348 | ||||||
| chr9:5555451
|
C | T | 1 | a0002c0004t0005g0229 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.632-2167C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555451 | ||||||
| chr9:5555452
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.632-2166G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555452 | ||||||
| chr9:5555489
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0144others(14): Show | 20 | HG00673.hp1 HG01123.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.632-2129G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555489 | ||||||
| chr9:5555554
|
G | A | 92 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(89): Show | 94 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.632-2064G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555554 | ||||||
| chr9:5555572
|
G | A | 15 | a0001c0001t0001g0067a0001c0001t0001g0182a0001c0001t0001g0194others(12): Show | 15 | HG00741.hp1 HG00741.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.632-2046G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555572 | ||||||
| chr9:5555572
|
G | T | 93 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(90): Show | 95 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.632-2046G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555572 | ||||||
| chr9:5555831
|
G | A | 93 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(90): Show | 95 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.632-1787G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555831 | ||||||
| chr9:5555897
|
C | T | 89 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(86): Show | 91 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.632-1721C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555897 | ||||||
| chr9:5555942
|
C | T | 1 | a0001c0001t0003g0361 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.632-1676C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555942 | ||||||
| chr9:5556024
|
G | A | 381 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(378): Show | 403 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.632-1594G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556024 | ||||||
| chr9:5556034
|
T | C | 173 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(170): Show | 182 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.632-1584T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556034 | ||||||
| chr9:5556122
|
T | G | 94 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(91): Show | 96 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.632-1496T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556122 | ||||||
| chr9:5556129
|
C | T | 1 | a0002c0002t0001g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.632-1489C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556129 | ||||||
| chr9:5556272
|
A | G | 2 | a0001c0001t0001g0115a0002c0002t0002g0045 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.632-1346A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556272 | ||||||
| chr9:5556372
|
CCTT | C | 8 | a0001c0001t0001g0069a0001c0001t0001g0253a0001c0001t0001g0254others(5): Show | 10 | HG02109.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.632-1245_632-1243d others(5): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556372 | ||||||
| chr9:5556406
|
T | C | 1 | a0001c0001t0004g0293 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.632-1212T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556406 | ||||||
| chr9:5556434
|
G | A | 94 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0083others(91): Show | 96 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.632-1184G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556434 | ||||||
| chr9:5556444
|
G | C | 1 | a0001c0001t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.632-1174G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556444 | ||||||
| chr9:5556514
|
A | C | 1 | a0002c0002t0001g0288 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.632-1104A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556514 | ||||||
| chr9:5556532
|
T | C | 2 | a0001c0001t0001g0115a0002c0002t0002g0045 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.632-1086T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556532 | ||||||
| chr9:5556677
|
C | T | 7 | a0001c0001t0001g0233a0002c0002t0001g0230a0002c0002t0005g0234others(4): Show | 8 | HG01243.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.632-941C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556677 | ||||||
| chr9:5556700
|
T | C | 1 | a0001c0001t0002g0088 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.632-918T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556700 | ||||||
| chr9:5556786
|
A | G | 186 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(183): Show | 198 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.632-832A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556786 | ||||||
| chr9:5556822
|
T | C | 99 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0069others(96): Show | 103 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.632-796T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556822 | ||||||
| chr9:5556999
|
A | C | 1 | a0008c0009t0001g0274 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.632-619A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556999 | ||||||
| chr9:5557104
|
G | C | 1 | a0001c0001t0003g0360 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.632-514G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557104 | ||||||
| chr9:5557108
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.632-510T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557108 | ||||||
| chr9:5557249
|
G | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0195a0001c0001t0001g0240 | 4 | NA18939.hp2 NA18943.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.632-369G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557249 | ||||||
| chr9:5557251
|
TGATA | T | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0042others(100): Show | 110 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.632-363_632-360del others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 5557251 | |||||
| chr9:5557255
|
A | G | 39 | a0001c0001t0001g0012a0001c0001t0001g0122a0001c0001t0001g0130others(36): Show | 42 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.632-363A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557255 | ||||||
| chr9:5557255
|
AGATG | A | 4 | a0001c0001t0001g0204a0001c0001t0002g0047a0002c0002t0002g0097others(1): Show | 4 | HG01978.hp1 HG02572.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.632-355_632-352del others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 5557255 | |||||
| chr9:5557263
|
G | T | 2 | a0001c0001t0001g0302a0001c0001t0001g0312 | 2 | HG02074.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.632-355G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557263 | ||||||
| chr9:5557267
|
T | G | 3 | a0001c0001t0001g0302a0001c0001t0001g0312a0001c0001t0002g0061 | 3 | HG02074.hp1 HG04228.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.632-351T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557267 | ||||||
| chr9:5557267
|
TGATG | T | 2 | a0001c0001t0003g0367a0001c0001t0004g0014 | 3 | HG00544.hp2 NA19077.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.632-340_632-337del others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 5557267 | |||||
| chr9:5557302
|
G | A | 1 | a0001c0001t0003g0337 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.632-316G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557302 | ||||||
| chr9:5557422
|
T | C | 25 | a0001c0001t0001g0120a0001c0001t0001g0130a0001c0001t0001g0132others(22): Show | 25 | HG00735.hp1 HG01081.hp1 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.632-196T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557422 | ||||||
| chr9:5557451
|
G | A | 1 | a0002c0002t0002g0320 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.632-167G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557451 | ||||||
| chr9:5557561
|
G | A | 2 | a0002c0002t0001g0347a0002c0002t0002g0097 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.632-57G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557561 | ||||||
| chr9:5557562
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0262 | 3 | HG00438.hp2 NA18949.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.632-56T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557562 | ||||||
| chr9:5557608
|
C | T | 1 | a0002c0002t0001g0323 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.632-10C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557608 | ||||||
| chr9:5557611
|
T | C | 1 | a0002c0002t0002g0097 | 1 | HG02572.hp2 | splice_region_variant&intron_variant | LOW | c.632-7T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557611 | ||||||
| chr9:5557768
|
T | G | 1 | a0003c0003t0003g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.766+16T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5557768 | ||||||
| chr9:5557793
|
T | A | 4 | a0001c0001t0001g0182a0001c0001t0001g0345a0001c0001t0001g0346others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+41T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5557793 | ||||||
| chr9:5557825
|
G | C | 13 | a0002c0002t0001g0230a0002c0002t0001g0270a0002c0002t0001g0271others(10): Show | 13 | HG02055.hp1 HG02109.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.766+73G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5557825 | ||||||
| chr9:5557926
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.766+174C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5557926 | ||||||
| chr9:5557962
|
A | C | 2 | a0002c0002t0001g0323a0002c0002t0002g0329 | 2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.766+210A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5557962 | ||||||
| chr9:5557975
|
G | C | 4 | a0001c0001t0002g0032a0001c0001t0002g0075a0001c0001t0002g0124others(1): Show | 4 | HG02523.hp2 NA18612.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+223G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5557975 | ||||||
| chr9:5558202
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.766+450G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558202 | ||||||
| chr9:5558224
|
G | T | 4 | a0001c0001t0001g0182a0001c0001t0001g0345a0001c0001t0001g0346others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+472G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558224 | ||||||
| chr9:5558347
|
G | A | 1 | a0001c0001t0002g0082 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.766+595G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558347 | ||||||
| chr9:5558360
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.766+608C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558360 | ||||||
| chr9:5558394
|
T | C | 1 | a0001c0001t0002g0096 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.766+642T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558394 | ||||||
| chr9:5558464
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.766+712T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558464 | ||||||
| chr9:5558793
|
CAGAG | C | 24 | a0002c0002t0001g0138a0002c0002t0001g0228a0002c0002t0001g0230others(21): Show | 25 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.766+1042_766+1045d others(6): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558793 | ||||||
| chr9:5558794
|
A | G | 5 | a0002c0002t0001g0251a0002c0002t0001g0252a0002c0002t0001g0323others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766+1042A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558794 | ||||||
| chr9:5558834
|
G | C | 24 | a0002c0002t0001g0138a0002c0002t0001g0228a0002c0002t0001g0230others(21): Show | 25 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.766+1082G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558834 | ||||||
| chr9:5558919
|
T | C | 1 | a0002c0002t0015g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.766+1167T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558919 | ||||||
| chr9:5559128
|
C | G | 1 | a0002c0002t0002g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.766+1376C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559128 | ||||||
| chr9:5559430
|
G | T | 1 | a0001c0001t0001g0195 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.766+1678G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559430 | ||||||
| chr9:5559495
|
T | G | 65 | a0001c0001t0001g0264a0001c0001t0002g0114a0001c0001t0003g0353others(62): Show | 70 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.766+1743T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559495 | ||||||
| chr9:5559539
|
T | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0083 | 2 | NA18981.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.766+1787T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559539 | ||||||
| chr9:5559835
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.766+2083C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559835 | ||||||
| chr9:5559893
|
C | T | 90 | a0001c0001t0002g0114a0001c0001t0003g0353a0002c0002t0001g0011others(87): Show | 96 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.766+2141C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559893 | ||||||
| chr9:5559937
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0154a0001c0001t0001g0185others(3): Show | 8 | NA18989.hp2 NA19001.hp1 NA19006.hp1 others(5): Show |
intron_variant | MODIFIER | c.766+2185C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559937 | ||||||
| chr9:5559962
|
C | G | 5 | a0002c0002t0001g0270a0002c0002t0001g0271a0002c0002t0001g0272others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.766+2210C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559962 | ||||||
| chr9:5560232
|
C | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0223a0001c0001t0001g0308others(1): Show | 4 | HG00140.hp2 HG02735.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+2480C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560232 | ||||||
| chr9:5560320
|
C | A | 1 | a0001c0001t0002g0103 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.766+2568C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560320 | ||||||
| chr9:5560372
|
T | G | 1 | a0002c0002t0001g0348 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.766+2620T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560372 | ||||||
| chr9:5560392
|
C | T | 11 | a0002c0002t0001g0138a0002c0002t0001g0228a0002c0002t0001g0266others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.766+2640C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560392 | ||||||
| chr9:5560469
|
C | T | 6 | a0002c0002t0005g0160a0002c0002t0005g0234a0002c0002t0023g0118others(3): Show | 7 | HG00741.hp2 HG01243.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.767-2693C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560469 | ||||||
| chr9:5560581
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0002g0089 | 2 | HG00621.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.767-2581C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560581 | ||||||
| chr9:5560607
|
C | G | 1 | a0002c0002t0001g0230 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.767-2555C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560607 | ||||||
| chr9:5560632
|
G | C | 1 | a0002c0002t0001g0323 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.767-2530G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560632 | ||||||
| chr9:5560635
|
C | T | 2 | a0002c0002t0001g0251a0002c0002t0001g0252 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.767-2527C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560635 | ||||||
| chr9:5560685
|
T | TGGTATCC others(324): Show |
3 | a0002c0002t0001g0271a0002c0002t0001g0273a0002c0002t0011g0043 | 3 | HG03139.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.767-2460_767-2459i others(333): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 5560685 | |||||
| chr9:5560685
|
T | TGGTATCC others(325): Show |
4 | a0002c0002t0001g0270a0002c0002t0001g0272a0003c0003t0003g0248others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.767-2460_767-2459i others(334): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 5560685 | |||||
| chr9:5560685
|
T | TGGTATCC others(326): Show |
4 | a0002c0002t0002g0045a0003c0003t0001g0029a0003c0003t0003g0249others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-2460_767-2459i others(335): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 5560685 | |||||
| chr9:5560685
|
T | TGGTATCC others(327): Show |
1 | a0002c0002t0014g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.767-2460_767-2459i others(336): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 5560685 | |||||
| chr9:5560685
|
T | TGGTATCC others(329): Show |
1 | a0002c0002t0001g0230 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.767-2460_767-2459i others(338): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 5560685 | |||||
| chr9:5560777
|
C | A | 2 | a0002c0002t0001g0172a0002c0002t0001g0187 | 2 | HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.767-2385C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560777 | ||||||
| chr9:5560822
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.767-2340G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560822 | ||||||
| chr9:5560892
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.767-2270T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560892 | ||||||
| chr9:5560922
|
C | G | 1 | a0002c0002t0001g0323 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.767-2240C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560922 | ||||||
| chr9:5561225
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.767-1937C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5561225 | ||||||
| chr9:5561356
|
A | C | 1 | a0001c0001t0002g0084 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.767-1806A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5561356 | ||||||
| chr9:5561423
|
A | C | 1 | a0001c0001t0001g0189 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.767-1739A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5561423 | ||||||
| chr9:5561616
|
G | C | 1 | a0001c0001t0002g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.767-1546G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5561616 | ||||||
| chr9:5561755
|
A | G | 3 | a0002c0002t0002g0329a0002c0002t0007g0001a0002c0002t0007g0116 | 5 | HG02145.hp2 HG02809.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.767-1407A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5561755 | ||||||
| chr9:5561851
|
T | C | 1 | a0002c0002t0001g0323 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.767-1311T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5561851 | ||||||
| chr9:5561962
|
C | T | 55 | a0001c0001t0002g0114a0001c0001t0003g0353a0002c0002t0001g0011others(52): Show | 59 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.767-1200C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5561962 | ||||||
| chr9:5562075
|
G | A | 2 | a0002c0002t0006g0068a0002c0002t0006g0071 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.767-1087G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5562075 | ||||||
| chr9:5562252
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.767-910G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5562252 | ||||||
| chr9:5562327
|
G | A | 1 | a0002c0002t0022g0355 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.767-835G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5562327 | ||||||
| chr9:5562563
|
T | A | 1 | a0002c0002t0001g0323 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.767-599T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5562563 | ||||||
| chr9:5562642
|
TA | T | 341 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(338): Show | 357 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(354): Show |
intron_variant | MODIFIER | c.767-510delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 5562642 | |||||
| chr9:5562713
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.767-449T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5562713 | ||||||
| chr9:5562762
|
C | A | 1 | a0002c0002t0001g0288 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.767-400C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5562762 | ||||||
| chr9:5563115
|
A | T | 11 | a0002c0002t0001g0138a0002c0002t0001g0228a0002c0002t0001g0266others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.767-47A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5563115 | ||||||
| chr9:5563217
|
T | C | 1 | a0002c0002t0001g0187 | 1 | HG03927.hp1 | splice_region_variant&intron_variant | LOW | c.816+6T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563217 | ||||||
| chr9:5563364
|
C | G | 1 | a0001c0001t0002g0084 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.816+153C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563364 | ||||||
| chr9:5563438
|
C | A | 1 | a0001c0001t0002g0096 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.816+227C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563438 | ||||||
| chr9:5563645
|
G | A | 1 | a0002c0002t0002g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.816+434G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563645 | ||||||
| chr9:5563769
|
T | C | 1 | a0001c0001t0010g0039 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.816+558T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563769 | ||||||
| chr9:5563881
|
C | G | 13 | a0001c0001t0002g0114a0001c0001t0017g0309a0002c0002t0001g0172others(10): Show | 13 | HG00735.hp1 HG01358.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.816+670C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563881 | ||||||
| chr9:5563942
|
T | C | 2 | a0002c0002t0001g0251a0002c0002t0001g0252 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.816+731T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563942 | ||||||
| chr9:5563988
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.816+777A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563988 | ||||||
| chr9:5564596
|
T | C | 1 | a0002c0002t0001g0197 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.816+1385T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5564596 | ||||||
| chr9:5564616
|
C | G | 1 | a0009c0008t0001g0245 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.816+1405C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5564616 | ||||||
| chr9:5564668
|
A | T | 1 | a0010c0005t0007g0117 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.816+1457A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5564668 | ||||||
| chr9:5564748
|
A | C | 61 | a0001c0001t0001g0264a0001c0001t0001g0336a0001c0001t0002g0114others(58): Show | 65 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.816+1537A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5564748 | ||||||
| chr9:5564817
|
G | C | 2 | a0002c0002t0001g0251a0002c0002t0001g0252 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.816+1606G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5564817 | ||||||
| chr9:5565172
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.816+1961T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565172 | ||||||
| chr9:5565316
|
G | A | 1 | a0002c0002t0001g0348 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.816+2105G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565316 | ||||||
| chr9:5565412
|
C | T | 5 | a0001c0001t0001g0203a0001c0001t0001g0226a0001c0001t0002g0037others(2): Show | 5 | NA18977.hp2 NA18980.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+2201C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565412 | ||||||
| chr9:5565413
|
G | A | 1 | a0002c0002t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.816+2202G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565413 | ||||||
| chr9:5565472
|
C | T | 5 | a0001c0001t0001g0123a0001c0001t0001g0215a0001c0001t0002g0005others(2): Show | 6 | HG00639.hp1 HG01257.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+2261C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565472 | ||||||
| chr9:5565601
|
G | A | 75 | a0001c0001t0002g0114a0002c0002t0001g0011a0002c0002t0001g0048others(72): Show | 81 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.816+2390G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565601 | ||||||
| chr9:5565684
|
C | A | 1 | a0002c0002t0001g0323 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.816+2473C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565684 | ||||||
| chr9:5565716
|
G | A | 17 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0174others(14): Show | 17 | HG00423.hp2 HG01099.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.816+2505G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565716 | ||||||
| chr9:5565860
|
G | C | 381 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(378): Show | 403 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.816+2649G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565860 | ||||||
| chr9:5565866
|
CAAT | C | 6 | a0002c0002t0005g0160a0002c0002t0005g0234a0002c0002t0023g0118others(3): Show | 7 | HG00741.hp2 HG01243.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.816+2658_816+2660d others(5): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr9 | 5565866 | |||||
| chr9:5566069
|
A | G | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.816+2858A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566069 | ||||||
| chr9:5566113
|
GC | G | 72 | a0001c0001t0002g0114a0002c0002t0001g0011a0002c0002t0001g0048others(69): Show | 78 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.816+2905delC | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr9 | 5566113 | |||||
| chr9:5566129
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.816+2918G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566129 | ||||||
| chr9:5566148
|
C | T | 1 | a0002c0002t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.816+2937C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566148 | ||||||
| chr9:5566192
|
C | G | 1 | a0002c0002t0002g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.816+2981C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566192 | ||||||
| chr9:5566240
|
C | T | 1 | a0002c0002t0006g0105 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.816+3029C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566240 | ||||||
| chr9:5566249
|
T | G | 2 | a0002c0002t0001g0251a0002c0002t0001g0252 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.816+3038T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566249 | ||||||
| chr9:5566281
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.816+3070C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566281 | ||||||
| chr9:5566334
|
G | C | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.816+3123G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566334 | ||||||
| chr9:5566381
|
A | T | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.816+3170A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566381 | ||||||
| chr9:5566393
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.816+3182C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566393 | ||||||
| chr9:5566465
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.816+3254G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566465 | ||||||
| chr9:5566474
|
G | C | 1 | a0002c0002t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.816+3263G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566474 | ||||||
| chr9:5566868
|
C | G | 1 | a0001c0001t0004g0305 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.817-3086C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566868 | ||||||
| chr9:5566929
|
C | T | 381 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(378): Show | 403 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.817-3025C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566929 | ||||||
| chr9:5567073
|
G | C | 6 | a0001c0001t0001g0147a0001c0001t0001g0165a0001c0001t0001g0168others(3): Show | 6 | HG00738.hp1 HG01074.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-2881G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567073 | ||||||
| chr9:5567182
|
G | A | 13 | a0002c0002t0001g0230a0002c0002t0001g0270a0002c0002t0001g0271others(10): Show | 13 | HG02055.hp1 HG02109.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.817-2772G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567182 | ||||||
| chr9:5567237
|
C | T | 2 | a0001c0001t0002g0004a0001c0001t0002g0059 | 3 | NA18965.hp2 NA18969.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.817-2717C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567237 | ||||||
| chr9:5567389
|
G | C | 2 | a0002c0002t0007g0001a0002c0002t0007g0116 | 4 | HG02809.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-2565G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567389 | ||||||
| chr9:5567471
|
C | G | 1 | a0001c0001t0010g0039 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.817-2483C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567471 | ||||||
| chr9:5567623
|
G | C | 1 | a0001c0001t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.817-2331G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567623 | ||||||
| chr9:5567678
|
C | T | 2 | a0002c0002t0007g0001a0002c0002t0007g0116 | 4 | HG02809.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-2276C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567678 | ||||||
| chr9:5567808
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.817-2146C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567808 | ||||||
| chr9:5568222
|
C | T | 69 | a0001c0001t0001g0258a0001c0001t0002g0114a0002c0002t0001g0011others(66): Show | 75 | HG00597.hp2 HG00609.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.817-1732C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5568222 | ||||||
| chr9:5568230
|
C | T | 1 | a0002c0002t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.817-1724C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5568230 | ||||||
| chr9:5568338
|
T | C | 2 | a0002c0002t0001g0251a0002c0002t0001g0252 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.817-1616T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5568338 | ||||||
| chr9:5568737
|
G | T | 45 | a0001c0001t0001g0258a0001c0001t0002g0114a0002c0002t0001g0011others(42): Show | 47 | HG00597.hp2 HG00609.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.817-1217G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5568737 | ||||||
| chr9:5569155
|
A | G | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.817-799A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5569155 | ||||||
| chr9:5569255
|
G | C | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.817-699G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5569255 | ||||||
| chr9:5569406
|
G | A | 33 | a0002c0002t0001g0011a0002c0002t0001g0070a0002c0002t0001g0127others(30): Show | 35 | HG00597.hp2 HG00609.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.817-548G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5569406 | ||||||
| chr9:5569495
|
A | G | 8 | a0001c0001t0001g0069a0001c0001t0001g0253a0001c0001t0001g0254others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-459A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5569495 | ||||||
| chr9:5569860
|
T | A | 52 | a0001c0001t0001g0258a0001c0001t0001g0264a0001c0001t0002g0114others(49): Show | 56 | HG00597.hp2 HG00609.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.817-94T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5569860 | ||||||
| chr9:5569871
|
G | C | 1 | a0002c0002t0001g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.817-83G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5569871 |