| geneid | 9360 |
|---|---|
| ensemblid | ENSG00000138398.17 |
| hgncid | 14650 |
| symbol | PPIG |
| name | peptidylprolyl isomerase G |
| refseq_nuc | NM_004792.3 |
| refseq_prot | NP_004783.2 |
| ensembl_nuc | ENST00000260970.8 |
| ensembl_prot | ENSP00000260970.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 169584351 |
| end | 169641406 |
| strand | + |
| ver | v1.2 |
| region | chr2:169584351-169641406 |
| region5000 | chr2:169579351-169646406 |
| regionname0 | PPIG_chr2_169584351_169641406 |
| regionname5000 | PPIG_chr2_169579351_169646406 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 754 | 161 | 45 | 19 | 78 | 4 | 14 | 60 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0002 | 1/0 | 754 | 160 | 23 | 30 | 85 | 6 | 15 | 69 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0003 | 0/0 | 754 | 57 | 24 | 13 | 6 | 4 | 10 | 4 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0004 | 0/0 | 754 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0005 | 0/0 | 754 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2265 | 156 | 43 | 19 | 75 | 4 | 14 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| c0002 | 1/0 | 2265 | 151 | 23 | 28 | 78 | 6 | 15 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| c0003 | 0/0 | 2265 | 57 | 24 | 13 | 6 | 4 | 10 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| c0004 | 0/0 | 2265 | 9 | 0 | 2 | 7 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| c0005 | 0/0 | 2265 | 3 | 0 | 0 | 3 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| c0006 | 0/0 | 2265 | 2 | 0 | 0 | 1 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| c0007 | 0/0 | 2265 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| c0008 | 0/0 | 2265 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 4093 | 103 | 18 | 28 | 40 | 4 | 12 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0002 | 0/0 | 4092 | 51 | 0 | 8 | 33 | 3 | 7 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0003 | 0/0 | 4094 | 44 | 6 | 2 | 32 | 1 | 3 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0004 | 0/0 | 4090 | 36 | 22 | 6 | 1 | 2 | 5 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0005 | 0/0 | 4092 | 26 | 0 | 0 | 22 | 1 | 3 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0006 | 0/1 | 4093 | 22 | 1 | 9 | 8 | 0 | 3 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0007 | 0/0 | 4093 | 20 | 20 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0008 | 0/0 | 4090 | 17 | 2 | 7 | 2 | 2 | 4 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0009 | 0/0 | 4092 | 10 | 0 | 0 | 9 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0010 | 0/0 | 4093 | 8 | 0 | 0 | 8 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0011 | 0/0 | 4093 | 8 | 8 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0012 | 0/0 | 4093 | 5 | 5 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0013 | 0/0 | 4092 | 4 | 4 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0014 | 0/0 | 4093 | 3 | 1 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0015 | 0/0 | 4093 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0016 | 0/0 | 4090 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0017 | 0/0 | 4092 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0018 | 0/0 | 4090 | 2 | 0 | 0 | 1 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0019 | 0/0 | 4093 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0020 | 0/0 | 4093 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0021 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0022 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0023 | 0/0 | 4093 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0024 | 0/0 | 4090 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0025 | 0/0 | 4093 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0026 | 0/0 | 4094 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0027 | 0/0 | 4093 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0028 | 0/0 | 4093 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0029 | 0/0 | 4093 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0030 | 0/0 | 4094 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0031 | 0/0 | 4090 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0032 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0033 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| t0034 | 0/0 | 4093 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2265 | 156 | 43 | 19 | 75 | 4 | 14 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0005 | 0/0 | 2265 | 3 | 0 | 0 | 3 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0007 | 0/0 | 2265 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0002c0002 | 1/0 | 2265 | 151 | 23 | 28 | 78 | 6 | 15 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0002c0004 | 0/0 | 2265 | 9 | 0 | 2 | 7 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0003c0003 | 0/0 | 2265 | 57 | 24 | 13 | 6 | 4 | 10 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0004c0008 | 0/0 | 2265 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0005c0006 | 0/0 | 2265 | 2 | 0 | 0 | 1 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 6356 | 48 | 0 | 8 | 30 | 3 | 7 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0005 | 0/0 | 6356 | 26 | 0 | 0 | 22 | 1 | 3 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0006 | 0/1 | 6357 | 22 | 1 | 9 | 8 | 0 | 3 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0007 | 0/0 | 6357 | 20 | 20 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0009 | 0/0 | 6356 | 10 | 0 | 0 | 9 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0011 | 0/0 | 6357 | 8 | 8 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0012 | 0/0 | 6357 | 5 | 5 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0013 | 0/0 | 6356 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0015 | 0/0 | 6357 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0017 | 0/0 | 6356 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0019 | 0/0 | 6357 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0021 | 0/0 | 6356 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0022 | 0/0 | 6356 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0025 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0026 | 0/0 | 6358 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0027 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0028 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0029 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0032 | 0/0 | 6356 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0001t0033 | 0/0 | 6356 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0005t0002 | 0/0 | 6356 | 3 | 0 | 0 | 3 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0001c0007t0013 | 0/0 | 6356 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0002c0002t0001 | 1/0 | 6357 | 101 | 16 | 28 | 40 | 4 | 12 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0002c0002t0003 | 0/0 | 6358 | 35 | 6 | 0 | 25 | 1 | 3 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0002c0002t0010 | 0/0 | 6357 | 8 | 0 | 0 | 8 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0002c0002t0014 | 0/0 | 6357 | 3 | 1 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0002c0002t0020 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0002c0002t0023 | 0/0 | 6357 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0002c0002t0030 | 0/0 | 6358 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0002c0002t0034 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0002c0004t0003 | 0/0 | 6358 | 9 | 0 | 2 | 7 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0003c0003t0004 | 0/0 | 6354 | 36 | 22 | 6 | 1 | 2 | 5 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0003c0003t0008 | 0/0 | 6354 | 17 | 2 | 7 | 2 | 2 | 4 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0003c0003t0016 | 0/0 | 6354 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0003c0003t0024 | 0/0 | 6354 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0003c0003t0031 | 0/0 | 6354 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0004c0008t0001 | 0/0 | 6357 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| a0005c0006t0018 | 0/0 | 6354 | 2 | 0 | 0 | 1 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | copy fasta | chr2 | 169579351 | 169646406 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0005g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0009g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0009g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0009g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0009g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0009g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0009g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0009g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0009g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0009g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0011g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0011g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0011g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0011g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0011g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0011g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0012g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0012g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0012g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0012g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0012g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0013g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0013g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0015g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0017g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0019g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0019g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0021g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0022g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0025g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0026g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0027g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0028g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0029g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0032g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0001t0033g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0005t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0005t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0005t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0007t0013g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0001c0007t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0001 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0010g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0010g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0010g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0010g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0010g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0010g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0010g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0010g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0014g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0014g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0014g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0020g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0023g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0030g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0002t0034g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0004t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0004t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0004t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0004t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0004t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0004t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0004t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0002c0004t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0004g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0008g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0016g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0016g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0024g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0003c0003t0031g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0004c0008t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0004c0008t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0005c0006t0018g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| a0005c0006t0018g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0089 | EUR | GBR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0239 | EUR | GBR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0345 | EUR | GBR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00140 | hp2 | a0003 | c0003 | t0008 | g0322 | EUR | GBR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0277 | EUR | FIN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00280 | hp2 | a0003 | c0003 | t0004 | g0113 | EUR | FIN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0082 | EUR | FIN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00323 | hp2 | a0003 | c0003 | t0004 | g0095 | EUR | FIN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00423 | hp1 | a0002 | c0002 | t0003 | g0176 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00438 | hp1 | a0001 | c0001 | t0019 | g0305 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0339 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00558 | hp2 | a0003 | c0003 | t0031 | g0360 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0334 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00609 | hp2 | a0002 | c0002 | t0010 | g0266 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00621 | hp1 | a0001 | c0001 | t0019 | g0131 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0349 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00733 | hp1 | a0003 | c0003 | t0004 | g0096 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0134 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00735 | hp1 | a0003 | c0003 | t0008 | g0324 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01069 | hp1 | a0003 | c0003 | t0008 | g0326 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0132 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0246 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01070 | hp2 | a0001 | c0001 | t0033 | g0140 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01071 | hp1 | a0001 | c0001 | t0029 | g0133 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0148 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0232 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0135 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0145 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0248 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01099 | hp1 | a0003 | c0003 | t0004 | g0128 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0153 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01106 | hp1 | a0003 | c0003 | t0008 | g0130 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01109 | hp1 | a0003 | c0003 | t0008 | g0361 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0264 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01168 | hp1 | a0003 | c0003 | t0008 | g0319 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0155 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0141 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0159 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0213 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0317 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01192 | hp2 | a0002 | c0004 | t0003 | g0012 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0230 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01255 | hp2 | a0003 | c0003 | t0004 | g0003 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01256 | hp1 | a0003 | c0003 | t0004 | g0010 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01256 | hp2 | a0003 | c0003 | t0008 | g0122 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01258 | hp1 | a0003 | c0003 | t0004 | g0010 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0275 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0278 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0303 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0147 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0233 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0224 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01358 | hp2 | a0002 | c0004 | t0003 | g0012 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0206 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01496 | hp1 | a0003 | c0003 | t0004 | g0357 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0279 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0297 | EUR | IBS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0283 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01884 | hp2 | a0003 | c0003 | t0004 | g0127 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0205 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01891 | hp2 | a0003 | c0003 | t0004 | g0108 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0270 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01978 | hp2 | a0003 | c0003 | t0008 | g0328 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02027 | hp1 | a0003 | c0003 | t0004 | g0098 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02055 | hp1 | a0003 | c0003 | t0004 | g0097 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02056 | hp1 | a0002 | c0002 | t0003 | g0189 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0139 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0346 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0154 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02129 | hp1 | a0002 | c0002 | t0003 | g0170 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02132 | hp1 | a0002 | c0002 | t0020 | g0234 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02132 | hp2 | a0001 | c0001 | t0006 | g0156 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0344 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02135 | hp2 | a0002 | c0002 | t0030 | g0193 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0254 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CDX | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | CDX | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0298 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0311 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02258 | hp2 | a0001 | c0007 | t0013 | g0028 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0249 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02280 | hp1 | a0001 | c0001 | t0028 | g0137 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0273 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0253 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02451 | hp1 | a0003 | c0003 | t0008 | g0321 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02451 | hp2 | a0001 | c0001 | t0015 | g0032 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02523 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02523 | hp2 | a0001 | c0001 | t0009 | g0066 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02572 | hp1 | a0003 | c0003 | t0004 | g0100 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02602 | hp1 | a0003 | c0003 | t0008 | g0327 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0093 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02615 | hp2 | a0003 | c0003 | t0004 | g0116 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0304 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0161 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0289 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0163 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0350 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02698 | hp2 | a0003 | c0003 | t0024 | g0117 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0030 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0023 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0296 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0094 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02735 | hp1 | a0002 | c0002 | t0003 | g0182 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0146 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02738 | hp1 | a0003 | c0003 | t0008 | g0358 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0215 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0290 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02809 | hp2 | a0003 | c0003 | t0004 | g0123 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02886 | hp1 | a0003 | c0003 | t0004 | g0107 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0150 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02895 | hp1 | a0002 | c0002 | t0003 | g0173 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02895 | hp2 | a0003 | c0003 | t0004 | g0355 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02896 | hp1 | a0003 | c0003 | t0004 | g0099 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02897 | hp1 | a0002 | c0002 | t0014 | g0177 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02922 | hp1 | a0003 | c0003 | t0004 | g0126 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02922 | hp2 | a0003 | c0003 | t0004 | g0104 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02965 | hp1 | a0001 | c0001 | t0015 | g0031 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02965 | hp2 | a0003 | c0003 | t0004 | g0003 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02970 | hp1 | a0001 | c0001 | t0012 | g0041 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02970 | hp2 | a0004 | c0008 | t0001 | g0302 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02976 | hp1 | a0003 | c0003 | t0008 | g0329 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0294 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0342 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03041 | hp1 | a0002 | c0002 | t0003 | g0178 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0040 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03130 | hp1 | a0003 | c0003 | t0004 | g0125 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03130 | hp2 | a0004 | c0008 | t0001 | g0301 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03139 | hp1 | a0001 | c0007 | t0013 | g0029 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0091 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03195 | hp1 | a0001 | c0001 | t0012 | g0035 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03195 | hp2 | a0003 | c0003 | t0004 | g0356 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03209 | hp1 | a0002 | c0002 | t0003 | g0308 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03209 | hp2 | a0001 | c0001 | t0025 | g0033 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0014 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03225 | hp2 | a0002 | c0002 | t0003 | g0309 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03239 | hp1 | a0003 | c0003 | t0004 | g0111 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03239 | hp2 | a0002 | c0002 | t0003 | g0179 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0287 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03453 | hp2 | a0003 | c0003 | t0004 | g0106 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0306 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03486 | hp2 | a0001 | c0001 | t0026 | g0034 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03490 | hp1 | a0003 | c0003 | t0008 | g0320 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03490 | hp2 | a0003 | c0003 | t0004 | g0119 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0332 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0245 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0244 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03492 | hp2 | a0003 | c0003 | t0004 | g0121 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0312 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0241 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03540 | hp1 | a0003 | c0003 | t0004 | g0003 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0285 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03654 | hp1 | a0005 | c0006 | t0018 | g0114 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0276 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0160 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0138 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03831 | hp2 | a0003 | c0003 | t0004 | g0120 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0252 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0220 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0235 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03927 | hp2 | a0001 | c0001 | t0009 | g0068 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0280 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0209 | SAS | STU | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | STU | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0318 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | STU | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG04199 | hp2 | a0002 | c0002 | t0003 | g0186 | SAS | STU | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG04228 | hp1 | a0003 | c0003 | t0004 | g0115 | SAS | STU | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0242 | SAS | STU | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18522 | hp1 | a0001 | c0001 | t0013 | g0027 | AFR | YRI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0092 | AFR | YRI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18612 | hp1 | a0002 | c0002 | t0003 | g0190 | EAS | CHB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18612 | hp2 | a0001 | c0005 | t0002 | g0079 | EAS | CHB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0335 | EAS | CHB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18747 | hp2 | a0002 | c0002 | t0010 | g0238 | EAS | CHB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0202 | AFR | YRI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0299 | AFR | YRI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18939 | hp2 | a0002 | c0002 | t0003 | g0200 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18942 | hp2 | a0001 | c0001 | t0009 | g0076 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18943 | hp2 | a0001 | c0001 | t0022 | g0059 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18945 | hp1 | a0002 | c0002 | t0010 | g0013 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18945 | hp2 | a0001 | c0001 | t0017 | g0004 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18946 | hp1 | a0002 | c0004 | t0003 | g0195 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18946 | hp2 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18947 | hp1 | a0002 | c0002 | t0034 | g0231 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18948 | hp1 | a0002 | c0002 | t0010 | g0313 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18948 | hp2 | a0002 | c0002 | t0003 | g0180 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18950 | hp2 | a0002 | c0002 | t0003 | g0187 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18951 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0331 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18953 | hp1 | a0002 | c0002 | t0010 | g0237 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18953 | hp2 | a0002 | c0002 | t0003 | g0172 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18954 | hp1 | a0002 | c0002 | t0003 | g0183 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18957 | hp2 | a0002 | c0002 | t0010 | g0295 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18960 | hp1 | a0002 | c0002 | t0003 | g0199 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18961 | hp1 | a0002 | c0002 | t0003 | g0184 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18962 | hp2 | a0002 | c0002 | t0003 | g0185 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18965 | hp1 | a0002 | c0004 | t0003 | g0191 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18965 | hp2 | a0001 | c0001 | t0006 | g0143 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18966 | hp2 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18972 | hp2 | a0002 | c0002 | t0010 | g0208 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0352 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18982 | hp2 | a0002 | c0002 | t0014 | g0201 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18984 | hp1 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18985 | hp2 | a0001 | c0001 | t0009 | g0026 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18986 | hp1 | a0002 | c0002 | t0003 | g0198 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18986 | hp2 | a0002 | c0002 | t0003 | g0167 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18990 | hp2 | a0001 | c0001 | t0005 | g0347 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0348 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0333 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18993 | hp2 | a0002 | c0002 | t0003 | g0194 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18995 | hp2 | a0001 | c0001 | t0005 | g0336 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18997 | hp2 | a0003 | c0003 | t0008 | g0325 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18998 | hp2 | a0003 | c0003 | t0008 | g0359 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0337 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18999 | hp2 | a0001 | c0001 | t0021 | g0007 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19000 | hp1 | a0001 | c0005 | t0002 | g0077 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19000 | hp2 | a0002 | c0004 | t0003 | g0192 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19001 | hp1 | a0001 | c0001 | t0005 | g0341 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19001 | hp2 | a0001 | c0001 | t0009 | g0051 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0149 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19002 | hp2 | a0002 | c0002 | t0003 | g0169 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19003 | hp1 | a0005 | c0006 | t0018 | g0109 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19003 | hp2 | a0001 | c0001 | t0009 | g0038 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19004 | hp2 | a0002 | c0004 | t0003 | g0196 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19006 | hp1 | a0001 | c0001 | t0006 | g0152 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19006 | hp2 | a0002 | c0002 | t0003 | g0164 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19007 | hp1 | a0002 | c0002 | t0003 | g0168 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0343 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19009 | hp2 | a0003 | c0003 | t0016 | g0112 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19010 | hp2 | a0002 | c0004 | t0003 | g0364 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0338 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0203 | AFR | LWK | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19030 | hp2 | a0001 | c0001 | t0013 | g0037 | AFR | LWK | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0288 | AFR | LWK | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19043 | hp2 | a0003 | c0003 | t0004 | g0105 | AFR | LWK | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19056 | hp1 | a0002 | c0002 | t0014 | g0166 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0340 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19062 | hp2 | a0002 | c0004 | t0003 | g0174 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19064 | hp2 | a0002 | c0004 | t0003 | g0363 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0351 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19068 | hp1 | a0002 | c0002 | t0010 | g0211 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19070 | hp1 | a0001 | c0001 | t0009 | g0005 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19074 | hp1 | a0003 | c0003 | t0016 | g0110 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0354 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19075 | hp1 | a0002 | c0002 | t0003 | g0197 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19077 | hp1 | a0002 | c0002 | t0003 | g0175 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19077 | hp2 | a0001 | c0001 | t0009 | g0058 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0362 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19083 | hp1 | a0002 | c0002 | t0003 | g0165 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19088 | hp1 | a0001 | c0005 | t0002 | g0078 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19088 | hp2 | a0002 | c0002 | t0003 | g0188 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19091 | hp1 | a0001 | c0001 | t0009 | g0073 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0353 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0284 | AFR | YRI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA19240 | hp2 | a0003 | c0003 | t0004 | g0129 | AFR | YRI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0310 | AFR | ASW | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0157 | AFR | ASW | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0181 | EUR | TSI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA20805 | hp1 | a0002 | c0002 | t0023 | g0218 | EUR | TSI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA20805 | hp2 | a0003 | c0003 | t0008 | g0330 | EUR | TSI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | GIH | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA20905 | hp2 | a0003 | c0003 | t0008 | g0323 | SAS | GIH | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0226 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02109 | hp1 | a0003 | c0003 | t0004 | g0102 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02109 | hp2 | a0001 | c0001 | t0027 | g0017 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0292 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0162 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02559 | hp1 | a0003 | c0003 | t0004 | g0124 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG02559 | hp2 | a0001 | c0001 | t0012 | g0036 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0014 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0307 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG06807 | hp1 | a0003 | c0003 | t0004 | g0103 | AFR | USA | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0300 | AFR | USA | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18955 | hp1 | a0002 | c0002 | t0003 | g0171 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA18955 | hp2 | a0001 | c0001 | t0017 | g0004 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA20300 | hp1 | a0003 | c0003 | t0004 | g0101 | AFR | USA | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0204 | AFR | USA | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0286 | AFR | LWK | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| NA21309 | hp2 | a0001 | c0001 | t0032 | g0136 | AFR | LWK | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0006 | g0151 | REF | REF | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0118 | REF | REF | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169604026
|
A | C | 1 | a0001 | 8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
splice_region_variant | LOW | c.-16A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 3/14 | chr2 | 169604026 | ||||||
| chr2:169636593
|
T | A | 3 | a0001a0003a0005 | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
missense_variant | MODERATE | c.1335T>A | p.Asp445Glu | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1544/6357 | 1335/2265 | 445/754 | chr2 | 169636593 | ||
| chr2:169637057
|
G | C | 1 | a0005 | 2 | HG03654.hp1 NA19003.hp1 |
missense_variant | MODERATE | c.1799G>C | p.Arg600Thr | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2008/6357 | 1799/2265 | 600/754 | chr2 | 169637057 | ||
| chr2:169637167
|
C | G | 1 | a0004 | 2 | HG02970.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.1909C>G | p.Gln637Glu | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2118/6357 | 1909/2265 | 637/754 | chr2 | 169637167 | ||
| chr2:169637353
|
A | G | 2 | a0003a0005 | 59 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
missense_variant | MODERATE | c.2095A>G | p.Asn699Asp | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2304/6357 | 2095/2265 | 699/754 | chr2 | 169637353 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169608672
|
C | T | 1 | a0001c0005 | 3 | NA18612.hp2 NA19000.hp1 NA19088.hp1 |
splice_region_variant&synonymous_variant | LOW | c.291C>T | p.Asp97Asp | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/14 | 500/6357 | 291/2265 | 97/754 | chr2 | 169608672 | ||
| chr2:169636743
|
A | G | 1 | a0002c0004 | 9 | HG01192.hp2 HG01358.hp2 NA18946.hp1 others(6): Show |
synonymous_variant | LOW | c.1485A>G | p.Glu495Glu | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1694/6357 | 1485/2265 | 495/754 | chr2 | 169636743 | ||
| chr2:169637274
|
T | C | 1 | a0001c0007 | 2 | HG02258.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.2016T>C | p.Asn672Asn | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2225/6357 | 2016/2265 | 672/754 | chr2 | 169637274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169584385
|
G | T | 1 | a0001c0001t0019 | 2 | HG00438.hp1 HG00621.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-175G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/14 | chr2 | 169584385 | ||||||
| chr2:169584406
|
G | A | 1 | a0002c0002t0020 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-154G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/14 | 19636 | chr2 | 169584406 | |||||
| chr2:169584452
|
G | A | 1 | a0001c0001t0021 | 1 | NA18999.hp2 | 5_prime_UTR_variant | MODIFIER | c.-108G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/14 | 19590 | chr2 | 169584452 | |||||
| chr2:169637557
|
G | A | 2 | a0001c0001t0009a0001c0001t0022 | 11 | HG02523.hp2 HG03927.hp2 NA18942.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*34G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 34 | chr2 | 169637557 | |||||
| chr2:169637935
|
T | C | 1 | a0002c0002t0023 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 412 | chr2 | 169637935 | |||||
| chr2:169638324
|
T | G | 1 | a0003c0003t0024 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*801T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 801 | chr2 | 169638324 | |||||
| chr2:169638341
|
T | TA | 14 | a0001c0001t0006a0001c0001t0007a0001c0001t0011others(11): Show | 109 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*830dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 831 | INFO_REALIGN_3_PRIME | chr2 | 169638341 | ||||
| chr2:169638747
|
A | G | 1 | a0001c0001t0022 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1224A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1224 | chr2 | 169638747 | |||||
| chr2:169638856
|
A | G | 1 | a0002c0002t0034 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1333A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1333 | chr2 | 169638856 | |||||
| chr2:169639157
|
C | A | 4 | a0001c0001t0012a0001c0001t0015a0001c0001t0025others(1): Show | 9 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1634C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1634 | chr2 | 169639157 | |||||
| chr2:169639294
|
T | C | 1 | a0001c0001t0015 | 2 | HG02451.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1771T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1771 | chr2 | 169639294 | |||||
| chr2:169639299
|
T | A | 1 | a0002c0002t0010 | 8 | HG00609.hp2 NA18747.hp2 NA18945.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1776T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1776 | chr2 | 169639299 | |||||
| chr2:169639418
|
AT | A | 27 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(24): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1903delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1903 | INFO_REALIGN_3_PRIME | chr2 | 169639418 | ||||
| chr2:169639505
|
C | T | 4 | a0001c0001t0006a0001c0001t0019a0001c0001t0029others(1): Show | 26 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1982C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1982 | chr2 | 169639505 | |||||
| chr2:169639976
|
C | T | 1 | a0005c0006t0018 | 2 | HG03654.hp1 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2453C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2453 | chr2 | 169639976 | |||||
| chr2:169640080
|
C | T | 1 | a0001c0001t0025 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2557C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2557 | chr2 | 169640080 | |||||
| chr2:169640102
|
G | T | 2 | a0001c0001t0013a0001c0007t0013 | 4 | HG02258.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2579G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2579 | chr2 | 169640102 | |||||
| chr2:169640171
|
A | G | 2 | a0001c0001t0028a0001c0001t0032 | 2 | HG02280.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2648A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2648 | chr2 | 169640171 | |||||
| chr2:169640535
|
G | T | 1 | a0002c0002t0030 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3012G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3012 | chr2 | 169640535 | |||||
| chr2:169640669
|
T | C | 1 | a0001c0001t0005 | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3146T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3146 | chr2 | 169640669 | |||||
| chr2:169640911
|
G | A | 2 | a0003c0003t0008a0003c0003t0031 | 18 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3388G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3388 | chr2 | 169640911 | |||||
| chr2:169640989
|
T | G | 1 | a0003c0003t0031 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3466T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3466 | chr2 | 169640989 | |||||
| chr2:169641024
|
A | G | 5 | a0001c0001t0017a0002c0002t0003a0002c0002t0014others(2): Show | 50 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*3501A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3501 | chr2 | 169641024 | |||||
| chr2:169641043
|
T | C | 1 | a0003c0003t0016 | 2 | NA19009.hp2 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3520T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3520 | chr2 | 169641043 | |||||
| chr2:169641136
|
G | A | 1 | a0001c0001t0027 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3613G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3613 | chr2 | 169641136 | |||||
| chr2:169641136
|
GCT | G | 6 | a0003c0003t0004a0003c0003t0008a0003c0003t0016others(3): Show | 59 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3618_*3619delCT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3618 | INFO_REALIGN_3_PRIME | chr2 | 169641136 | ||||
| chr2:169641254
|
A | C | 2 | a0001c0001t0028a0001c0001t0032 | 2 | HG02280.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3731A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3731 | chr2 | 169641254 | |||||
| chr2:169641254
|
A | G | 2 | a0001c0001t0029a0001c0001t0033 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3731A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3731 | chr2 | 169641254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169584491
|
G | A | 83 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(80): Show | 88 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(85): Show |
splice_donor_variant&intron_variant | HIGH | c.-70+1G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169584491 | ||||||
| chr2:169584508
|
C | G | 2 | a0002c0004t0003g0363a0002c0004t0003g0364 | 2 | NA19010.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-70+18C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169584508 | ||||||
| chr2:169584916
|
G | A | 10 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70+426G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169584916 | ||||||
| chr2:169584952
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-70+462C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169584952 | ||||||
| chr2:169585020
|
C | A | 1 | a0001c0001t0005g0090 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-70+530C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585020 | ||||||
| chr2:169585050
|
T | C | 5 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(2): Show | 6 | HG02145.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70+560T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585050 | ||||||
| chr2:169585253
|
T | C | 1 | a0001c0001t0002g0025 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-70+763T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585253 | ||||||
| chr2:169585270
|
C | CCTTTTTT others(5): Show |
1 | a0001c0001t0009g0026 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-70+780_-70+781ins others(12): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585270 | ||||||
| chr2:169585270
|
C | CTTTTTTT others(3): Show |
33 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(30): Show | 33 | HG00621.hp1 HG00733.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(10): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | |||||
| chr2:169585270
|
C | CTTTTTTT others(4): Show |
161 | a0001c0001t0002g0039a0001c0001t0007g0202a0001c0001t0007g0203others(158): Show | 166 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(11): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | |||||
| chr2:169585270
|
C | CTTTTTTT others(5): Show |
74 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(71): Show | 81 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(12): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | |||||
| chr2:169585270
|
C | CTTTTTTT others(6): Show |
13 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0088others(10): Show | 13 | HG01433.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(13): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | |||||
| chr2:169585270
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0007g0023a0001c0001t0007g0024 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(14): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | |||||
| chr2:169585270
|
C | CTTTTTTT others(8): Show |
2 | a0003c0003t0008g0319a0003c0003t0008g0320 | 2 | HG01168.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(15): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | |||||
| chr2:169585270
|
C | CTTTTTTT others(9): Show |
35 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(32): Show | 35 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(16): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | |||||
| chr2:169585270
|
C | CTTTTTTT others(10): Show |
8 | a0001c0001t0005g0362a0003c0003t0004g0355a0003c0003t0004g0356others(5): Show | 8 | HG00558.hp2 HG01109.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(17): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | |||||
| chr2:169585533
|
A | G | 7 | a0002c0002t0001g0298a0002c0002t0001g0299a0002c0002t0001g0300others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70+1043A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585533 | ||||||
| chr2:169585591
|
G | C | 2 | a0001c0001t0019g0131a0001c0001t0019g0305 | 2 | HG00438.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.-70+1101G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585591 | ||||||
| chr2:169585657
|
A | G | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.-70+1167A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585657 | ||||||
| chr2:169585827
|
A | T | 1 | a0001c0001t0006g0160 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-70+1337A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585827 | ||||||
| chr2:169586077
|
T | C | 310 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(307): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-70+1587T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586077 | ||||||
| chr2:169586078
|
G | C | 4 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(1): Show | 4 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70+1588G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586078 | ||||||
| chr2:169586112
|
A | G | 1 | a0001c0001t0002g0085 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-70+1622A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586112 | ||||||
| chr2:169586130
|
C | T | 1 | a0001c0001t0002g0025 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-70+1640C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586130 | ||||||
| chr2:169586132
|
TAAAC | T | 17 | a0003c0003t0008g0130a0003c0003t0008g0319a0003c0003t0008g0320others(14): Show | 17 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-70+1645_-70+1648d others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169586132 | |||||
| chr2:169586165
|
T | A | 4 | a0001c0001t0011g0161a0001c0001t0011g0162a0001c0001t0011g0163others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+1675T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586165 | ||||||
| chr2:169586200
|
C | A | 7 | a0002c0002t0003g0164a0002c0002t0003g0165a0002c0002t0003g0167others(4): Show | 7 | HG02129.hp1 NA18986.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+1710C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586200 | ||||||
| chr2:169586230
|
A | G | 4 | a0001c0001t0005g0351a0001c0001t0005g0352a0001c0001t0005g0353others(1): Show | 4 | NA18981.hp2 NA19066.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+1740A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586230 | ||||||
| chr2:169586238
|
T | A | 1 | a0002c0002t0003g0171 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-70+1748T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586238 | ||||||
| chr2:169586241
|
T | C | 28 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(25): Show | 28 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.-70+1751T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586241 | ||||||
| chr2:169586249
|
T | C | 46 | a0002c0002t0003g0011a0002c0002t0003g0164a0002c0002t0003g0165others(43): Show | 48 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.-70+1759T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586249 | ||||||
| chr2:169586265
|
A | C | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+1775A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586265 | ||||||
| chr2:169586266
|
G | T | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+1776G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586266 | ||||||
| chr2:169586275
|
T | TTGTCAGG others(11): Show |
1 | a0002c0002t0003g0172 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-70+1797_-70+1814d others(20): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169586275 | |||||
| chr2:169586503
|
A | T | 1 | a0002c0002t0001g0297 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-70+2013A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586503 | ||||||
| chr2:169586525
|
A | C | 40 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(37): Show | 41 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.-70+2035A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586525 | ||||||
| chr2:169586555
|
G | C | 31 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(28): Show | 32 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-70+2065G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586555 | ||||||
| chr2:169586560
|
G | T | 1 | a0001c0001t0005g0350 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-70+2070G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586560 | ||||||
| chr2:169586619
|
A | C | 1 | a0001c0001t0007g0205 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-70+2129A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586619 | ||||||
| chr2:169586738
|
C | T | 1 | a0002c0002t0001g0296 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-70+2248C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586738 | ||||||
| chr2:169586742
|
TTTAG | T | 6 | a0001c0001t0012g0030a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-70+2257_-70+2260d others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169586742 | |||||
| chr2:169586933
|
T | G | 9 | a0001c0001t0012g0030a0001c0001t0012g0035a0001c0001t0012g0036others(6): Show | 9 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-70+2443T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586933 | ||||||
| chr2:169587023
|
T | C | 1 | a0002c0002t0001g0206 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-70+2533T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587023 | ||||||
| chr2:169587177
|
T | C | 3 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0026g0034 | 3 | HG02559.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-70+2687T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587177 | ||||||
| chr2:169587233
|
C | T | 2 | a0001c0001t0007g0021a0001c0001t0007g0022 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-70+2743C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587233 | ||||||
| chr2:169587249
|
C | CT | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.-70+2769dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169587249 | |||||
| chr2:169587308
|
C | G | 111 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(108): Show | 114 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-70+2818C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587308 | ||||||
| chr2:169587435
|
T | A | 1 | a0001c0001t0012g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-70+2945T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587435 | ||||||
| chr2:169587511
|
A | G | 88 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 94 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.-70+3021A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587511 | ||||||
| chr2:169587691
|
C | G | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.-70+3201C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587691 | ||||||
| chr2:169587894
|
A | G | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+3404A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587894 | ||||||
| chr2:169588004
|
G | C | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-70+3514G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588004 | ||||||
| chr2:169588146
|
C | CAA | 283 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(280): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.-70+3656_-70+3657i others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588146 | ||||||
| chr2:169588234
|
C | CGT | 4 | a0001c0001t0002g0008a0001c0001t0002g0082a0001c0001t0002g0083others(1): Show | 5 | HG00323.hp1 HG01123.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+3757_-70+3758d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169588234 | |||||
| chr2:169588239
|
G | A | 1 | a0001c0001t0005g0331 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-70+3749G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588239 | ||||||
| chr2:169588247
|
G | A | 155 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(152): Show | 160 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.-70+3757G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588247 | ||||||
| chr2:169588249
|
A | G | 1 | a0003c0003t0008g0330 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-70+3759A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588249 | ||||||
| chr2:169588359
|
A | T | 1 | a0001c0001t0012g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-70+3869A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588359 | ||||||
| chr2:169588478
|
A | C | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-70+3988A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588478 | ||||||
| chr2:169588536
|
A | T | 4 | a0002c0002t0003g0198a0002c0002t0003g0199a0002c0002t0003g0200others(1): Show | 4 | NA18939.hp2 NA18960.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+4046A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588536 | ||||||
| chr2:169588546
|
G | A | 2 | a0002c0002t0003g0164a0002c0002t0003g0165 | 2 | NA19006.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-70+4056G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588546 | ||||||
| chr2:169588690
|
A | G | 310 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(307): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-70+4200A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588690 | ||||||
| chr2:169588752
|
G | A | 46 | a0002c0002t0003g0011a0002c0002t0003g0164a0002c0002t0003g0165others(43): Show | 48 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.-70+4262G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588752 | ||||||
| chr2:169588803
|
A | G | 7 | a0001c0001t0011g0014a0001c0001t0011g0161a0001c0001t0011g0162others(4): Show | 8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-70+4313A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588803 | ||||||
| chr2:169588928
|
C | A | 1 | a0003c0003t0004g0095 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-70+4438C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588928 | ||||||
| chr2:169588958
|
C | CA | 12 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(9): Show | 12 | HG00733.hp1 HG01255.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-70+4493dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169588958 | |||||
| chr2:169588958
|
CA | C | 129 | a0001c0001t0002g0050a0001c0001t0002g0052a0001c0001t0002g0053others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.-70+4493delA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169588958 | |||||
| chr2:169588958
|
CAA | C | 100 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(97): Show | 105 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-70+4492_-70+4493d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169588958 | |||||
| chr2:169588958
|
CAAA | C | 46 | a0001c0001t0006g0155a0002c0002t0001g0293a0002c0002t0001g0294others(43): Show | 48 | HG01168.hp2 HG01192.hp2 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.-70+4491_-70+4493d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169588958 | |||||
| chr2:169588958
|
CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0007g0205a0001c0001t0011g0014a0001c0001t0011g0161others(4): Show | 8 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-70+4485_-70+4493d others(11): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169588958 | |||||
| chr2:169589104
|
T | C | 1 | a0002c0002t0001g0214 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-70+4614T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589104 | ||||||
| chr2:169589272
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0080a0001c0001t0002g0081 | 5 | NA18947.hp2 NA18964.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70+4782A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589272 | ||||||
| chr2:169589286
|
C | T | 4 | a0001c0001t0007g0157a0001c0001t0007g0202a0001c0001t0007g0203others(1): Show | 4 | NA18906.hp1 NA19030.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+4796C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589286 | ||||||
| chr2:169589370
|
T | C | 26 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(23): Show | 26 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.-70+4880T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589370 | ||||||
| chr2:169589409
|
G | A | 1 | a0002c0002t0003g0175 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-70+4919G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589409 | ||||||
| chr2:169589545
|
A | G | 3 | a0001c0005t0002g0077a0001c0005t0002g0078a0001c0005t0002g0079 | 3 | NA18612.hp2 NA19000.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-70+5055A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589545 | ||||||
| chr2:169589652
|
G | GT | 4 | a0001c0001t0006g0160a0001c0001t0009g0076a0002c0002t0001g0274others(1): Show | 4 | HG03669.hp2 HG04184.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+5169dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169589652 | |||||
| chr2:169589660
|
G | T | 3 | a0003c0003t0004g0355a0003c0003t0004g0356a0003c0003t0004g0357 | 3 | HG01496.hp1 HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-70+5170G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589660 | ||||||
| chr2:169589667
|
G | T | 1 | a0001c0001t0006g0154 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-70+5177G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589667 | ||||||
| chr2:169589680
|
G | A | 4 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(1): Show | 4 | NA18939.hp1 NA19005.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+5190G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589680 | ||||||
| chr2:169589689
|
C | A | 10 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70+5199C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589689 | ||||||
| chr2:169589811
|
A | G | 7 | a0003c0003t0004g0123a0003c0003t0004g0124a0003c0003t0004g0125others(4): Show | 7 | HG01099.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70+5321A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589811 | ||||||
| chr2:169589861
|
A | G | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+5371A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589861 | ||||||
| chr2:169590085
|
G | A | 9 | a0002c0002t0001g0215a0002c0002t0001g0275a0002c0002t0001g0276others(6): Show | 9 | HG00280.hp1 HG01192.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-70+5595G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590085 | ||||||
| chr2:169590129
|
C | CA | 13 | a0001c0001t0005g0334a0001c0001t0007g0009a0001c0001t0007g0091others(10): Show | 15 | HG00609.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-70+5651dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169590129 | |||||
| chr2:169590129
|
C | CAA | 152 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(149): Show | 157 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.-70+5650_-70+5651d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169590129 | |||||
| chr2:169590136
|
A | C | 82 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(79): Show | 87 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-70+5646A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590136 | ||||||
| chr2:169590158
|
G | A | 13 | a0003c0003t0004g0003a0003c0003t0004g0096a0003c0003t0004g0097others(10): Show | 15 | HG00733.hp1 HG01255.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-70+5668G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590158 | ||||||
| chr2:169590289
|
G | A | 70 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(67): Show | 75 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-70+5799G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590289 | ||||||
| chr2:169590369
|
A | G | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+5879A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590369 | ||||||
| chr2:169590388
|
G | A | 3 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0026g0034 | 3 | HG02559.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-70+5898G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590388 | ||||||
| chr2:169590403
|
G | A | 1 | a0003c0003t0004g0098 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-70+5913G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590403 | ||||||
| chr2:169590534
|
C | T | 1 | a0001c0001t0013g0037 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-70+6044C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590534 | ||||||
| chr2:169590784
|
C | G | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-70+6294C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590784 | ||||||
| chr2:169590847
|
A | T | 6 | a0001c0001t0006g0153a0001c0001t0007g0157a0001c0001t0007g0202others(3): Show | 6 | HG01099.hp2 HG01891.hp1 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.-70+6357A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590847 | ||||||
| chr2:169590848
|
T | A | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+6358T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590848 | ||||||
| chr2:169590877
|
C | T | 1 | a0002c0002t0001g0271 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-70+6387C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590877 | ||||||
| chr2:169590879
|
C | T | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-70+6389C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590879 | ||||||
| chr2:169591026
|
C | T | 3 | a0002c0004t0003g0012a0002c0004t0003g0195a0002c0004t0003g0196 | 4 | HG01192.hp2 HG01358.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70+6536C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591026 | ||||||
| chr2:169591035
|
T | C | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+6545T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591035 | ||||||
| chr2:169591065
|
G | A | 1 | a0003c0003t0004g0355 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-70+6575G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591065 | ||||||
| chr2:169591186
|
G | A | 3 | a0002c0002t0003g0173a0002c0002t0003g0178a0002c0002t0014g0177 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-70+6696G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591186 | ||||||
| chr2:169591188
|
C | T | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+6698C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591188 | ||||||
| chr2:169591224
|
T | C | 1 | a0002c0002t0001g0216 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-70+6734T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591224 | ||||||
| chr2:169591271
|
A | G | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-70+6781A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591271 | ||||||
| chr2:169591341
|
A | C | 1 | a0001c0001t0002g0075 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-70+6851A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591341 | ||||||
| chr2:169591677
|
G | A | 4 | a0001c0001t0007g0157a0001c0001t0007g0202a0001c0001t0007g0203others(1): Show | 4 | NA18906.hp1 NA19030.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+7187G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591677 | ||||||
| chr2:169591754
|
A | C | 1 | a0001c0001t0002g0075 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-70+7264A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591754 | ||||||
| chr2:169591781
|
A | AT | 281 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(278): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-70+7302dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591781 | |||||
| chr2:169591781
|
A | ATT | 22 | a0001c0001t0006g0135a0001c0001t0006g0138a0001c0001t0006g0141others(19): Show | 22 | HG00438.hp1 HG00621.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-70+7301_-70+7302d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591781 | |||||
| chr2:169591920
|
A | AT | 32 | a0001c0001t0005g0333a0001c0001t0006g0132a0001c0001t0006g0135others(29): Show | 34 | HG00438.hp1 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-70+7455dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591920 | |||||
| chr2:169591920
|
A | ATT | 42 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(39): Show | 46 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-70+7454_-70+7455d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591920 | |||||
| chr2:169591920
|
A | ATTT | 27 | a0001c0001t0002g0006a0001c0001t0002g0025a0001c0001t0002g0044others(24): Show | 28 | HG00438.hp2 HG00733.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.-70+7453_-70+7455d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591920 | |||||
| chr2:169591920
|
AT | A | 49 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0334others(46): Show | 52 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-70+7455delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591920 | |||||
| chr2:169591920
|
ATT | A | 44 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(41): Show | 45 | HG00609.hp2 HG00673.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.-70+7454_-70+7455d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591920 | |||||
| chr2:169591920
|
ATTT | A | 124 | a0001c0001t0012g0030a0001c0001t0015g0031a0001c0001t0015g0032others(121): Show | 128 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.-70+7453_-70+7455d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591920 | |||||
| chr2:169591920
|
ATTTTTTT others(2): Show |
A | 21 | a0003c0003t0004g0355a0003c0003t0004g0356a0003c0003t0004g0357others(18): Show | 21 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.-70+7447_-70+7455d others(11): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591920 | |||||
| chr2:169592007
|
A | G | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+7517A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592007 | ||||||
| chr2:169592099
|
AT | A | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+7619delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169592099 | |||||
| chr2:169592192
|
C | T | 19 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(16): Show | 19 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-70+7702C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592192 | ||||||
| chr2:169592207
|
T | C | 1 | a0003c0003t0004g0099 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-70+7717T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592207 | ||||||
| chr2:169592267
|
T | C | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+7777T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592267 | ||||||
| chr2:169592272
|
C | T | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+7782C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592272 | ||||||
| chr2:169592303
|
C | CT | 66 | a0001c0001t0007g0018a0001c0001t0007g0024a0001c0001t0007g0093others(63): Show | 69 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(66): Show |
intron_variant | MODIFIER | c.-70+7832dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169592303 | |||||
| chr2:169592303
|
C | CTT | 133 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(130): Show | 136 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.-70+7831_-70+7832d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169592303 | |||||
| chr2:169592303
|
C | CTTT | 15 | a0001c0001t0005g0344a0001c0001t0005g0345a0001c0001t0005g0349others(12): Show | 15 | HG00140.hp1 HG00621.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-70+7830_-70+7832d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169592303 | |||||
| chr2:169592303
|
CT | C | 57 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(54): Show | 62 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-70+7832delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169592303 | |||||
| chr2:169592306
|
T | TC | 5 | a0001c0001t0007g0015a0001c0001t0007g0019a0001c0001t0007g0021others(2): Show | 5 | HG02280.hp2 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+7816_-70+7817i others(3): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592306 | ||||||
| chr2:169592402
|
T | G | 1 | a0002c0002t0001g0220 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-70+7912T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592402 | ||||||
| chr2:169592492
|
G | A | 1 | a0001c0001t0013g0037 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-70+8002G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592492 | ||||||
| chr2:169592565
|
G | A | 279 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(276): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-70+8075G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592565 | ||||||
| chr2:169592755
|
C | A | 1 | a0001c0001t0027g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-70+8265C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592755 | ||||||
| chr2:169592771
|
A | G | 4 | a0001c0001t0007g0157a0001c0001t0007g0202a0001c0001t0007g0203others(1): Show | 4 | NA18906.hp1 NA19030.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+8281A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592771 | ||||||
| chr2:169593037
|
A | G | 100 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(97): Show | 106 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-70+8547A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593037 | ||||||
| chr2:169593050
|
C | T | 1 | a0002c0002t0003g0167 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-70+8560C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593050 | ||||||
| chr2:169593056
|
G | C | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-70+8566G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593056 | ||||||
| chr2:169593126
|
G | GTA | 32 | a0001c0001t0002g0084a0003c0003t0004g0003a0003c0003t0004g0096others(29): Show | 34 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.-70+8652_-70+8653d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593126 | |||||
| chr2:169593126
|
GTA | G | 66 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(63): Show | 68 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(65): Show |
intron_variant | MODIFIER | c.-70+8652_-70+8653d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593126 | |||||
| chr2:169593128
|
A | G | 111 | a0001c0001t0006g0153a0002c0002t0001g0001a0002c0002t0001g0013others(108): Show | 114 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-70+8638A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593128 | ||||||
| chr2:169593130
|
A | G | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+8640A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593130 | ||||||
| chr2:169593142
|
A | ATC | 3 | a0003c0003t0008g0326a0003c0003t0008g0327a0003c0003t0008g0361 | 3 | HG01069.hp1 HG01109.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-70+8654_-70+8655d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593142 | |||||
| chr2:169593174
|
C | G | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.-70+8684C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593174 | ||||||
| chr2:169593338
|
A | G | 284 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(281): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.-70+8848A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593338 | ||||||
| chr2:169593398
|
A | G | 5 | a0001c0001t0007g0157a0001c0001t0007g0202a0001c0001t0007g0203others(2): Show | 5 | HG01891.hp1 NA18906.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70+8908A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593398 | ||||||
| chr2:169593491
|
G | C | 1 | a0002c0002t0001g0214 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-70+9001G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593491 | ||||||
| chr2:169593511
|
C | G | 4 | a0001c0001t0007g0157a0001c0001t0007g0202a0001c0001t0007g0203others(1): Show | 4 | NA18906.hp1 NA19030.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+9021C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593511 | ||||||
| chr2:169593517
|
A | T | 3 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0026g0034 | 3 | HG02559.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-70+9027A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593517 | ||||||
| chr2:169593650
|
C | CTT | 39 | a0001c0001t0002g0075a0001c0001t0002g0082a0001c0001t0006g0132others(36): Show | 40 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-70+9178_-70+9179d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593650 | |||||
| chr2:169593650
|
C | CTTT | 58 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(55): Show | 63 | HG00099.hp1 HG00639.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.-70+9177_-70+9179d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593650 | |||||
| chr2:169593650
|
CT | C | 167 | a0001c0001t0005g0335a0001c0001t0007g0021a0001c0001t0012g0030others(164): Show | 172 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.-70+9179delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593650 | |||||
| chr2:169593674
|
C | T | 4 | a0002c0002t0001g0216a0002c0002t0001g0255a0002c0002t0001g0256others(1): Show | 4 | HG02155.hp2 NA18942.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70+9184C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593674 | ||||||
| chr2:169593720
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-70+9230C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593720 | ||||||
| chr2:169593813
|
A | AT | 192 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(189): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-70+9338dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593813 | |||||
| chr2:169593813
|
A | ATT | 6 | a0001c0001t0006g0152a0002c0002t0001g0253a0002c0002t0001g0254others(3): Show | 6 | HG01261.hp1 HG02148.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.-70+9337_-70+9338d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593813 | |||||
| chr2:169593875
|
T | C | 9 | a0001c0001t0012g0030a0001c0001t0012g0035a0001c0001t0012g0036others(6): Show | 9 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-70+9385T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593875 | ||||||
| chr2:169593950
|
C | T | 9 | a0001c0001t0002g0053a0002c0004t0003g0012a0002c0004t0003g0174others(6): Show | 10 | HG01175.hp2 HG01192.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70+9460C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593950 | ||||||
| chr2:169594028
|
G | A | 7 | a0002c0002t0001g0298a0002c0002t0001g0299a0002c0002t0001g0300others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70+9538G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594028 | ||||||
| chr2:169594074
|
T | C | 7 | a0003c0003t0004g0123a0003c0003t0004g0124a0003c0003t0004g0125others(4): Show | 7 | HG01099.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-9568T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594074 | ||||||
| chr2:169594099
|
C | G | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-9543C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594099 | ||||||
| chr2:169594189
|
T | C | 1 | a0002c0002t0003g0179 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-69-9453T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594189 | ||||||
| chr2:169594324
|
C | CA | 137 | a0001c0001t0002g0008a0001c0001t0002g0055a0001c0001t0002g0082others(134): Show | 142 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-69-9305dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594324 | |||||
| chr2:169594324
|
C | CAA | 128 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0039others(125): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-69-9306_-69-9305d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594324 | |||||
| chr2:169594324
|
C | CAAA | 62 | a0001c0001t0002g0002a0001c0001t0002g0025a0001c0001t0002g0042others(59): Show | 64 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.-69-9307_-69-9305d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594324 | |||||
| chr2:169594359
|
T | A | 3 | a0001c0001t0011g0161a0001c0001t0011g0162a0001c0001t0011g0163 | 3 | HG02486.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-69-9283T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594359 | ||||||
| chr2:169594392
|
G | C | 2 | a0002c0002t0003g0168a0002c0002t0003g0169 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-69-9250G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594392 | ||||||
| chr2:169594438
|
G | A | 1 | a0002c0002t0001g0296 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-69-9204G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594438 | ||||||
| chr2:169594502
|
C | A | 1 | a0002c0002t0001g0265 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-69-9140C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594502 | ||||||
| chr2:169594625
|
C | CT | 22 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(19): Show | 23 | HG00280.hp2 HG00735.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.-69-8996dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594625 | |||||
| chr2:169594625
|
CT | C | 82 | a0001c0001t0002g0050a0001c0001t0002g0081a0001c0001t0005g0090others(79): Show | 83 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-69-8996delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594625 | |||||
| chr2:169594625
|
CTT | C | 72 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(69): Show | 77 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-69-8997_-69-8996d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594625 | |||||
| chr2:169594625
|
CTTT | C | 137 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(134): Show | 142 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-69-8998_-69-8996d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594625 | |||||
| chr2:169594625
|
CTTTT | C | 6 | a0002c0002t0001g0232a0002c0002t0001g0263a0002c0002t0003g0197others(3): Show | 6 | HG01074.hp1 HG02897.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.-69-8999_-69-8996d others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594625 | |||||
| chr2:169594631
|
T | C | 41 | a0001c0001t0002g0050a0001c0001t0002g0081a0001c0001t0006g0134others(38): Show | 42 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.-69-9011T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594631 | ||||||
| chr2:169594632
|
T | C | 59 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(56): Show | 64 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-69-9010T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594632 | ||||||
| chr2:169594755
|
G | C | 1 | a0001c0001t0007g0205 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-69-8887G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594755 | ||||||
| chr2:169594762
|
T | G | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-8880T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594762 | ||||||
| chr2:169594883
|
A | T | 10 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-69-8759A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594883 | ||||||
| chr2:169595022
|
G | A | 2 | a0001c0001t0002g0060a0001c0001t0002g0069 | 2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-69-8620G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595022 | ||||||
| chr2:169595032
|
G | A | 1 | a0001c0001t0005g0331 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-69-8610G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595032 | ||||||
| chr2:169595053
|
T | C | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-8589T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595053 | ||||||
| chr2:169595359
|
G | A | 331 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(328): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-69-8283G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595359 | ||||||
| chr2:169595380
|
G | A | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-69-8262G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595380 | ||||||
| chr2:169595456
|
T | C | 2 | a0002c0002t0001g0300a0002c0002t0001g0303 | 2 | HG01261.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-69-8186T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595456 | ||||||
| chr2:169595516
|
A | T | 7 | a0001c0001t0011g0014a0001c0001t0011g0161a0001c0001t0011g0162others(4): Show | 8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-69-8126A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595516 | ||||||
| chr2:169595539
|
C | T | 21 | a0002c0002t0001g0216a0002c0002t0001g0217a0002c0002t0001g0247others(18): Show | 21 | HG00673.hp1 HG01081.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.-69-8103C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595539 | ||||||
| chr2:169595632
|
G | T | 4 | a0001c0001t0013g0027a0001c0001t0013g0037a0001c0007t0013g0028others(1): Show | 4 | HG02258.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69-8010G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595632 | ||||||
| chr2:169595661
|
G | C | 1 | a0002c0002t0010g0295 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-69-7981G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595661 | ||||||
| chr2:169595801
|
T | C | 28 | a0001c0001t0007g0009a0001c0001t0007g0015a0001c0001t0007g0016others(25): Show | 29 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.-69-7841T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595801 | ||||||
| chr2:169595865
|
G | A | 2 | a0002c0002t0003g0180a0002c0002t0010g0313 | 2 | NA18948.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-69-7777G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595865 | ||||||
| chr2:169595966
|
G | A | 1 | a0002c0002t0001g0253 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-69-7676G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595966 | ||||||
| chr2:169595977
|
T | A | 2 | a0002c0002t0001g0247a0002c0002t0001g0315 | 2 | NA18954.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-69-7665T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595977 | ||||||
| chr2:169595996
|
G | C | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-7646G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595996 | ||||||
| chr2:169596095
|
C | T | 2 | a0001c0007t0013g0028a0001c0007t0013g0029 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-69-7547C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596095 | ||||||
| chr2:169596104
|
T | G | 1 | a0003c0003t0008g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-69-7538T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596104 | ||||||
| chr2:169596253
|
C | T | 9 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(6): Show | 10 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-7389C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596253 | ||||||
| chr2:169596404
|
C | T | 10 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-69-7238C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596404 | ||||||
| chr2:169596414
|
G | A | 4 | a0001c0001t0005g0351a0001c0001t0005g0352a0001c0001t0005g0353others(1): Show | 4 | NA18981.hp2 NA19066.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-7228G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596414 | ||||||
| chr2:169596657
|
G | A | 4 | a0001c0001t0011g0161a0001c0001t0011g0162a0001c0001t0011g0163others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-6985G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596657 | ||||||
| chr2:169596677
|
G | C | 310 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(307): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-69-6965G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596677 | ||||||
| chr2:169596715
|
T | C | 1 | a0001c0001t0015g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-69-6927T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596715 | ||||||
| chr2:169596760
|
C | T | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-69-6882C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596760 | ||||||
| chr2:169596802
|
C | T | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-69-6840C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596802 | ||||||
| chr2:169596982
|
G | A | 1 | a0002c0002t0003g0181 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-69-6660G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596982 | ||||||
| chr2:169597005
|
A | G | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-6637A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597005 | ||||||
| chr2:169597035
|
TA | T | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-6606delA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597035 | ||||||
| chr2:169597159
|
T | C | 34 | a0003c0003t0004g0003a0003c0003t0004g0096a0003c0003t0004g0097others(31): Show | 36 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.-69-6483T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597159 | ||||||
| chr2:169597243
|
C | T | 2 | a0005c0006t0018g0109a0005c0006t0018g0114 | 2 | HG03654.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-69-6399C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597243 | ||||||
| chr2:169597315
|
T | A | 1 | a0003c0003t0008g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-69-6327T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597315 | ||||||
| chr2:169597388
|
G | A | 6 | a0001c0001t0012g0030a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-69-6254G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597388 | ||||||
| chr2:169597458
|
C | T | 2 | a0002c0002t0001g0230a0002c0002t0001g0246 | 2 | HG01070.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-69-6184C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597458 | ||||||
| chr2:169597491
|
CCTTTT | C | 5 | a0001c0001t0007g0157a0001c0001t0007g0202a0001c0001t0007g0203others(2): Show | 5 | HG01891.hp1 NA18906.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.-69-6140_-69-6136d others(7): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597491 | |||||
| chr2:169597496
|
T | C | 1 | a0001c0001t0002g0070 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-69-6146T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597496 | ||||||
| chr2:169597502
|
C | CT | 40 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0333others(37): Show | 41 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.-69-6126dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597502 | |||||
| chr2:169597502
|
CT | C | 157 | a0001c0001t0002g0071a0001c0001t0007g0091a0001c0001t0009g0038others(154): Show | 162 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-69-6126delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597502 | |||||
| chr2:169597521
|
CAG | C | 26 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(23): Show | 26 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.-69-6118_-69-6117d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597521 | |||||
| chr2:169597584
|
C | T | 26 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(23): Show | 26 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.-69-6058C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597584 | ||||||
| chr2:169597642
|
C | T | 3 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0252 | 3 | HG03491.hp2 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-69-6000C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597642 | ||||||
| chr2:169597643
|
G | A | 10 | a0002c0002t0001g0159a0002c0002t0001g0206a0002c0002t0001g0210others(7): Show | 10 | HG00642.hp1 HG00735.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-69-5999G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597643 | ||||||
| chr2:169597678
|
T | C | 4 | a0002c0002t0001g0278a0002c0002t0001g0280a0002c0002t0001g0317others(1): Show | 4 | HG01192.hp1 HG01261.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-5964T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597678 | ||||||
| chr2:169597850
|
CCTTG | C | 5 | a0001c0001t0005g0332a0001c0001t0005g0342a0001c0001t0005g0347others(2): Show | 5 | HG00621.hp2 HG03017.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.-69-5787_-69-5784d others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597850 | |||||
| chr2:169597855
|
C | CTTGCTTG others(1): Show |
3 | a0003c0003t0004g0096a0003c0003t0004g0099a0003c0003t0004g0104 | 3 | HG00733.hp1 HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-69-5784_-69-5783i others(10): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597855 | |||||
| chr2:169597855
|
C | CTTGCTTG others(5): Show |
1 | a0003c0003t0004g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-69-5784_-69-5783i others(14): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597855 | |||||
| chr2:169597855
|
C | CTTGT | 18 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0007g0157others(15): Show | 20 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-69-5751_-69-5748d others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597855 | |||||
| chr2:169597855
|
CTTGT | C | 116 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-69-5751_-69-5748d others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597855 | |||||
| chr2:169597855
|
CTTGTTTG others(1): Show |
C | 13 | a0001c0001t0002g0039a0001c0001t0002g0061a0001c0001t0007g0205others(10): Show | 14 | HG00639.hp1 HG01106.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-69-5755_-69-5748d others(10): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597855 | |||||
| chr2:169597855
|
CTTGTTTG others(5): Show |
C | 6 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(3): Show | 7 | HG00323.hp2 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-5759_-69-5748d others(14): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597855 | |||||
| chr2:169597855
|
CTTGTTTG others(9): Show |
C | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-5763_-69-5748d others(18): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597855 | |||||
| chr2:169597912
|
T | C | 1 | a0003c0003t0008g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-69-5730T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597912 | ||||||
| chr2:169597913
|
C | T | 1 | a0003c0003t0008g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-69-5729C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597913 | ||||||
| chr2:169597940
|
A | G | 157 | a0001c0001t0002g0063a0002c0002t0001g0001a0002c0002t0001g0013others(154): Show | 162 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-69-5702A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597940 | ||||||
| chr2:169597952
|
C | T | 1 | a0002c0002t0003g0188 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-69-5690C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597952 | ||||||
| chr2:169598004
|
C | CT | 153 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(150): Show | 158 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.-69-5624dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169598004 | |||||
| chr2:169598024
|
A | T | 79 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(76): Show | 84 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-69-5618A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598024 | ||||||
| chr2:169598087
|
G | A | 2 | a0001c0001t0005g0347a0001c0001t0005g0362 | 2 | NA18990.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-69-5555G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598087 | ||||||
| chr2:169598381
|
C | T | 1 | a0003c0003t0008g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-69-5261C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598381 | ||||||
| chr2:169598384
|
G | A | 7 | a0001c0001t0011g0014a0001c0001t0011g0161a0001c0001t0011g0162others(4): Show | 8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-69-5258G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598384 | ||||||
| chr2:169598482
|
G | A | 3 | a0001c0001t0011g0014a0001c0001t0011g0311a0001c0001t0011g0312 | 4 | HG02258.hp1 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69-5160G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598482 | ||||||
| chr2:169598493
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-69-5149G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598493 | ||||||
| chr2:169598541
|
G | A | 5 | a0001c0001t0005g0090a0001c0001t0005g0333a0001c0001t0005g0338others(2): Show | 5 | HG02280.hp1 NA18993.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-69-5101G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598541 | ||||||
| chr2:169598542
|
C | A | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-69-5100C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598542 | ||||||
| chr2:169598697
|
A | C | 5 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(2): Show | 6 | HG02145.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-69-4945A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598697 | ||||||
| chr2:169598814
|
T | C | 155 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(152): Show | 160 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.-69-4828T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598814 | ||||||
| chr2:169598815
|
T | G | 34 | a0003c0003t0004g0003a0003c0003t0004g0096a0003c0003t0004g0097others(31): Show | 36 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.-69-4827T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598815 | ||||||
| chr2:169598836
|
T | TATGTATA others(13): Show |
9 | a0001c0001t0002g0006a0001c0001t0002g0067a0001c0001t0002g0070others(6): Show | 11 | NA18941.hp2 NA18945.hp2 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.-69-4806_-69-4805i others(22): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598836 | ||||||
| chr2:169598837
|
T | A | 9 | a0001c0001t0002g0006a0001c0001t0002g0067a0001c0001t0002g0070others(6): Show | 11 | NA18941.hp2 NA18945.hp2 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.-69-4805T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598837 | ||||||
| chr2:169598837
|
T | TTATATGT others(17): Show |
1 | a0001c0001t0006g0156 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-69-4799_-69-4776d others(26): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169598837 | |||||
| chr2:169598843
|
G | GTATATAA others(17): Show |
62 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(59): Show | 63 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.-69-4771_-69-4748d others(26): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169598843 | |||||
| chr2:169598843
|
G | GTATATAA others(45): Show |
3 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0029g0133 | 3 | HG00733.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-69-4778_-69-4777i others(54): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169598843 | |||||
| chr2:169598843
|
G | T | 9 | a0001c0001t0002g0006a0001c0001t0002g0067a0001c0001t0002g0070others(6): Show | 11 | NA18941.hp2 NA18945.hp2 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.-69-4799G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598843 | ||||||
| chr2:169598869
|
A | ATATAAAT others(41): Show |
4 | a0001c0001t0013g0027a0001c0001t0013g0037a0001c0007t0013g0028others(1): Show | 4 | HG02258.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69-4748_-69-4747i others(50): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169598869 | |||||
| chr2:169598869
|
A | ATATAAAT others(17): Show |
75 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(72): Show | 79 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-69-4750_-69-4749i others(26): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169598869 | |||||
| chr2:169598869
|
A | G | 9 | a0001c0001t0002g0006a0001c0001t0002g0067a0001c0001t0002g0070others(6): Show | 11 | NA18941.hp2 NA18945.hp2 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.-69-4773A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598869 | ||||||
| chr2:169598871
|
A | G | 1 | a0001c0001t0006g0156 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-69-4771A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598871 | ||||||
| chr2:169599354
|
A | C | 7 | a0001c0001t0011g0014a0001c0001t0011g0161a0001c0001t0011g0162others(4): Show | 8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-69-4288A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599354 | ||||||
| chr2:169599419
|
T | G | 10 | a0001c0001t0012g0030a0001c0001t0012g0035a0001c0001t0012g0036others(7): Show | 10 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-4223T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599419 | ||||||
| chr2:169599670
|
C | T | 331 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(328): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-69-3972C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599670 | ||||||
| chr2:169599707
|
A | G | 361 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(358): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-69-3935A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599707 | ||||||
| chr2:169599732
|
C | A | 1 | a0001c0001t0002g0053 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-69-3910C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599732 | ||||||
| chr2:169599812
|
G | A | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-69-3830G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599812 | ||||||
| chr2:169599923
|
T | A | 1 | a0005c0006t0018g0109 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-69-3719T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599923 | ||||||
| chr2:169599957
|
A | G | 2 | a0001c0001t0002g0039a0001c0001t0002g0061 | 2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-69-3685A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599957 | ||||||
| chr2:169599973
|
A | G | 3 | a0002c0002t0003g0308a0002c0002t0003g0309a0002c0002t0003g0310 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-69-3669A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599973 | ||||||
| chr2:169600006
|
G | A | 4 | a0002c0002t0001g0281a0002c0002t0001g0282a0002c0002t0001g0291others(1): Show | 4 | NA18980.hp1 NA19056.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69-3636G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600006 | ||||||
| chr2:169600078
|
A | AT | 6 | a0001c0001t0002g0080a0001c0001t0028g0137a0001c0001t0032g0136others(3): Show | 6 | HG01496.hp1 HG02027.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-69-3548dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169600078 | |||||
| chr2:169600078
|
AT | A | 158 | a0001c0001t0002g0045a0001c0001t0002g0072a0001c0001t0005g0352others(155): Show | 163 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.-69-3548delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169600078 | |||||
| chr2:169600079
|
T | A | 1 | a0005c0006t0018g0109 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-69-3563T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600079 | ||||||
| chr2:169600405
|
A | T | 4 | a0001c0001t0011g0161a0001c0001t0011g0162a0001c0001t0011g0163others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-3237A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600405 | ||||||
| chr2:169600507
|
C | T | 1 | a0002c0002t0003g0194 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-69-3135C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600507 | ||||||
| chr2:169600620
|
G | GTTTTTCA others(4): Show |
1 | a0001c0001t0009g0038 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-69-3021_-69-3020i others(13): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169600620 | |||||
| chr2:169600646
|
T | C | 4 | a0002c0002t0001g0206a0002c0002t0001g0221a0002c0002t0001g0222others(1): Show | 4 | HG00642.hp1 HG01346.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-2996T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600646 | ||||||
| chr2:169600789
|
C | T | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-2853C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600789 | ||||||
| chr2:169600865
|
T | G | 128 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(125): Show | 135 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.-69-2777T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600865 | ||||||
| chr2:169600937
|
T | TA | 128 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(125): Show | 135 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.-69-2704dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169600937 | |||||
| chr2:169600941
|
C | T | 128 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(125): Show | 135 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.-69-2701C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600941 | ||||||
| chr2:169601078
|
G | T | 1 | a0002c0002t0001g0297 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-69-2564G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601078 | ||||||
| chr2:169601105
|
T | C | 4 | a0002c0002t0001g0225a0002c0002t0001g0265a0002c0002t0001g0316others(1): Show | 4 | HG02132.hp1 NA18943.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69-2537T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601105 | ||||||
| chr2:169601302
|
A | G | 4 | a0001c0001t0012g0030a0001c0001t0015g0031a0001c0001t0015g0032others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69-2340A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601302 | ||||||
| chr2:169601450
|
C | G | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-2192C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601450 | ||||||
| chr2:169601484
|
A | G | 92 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(89): Show | 98 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.-69-2158A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601484 | ||||||
| chr2:169601504
|
G | A | 1 | a0001c0001t0005g0350 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-69-2138G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601504 | ||||||
| chr2:169601564
|
A | G | 18 | a0003c0003t0008g0122a0003c0003t0008g0130a0003c0003t0008g0319others(15): Show | 18 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-69-2078A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601564 | ||||||
| chr2:169601820
|
T | C | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-69-1822T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601820 | ||||||
| chr2:169601865
|
C | T | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-1777C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601865 | ||||||
| chr2:169601906
|
C | CA | 155 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(152): Show | 160 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.-69-1724dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169601906 | |||||
| chr2:169601922
|
A | T | 1 | a0001c0001t0007g0205 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-69-1720A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601922 | ||||||
| chr2:169601966
|
T | A | 310 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(307): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-69-1676T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601966 | ||||||
| chr2:169601967
|
T | C | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-1675T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601967 | ||||||
| chr2:169602206
|
A | C | 344 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(341): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-69-1436A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602206 | ||||||
| chr2:169602221
|
T | TA | 7 | a0002c0002t0003g0164a0002c0002t0003g0165a0002c0002t0003g0167others(4): Show | 7 | HG02129.hp1 NA18986.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.-69-1421_-69-1420i others(3): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602221 | ||||||
| chr2:169602222
|
C | A | 7 | a0002c0002t0003g0164a0002c0002t0003g0165a0002c0002t0003g0167others(4): Show | 7 | HG02129.hp1 NA18986.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.-69-1420C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602222 | ||||||
| chr2:169602222
|
C | CA | 146 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(143): Show | 151 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.-69-1410dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169602222 | |||||
| chr2:169602408
|
C | T | 26 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(23): Show | 26 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.-69-1234C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602408 | ||||||
| chr2:169602409
|
G | A | 1 | a0003c0003t0004g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-69-1233G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602409 | ||||||
| chr2:169602409
|
G | C | 1 | a0001c0001t0005g0333 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-69-1233G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602409 | ||||||
| chr2:169602461
|
A | G | 79 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(76): Show | 84 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-69-1181A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602461 | ||||||
| chr2:169602601
|
C | T | 4 | a0001c0001t0011g0161a0001c0001t0011g0162a0001c0001t0011g0163others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-1041C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602601 | ||||||
| chr2:169602607
|
C | T | 3 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0314 | 3 | NA18977.hp2 NA18985.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-69-1035C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602607 | ||||||
| chr2:169602612
|
C | G | 4 | a0002c0002t0001g0216a0002c0002t0001g0255a0002c0002t0001g0256others(1): Show | 4 | HG02155.hp2 NA18942.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69-1030C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602612 | ||||||
| chr2:169602763
|
A | C | 2 | a0001c0001t0011g0014a0001c0001t0011g0312 | 3 | HG03225.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-69-879A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602763 | ||||||
| chr2:169602881
|
A | G | 38 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(35): Show | 39 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.-69-761A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602881 | ||||||
| chr2:169602997
|
A | T | 1 | a0001c0001t0005g0335 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-69-645A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602997 | ||||||
| chr2:169603060
|
A | G | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.-69-582A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169603060 | ||||||
| chr2:169603061
|
G | C | 1 | a0001c0001t0002g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-69-581G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169603061 | ||||||
| chr2:169603141
|
T | C | 9 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(6): Show | 10 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-501T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169603141 | ||||||
| chr2:169603259
|
A | T | 1 | a0003c0003t0008g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-69-383A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169603259 | ||||||
| chr2:169603483
|
CATATACT others(30): Show |
C | 311 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(308): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-69-111_-69-75delT others(36): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169603483 | |||||
| chr2:169603581
|
C | T | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-61C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169603581 | ||||||
| chr2:169603831
|
A | G | 1 | a0001c0001t0006g0135 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-17+137A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 2/13 | chr2 | 169603831 | ||||||
| chr2:169604307
|
A | ATGGC | 8 | a0002c0002t0001g0228a0002c0002t0001g0314a0002c0002t0003g0164others(5): Show | 8 | HG04199.hp2 NA18948.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+48_136+51dupGG others(2): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604307 | |||||
| chr2:169604313
|
T | G | 148 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(145): Show | 153 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.136+52T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604313 | ||||||
| chr2:169604325
|
T | TG | 3 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0019 | 3 | HG02257.hp2 HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.136+66dupG | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604325 | |||||
| chr2:169604326
|
G | GCTT | 53 | a0002c0002t0001g0158a0002c0002t0001g0207a0002c0002t0001g0209others(50): Show | 55 | HG00423.hp1 HG01175.hp1 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.136+65_136+66insCT others(1): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604326 | ||||||
| chr2:169604327
|
G | C | 95 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0159others(92): Show | 98 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.136+66G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604327 | ||||||
| chr2:169604327
|
G | GGT | 7 | a0001c0001t0007g0016a0001c0001t0007g0020a0001c0001t0007g0021others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.136+66_136+67insGT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604327 | ||||||
| chr2:169604327
|
G | GT | 28 | a0001c0001t0002g0044a0001c0001t0002g0052a0001c0001t0002g0056others(25): Show | 28 | HG00733.hp1 HG01243.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.136+94dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604327 | |||||
| chr2:169604327
|
G | GTT | 7 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(4): Show | 8 | HG02615.hp1 HG02723.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+93_136+94dupTT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604327 | |||||
| chr2:169604327
|
G | GTTT | 9 | a0001c0001t0007g0009a0001c0001t0011g0161a0001c0001t0011g0162others(6): Show | 10 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.136+92_136+94dupTT others(1): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604327 | |||||
| chr2:169604327
|
GT | G | 9 | a0001c0001t0002g0072a0001c0001t0002g0082a0001c0001t0006g0132others(6): Show | 9 | HG00323.hp1 HG01069.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.136+94delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604327 | |||||
| chr2:169604327
|
GTT | G | 17 | a0001c0001t0005g0337a0001c0001t0005g0348a0003c0003t0004g0355others(14): Show | 17 | HG00735.hp1 HG01069.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.136+93_136+94delTT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604327 | |||||
| chr2:169604327
|
GTTT | G | 25 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(22): Show | 25 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.136+92_136+94delTT others(1): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604327 | |||||
| chr2:169604327
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0007g0202 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.136+84_136+94delTT others(9): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604327 | |||||
| chr2:169604328
|
T | G | 53 | a0002c0002t0001g0158a0002c0002t0001g0207a0002c0002t0001g0209others(50): Show | 55 | HG00423.hp1 HG01175.hp1 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.136+67T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604328 | ||||||
| chr2:169604329
|
T | TG | 6 | a0002c0002t0001g0290a0002c0002t0001g0296a0002c0002t0001g0300others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+68_136+69insG | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604329 | ||||||
| chr2:169604329
|
T | TGG | 89 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0159others(86): Show | 92 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.136+68_136+69insGG | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604329 | ||||||
| chr2:169604330
|
T | G | 6 | a0002c0002t0001g0290a0002c0002t0001g0296a0002c0002t0001g0300others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+69T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604330 | ||||||
| chr2:169604390
|
A | T | 1 | a0003c0003t0008g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.136+129A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604390 | ||||||
| chr2:169604391
|
G | A | 4 | a0003c0003t0004g0355a0003c0003t0004g0356a0003c0003t0004g0357others(1): Show | 4 | HG00140.hp2 HG01496.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+130G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604391 | ||||||
| chr2:169604425
|
G | A | 88 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 94 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.136+164G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604425 | ||||||
| chr2:169604657
|
C | T | 3 | a0001c0001t0006g0138a0001c0001t0006g0148a0001c0001t0033g0140 | 3 | HG01070.hp2 HG01071.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.136+396C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604657 | ||||||
| chr2:169604747
|
G | A | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.136+486G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604747 | ||||||
| chr2:169604797
|
C | G | 38 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(35): Show | 39 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.136+536C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604797 | ||||||
| chr2:169604904
|
T | G | 1 | a0003c0003t0008g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.136+643T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604904 | ||||||
| chr2:169605047
|
T | C | 9 | a0001c0001t0012g0030a0001c0001t0012g0035a0001c0001t0012g0036others(6): Show | 9 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+786T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605047 | ||||||
| chr2:169605163
|
A | G | 1 | a0002c0002t0003g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.137-876A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605163 | ||||||
| chr2:169605213
|
A | G | 2 | a0002c0002t0003g0173a0002c0002t0014g0177 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.137-826A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605213 | ||||||
| chr2:169605226
|
C | T | 3 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0252 | 3 | HG03491.hp2 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.137-813C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605226 | ||||||
| chr2:169605308
|
G | A | 6 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(3): Show | 7 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-731G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605308 | ||||||
| chr2:169605481
|
C | T | 3 | a0001c0001t0013g0027a0001c0001t0013g0037a0001c0007t0013g0029 | 3 | HG03139.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.137-558C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605481 | ||||||
| chr2:169605520
|
G | GC | 7 | a0001c0001t0011g0014a0001c0001t0011g0161a0001c0001t0011g0162others(4): Show | 8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.137-517dupC | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169605520 | |||||
| chr2:169605547
|
T | C | 1 | a0001c0001t0002g0088 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.137-492T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605547 | ||||||
| chr2:169605556
|
T | A | 3 | a0003c0003t0004g0355a0003c0003t0004g0356a0003c0003t0004g0357 | 3 | HG01496.hp1 HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.137-483T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605556 | ||||||
| chr2:169605566
|
C | T | 13 | a0003c0003t0004g0003a0003c0003t0004g0096a0003c0003t0004g0097others(10): Show | 15 | HG00733.hp1 HG01255.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.137-473C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605566 | ||||||
| chr2:169605591
|
A | G | 3 | a0002c0002t0003g0308a0002c0002t0003g0309a0002c0002t0003g0310 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.137-448A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605591 | ||||||
| chr2:169605611
|
G | C | 45 | a0002c0002t0003g0011a0002c0002t0003g0164a0002c0002t0003g0165others(42): Show | 47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.137-428G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605611 | ||||||
| chr2:169605638
|
C | CT | 195 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(192): Show | 201 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.137-401_137-400ins others(1): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605638 | ||||||
| chr2:169605639
|
G | A | 195 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(192): Show | 201 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.137-400G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605639 | ||||||
| chr2:169605639
|
G | T | 89 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(86): Show | 95 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.137-400G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605639 | ||||||
| chr2:169605732
|
C | G | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.137-307C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605732 | ||||||
| chr2:169605820
|
C | T | 9 | a0001c0001t0012g0030a0001c0001t0012g0035a0001c0001t0012g0036others(6): Show | 9 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.137-219C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605820 | ||||||
| chr2:169605838
|
A | G | 6 | a0001c0001t0012g0030a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.137-201A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605838 | ||||||
| chr2:169605902
|
A | T | 10 | a0003c0003t0004g0010a0003c0003t0004g0098a0003c0003t0004g0111others(7): Show | 11 | HG00280.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-137A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605902 | ||||||
| chr2:169605932
|
T | C | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.137-107T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605932 | ||||||
| chr2:169606321
|
C | T | 2 | a0002c0002t0001g0264a0002c0002t0023g0218 | 2 | HG01109.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.244+175C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169606321 | ||||||
| chr2:169606578
|
C | G | 10 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.244+432C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169606578 | ||||||
| chr2:169606587
|
G | T | 1 | a0003c0003t0004g0104 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.244+441G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169606587 | ||||||
| chr2:169606591
|
C | CAAAAAAA | 12 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(9): Show | 13 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.244+456_244+462dup others(7): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(1): Show |
43 | a0002c0002t0001g0272a0002c0002t0001g0314a0002c0002t0003g0011others(40): Show | 45 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(42): Show |
intron_variant | MODIFIER | c.244+455_244+462dup others(8): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(2): Show |
106 | a0001c0001t0005g0336a0001c0001t0005g0340a0001c0001t0005g0341others(103): Show | 109 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.244+454_244+462dup others(9): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(3): Show |
9 | a0001c0001t0006g0155a0002c0002t0001g0209a0002c0002t0001g0226others(6): Show | 9 | HG00423.hp2 HG01123.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+453_244+462dup others(10): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(4): Show |
19 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.244+452_244+462dup others(11): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(5): Show |
20 | a0001c0001t0005g0343a0001c0001t0005g0347a0001c0001t0005g0362others(17): Show | 21 | HG01081.hp1 HG02258.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.244+451_244+462dup others(12): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0007g0022 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.244+450_244+462dup others(13): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(7): Show |
15 | a0001c0001t0005g0348a0001c0001t0005g0351a0001c0001t0005g0352others(12): Show | 15 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.244+449_244+462dup others(14): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0005g0332a0001c0001t0007g0020a0001c0001t0007g0024others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+448_244+462dup others(15): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0005g0342a0001c0001t0005g0346 | 2 | HG02080.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.244+447_244+462dup others(16): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0012g0036 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.244+446_244+462dup others(17): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0012g0035 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(18): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0005g0345a0001c0001t0026g0034 | 2 | HG00140.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.244+462_244+463ins others(19): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0032g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.244+462_244+463ins others(23): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0028g0137 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(24): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0005g0333 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(25): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(21): Show |
1 | a0001c0001t0005g0335 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(28): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(23): Show |
2 | a0001c0001t0005g0090a0001c0001t0005g0350 | 2 | HG02698.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.244+462_244+463ins others(30): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(27): Show |
2 | a0001c0001t0005g0331a0001c0001t0005g0337 | 2 | NA18952.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.244+462_244+463ins others(34): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(28): Show |
1 | a0001c0001t0005g0338 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(35): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(29): Show |
1 | a0001c0001t0005g0339 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(36): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(30): Show |
1 | a0001c0001t0005g0344 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(37): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(38): Show |
1 | a0001c0001t0005g0334 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(45): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
C | CAAAAAAA others(39): Show |
1 | a0001c0001t0005g0349 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.244+462_244+463ins others(46): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606591
|
CA | C | 80 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(77): Show | 85 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.244+462delA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | |||||
| chr2:169606646
|
A | G | 26 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(23): Show | 26 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.245-458A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169606646 | ||||||
| chr2:169606873
|
T | C | 4 | a0002c0002t0003g0167a0002c0002t0003g0168a0002c0002t0003g0169others(1): Show | 4 | NA18986.hp2 NA19002.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-231T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169606873 | ||||||
| chr2:169606896
|
G | A | 3 | a0003c0003t0004g0111a0003c0003t0004g0115a0003c0003t0004g0120 | 3 | HG03239.hp1 HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.245-208G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169606896 | ||||||
| chr2:169606910
|
A | G | 4 | a0001c0001t0013g0027a0001c0001t0013g0037a0001c0007t0013g0028others(1): Show | 4 | HG02258.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-194A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169606910 | ||||||
| chr2:169607000
|
T | C | 1 | a0001c0001t0007g0205 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.245-104T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169607000 | ||||||
| chr2:169607037
|
T | C | 83 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(80): Show | 88 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.245-67T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169607037 | ||||||
| chr2:169607041
|
T | G | 111 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(108): Show | 114 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.245-63T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169607041 | ||||||
| chr2:169607169
|
A | G | 40 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(37): Show | 41 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.289+21A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607169 | ||||||
| chr2:169607320
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.289+172T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607320 | ||||||
| chr2:169607401
|
A | G | 1 | a0001c0001t0007g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.289+253A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607401 | ||||||
| chr2:169607418
|
G | A | 12 | a0001c0001t0007g0157a0001c0001t0007g0202a0001c0001t0007g0203others(9): Show | 13 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.289+270G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607418 | ||||||
| chr2:169607482
|
G | A | 1 | a0002c0002t0001g0314 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.289+334G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607482 | ||||||
| chr2:169607486
|
A | AT | 10 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.289+344dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 169607486 | |||||
| chr2:169607512
|
A | G | 10 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.289+364A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607512 | ||||||
| chr2:169607678
|
G | T | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.289+530G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607678 | ||||||
| chr2:169607694
|
C | T | 1 | a0002c0002t0001g0253 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.289+546C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607694 | ||||||
| chr2:169607706
|
T | G | 7 | a0001c0001t0011g0014a0001c0001t0011g0161a0001c0001t0011g0162others(4): Show | 8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+558T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607706 | ||||||
| chr2:169607750
|
G | A | 4 | a0001c0001t0011g0161a0001c0001t0011g0162a0001c0001t0011g0163others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+602G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607750 | ||||||
| chr2:169607996
|
T | C | 1 | a0002c0002t0003g0183 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.290-675T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607996 | ||||||
| chr2:169608113
|
A | G | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.290-558A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608113 | ||||||
| chr2:169608137
|
GATA | G | 3 | a0002c0002t0003g0173a0002c0002t0003g0178a0002c0002t0014g0177 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.290-530_290-528del others(3): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 169608137 | |||||
| chr2:169608218
|
C | T | 1 | a0002c0002t0003g0310 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.290-453C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608218 | ||||||
| chr2:169608223
|
G | A | 34 | a0003c0003t0004g0003a0003c0003t0004g0096a0003c0003t0004g0097others(31): Show | 36 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.290-448G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608223 | ||||||
| chr2:169608349
|
C | T | 13 | a0003c0003t0004g0003a0003c0003t0004g0096a0003c0003t0004g0097others(10): Show | 15 | HG00733.hp1 HG01255.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.290-322C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608349 | ||||||
| chr2:169608401
|
A | G | 1 | a0002c0002t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.290-270A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608401 | ||||||
| chr2:169608453
|
G | A | 1 | a0002c0002t0003g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.290-218G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608453 | ||||||
| chr2:169608454
|
C | CA | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.290-216dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 169608454 | |||||
| chr2:169608470
|
A | G | 5 | a0002c0002t0001g0278a0002c0002t0001g0279a0002c0002t0001g0280others(2): Show | 5 | HG01192.hp1 HG01261.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-201A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608470 | ||||||
| chr2:169608597
|
A | G | 1 | a0001c0001t0005g0345 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.290-74A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608597 | ||||||
| chr2:169608615
|
G | A | 46 | a0002c0002t0003g0011a0002c0002t0003g0164a0002c0002t0003g0165others(43): Show | 48 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.290-56G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608615 | ||||||
| chr2:169608636
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.290-35T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608636 | ||||||
| chr2:169608639
|
A | G | 1 | a0002c0002t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.290-32A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608639 | ||||||
| chr2:169608843
|
G | A | 1 | a0002c0002t0003g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.377+85G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169608843 | ||||||
| chr2:169608854
|
G | A | 3 | a0001c0001t0013g0027a0001c0001t0013g0037a0001c0007t0013g0029 | 3 | HG03139.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.377+96G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169608854 | ||||||
| chr2:169608898
|
C | T | 1 | a0002c0002t0003g0190 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.377+140C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169608898 | ||||||
| chr2:169609013
|
G | A | 1 | a0003c0003t0004g0111 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.377+255G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609013 | ||||||
| chr2:169609081
|
C | CA | 24 | a0001c0001t0002g0039a0001c0001t0002g0043a0001c0001t0002g0052others(21): Show | 24 | HG00438.hp1 HG00639.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.377+342dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169609081 | |||||
| chr2:169609081
|
CA | C | 151 | a0001c0001t0006g0155a0002c0002t0001g0001a0002c0002t0001g0013others(148): Show | 156 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.377+342delA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169609081 | |||||
| chr2:169609100
|
A | G | 1 | a0003c0003t0004g0096 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.377+342A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609100 | ||||||
| chr2:169609104
|
C | T | 1 | a0003c0003t0008g0130 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.377+346C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609104 | ||||||
| chr2:169609177
|
G | A | 6 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(3): Show | 7 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.377+419G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609177 | ||||||
| chr2:169609195
|
G | A | 1 | a0001c0001t0005g0334 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.377+437G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609195 | ||||||
| chr2:169609223
|
G | A | 2 | a0001c0001t0013g0027a0001c0007t0013g0029 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.377+465G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609223 | ||||||
| chr2:169609250
|
A | C | 1 | a0002c0002t0001g0315 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.377+492A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609250 | ||||||
| chr2:169609266
|
T | C | 1 | a0002c0002t0003g0172 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.377+508T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609266 | ||||||
| chr2:169609267
|
G | T | 110 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(107): Show | 113 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.377+509G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609267 | ||||||
| chr2:169609268
|
T | G | 310 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(307): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.377+510T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609268 | ||||||
| chr2:169609277
|
T | C | 2 | a0002c0002t0003g0168a0002c0002t0003g0169 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.377+519T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609277 | ||||||
| chr2:169609446
|
CAT | C | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.377+689_377+690del others(2): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609446 | ||||||
| chr2:169609518
|
T | C | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.377+760T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609518 | ||||||
| chr2:169609520
|
C | T | 2 | a0003c0003t0004g0355a0003c0003t0004g0356 | 2 | HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.377+762C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609520 | ||||||
| chr2:169609728
|
A | G | 88 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 94 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.377+970A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609728 | ||||||
| chr2:169609736
|
A | T | 2 | a0002c0002t0001g0230a0002c0002t0001g0246 | 2 | HG01070.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.377+978A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609736 | ||||||
| chr2:169609895
|
C | A | 4 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(1): Show | 4 | NA18939.hp1 NA19005.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.377+1137C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609895 | ||||||
| chr2:169609923
|
T | C | 1 | a0002c0002t0001g0287 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.377+1165T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609923 | ||||||
| chr2:169609939
|
C | A | 310 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(307): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.377+1181C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609939 | ||||||
| chr2:169610017
|
A | T | 40 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(37): Show | 41 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.377+1259A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610017 | ||||||
| chr2:169610063
|
A | G | 79 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(76): Show | 84 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.377+1305A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610063 | ||||||
| chr2:169610307
|
T | G | 1 | a0003c0003t0008g0319 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.377+1549T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610307 | ||||||
| chr2:169610479
|
A | ATT | 23 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(20): Show | 23 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.377+1730_377+1731d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169610479 | |||||
| chr2:169610512
|
T | C | 79 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(76): Show | 84 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.377+1754T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610512 | ||||||
| chr2:169610603
|
T | C | 43 | a0002c0002t0003g0011a0002c0002t0003g0164a0002c0002t0003g0165others(40): Show | 45 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(42): Show |
intron_variant | MODIFIER | c.377+1845T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610603 | ||||||
| chr2:169610641
|
A | C | 7 | a0001c0001t0011g0014a0001c0001t0011g0161a0001c0001t0011g0162others(4): Show | 8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.377+1883A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610641 | ||||||
| chr2:169610742
|
G | GTA | 4 | a0001c0001t0013g0027a0001c0001t0013g0037a0001c0007t0013g0028others(1): Show | 4 | HG02258.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+1987_377+1988d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169610742 | |||||
| chr2:169610787
|
C | T | 1 | a0001c0001t0005g0346 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.377+2029C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610787 | ||||||
| chr2:169610890
|
A | G | 1 | a0002c0004t0003g0174 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.377+2132A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610890 | ||||||
| chr2:169611101
|
G | A | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.377+2343G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611101 | ||||||
| chr2:169611120
|
G | T | 38 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(35): Show | 39 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.377+2362G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611120 | ||||||
| chr2:169611145
|
G | A | 7 | a0001c0001t0011g0014a0001c0001t0011g0161a0001c0001t0011g0162others(4): Show | 8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.377+2387G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611145 | ||||||
| chr2:169611181
|
C | T | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.377+2423C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611181 | ||||||
| chr2:169611261
|
A | G | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.377+2503A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611261 | ||||||
| chr2:169611343
|
A | G | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.377+2585A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611343 | ||||||
| chr2:169611443
|
TTAA | T | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.377+2687_377+2689d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169611443 | |||||
| chr2:169611605
|
T | C | 26 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(23): Show | 26 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.377+2847T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611605 | ||||||
| chr2:169611788
|
A | G | 1 | a0002c0002t0003g0171 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.378-2676A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611788 | ||||||
| chr2:169611883
|
A | T | 7 | a0001c0001t0011g0014a0001c0001t0011g0161a0001c0001t0011g0162others(4): Show | 8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.378-2581A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611883 | ||||||
| chr2:169612005
|
T | C | 1 | a0002c0004t0003g0195 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.378-2459T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612005 | ||||||
| chr2:169612011
|
T | G | 1 | a0002c0002t0001g0292 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.378-2453T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612011 | ||||||
| chr2:169612090
|
C | T | 9 | a0001c0001t0012g0030a0001c0001t0012g0035a0001c0001t0012g0036others(6): Show | 9 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.378-2374C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612090 | ||||||
| chr2:169612094
|
G | A | 6 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(3): Show | 7 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-2370G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612094 | ||||||
| chr2:169612249
|
T | C | 26 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(23): Show | 26 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.378-2215T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612249 | ||||||
| chr2:169612379
|
A | AT | 14 | a0001c0001t0005g0354a0001c0001t0006g0138a0001c0001t0006g0153others(11): Show | 16 | HG00733.hp1 HG01099.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.378-2063dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169612379 | |||||
| chr2:169612379
|
AT | A | 115 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(112): Show | 121 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.378-2063delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169612379 | |||||
| chr2:169612379
|
ATT | A | 16 | a0001c0001t0002g0054a0001c0001t0002g0069a0001c0001t0005g0362others(13): Show | 17 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.378-2064_378-2063d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169612379 | |||||
| chr2:169612379
|
ATTT | A | 6 | a0002c0002t0001g0243a0002c0002t0001g0259a0002c0002t0001g0298others(3): Show | 6 | HG00639.hp2 HG02074.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.378-2065_378-2063d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169612379 | |||||
| chr2:169612379
|
ATTTT | A | 147 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(144): Show | 152 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.378-2066_378-2063d others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169612379 | |||||
| chr2:169612493
|
C | T | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.378-1971C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612493 | ||||||
| chr2:169612601
|
C | T | 1 | a0002c0002t0003g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.378-1863C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612601 | ||||||
| chr2:169612664
|
G | A | 26 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(23): Show | 26 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.378-1800G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612664 | ||||||
| chr2:169612685
|
A | C | 1 | a0003c0003t0004g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.378-1779A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612685 | ||||||
| chr2:169612709
|
T | TA | 3 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092 | 4 | HG02145.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-1754dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169612709 | |||||
| chr2:169612788
|
G | C | 3 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0253 | 3 | HG01081.hp2 HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.378-1676G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612788 | ||||||
| chr2:169612802
|
A | G | 2 | a0001c0001t0006g0143a0001c0001t0006g0149 | 2 | NA18965.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.378-1662A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612802 | ||||||
| chr2:169612949
|
C | T | 1 | a0003c0003t0008g0329 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.378-1515C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612949 | ||||||
| chr2:169612957
|
A | G | 1 | a0001c0001t0005g0345 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.378-1507A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612957 | ||||||
| chr2:169613015
|
A | G | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.378-1449A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613015 | ||||||
| chr2:169613329
|
A | G | 38 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(35): Show | 39 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.378-1135A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613329 | ||||||
| chr2:169613387
|
C | T | 1 | a0002c0002t0001g0242 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.378-1077C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613387 | ||||||
| chr2:169613398
|
T | C | 2 | a0001c0001t0009g0026a0001c0001t0022g0059 | 2 | NA18943.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.378-1066T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613398 | ||||||
| chr2:169613420
|
G | GT | 40 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(37): Show | 41 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.378-1038dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169613420 | |||||
| chr2:169613550
|
T | A | 1 | a0002c0002t0001g0289 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.378-914T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613550 | ||||||
| chr2:169613688
|
A | G | 1 | a0002c0002t0001g0210 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.378-776A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613688 | ||||||
| chr2:169613792
|
G | C | 3 | a0001c0001t0005g0332a0001c0001t0005g0342a0001c0001t0005g0349 | 3 | HG00621.hp2 HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.378-672G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613792 | ||||||
| chr2:169613793
|
G | T | 3 | a0001c0001t0005g0332a0001c0001t0005g0342a0001c0001t0005g0349 | 3 | HG00621.hp2 HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.378-671G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613793 | ||||||
| chr2:169613911
|
A | G | 1 | a0001c0001t0006g0144 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.378-553A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613911 | ||||||
| chr2:169613993
|
C | T | 46 | a0002c0002t0003g0011a0002c0002t0003g0164a0002c0002t0003g0165others(43): Show | 48 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.378-471C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613993 | ||||||
| chr2:169614022
|
A | G | 5 | a0002c0002t0001g0207a0002c0002t0001g0212a0002c0002t0001g0236others(2): Show | 5 | HG00423.hp2 HG02027.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.378-442A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169614022 | ||||||
| chr2:169614116
|
A | G | 1 | a0002c0002t0034g0231 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.378-348A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169614116 | ||||||
| chr2:169614234
|
G | A | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.378-230G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169614234 | ||||||
| chr2:169614236
|
A | G | 3 | a0002c0002t0003g0308a0002c0002t0003g0309a0002c0002t0003g0310 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.378-228A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169614236 | ||||||
| chr2:169614452
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.378-12G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169614452 | ||||||
| chr2:169614760
|
A | G | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.547+36A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169614760 | ||||||
| chr2:169615036
|
G | GT | 16 | a0001c0001t0002g0070a0001c0001t0002g0081a0001c0001t0006g0148others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.547+322dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169615036 | |||||
| chr2:169615069
|
G | A | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.547+345G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615069 | ||||||
| chr2:169615109
|
C | T | 1 | a0003c0003t0004g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.547+385C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615109 | ||||||
| chr2:169615219
|
C | T | 156 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.547+495C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615219 | ||||||
| chr2:169615235
|
G | T | 7 | a0001c0001t0005g0331a0001c0001t0005g0334a0001c0001t0005g0337others(4): Show | 7 | HG00609.hp1 NA18952.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.547+511G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615235 | ||||||
| chr2:169615370
|
A | G | 284 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(281): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.547+646A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615370 | ||||||
| chr2:169615531
|
G | A | 1 | a0002c0002t0001g0259 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.547+807G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615531 | ||||||
| chr2:169615561
|
T | C | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.547+837T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615561 | ||||||
| chr2:169615720
|
CA | C | 56 | a0003c0003t0004g0003a0003c0003t0004g0010a0003c0003t0004g0095others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.547+997delA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615720 | ||||||
| chr2:169615784
|
C | T | 1 | a0002c0002t0003g0190 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.547+1060C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615784 | ||||||
| chr2:169615901
|
G | A | 82 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(79): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.547+1177G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615901 | ||||||
| chr2:169615926
|
C | T | 2 | a0001c0001t0005g0332a0001c0001t0005g0342 | 2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.547+1202C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615926 | ||||||
| chr2:169616031
|
A | G | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.547+1307A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616031 | ||||||
| chr2:169616363
|
A | G | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.547+1639A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616363 | ||||||
| chr2:169616453
|
C | T | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.547+1729C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616453 | ||||||
| chr2:169616502
|
G | A | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.547+1778G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616502 | ||||||
| chr2:169616545
|
C | A | 21 | a0003c0003t0004g0355a0003c0003t0004g0356a0003c0003t0004g0357others(18): Show | 21 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.547+1821C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616545 | ||||||
| chr2:169616561
|
A | G | 4 | a0001c0001t0007g0157a0001c0001t0007g0202a0001c0001t0007g0203others(1): Show | 4 | NA18906.hp1 NA19030.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+1837A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616561 | ||||||
| chr2:169616602
|
T | C | 12 | a0002c0002t0001g0013a0002c0002t0001g0281a0002c0002t0001g0282others(9): Show | 12 | HG00609.hp2 NA18747.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.547+1878T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616602 | ||||||
| chr2:169616695
|
T | G | 56 | a0003c0003t0004g0003a0003c0003t0004g0010a0003c0003t0004g0095others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.547+1971T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616695 | ||||||
| chr2:169616698
|
G | GT | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.547+1981dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169616698 | |||||
| chr2:169616754
|
G | T | 1 | a0001c0001t0006g0151 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.547+2030G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616754 | ||||||
| chr2:169616799
|
C | T | 1 | a0001c0001t0005g0345 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.547+2075C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616799 | ||||||
| chr2:169616802
|
G | A | 10 | a0003c0003t0004g0010a0003c0003t0004g0098a0003c0003t0004g0111others(7): Show | 11 | HG00280.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.547+2078G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616802 | ||||||
| chr2:169617056
|
G | A | 1 | a0002c0002t0001g0285 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.547+2332G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169617056 | ||||||
| chr2:169617293
|
T | A | 5 | a0002c0002t0001g0207a0002c0002t0001g0212a0002c0002t0001g0236others(2): Show | 5 | HG00423.hp2 HG02027.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+2569T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169617293 | ||||||
| chr2:169617309
|
G | C | 6 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(3): Show | 7 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.547+2585G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169617309 | ||||||
| chr2:169617619
|
A | G | 1 | a0003c0003t0008g0329 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.547+2895A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169617619 | ||||||
| chr2:169617792
|
T | C | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.547+3068T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169617792 | ||||||
| chr2:169617948
|
G | A | 1 | a0003c0003t0016g0112 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.547+3224G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169617948 | ||||||
| chr2:169618001
|
GTTC | G | 23 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(20): Show | 23 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.547+3280_547+3282d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169618001 | |||||
| chr2:169618179
|
A | C | 26 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(23): Show | 26 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.547+3455A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618179 | ||||||
| chr2:169618302
|
G | A | 1 | a0001c0001t0002g0008 | 2 | HG01123.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.547+3578G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618302 | ||||||
| chr2:169618365
|
C | T | 1 | a0004c0008t0001g0302 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.547+3641C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618365 | ||||||
| chr2:169618380
|
G | C | 5 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(2): Show | 6 | HG02145.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.547+3656G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618380 | ||||||
| chr2:169618431
|
C | A | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.547+3707C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618431 | ||||||
| chr2:169618552
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.547+3828G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618552 | ||||||
| chr2:169618639
|
G | A | 3 | a0001c0001t0013g0027a0001c0001t0013g0037a0001c0007t0013g0029 | 3 | HG03139.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.547+3915G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618639 | ||||||
| chr2:169618682
|
A | G | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.547+3958A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618682 | ||||||
| chr2:169618826
|
A | AT | 179 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(176): Show | 188 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.547+4115dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169618826 | |||||
| chr2:169618852
|
G | T | 9 | a0001c0001t0012g0030a0001c0001t0012g0035a0001c0001t0012g0036others(6): Show | 9 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.547+4128G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618852 | ||||||
| chr2:169618898
|
G | A | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.547+4174G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618898 | ||||||
| chr2:169619066
|
C | T | 1 | a0003c0003t0008g0327 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.547+4342C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619066 | ||||||
| chr2:169619156
|
A | G | 256 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(253): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.547+4432A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619156 | ||||||
| chr2:169619175
|
A | G | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.547+4451A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619175 | ||||||
| chr2:169619237
|
G | A | 1 | a0002c0002t0003g0185 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.547+4513G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619237 | ||||||
| chr2:169619318
|
C | A | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.547+4594C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619318 | ||||||
| chr2:169619357
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.547+4633G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619357 | ||||||
| chr2:169619422
|
C | T | 1 | a0003c0003t0004g0107 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.547+4698C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619422 | ||||||
| chr2:169619443
|
T | A | 1 | a0002c0002t0001g0283 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.547+4719T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619443 | ||||||
| chr2:169619568
|
A | G | 3 | a0001c0001t0005g0090a0001c0001t0005g0333a0001c0001t0005g0338 | 3 | NA18993.hp1 NA19007.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.547+4844A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619568 | ||||||
| chr2:169619575
|
T | G | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.547+4851T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619575 | ||||||
| chr2:169619628
|
C | T | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.547+4904C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619628 | ||||||
| chr2:169619661
|
A | G | 10 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.547+4937A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619661 | ||||||
| chr2:169619751
|
CT | C | 46 | a0001c0001t0002g0069a0002c0002t0003g0011a0002c0002t0003g0164others(43): Show | 48 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.547+5037delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169619751 | |||||
| chr2:169619755
|
T | C | 2 | a0003c0003t0008g0321a0003c0003t0008g0329 | 2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.547+5031T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619755 | ||||||
| chr2:169619983
|
G | A | 363 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(360): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.547+5259G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619983 | ||||||
| chr2:169620008
|
A | G | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.547+5284A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620008 | ||||||
| chr2:169620018
|
A | G | 3 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0252 | 3 | HG03491.hp2 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.547+5294A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620018 | ||||||
| chr2:169620032
|
A | G | 1 | a0002c0002t0003g0184 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.547+5308A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620032 | ||||||
| chr2:169620152
|
T | C | 31 | a0003c0003t0004g0003a0003c0003t0004g0096a0003c0003t0004g0097others(28): Show | 33 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.547+5428T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620152 | ||||||
| chr2:169620164
|
A | G | 79 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(76): Show | 84 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.547+5440A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620164 | ||||||
| chr2:169620169
|
A | G | 38 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(35): Show | 39 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.547+5445A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620169 | ||||||
| chr2:169620319
|
G | A | 1 | a0001c0001t0011g0312 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.547+5595G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620319 | ||||||
| chr2:169620347
|
T | C | 1 | a0002c0002t0010g0237 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.547+5623T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620347 | ||||||
| chr2:169620360
|
G | A | 1 | a0003c0003t0008g0324 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.547+5636G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620360 | ||||||
| chr2:169620391
|
C | T | 9 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(6): Show | 10 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.547+5667C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620391 | ||||||
| chr2:169620523
|
A | G | 26 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(23): Show | 26 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.547+5799A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620523 | ||||||
| chr2:169620665
|
G | A | 3 | a0001c0001t0013g0027a0001c0007t0013g0028a0001c0007t0013g0029 | 3 | HG02258.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.547+5941G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620665 | ||||||
| chr2:169620680
|
T | G | 1 | a0001c0001t0005g0351 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.547+5956T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620680 | ||||||
| chr2:169620884
|
C | A | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.547+6160C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620884 | ||||||
| chr2:169620888
|
G | T | 3 | a0003c0003t0008g0325a0003c0003t0008g0359a0003c0003t0031g0360 | 3 | HG00558.hp2 NA18997.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.547+6164G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620888 | ||||||
| chr2:169620961
|
A | G | 1 | a0003c0003t0004g0107 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.547+6237A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620961 | ||||||
| chr2:169621290
|
A | T | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.547+6566A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621290 | ||||||
| chr2:169621440
|
C | T | 1 | a0002c0002t0003g0183 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.547+6716C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621440 | ||||||
| chr2:169621544
|
G | C | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.547+6820G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621544 | ||||||
| chr2:169621608
|
AC | A | 6 | a0001c0001t0012g0030a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+6887delC | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169621608 | |||||
| chr2:169621619
|
A | G | 9 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(6): Show | 10 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.547+6895A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621619 | ||||||
| chr2:169621672
|
A | G | 1 | a0001c0001t0002g0062 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.547+6948A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621672 | ||||||
| chr2:169621734
|
A | ATT | 78 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(75): Show | 83 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.547+7023_547+7024d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169621734 | |||||
| chr2:169621776
|
G | A | 209 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(206): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.547+7052G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621776 | ||||||
| chr2:169621923
|
C | T | 363 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(360): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.547+7199C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621923 | ||||||
| chr2:169621942
|
A | T | 7 | a0002c0002t0001g0241a0002c0002t0001g0243a0002c0002t0001g0259others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.547+7218A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621942 | ||||||
| chr2:169621942
|
AT | A | 207 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(204): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.547+7227delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169621942 | |||||
| chr2:169621943
|
T | A | 1 | a0001c0001t0005g0338 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.547+7219T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621943 | ||||||
| chr2:169621944
|
T | A | 11 | a0001c0001t0005g0090a0001c0001t0005g0333a0001c0001t0005g0336others(8): Show | 11 | HG00558.hp1 HG02080.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.547+7220T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621944 | ||||||
| chr2:169621999
|
A | C | 31 | a0003c0003t0004g0003a0003c0003t0004g0096a0003c0003t0004g0097others(28): Show | 33 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.547+7275A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621999 | ||||||
| chr2:169622009
|
C | G | 6 | a0001c0001t0012g0030a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+7285C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622009 | ||||||
| chr2:169622019
|
G | C | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.547+7295G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622019 | ||||||
| chr2:169622066
|
A | G | 6 | a0001c0001t0012g0030a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+7342A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622066 | ||||||
| chr2:169622088
|
A | G | 3 | a0002c0002t0003g0308a0002c0002t0003g0309a0002c0002t0003g0310 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.547+7364A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622088 | ||||||
| chr2:169622105
|
T | C | 1 | a0001c0005t0002g0077 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.547+7381T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622105 | ||||||
| chr2:169622186
|
C | T | 78 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(75): Show | 83 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.547+7462C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622186 | ||||||
| chr2:169622303
|
A | G | 209 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(206): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.547+7579A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622303 | ||||||
| chr2:169622487
|
T | C | 1 | a0002c0002t0001g0252 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.547+7763T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622487 | ||||||
| chr2:169622534
|
A | G | 60 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(57): Show | 65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.547+7810A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622534 | ||||||
| chr2:169622794
|
C | T | 209 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(206): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-7980C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622794 | ||||||
| chr2:169622858
|
A | C | 1 | a0002c0002t0001g0235 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.548-7916A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622858 | ||||||
| chr2:169622866
|
A | G | 1 | a0002c0002t0001g0296 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.548-7908A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622866 | ||||||
| chr2:169622911
|
C | T | 3 | a0003c0003t0004g0355a0003c0003t0004g0356a0003c0003t0004g0357 | 3 | HG01496.hp1 HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.548-7863C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622911 | ||||||
| chr2:169622942
|
T | A | 1 | a0002c0002t0001g0275 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.548-7832T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622942 | ||||||
| chr2:169623002
|
TA | T | 6 | a0001c0001t0012g0030a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.548-7771delA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623002 | ||||||
| chr2:169623015
|
G | T | 153 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(150): Show | 160 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.548-7759G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623015 | ||||||
| chr2:169623108
|
A | C | 1 | a0001c0001t0007g0205 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.548-7666A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623108 | ||||||
| chr2:169623152
|
T | C | 35 | a0003c0003t0004g0003a0003c0003t0004g0010a0003c0003t0004g0095others(32): Show | 38 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.548-7622T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623152 | ||||||
| chr2:169623154
|
G | A | 1 | a0001c0001t0006g0134 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.548-7620G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623154 | ||||||
| chr2:169623241
|
C | A | 1 | a0002c0002t0003g0197 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.548-7533C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623241 | ||||||
| chr2:169623429
|
G | A | 70 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(67): Show | 75 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.548-7345G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623429 | ||||||
| chr2:169623453
|
G | A | 2 | a0002c0002t0003g0164a0002c0002t0003g0165 | 2 | NA19006.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.548-7321G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623453 | ||||||
| chr2:169623513
|
C | T | 45 | a0002c0002t0003g0011a0002c0002t0003g0164a0002c0002t0003g0165others(42): Show | 47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.548-7261C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623513 | ||||||
| chr2:169623707
|
T | C | 5 | a0001c0001t0011g0161a0001c0001t0011g0162a0001c0001t0011g0163others(2): Show | 5 | HG00099.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.548-7067T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623707 | ||||||
| chr2:169623892
|
G | T | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.548-6882G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623892 | ||||||
| chr2:169623953
|
T | G | 1 | a0001c0001t0012g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.548-6821T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623953 | ||||||
| chr2:169623955
|
C | T | 26 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(23): Show | 26 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.548-6819C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623955 | ||||||
| chr2:169624000
|
T | C | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.548-6774T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624000 | ||||||
| chr2:169624010
|
A | T | 1 | a0001c0005t0002g0077 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.548-6764A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624010 | ||||||
| chr2:169624157
|
A | G | 10 | a0002c0002t0001g0159a0002c0002t0001g0206a0002c0002t0001g0210others(7): Show | 10 | HG00642.hp1 HG00735.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.548-6617A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624157 | ||||||
| chr2:169624160
|
TCTCGCTA others(5): Show |
T | 2 | a0005c0006t0018g0109a0005c0006t0018g0114 | 2 | HG03654.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.548-6612_548-6601d others(14): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169624160 | |||||
| chr2:169624223
|
A | C | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.548-6551A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624223 | ||||||
| chr2:169624244
|
A | G | 256 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(253): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.548-6530A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624244 | ||||||
| chr2:169624368
|
C | A | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.548-6406C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624368 | ||||||
| chr2:169624388
|
T | A | 1 | a0003c0003t0004g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.548-6386T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624388 | ||||||
| chr2:169624464
|
C | T | 363 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(360): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.548-6310C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624464 | ||||||
| chr2:169624650
|
C | T | 4 | a0002c0002t0001g0281a0002c0002t0001g0282a0002c0002t0001g0291others(1): Show | 4 | NA18980.hp1 NA19056.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.548-6124C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624650 | ||||||
| chr2:169624737
|
A | G | 4 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0253others(1): Show | 4 | HG01081.hp2 HG02273.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-6037A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624737 | ||||||
| chr2:169624932
|
C | T | 1 | a0002c0002t0001g0303 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.548-5842C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624932 | ||||||
| chr2:169624939
|
G | A | 3 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092 | 4 | HG02145.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-5835G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624939 | ||||||
| chr2:169624946
|
A | T | 1 | a0002c0002t0001g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.548-5828A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624946 | ||||||
| chr2:169625026
|
A | G | 1 | a0001c0001t0011g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.548-5748A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625026 | ||||||
| chr2:169625217
|
G | A | 72 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(69): Show | 74 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.548-5557G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625217 | ||||||
| chr2:169625259
|
A | G | 56 | a0003c0003t0004g0003a0003c0003t0004g0010a0003c0003t0004g0095others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.548-5515A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625259 | ||||||
| chr2:169625565
|
G | A | 60 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(57): Show | 65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.548-5209G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625565 | ||||||
| chr2:169625586
|
A | C | 60 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(57): Show | 65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.548-5188A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625586 | ||||||
| chr2:169625726
|
C | T | 1 | a0001c0001t0025g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.548-5048C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625726 | ||||||
| chr2:169625728
|
AT | A | 7 | a0001c0001t0002g0072a0001c0001t0005g0362a0002c0002t0001g0278others(4): Show | 7 | HG01192.hp1 HG01261.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.548-5035delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169625728 | |||||
| chr2:169625841
|
A | G | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.548-4933A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625841 | ||||||
| chr2:169625989
|
T | C | 14 | a0001c0001t0007g0157a0001c0001t0007g0202a0001c0001t0007g0203others(11): Show | 15 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.548-4785T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625989 | ||||||
| chr2:169626047
|
G | T | 104 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0158others(101): Show | 107 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.548-4727G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169626047 | ||||||
| chr2:169626081
|
T | C | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.548-4693T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169626081 | ||||||
| chr2:169626535
|
A | G | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.548-4239A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169626535 | ||||||
| chr2:169626581
|
G | T | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.548-4193G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169626581 | ||||||
| chr2:169626732
|
C | T | 1 | a0003c0003t0004g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.548-4042C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169626732 | ||||||
| chr2:169626956
|
T | A | 3 | a0002c0002t0001g0225a0002c0002t0001g0265a0002c0002t0001g0316 | 3 | NA18943.hp1 NA19005.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.548-3818T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169626956 | ||||||
| chr2:169627047
|
T | C | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.548-3727T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627047 | ||||||
| chr2:169627049
|
A | G | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.548-3725A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627049 | ||||||
| chr2:169627150
|
T | G | 13 | a0003c0003t0004g0003a0003c0003t0004g0096a0003c0003t0004g0097others(10): Show | 15 | HG00733.hp1 HG01255.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.548-3624T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627150 | ||||||
| chr2:169627239
|
C | T | 56 | a0003c0003t0004g0003a0003c0003t0004g0010a0003c0003t0004g0095others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.548-3535C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627239 | ||||||
| chr2:169627285
|
G | A | 1 | a0001c0001t0013g0037 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.548-3489G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627285 | ||||||
| chr2:169627309
|
C | T | 2 | a0001c0001t0007g0093a0001c0001t0007g0094 | 2 | HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.548-3465C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627309 | ||||||
| chr2:169627411
|
T | C | 1 | a0002c0002t0003g0171 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.548-3363T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627411 | ||||||
| chr2:169627470
|
T | A | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.548-3304T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627470 | ||||||
| chr2:169627598
|
C | T | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.548-3176C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627598 | ||||||
| chr2:169627704
|
C | CTTTTT | 70 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(67): Show | 75 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.548-3053_548-3049d others(7): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169627704 | |||||
| chr2:169627704
|
C | CTTTTTT | 35 | a0001c0001t0002g0053a0001c0001t0002g0062a0001c0001t0002g0075others(32): Show | 38 | HG00323.hp2 HG00438.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.548-3054_548-3049d others(8): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169627704 | |||||
| chr2:169627704
|
C | CTTTTTTT | 12 | a0001c0001t0012g0030a0001c0001t0012g0041a0001c0001t0015g0032others(9): Show | 12 | HG01099.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.548-3055_548-3049d others(9): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169627704 | |||||
| chr2:169627704
|
CT | C | 35 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(32): Show | 35 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.548-3049delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169627704 | |||||
| chr2:169627725
|
T | A | 25 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(22): Show | 25 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.548-3049T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627725 | ||||||
| chr2:169627725
|
T | TTTTTTA | 9 | a0001c0001t0005g0353a0001c0001t0005g0354a0001c0001t0007g0091others(6): Show | 9 | HG02630.hp2 HG02647.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.548-3049_548-3048i others(8): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627725 | ||||||
| chr2:169627725
|
T | TTTTTTTA | 27 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(24): Show | 28 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.548-3049_548-3048i others(9): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627725 | ||||||
| chr2:169627808
|
A | G | 4 | a0001c0001t0009g0058a0001c0001t0009g0066a0001c0001t0009g0068others(1): Show | 4 | HG02523.hp2 HG03927.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-2966A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627808 | ||||||
| chr2:169627965
|
T | A | 1 | a0002c0002t0003g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.548-2809T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627965 | ||||||
| chr2:169628146
|
A | G | 256 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(253): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.548-2628A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628146 | ||||||
| chr2:169628214
|
A | G | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.548-2560A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628214 | ||||||
| chr2:169628272
|
G | A | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.548-2502G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628272 | ||||||
| chr2:169628370
|
C | T | 1 | a0002c0002t0001g0210 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.548-2404C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628370 | ||||||
| chr2:169628422
|
T | A | 1 | a0002c0004t0003g0192 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.548-2352T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628422 | ||||||
| chr2:169628534
|
A | G | 21 | a0003c0003t0004g0355a0003c0003t0004g0356a0003c0003t0004g0357others(18): Show | 21 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.548-2240A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628534 | ||||||
| chr2:169628698
|
C | T | 4 | a0001c0001t0013g0027a0001c0001t0013g0037a0001c0007t0013g0028others(1): Show | 4 | HG02258.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.548-2076C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628698 | ||||||
| chr2:169628731
|
G | A | 1 | a0004c0008t0001g0302 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.548-2043G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628731 | ||||||
| chr2:169628808
|
T | C | 10 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.548-1966T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628808 | ||||||
| chr2:169628930
|
C | A | 54 | a0003c0003t0004g0003a0003c0003t0004g0010a0003c0003t0004g0095others(51): Show | 57 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.548-1844C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628930 | ||||||
| chr2:169628939
|
C | CA | 52 | a0001c0001t0005g0339a0001c0001t0012g0030a0002c0002t0001g0207others(49): Show | 52 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.548-1806dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | |||||
| chr2:169628939
|
C | CAA | 8 | a0002c0002t0001g0287a0002c0002t0001g0298a0002c0002t0001g0304others(5): Show | 8 | HG01192.hp1 HG02135.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.548-1807_548-1806d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | |||||
| chr2:169628939
|
C | CAAA | 7 | a0001c0001t0012g0035a0001c0001t0026g0034a0002c0002t0001g0267others(4): Show | 7 | HG00673.hp1 HG02735.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.548-1808_548-1806d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | |||||
| chr2:169628939
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0028g0137 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.548-1815_548-1806d others(12): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | |||||
| chr2:169628939
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0007g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.548-1816_548-1806d others(13): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | |||||
| chr2:169628939
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0007g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.548-1817_548-1806d others(14): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | |||||
| chr2:169628939
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0007g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.548-1818_548-1806d others(15): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | |||||
| chr2:169628939
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0027g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.548-1823_548-1806d others(20): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | |||||
| chr2:169628939
|
CA | C | 21 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0334others(18): Show | 21 | HG00140.hp1 HG00609.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.548-1806delA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | |||||
| chr2:169628939
|
CAAAAAAA others(3): Show |
C | 26 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0019others(23): Show | 27 | HG00280.hp2 HG01099.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.548-1815_548-1806d others(12): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | |||||
| chr2:169628939
|
CAAAAAAA others(4): Show |
C | 39 | a0001c0001t0002g0043a0001c0001t0002g0045a0001c0001t0002g0053others(36): Show | 41 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.548-1816_548-1806d others(13): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | |||||
| chr2:169628939
|
CAAAAAAA others(5): Show |
C | 94 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(91): Show | 101 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.548-1817_548-1806d others(14): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | |||||
| chr2:169628939
|
CAAAAAAA others(6): Show |
C | 4 | a0001c0001t0011g0161a0001c0001t0011g0162a0001c0001t0011g0163others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-1818_548-1806d others(15): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | |||||
| chr2:169628966
|
A | G | 1 | a0003c0003t0008g0325 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.548-1808A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628966 | ||||||
| chr2:169628968
|
A | G | 1 | a0002c0002t0001g0262 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.548-1806A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628968 | ||||||
| chr2:169629041
|
A | G | 208 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(205): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.548-1733A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169629041 | ||||||
| chr2:169629237
|
A | G | 1 | a0003c0003t0008g0319 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.548-1537A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169629237 | ||||||
| chr2:169629662
|
A | G | 10 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092others(7): Show | 12 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.548-1112A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169629662 | ||||||
| chr2:169629757
|
C | T | 1 | a0001c0001t0007g0205 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.548-1017C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169629757 | ||||||
| chr2:169629830
|
T | C | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.548-944T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169629830 | ||||||
| chr2:169629925
|
T | C | 3 | a0002c0002t0001g0285a0002c0002t0001g0286a0002c0002t0001g0294 | 3 | HG02976.hp2 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.548-849T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169629925 | ||||||
| chr2:169629935
|
T | C | 26 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(23): Show | 26 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.548-839T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169629935 | ||||||
| chr2:169630081
|
C | G | 2 | a0003c0003t0004g0124a0003c0003t0004g0129 | 2 | HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.548-693C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169630081 | ||||||
| chr2:169630141
|
G | GT | 6 | a0002c0002t0001g0013a0002c0002t0003g0173a0002c0002t0010g0013others(3): Show | 6 | HG02895.hp1 HG02897.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.548-620dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169630141 | |||||
| chr2:169630141
|
GT | G | 195 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0008others(192): Show | 203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.548-620delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169630141 | |||||
| chr2:169630141
|
GTT | G | 6 | a0001c0001t0002g0002a0001c0001t0002g0067a0001c0001t0002g0080others(3): Show | 8 | NA18943.hp2 NA18947.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.548-621_548-620del others(2): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169630141 | |||||
| chr2:169630274
|
C | G | 78 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(75): Show | 83 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.548-500C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169630274 | ||||||
| chr2:169630497
|
A | T | 209 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(206): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-277A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169630497 | ||||||
| chr2:169630586
|
C | T | 4 | a0001c0001t0013g0027a0001c0001t0013g0037a0001c0007t0013g0028others(1): Show | 4 | HG02258.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.548-188C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169630586 | ||||||
| chr2:169630644
|
C | G | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.548-130C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169630644 | ||||||
| chr2:169630660
|
G | T | 5 | a0001c0001t0006g0146a0001c0001t0006g0147a0001c0001t0006g0150others(2): Show | 5 | HG01099.hp2 HG01346.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.548-114G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169630660 | ||||||
| chr2:169630746
|
G | A | 1 | a0002c0002t0003g0176 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.548-28G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169630746 | ||||||
| chr2:169631089
|
G | T | 1 | a0001c0001t0007g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.761+102G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 10/13 | chr2 | 169631089 | ||||||
| chr2:169631170
|
G | C | 254 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(251): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.761+183G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 10/13 | chr2 | 169631170 | ||||||
| chr2:169631329
|
G | A | 78 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(75): Show | 83 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.761+342G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 10/13 | chr2 | 169631329 | ||||||
| chr2:169631477
|
T | C | 5 | a0001c0001t0007g0157a0001c0001t0007g0202a0001c0001t0007g0203others(2): Show | 5 | HG01891.hp1 NA18906.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.762-289T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 10/13 | chr2 | 169631477 | ||||||
| chr2:169631721
|
A | G | 1 | a0003c0003t0008g0358 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.762-45A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 10/13 | chr2 | 169631721 | ||||||
| chr2:169631944
|
A | G | 209 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(206): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.929+11A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169631944 | ||||||
| chr2:169632058
|
A | C | 3 | a0002c0002t0001g0285a0002c0002t0001g0286a0002c0002t0001g0294 | 3 | HG02976.hp2 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.929+125A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632058 | ||||||
| chr2:169632117
|
A | C | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.929+184A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632117 | ||||||
| chr2:169632149
|
A | G | 6 | a0001c0001t0012g0030a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.929+216A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632149 | ||||||
| chr2:169632173
|
A | G | 1 | a0002c0002t0003g0183 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.929+240A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632173 | ||||||
| chr2:169632182
|
G | A | 1 | a0002c0002t0001g0220 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.929+249G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632182 | ||||||
| chr2:169632189
|
T | C | 60 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(57): Show | 65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.929+256T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632189 | ||||||
| chr2:169632209
|
C | A | 60 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(57): Show | 65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.929+276C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632209 | ||||||
| chr2:169632230
|
A | G | 60 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(57): Show | 65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.929+297A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632230 | ||||||
| chr2:169632249
|
T | C | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.929+316T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632249 | ||||||
| chr2:169632260
|
T | G | 78 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(75): Show | 83 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.929+327T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632260 | ||||||
| chr2:169632356
|
T | G | 90 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(87): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.929+423T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632356 | ||||||
| chr2:169632467
|
C | T | 209 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(206): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.929+534C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632467 | ||||||
| chr2:169632590
|
A | T | 4 | a0002c0002t0001g0281a0002c0002t0001g0282a0002c0002t0001g0291others(1): Show | 4 | NA18980.hp1 NA19056.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.930-570A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632590 | ||||||
| chr2:169632677
|
G | A | 45 | a0002c0002t0003g0011a0002c0002t0003g0164a0002c0002t0003g0165others(42): Show | 47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.930-483G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632677 | ||||||
| chr2:169632701
|
C | T | 1 | a0001c0001t0007g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.930-459C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632701 | ||||||
| chr2:169632747
|
A | AAATAAT | 199 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(196): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.930-398_930-393dup others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 169632747 | |||||
| chr2:169632747
|
A | AAATAATA others(2): Show |
10 | a0001c0001t0002g0067a0001c0001t0007g0009a0001c0001t0007g0091others(7): Show | 11 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.930-401_930-393dup others(9): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 169632747 | |||||
| chr2:169632796
|
T | G | 3 | a0001c0001t0007g0009a0001c0001t0007g0091a0001c0001t0007g0092 | 4 | HG02145.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.930-364T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632796 | ||||||
| chr2:169632864
|
G | C | 1 | a0002c0002t0003g0172 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.930-296G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632864 | ||||||
| chr2:169633315
|
T | A | 5 | a0001c0001t0007g0015a0001c0001t0007g0019a0001c0001t0007g0021others(2): Show | 5 | HG02280.hp2 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+68T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633315 | ||||||
| chr2:169633460
|
A | G | 28 | a0003c0003t0004g0003a0003c0003t0004g0010a0003c0003t0004g0095others(25): Show | 31 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1017+213A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633460 | ||||||
| chr2:169633656
|
C | T | 2 | a0003c0003t0004g0119a0003c0003t0004g0121 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1017+409C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633656 | ||||||
| chr2:169633663
|
T | TA | 40 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0135others(37): Show | 41 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1017+417dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 169633663 | |||||
| chr2:169633693
|
C | T | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1017+446C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633693 | ||||||
| chr2:169633830
|
C | T | 1 | a0002c0002t0034g0231 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1017+583C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633830 | ||||||
| chr2:169633835
|
CCT | C | 207 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(204): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1017+589_1017+590d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633835 | ||||||
| chr2:169633837
|
T | C | 1 | a0002c0002t0001g0255 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1017+590T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633837 | ||||||
| chr2:169633900
|
G | A | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1017+653G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633900 | ||||||
| chr2:169634143
|
C | T | 6 | a0003c0003t0008g0320a0003c0003t0008g0324a0003c0003t0008g0326others(3): Show | 6 | HG00735.hp1 HG01069.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+896C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634143 | ||||||
| chr2:169634159
|
C | T | 26 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.1017+912C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634159 | ||||||
| chr2:169634604
|
G | A | 8 | a0001c0001t0012g0030a0001c0001t0012g0035a0001c0001t0012g0036others(5): Show | 8 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1017+1357G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634604 | ||||||
| chr2:169634643
|
T | G | 1 | a0002c0002t0001g0277 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1017+1396T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634643 | ||||||
| chr2:169634739
|
TCTGCCTC others(1): Show |
T | 45 | a0002c0002t0003g0011a0002c0002t0003g0164a0002c0002t0003g0165others(42): Show | 47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.1018-1352_1018-134 others(12): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634739 | ||||||
| chr2:169634748
|
T | A | 45 | a0002c0002t0003g0011a0002c0002t0003g0164a0002c0002t0003g0165others(42): Show | 47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.1018-1344T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634748 | ||||||
| chr2:169634750
|
A | C | 45 | a0002c0002t0003g0011a0002c0002t0003g0164a0002c0002t0003g0165others(42): Show | 47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.1018-1342A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634750 | ||||||
| chr2:169634752
|
T | C | 45 | a0002c0002t0003g0011a0002c0002t0003g0164a0002c0002t0003g0165others(42): Show | 47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.1018-1340T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634752 | ||||||
| chr2:169635006
|
A | G | 1 | a0003c0003t0008g0358 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1018-1086A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635006 | ||||||
| chr2:169635053
|
TAATGA | T | 82 | a0001c0001t0005g0090a0001c0001t0005g0331a0001c0001t0005g0332others(79): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1018-1035_1018-103 others(9): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 169635053 | |||||
| chr2:169635135
|
A | G | 4 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0253others(1): Show | 4 | HG01081.hp2 HG02273.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018-957A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635135 | ||||||
| chr2:169635268
|
G | A | 209 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(206): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1018-824G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635268 | ||||||
| chr2:169635313
|
G | A | 60 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(57): Show | 65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1018-779G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635313 | ||||||
| chr2:169635317
|
T | C | 1 | a0003c0003t0008g0358 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1018-775T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635317 | ||||||
| chr2:169635329
|
T | C | 2 | a0001c0001t0028g0137a0001c0001t0032g0136 | 2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1018-763T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635329 | ||||||
| chr2:169635569
|
G | A | 209 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(206): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1018-523G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635569 | ||||||
| chr2:169635745
|
G | A | 1 | a0002c0002t0010g0266 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1018-347G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635745 | ||||||
| chr2:169636026
|
C | T | 1 | a0003c0003t0004g0356 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1018-66C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169636026 | ||||||
| chr2:169636057
|
A | G | 210 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1018-35A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169636057 | ||||||
| chr2:169636074
|
T | C | 256 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(253): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.1018-18T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169636074 |