| geneid | 27043 |
|---|---|
| ensemblid | ENSG00000141456.16 |
| hgncid | 30134 |
| symbol | PELP1 |
| name | proline, glutamate and leucine rich protein 1 |
| refseq_nuc | NM_014389.3 |
| refseq_prot | NP_055204.4 |
| ensembl_nuc | ENST00000572293.7 |
| ensembl_prot | ENSP00000460300.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 4669774 |
| end | 4704137 |
| strand | - |
| ver | v1.2 |
| region | chr17:4669774-4704137 |
| region5000 | chr17:4664774-4709137 |
| regionname0 | PELP1_chr17_4669774_4704137 |
| regionname5000 | PELP1_chr17_4664774_4709137 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1130 | 271 | 81 | 50 | 101 | 5 | 32 | 74 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0002 | 0/0 | 1130 | 15 | 1 | 5 | 1 | 3 | 5 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0003 | 0/0 | 1126 | 9 | 0 | 0 | 9 | 0 | 0 | 7 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0004 | 0/0 | 1129 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0005 | 0/0 | 1130 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0006 | 0/0 | 1130 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0007 | 0/0 | 1130 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0008 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0009 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0010 | 0/0 | 1130 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0011 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0012 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0013 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0014 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0015 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| 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 | 3393 | 201 | 36 | 39 | 100 | 3 | 22 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0002 | 1/0 | 3393 | 33 | 31 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0003 | 0/0 | 3393 | 14 | 1 | 4 | 1 | 3 | 5 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0004 | 0/0 | 3393 | 10 | 2 | 6 | 0 | 1 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0005 | 0/0 | 3381 | 9 | 0 | 0 | 9 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0006 | 0/0 | 3393 | 5 | 2 | 2 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0007 | 0/0 | 3393 | 5 | 5 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0008 | 0/0 | 3393 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0009 | 0/0 | 3390 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0010 | 0/0 | 3393 | 3 | 0 | 0 | 0 | 0 | 3 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0011 | 0/0 | 3393 | 3 | 0 | 0 | 3 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0012 | 0/0 | 3393 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0013 | 0/0 | 3393 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0014 | 0/0 | 3393 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0015 | 0/0 | 3393 | 2 | 0 | 1 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0016 | 0/0 | 3393 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0017 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0018 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0019 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0020 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0021 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0022 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0023 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0024 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0025 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0026 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0027 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0028 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0029 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0030 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0031 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0032 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| c0033 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1692 | 184 | 36 | 38 | 75 | 4 | 30 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0002 | 0/0 | 1692 | 30 | 2 | 1 | 25 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0003 | 0/0 | 1692 | 16 | 1 | 6 | 1 | 3 | 5 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0004 | 0/0 | 1692 | 15 | 5 | 8 | 0 | 1 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0005 | 1/0 | 1692 | 12 | 11 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0006 | 0/0 | 1686 | 11 | 11 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0007 | 0/0 | 1688 | 11 | 9 | 2 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0008 | 0/0 | 1692 | 8 | 8 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0009 | 0/0 | 1693 | 7 | 1 | 0 | 6 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0010 | 0/0 | 1693 | 5 | 0 | 2 | 3 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0011 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0012 | 0/0 | 1692 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0013 | 0/0 | 1692 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0014 | 0/0 | 1692 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0015 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0016 | 0/0 | 1688 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0017 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0018 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0019 | 0/0 | 1693 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0020 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| t0021 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| 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 | 5 | 1 | 0 | 2 | 1 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0009 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0033 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| 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 | 3393 | 201 | 36 | 39 | 100 | 3 | 22 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0002 | 1/0 | 3393 | 33 | 31 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0004 | 0/0 | 3393 | 10 | 2 | 6 | 0 | 1 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0006 | 0/0 | 3393 | 5 | 2 | 2 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0007 | 0/0 | 3393 | 5 | 5 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0010 | 0/0 | 3393 | 3 | 0 | 0 | 0 | 0 | 3 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0013 | 0/0 | 3393 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0014 | 0/0 | 3393 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0015 | 0/0 | 3393 | 2 | 0 | 1 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0016 | 0/0 | 3393 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0023 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0025 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0028 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0029 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0030 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0032 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0002c0003 | 0/0 | 3393 | 14 | 1 | 4 | 1 | 3 | 5 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0002c0022 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0003c0005 | 0/0 | 3381 | 9 | 0 | 0 | 9 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0004c0009 | 0/0 | 3390 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0004c0017 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0004c0018 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0005c0011 | 0/0 | 3393 | 3 | 0 | 0 | 3 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0006c0008 | 0/0 | 3393 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0007c0012 | 0/0 | 3393 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0008c0033 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0009c0026 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0010c0020 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0011c0024 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0012c0027 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0013c0021 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0014c0031 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0015c0019 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5084 | 155 | 32 | 36 | 65 | 3 | 18 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0001t0002 | 0/0 | 5084 | 27 | 1 | 1 | 23 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0001t0007 | 0/0 | 5080 | 3 | 2 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0001t0009 | 0/0 | 5085 | 7 | 1 | 0 | 6 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0001t0010 | 0/0 | 5085 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0001t0012 | 0/0 | 5084 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0001t0013 | 0/0 | 5084 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0001t0014 | 0/0 | 5084 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0001t0020 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0001t0021 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0002t0005 | 1/0 | 5084 | 11 | 10 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0002t0006 | 0/0 | 5078 | 11 | 11 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0002t0007 | 0/0 | 5080 | 2 | 1 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0002t0008 | 0/0 | 5084 | 8 | 8 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0002t0017 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0004t0004 | 0/0 | 5084 | 10 | 2 | 6 | 0 | 1 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0006t0001 | 0/0 | 5084 | 5 | 2 | 2 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0007t0011 | 0/0 | 5084 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0007t0016 | 0/0 | 5080 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0007t0019 | 0/0 | 5085 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0010t0001 | 0/0 | 5084 | 3 | 0 | 0 | 0 | 0 | 3 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0013t0015 | 0/0 | 5084 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0014t0001 | 0/0 | 5084 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0015t0001 | 0/0 | 5084 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0015t0018 | 0/0 | 5084 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0016t0001 | 0/0 | 5084 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0023t0005 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0025t0007 | 0/0 | 5080 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0028t0001 | 0/0 | 5084 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0029t0001 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0030t0004 | 0/0 | 5084 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0001c0032t0002 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0002c0003t0003 | 0/0 | 5084 | 14 | 1 | 4 | 1 | 3 | 5 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0002c0022t0003 | 0/0 | 5084 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0003c0005t0001 | 0/0 | 5072 | 9 | 0 | 0 | 9 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0004c0009t0007 | 0/0 | 5077 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0004c0017t0007 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0004c0018t0007 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0005c0011t0010 | 0/0 | 5085 | 3 | 0 | 0 | 3 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0006c0008t0004 | 0/0 | 5084 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0007c0012t0001 | 0/0 | 5084 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0008c0033t0003 | 0/0 | 5084 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0009c0026t0001 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0010c0020t0001 | 0/0 | 5084 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0011c0024t0002 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0012c0027t0002 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0013c0021t0010 | 0/0 | 5085 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0014c0031t0004 | 0/0 | 5084 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| a0015c0019t0001 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | copy fasta | chr17 | 4664774 | 4709137 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 1 | 0 | 2 | 1 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0009g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0009g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0009g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0009g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0009g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0010g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0012g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0012g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0013g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0013g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0014g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0014g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0020g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0001t0021g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0005g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0005g0033 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0006g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0007g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0008g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0008g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0008g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0002t0017g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0004t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0004t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0004t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0004t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0004t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0004t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0004t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0004t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0004t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0004t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0006t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0006t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0006t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0006t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0006t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0007t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0007t0011g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0007t0016g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0007t0016g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0007t0019g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0010t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0010t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0010t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0013t0015g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0014t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0014t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0015t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0015t0018g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0016t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0016t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0023t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0025t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0028t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0029t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0030t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0001c0032t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0002c0003t0003g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0002c0003t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0002c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0002c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0002c0003t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0002c0003t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0002c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0002c0003t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0002c0003t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0002c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0002c0003t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0002c0003t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0002c0003t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0002c0022t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0003c0005t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0003c0005t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0003c0005t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0003c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0003c0005t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0003c0005t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0003c0005t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0003c0005t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0004c0009t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0004c0009t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0004c0009t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0004c0017t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0004c0018t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0005c0011t0010g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0005c0011t0010g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0005c0011t0010g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0006c0008t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0006c0008t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0006c0008t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0007c0012t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0007c0012t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0008c0033t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0009c0026t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0010c0020t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0011c0024t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0012c0027t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0013c0021t0010g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0014c0031t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| a0015c0019t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0003 | g0017 | EUR | GBR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | GBR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00140 | hp2 | a0001 | c0004 | t0004 | g0210 | EUR | GBR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00423 | hp2 | a0003 | c0005 | t0001 | g0112 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00438 | hp2 | a0001 | c0001 | t0009 | g0023 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00597 | hp1 | a0001 | c0001 | t0009 | g0177 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00642 | hp1 | a0001 | c0004 | t0004 | g0035 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00673 | hp1 | a0001 | c0001 | t0020 | g0152 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00735 | hp2 | a0001 | c0004 | t0004 | g0212 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG00741 | hp2 | a0014 | c0031 | t0004 | g0205 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01070 | hp2 | a0001 | c0015 | t0018 | g0239 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01099 | hp2 | a0001 | c0004 | t0004 | g0122 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01106 | hp1 | a0001 | c0004 | t0004 | g0217 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01109 | hp1 | a0002 | c0003 | t0003 | g0244 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0207 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01167 | hp2 | a0001 | c0002 | t0007 | g0209 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01168 | hp1 | a0001 | c0030 | t0004 | g0219 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01175 | hp2 | a0002 | c0022 | t0003 | g0237 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01243 | hp1 | a0001 | c0004 | t0004 | g0204 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01256 | hp1 | a0002 | c0003 | t0003 | g0235 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01258 | hp2 | a0002 | c0003 | t0003 | g0234 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01261 | hp2 | a0002 | c0003 | t0003 | g0017 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01346 | hp1 | a0013 | c0021 | t0010 | g0176 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01361 | hp1 | a0001 | c0006 | t0001 | g0106 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01515 | hp1 | a0001 | c0015 | t0001 | g0098 | EUR | IBS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01515 | hp2 | a0002 | c0003 | t0003 | g0233 | EUR | IBS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01517 | hp1 | a0002 | c0003 | t0003 | g0241 | EUR | IBS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | IBS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01884 | hp1 | a0001 | c0002 | t0006 | g0228 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01884 | hp2 | a0001 | c0007 | t0016 | g0246 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01952 | hp1 | a0001 | c0004 | t0004 | g0216 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01978 | hp2 | a0001 | c0006 | t0001 | g0096 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG01981 | hp2 | a0008 | c0033 | t0003 | g0289 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02055 | hp1 | a0001 | c0002 | t0008 | g0093 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02129 | hp2 | a0003 | c0005 | t0001 | g0014 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02145 | hp1 | a0001 | c0002 | t0005 | g0032 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02145 | hp2 | a0001 | c0007 | t0011 | g0247 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02155 | hp1 | a0001 | c0001 | t0009 | g0163 | EAS | CDX | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | CDX | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02257 | hp1 | a0001 | c0002 | t0006 | g0227 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02257 | hp2 | a0001 | c0002 | t0008 | g0086 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02258 | hp1 | a0004 | c0009 | t0007 | g0027 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02273 | hp2 | a0001 | c0001 | t0010 | g0053 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02280 | hp1 | a0006 | c0008 | t0004 | g0220 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02280 | hp2 | a0001 | c0002 | t0008 | g0090 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02451 | hp1 | a0001 | c0002 | t0005 | g0003 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02451 | hp2 | a0001 | c0002 | t0006 | g0225 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02523 | hp1 | a0002 | c0003 | t0003 | g0231 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0208 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02572 | hp2 | a0006 | c0008 | t0004 | g0214 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02602 | hp1 | a0002 | c0003 | t0003 | g0232 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02602 | hp2 | a0001 | c0016 | t0001 | g0172 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02615 | hp1 | a0001 | c0013 | t0015 | g0007 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0081 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02630 | hp2 | a0001 | c0002 | t0006 | g0005 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02647 | hp2 | a0002 | c0003 | t0003 | g0242 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02717 | hp1 | a0001 | c0002 | t0006 | g0226 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02723 | hp2 | a0001 | c0002 | t0006 | g0080 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02738 | hp1 | a0001 | c0006 | t0001 | g0103 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02738 | hp2 | a0002 | c0003 | t0003 | g0236 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02809 | hp2 | a0004 | c0017 | t0007 | g0021 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0031 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02886 | hp1 | a0001 | c0002 | t0008 | g0094 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02886 | hp2 | a0001 | c0002 | t0005 | g0230 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0029 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02895 | hp2 | a0001 | c0002 | t0005 | g0229 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02896 | hp1 | a0001 | c0002 | t0017 | g0087 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02897 | hp2 | a0001 | c0002 | t0005 | g0030 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02922 | hp1 | a0001 | c0004 | t0004 | g0036 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02976 | hp1 | a0001 | c0002 | t0008 | g0092 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02976 | hp2 | a0004 | c0009 | t0007 | g0026 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03017 | hp1 | a0001 | c0010 | t0001 | g0129 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03041 | hp1 | a0001 | c0006 | t0001 | g0113 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03041 | hp2 | a0004 | c0009 | t0007 | g0025 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03098 | hp2 | a0004 | c0018 | t0007 | g0022 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03130 | hp1 | a0001 | c0002 | t0007 | g0037 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03139 | hp1 | a0006 | c0008 | t0004 | g0213 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03209 | hp1 | a0001 | c0002 | t0006 | g0005 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0003 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03225 | hp2 | a0001 | c0002 | t0005 | g0034 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03453 | hp1 | a0001 | c0002 | t0005 | g0003 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03486 | hp1 | a0001 | c0023 | t0005 | g0088 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03490 | hp1 | a0002 | c0003 | t0003 | g0240 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03490 | hp2 | a0001 | c0001 | t0012 | g0179 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03491 | hp1 | a0007 | c0012 | t0001 | g0019 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03492 | hp1 | a0007 | c0012 | t0001 | g0020 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03492 | hp2 | a0001 | c0001 | t0012 | g0154 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03516 | hp1 | a0001 | c0002 | t0006 | g0221 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03579 | hp1 | a0001 | c0002 | t0008 | g0091 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03579 | hp2 | a0001 | c0002 | t0006 | g0224 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03654 | hp1 | a0001 | c0014 | t0001 | g0222 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03654 | hp2 | a0001 | c0010 | t0001 | g0127 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03669 | hp1 | a0010 | c0020 | t0001 | g0147 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03704 | hp2 | a0001 | c0004 | t0004 | g0215 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03831 | hp2 | a0002 | c0003 | t0003 | g0243 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03927 | hp2 | a0002 | c0003 | t0003 | g0238 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03942 | hp2 | a0001 | c0028 | t0001 | g0191 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG04204 | hp1 | a0001 | c0014 | t0001 | g0223 | SAS | STU | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | STU | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG04228 | hp2 | a0001 | c0010 | t0001 | g0065 | SAS | STU | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18522 | hp1 | a0001 | c0002 | t0008 | g0085 | AFR | YRI | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18522 | hp2 | a0001 | c0007 | t0019 | g0245 | AFR | YRI | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | CHB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18906 | hp2 | a0001 | c0013 | t0015 | g0007 | AFR | YRI | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18946 | hp2 | a0005 | c0011 | t0010 | g0054 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18979 | hp1 | a0003 | c0005 | t0001 | g0184 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18981 | hp2 | a0003 | c0005 | t0001 | g0158 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18983 | hp1 | a0001 | c0001 | t0009 | g0185 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18985 | hp1 | a0005 | c0011 | t0010 | g0052 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18990 | hp1 | a0003 | c0005 | t0001 | g0014 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18991 | hp2 | a0003 | c0005 | t0001 | g0169 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18993 | hp1 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18993 | hp2 | a0005 | c0011 | t0010 | g0051 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18995 | hp1 | a0001 | c0001 | t0009 | g0160 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19003 | hp2 | a0001 | c0001 | t0013 | g0135 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19006 | hp1 | a0012 | c0027 | t0002 | g0259 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19006 | hp2 | a0015 | c0019 | t0001 | g0062 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19011 | hp1 | a0001 | c0032 | t0002 | g0271 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19043 | hp1 | a0011 | c0024 | t0002 | g0263 | AFR | LWK | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0218 | AFR | LWK | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19064 | hp1 | a0001 | c0001 | t0014 | g0039 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19070 | hp2 | a0001 | c0001 | t0021 | g0117 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19082 | hp2 | a0001 | c0001 | t0013 | g0102 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19083 | hp2 | a0003 | c0005 | t0001 | g0193 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19085 | hp2 | a0001 | c0001 | t0014 | g0042 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19090 | hp1 | a0003 | c0005 | t0001 | g0190 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | YRI | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA19240 | hp2 | a0001 | c0029 | t0001 | g0141 | AFR | YRI | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA20129 | hp2 | a0001 | c0002 | t0006 | g0082 | AFR | ASW | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA20905 | hp1 | a0001 | c0016 | t0001 | g0171 | SAS | GIH | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | GIH | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02486 | hp1 | a0001 | c0002 | t0008 | g0089 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG02559 | hp2 | a0009 | c0026 | t0001 | g0097 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03471 | hp1 | a0001 | c0002 | t0006 | g0005 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG06807 | hp1 | a0001 | c0025 | t0007 | g0149 | AFR | USA | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| HG06807 | hp2 | a0001 | c0007 | t0016 | g0279 | AFR | USA | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA18955 | hp2 | a0003 | c0005 | t0001 | g0175 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA20300 | hp1 | a0001 | c0007 | t0011 | g0248 | AFR | USA | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA20300 | hp2 | a0001 | c0006 | t0001 | g0104 | AFR | USA | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| NA21309 | hp2 | a0001 | c0004 | t0004 | g0206 | AFR | LWK | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0166 | REF | REF | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0005 | g0033 | REF | REF | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4671456
|
T | A | 2 | a0002a0008 | 16 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(13): Show |
missense_variant | MODERATE | c.3376A>T | p.Thr1126Ser | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 3402/5084 | 3376/3393 | 1126/1130 | chr17 | 4671456 | ||
| chr17:4672027
|
GGGAGGCA others(5): Show |
G | 1 | a0003 | 9 | HG00423.hp2 HG02129.hp2 NA18955.hp2 others(6): Show |
disruptive_inframe_deletion | MODERATE | c.2952_2963delAGCTCT others(6): Show |
p.Ala985_Pro988del | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2989/5084 | 2952/3393 | 984/1130 | chr17 | 4672027 | ||
| chr17:4672141
|
ATCC | A | 1 | a0004 | 5 | HG02258.hp1 HG02809.hp2 HG02976.hp2 others(2): Show |
disruptive_inframe_deletion | MODERATE | c.2847_2849delGGA | p.Glu949del | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2875/5084 | 2847/3393 | 949/1130 | chr17 | 4672141 | ||
| chr17:4672422
|
G | A | 1 | a0011 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.2569C>T | p.Pro857Ser | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2595/5084 | 2569/3393 | 857/1130 | chr17 | 4672422 | ||
| chr17:4672463
|
G | T | 1 | a0012 | 1 | NA19006.hp1 | missense_variant | MODERATE | c.2528C>A | p.Pro843Gln | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2554/5084 | 2528/3393 | 843/1130 | chr17 | 4672463 | ||
| chr17:4672487
|
G | C | 1 | a0012 | 1 | NA19006.hp1 | missense_variant | MODERATE | c.2504C>G | p.Ala835Gly | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2530/5084 | 2504/3393 | 835/1130 | chr17 | 4672487 | ||
| chr17:4672488
|
C | A | 1 | a0012 | 1 | NA19006.hp1 | missense_variant | MODERATE | c.2503G>T | p.Ala835Ser | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2529/5084 | 2503/3393 | 835/1130 | chr17 | 4672488 | ||
| chr17:4672491
|
C | T | 1 | a0013 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.2500G>A | p.Ala834Thr | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2526/5084 | 2500/3393 | 834/1130 | chr17 | 4672491 | ||
| chr17:4672799
|
C | T | 1 | a0010 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.2192G>A | p.Arg731Gln | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2218/5084 | 2192/3393 | 731/1130 | chr17 | 4672799 | ||
| chr17:4673000
|
G | A | 1 | a0009 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1991C>T | p.Pro664Leu | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2017/5084 | 1991/3393 | 664/1130 | chr17 | 4673000 | ||
| chr17:4673250
|
C | A | 1 | a0015 | 1 | NA19006.hp2 | missense_variant&splice_region_variant | MODERATE | c.1845G>T | p.Glu615Asp | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 15/17 | 1871/5084 | 1845/3393 | 615/1130 | chr17 | 4673250 | ||
| chr17:4674659
|
G | A | 1 | a0005 | 3 | NA18946.hp2 NA18985.hp1 NA18993.hp2 |
missense_variant | MODERATE | c.1433C>T | p.Pro478Leu | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/17 | 1459/5084 | 1433/3393 | 478/1130 | chr17 | 4674659 | ||
| chr17:4675274
|
G | A | 1 | a0014 | 1 | HG00741.hp2 | missense_variant&splice_region_variant | MODERATE | c.1157C>T | p.Ala386Val | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 10/17 | 1183/5084 | 1157/3393 | 386/1130 | chr17 | 4675274 | ||
| chr17:4676389
|
A | C | 1 | a0015 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.821T>G | p.Leu274Arg | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 7/17 | 847/5084 | 821/3393 | 274/1130 | chr17 | 4676389 | ||
| chr17:4676405
|
C | T | 1 | a0006 | 3 | HG02280.hp1 HG02572.hp2 HG03139.hp1 |
missense_variant | MODERATE | c.805G>A | p.Ala269Thr | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 7/17 | 831/5084 | 805/3393 | 269/1130 | chr17 | 4676405 | ||
| chr17:4676462
|
A | T | 1 | a0015 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.748T>A | p.Phe250Ile | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 7/17 | 774/5084 | 748/3393 | 250/1130 | chr17 | 4676462 | ||
| chr17:4703943
|
G | C | 1 | a0008 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.169C>G | p.His57Asp | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/17 | 195/5084 | 169/3393 | 57/1130 | chr17 | 4703943 | ||
| chr17:4704077
|
C | G | 1 | a0007 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.35G>C | p.Gly12Ala | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/17 | 61/5084 | 35/3393 | 12/1130 | chr17 | 4704077 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4671844
|
A | T | 1 | a0001c0023 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.3147T>A | p.Pro1049Pro | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 3173/5084 | 3147/3393 | 1049/1130 | chr17 | 4671844 | ||
| chr17:4671988
|
A | G | 22 | a0001c0001a0001c0006a0001c0010others(19): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
synonymous_variant | LOW | c.3003T>C | p.Pro1001Pro | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 3029/5084 | 3003/3393 | 1001/1130 | chr17 | 4671988 | ||
| chr17:4672396
|
A | T | 1 | a0012c0027 | 1 | NA19006.hp1 | synonymous_variant | LOW | c.2595T>A | p.Thr865Thr | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2621/5084 | 2595/3393 | 865/1130 | chr17 | 4672396 | ||
| chr17:4672450
|
C | T | 1 | a0001c0016 | 2 | HG02602.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.2541G>A | p.Pro847Pro | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2567/5084 | 2541/3393 | 847/1130 | chr17 | 4672450 | ||
| chr17:4672615
|
G | A | 1 | a0001c0013 | 2 | HG02615.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.2376C>T | p.Pro792Pro | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2402/5084 | 2376/3393 | 792/1130 | chr17 | 4672615 | ||
| chr17:4672864
|
T | A | 1 | a0012c0027 | 1 | NA19006.hp1 | synonymous_variant | LOW | c.2127A>T | p.Leu709Leu | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2153/5084 | 2127/3393 | 709/1130 | chr17 | 4672864 | ||
| chr17:4672894
|
G | A | 1 | a0001c0025 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.2097C>T | p.Arg699Arg | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2123/5084 | 2097/3393 | 699/1130 | chr17 | 4672894 | ||
| chr17:4672921
|
G | A | 1 | a0001c0010 | 3 | HG03017.hp1 HG03654.hp2 HG04228.hp2 |
synonymous_variant | LOW | c.2070C>T | p.Pro690Pro | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2096/5084 | 2070/3393 | 690/1130 | chr17 | 4672921 | ||
| chr17:4673325
|
C | T | 3 | a0001c0013a0002c0003a0008c0033 | 17 | HG00099.hp1 HG01109.hp1 HG01256.hp1 others(14): Show |
synonymous_variant | LOW | c.1770G>A | p.Pro590Pro | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 15/17 | 1796/5084 | 1770/3393 | 590/1130 | chr17 | 4673325 | ||
| chr17:4673376
|
G | C | 1 | a0012c0027 | 1 | NA19006.hp1 | synonymous_variant | LOW | c.1719C>G | p.Ser573Ser | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 15/17 | 1745/5084 | 1719/3393 | 573/1130 | chr17 | 4673376 | ||
| chr17:4674532
|
G | A | 1 | a0001c0028 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.1560C>T | p.Asp520Asp | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/17 | 1586/5084 | 1560/3393 | 520/1130 | chr17 | 4674532 | ||
| chr17:4674589
|
C | G | 1 | a0001c0015 | 2 | HG01070.hp2 HG01515.hp1 |
synonymous_variant | LOW | c.1503G>C | p.Val501Val | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/17 | 1529/5084 | 1503/3393 | 501/1130 | chr17 | 4674589 | ||
| chr17:4674655
|
C | A | 4 | a0001c0004a0001c0030a0006c0008others(1): Show | 15 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(12): Show |
synonymous_variant | LOW | c.1437G>T | p.Arg479Arg | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/17 | 1463/5084 | 1437/3393 | 479/1130 | chr17 | 4674655 | ||
| chr17:4674839
|
G | A | 1 | a0001c0029 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.1392C>T | p.Ser464Ser | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 12/17 | 1418/5084 | 1392/3393 | 464/1130 | chr17 | 4674839 | ||
| chr17:4682526
|
G | A | 1 | a0001c0006 | 5 | HG01361.hp1 HG01978.hp2 HG02738.hp1 others(2): Show |
synonymous_variant | LOW | c.618C>T | p.Phe206Phe | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/17 | 644/5084 | 618/3393 | 206/1130 | chr17 | 4682526 | ||
| chr17:4682925
|
G | A | 1 | a0001c0007 | 5 | HG01884.hp2 HG02145.hp2 HG06807.hp2 others(2): Show |
synonymous_variant | LOW | c.448C>T | p.Leu150Leu | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 4/17 | 474/5084 | 448/3393 | 150/1130 | chr17 | 4682925 | ||
| chr17:4682950
|
G | C | 2 | a0001c0030a0014c0031 | 2 | HG00741.hp2 HG01168.hp1 |
splice_region_variant&synonymous_variant | LOW | c.423C>G | p.Thr141Thr | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 4/17 | 449/5084 | 423/3393 | 141/1130 | chr17 | 4682950 | ||
| chr17:4690933
|
C | T | 1 | a0001c0014 | 2 | HG03654.hp1 HG04204.hp1 |
synonymous_variant | LOW | c.375G>A | p.Gln125Gln | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/17 | 401/5084 | 375/3393 | 125/1130 | chr17 | 4690933 | ||
| chr17:4691422
|
T | C | 1 | a0001c0032 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.270A>G | p.Ala90Ala | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 2/17 | 296/5084 | 270/3393 | 90/1130 | chr17 | 4691422 | ||
| chr17:4703995
|
C | T | 1 | a0004c0018 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.117G>A | p.Glu39Glu | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/17 | 143/5084 | 117/3393 | 39/1130 | chr17 | 4703995 | ||
| chr17:4704055
|
G | T | 2 | a0001c0013a0004c0017 | 3 | HG02615.hp1 HG02809.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.57C>A | p.Gly19Gly | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/17 | 83/5084 | 57/3393 | 19/1130 | chr17 | 4704055 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4669779
|
GAATT | G | 8 | a0001c0001t0007a0001c0002t0006a0001c0002t0007others(5): Show | 24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1656_*1659delAATT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1656 | chr17 | 4669779 | |||||
| chr17:4669840
|
T | G | 2 | a0001c0002t0008a0001c0002t0017 | 9 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1599A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1599 | chr17 | 4669840 | |||||
| chr17:4669884
|
G | A | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(24): Show | 235 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*1555C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1555 | chr17 | 4669884 | |||||
| chr17:4669986
|
GTA | G | 1 | a0001c0002t0006 | 11 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1451_*1452delTA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1451 | chr17 | 4669986 | |||||
| chr17:4670004
|
T | C | 1 | a0001c0001t0014 | 2 | NA19064.hp1 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1435A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1435 | chr17 | 4670004 | |||||
| chr17:4670041
|
C | T | 1 | a0001c0001t0013 | 2 | NA19003.hp2 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1398G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1398 | chr17 | 4670041 | |||||
| chr17:4670112
|
T | C | 3 | a0002c0003t0003a0002c0022t0003a0008c0033t0003 | 16 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1327A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1327 | chr17 | 4670112 | |||||
| chr17:4670113
|
A | G | 1 | a0001c0001t0021 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1326T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1326 | chr17 | 4670113 | |||||
| chr17:4670119
|
C | G | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(24): Show | 235 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*1320G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1320 | chr17 | 4670119 | |||||
| chr17:4670248
|
T | C | 4 | a0001c0001t0002a0001c0032t0002a0011c0024t0002others(1): Show | 30 | HG00544.hp2 HG01943.hp1 HG02027.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1191A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1191 | chr17 | 4670248 | |||||
| chr17:4670264
|
C | T | 1 | a0001c0001t0020 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1175G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1175 | chr17 | 4670264 | |||||
| chr17:4670281
|
C | T | 1 | a0001c0001t0012 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1158G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1158 | chr17 | 4670281 | |||||
| chr17:4670316
|
C | T | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(24): Show | 235 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*1123G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1123 | chr17 | 4670316 | |||||
| chr17:4670317
|
G | A | 4 | a0001c0013t0015a0002c0003t0003a0002c0022t0003others(1): Show | 18 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1122C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1122 | chr17 | 4670317 | |||||
| chr17:4670372
|
G | A | 4 | a0001c0013t0015a0002c0003t0003a0002c0022t0003others(1): Show | 18 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1067C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1067 | chr17 | 4670372 | |||||
| chr17:4670377
|
A | C | 2 | a0001c0007t0011a0001c0007t0019 | 3 | HG02145.hp2 NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1062T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1062 | chr17 | 4670377 | |||||
| chr17:4670503
|
C | T | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(42): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*936G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 936 | chr17 | 4670503 | |||||
| chr17:4670551
|
C | G | 3 | a0002c0003t0003a0002c0022t0003a0008c0033t0003 | 16 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*888G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 888 | chr17 | 4670551 | |||||
| chr17:4670560
|
T | C | 3 | a0001c0001t0010a0005c0011t0010a0013c0021t0010 | 5 | HG01346.hp1 HG02273.hp2 NA18946.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*879A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 879 | chr17 | 4670560 | |||||
| chr17:4670573
|
A | G | 8 | a0001c0001t0007a0001c0002t0006a0001c0002t0007others(5): Show | 24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*866T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 866 | chr17 | 4670573 | |||||
| chr17:4670697
|
G | A | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(24): Show | 235 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*742C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 742 | chr17 | 4670697 | |||||
| chr17:4670699
|
G | A | 10 | a0001c0004t0004a0001c0007t0011a0001c0007t0019others(7): Show | 36 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*740C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 740 | chr17 | 4670699 | |||||
| chr17:4670719
|
C | CA | 5 | a0001c0001t0009a0001c0001t0010a0001c0007t0019others(2): Show | 13 | HG00438.hp2 HG00597.hp1 HG01346.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*719dupT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 719 | chr17 | 4670719 | |||||
| chr17:4670738
|
A | C | 2 | a0001c0007t0011a0001c0007t0019 | 3 | HG02145.hp2 NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*701T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 701 | chr17 | 4670738 | |||||
| chr17:4670758
|
A | G | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(34): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*681T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 681 | chr17 | 4670758 | |||||
| chr17:4670774
|
T | C | 1 | a0001c0007t0016 | 2 | HG01884.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*665A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 665 | chr17 | 4670774 | |||||
| chr17:4670922
|
C | T | 1 | a0001c0015t0018 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*517G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 517 | chr17 | 4670922 | |||||
| chr17:4671027
|
C | T | 1 | a0001c0002t0017 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 412 | chr17 | 4671027 | |||||
| chr17:4671171
|
G | A | 8 | a0001c0001t0007a0001c0002t0006a0001c0002t0007others(5): Show | 24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*268C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 268 | chr17 | 4671171 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4671536
|
T | C | 1 | a0009c0026t0001g0097 | 1 | HG02559.hp2 | splice_region_variant&intron_variant | LOW | c.3301-5A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/16 | chr17 | 4671536 | ||||||
| chr17:4673542
|
C | T | 1 | a0001c0001t0002g0165 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1638+77G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 14/16 | chr17 | 4673542 | ||||||
| chr17:4673817
|
G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(211): Show | 235 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1583-143C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4673817 | ||||||
| chr17:4673844
|
G | T | 1 | a0015c0019t0001g0062 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1583-170C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4673844 | ||||||
| chr17:4674049
|
T | C | 2 | a0003c0005t0001g0014a0003c0005t0001g0158 | 3 | HG02129.hp2 NA18981.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1583-375A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4674049 | ||||||
| chr17:4674083
|
T | G | 1 | a0015c0019t0001g0062 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1583-409A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4674083 | ||||||
| chr17:4674171
|
A | C | 1 | a0015c0019t0001g0062 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1582+339T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4674171 | ||||||
| chr17:4674176
|
G | A | 1 | a0001c0001t0007g0208 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1582+334C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4674176 | ||||||
| chr17:4674241
|
C | T | 1 | a0002c0003t0003g0238 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1582+269G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4674241 | ||||||
| chr17:4674312
|
G | A | 15 | a0001c0004t0004g0035a0001c0004t0004g0036a0001c0004t0004g0122others(12): Show | 15 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1582+198C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4674312 | ||||||
| chr17:4674441
|
G | C | 1 | a0012c0027t0002g0259 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1582+69C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4674441 | ||||||
| chr17:4674688
|
T | G | 1 | a0001c0001t0001g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1423-19A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 12/16 | chr17 | 4674688 | ||||||
| chr17:4674712
|
C | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1423-43G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 12/16 | chr17 | 4674712 | ||||||
| chr17:4674992
|
G | T | 1 | a0001c0001t0001g0170 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1275-36C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 11/16 | chr17 | 4674992 | ||||||
| chr17:4675012
|
C | T | 3 | a0006c0008t0004g0213a0006c0008t0004g0214a0006c0008t0004g0220 | 3 | HG02280.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1275-56G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 11/16 | chr17 | 4675012 | ||||||
| chr17:4675446
|
A | G | 2 | a0001c0007t0016g0246a0001c0007t0016g0279 | 2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1069-84T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 9/16 | chr17 | 4675446 | ||||||
| chr17:4675598
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1068+199G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 9/16 | chr17 | 4675598 | ||||||
| chr17:4675635
|
T | C | 32 | a0001c0001t0002g0252a0001c0001t0002g0253a0001c0001t0002g0254others(29): Show | 34 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.1068+162A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 9/16 | chr17 | 4675635 | ||||||
| chr17:4675636
|
G | A | 1 | a0001c0001t0007g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1068+161C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 9/16 | chr17 | 4675636 | ||||||
| chr17:4675643
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1068+154C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 9/16 | chr17 | 4675643 | ||||||
| chr17:4675668
|
G | A | 1 | a0001c0001t0009g0177 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1068+129C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 9/16 | chr17 | 4675668 | ||||||
| chr17:4675902
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.981-18T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 8/16 | chr17 | 4675902 | ||||||
| chr17:4675921
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.981-37C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 8/16 | chr17 | 4675921 | ||||||
| chr17:4676002
|
C | G | 1 | a0001c0013t0015g0007 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.980+34G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 8/16 | chr17 | 4676002 | ||||||
| chr17:4676006
|
G | A | 14 | a0002c0003t0003g0017a0002c0003t0003g0231a0002c0003t0003g0232others(11): Show | 15 | HG00099.hp1 HG01109.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.980+30C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 8/16 | chr17 | 4676006 | ||||||
| chr17:4676011
|
C | T | 5 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0283others(2): Show | 5 | HG02559.hp1 HG02647.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.980+25G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 8/16 | chr17 | 4676011 | ||||||
| chr17:4676343
|
G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(211): Show | 235 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.853+14C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 7/16 | chr17 | 4676343 | ||||||
| chr17:4676575
|
C | T | 2 | a0007c0012t0001g0019a0007c0012t0001g0020 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.703-68G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 6/16 | chr17 | 4676575 | ||||||
| chr17:4676642
|
G | A | 15 | a0001c0004t0004g0035a0001c0004t0004g0036a0001c0004t0004g0122others(12): Show | 15 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.702+111C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 6/16 | chr17 | 4676642 | ||||||
| chr17:4676842
|
A | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(277): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.643-30T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4676842 | ||||||
| chr17:4676929
|
C | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.643-117G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4676929 | ||||||
| chr17:4677034
|
C | T | 5 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0283others(2): Show | 5 | HG02559.hp1 HG02647.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-222G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677034 | ||||||
| chr17:4677124
|
AC | A | 11 | a0001c0004t0004g0035a0001c0004t0004g0036a0001c0004t0004g0122others(8): Show | 11 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.643-313delG | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677124 | ||||||
| chr17:4677244
|
C | A | 22 | a0001c0001t0007g0207a0001c0001t0007g0208a0001c0001t0007g0218others(19): Show | 24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.643-432G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677244 | ||||||
| chr17:4677275
|
G | A | 2 | a0001c0001t0001g0183a0003c0005t0001g0112 | 2 | HG00423.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.643-463C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677275 | ||||||
| chr17:4677284
|
A | G | 19 | a0001c0004t0004g0035a0001c0004t0004g0036a0001c0004t0004g0122others(16): Show | 20 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.643-472T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677284 | ||||||
| chr17:4677295
|
G | A | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.643-483C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677295 | ||||||
| chr17:4677490
|
A | C | 6 | a0001c0002t0007g0037a0004c0009t0007g0025a0004c0009t0007g0026others(3): Show | 6 | HG02258.hp1 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-678T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677490 | ||||||
| chr17:4677537
|
A | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(214): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.643-725T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677537 | ||||||
| chr17:4677787
|
G | A | 14 | a0001c0001t0007g0207a0001c0001t0007g0208a0001c0001t0007g0218others(11): Show | 16 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.643-975C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677787 | ||||||
| chr17:4677808
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(169): Show | 190 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.643-996A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677808 | ||||||
| chr17:4677817
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.643-1005G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677817 | ||||||
| chr17:4677836
|
G | A | 22 | a0001c0001t0007g0207a0001c0001t0007g0208a0001c0001t0007g0218others(19): Show | 24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.643-1024C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677836 | ||||||
| chr17:4677866
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0157a0001c0001t0001g0168 | 3 | NA18968.hp2 NA18991.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.643-1054G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677866 | ||||||
| chr17:4678042
|
C | A | 1 | a0015c0019t0001g0062 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.643-1230G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678042 | ||||||
| chr17:4678051
|
T | C | 3 | a0001c0002t0005g0003a0001c0002t0005g0029a0001c0002t0005g0030 | 5 | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-1239A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678051 | ||||||
| chr17:4678080
|
G | A | 1 | a0001c0004t0004g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.643-1268C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678080 | ||||||
| chr17:4678163
|
G | A | 4 | a0001c0004t0004g0206a0006c0008t0004g0213a0006c0008t0004g0214others(1): Show | 4 | HG02280.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-1351C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678163 | ||||||
| chr17:4678224
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.643-1412T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678224 | ||||||
| chr17:4678382
|
G | C | 6 | a0001c0002t0007g0037a0004c0009t0007g0025a0004c0009t0007g0026others(3): Show | 6 | HG02258.hp1 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-1570C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678382 | ||||||
| chr17:4678468
|
C | A | 1 | a0001c0001t0002g0277 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.643-1656G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678468 | ||||||
| chr17:4678494
|
C | A | 22 | a0001c0001t0007g0207a0001c0001t0007g0208a0001c0001t0007g0218others(19): Show | 24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.643-1682G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678494 | ||||||
| chr17:4678525
|
G | A | 2 | a0001c0007t0016g0246a0001c0007t0016g0279 | 2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.643-1713C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678525 | ||||||
| chr17:4678549
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.643-1737G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678549 | ||||||
| chr17:4678603
|
A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.643-1791T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678603 | ||||||
| chr17:4678724
|
C | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.643-1912G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678724 | ||||||
| chr17:4678731
|
G | C | 3 | a0001c0007t0011g0247a0001c0007t0011g0248a0001c0007t0019g0245 | 3 | HG02145.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.643-1919C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678731 | ||||||
| chr17:4678738
|
C | A | 3 | a0001c0001t0002g0264a0001c0001t0002g0276a0001c0001t0002g0277 | 3 | NA18946.hp1 NA18948.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.643-1926G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678738 | ||||||
| chr17:4678754
|
T | C | 1 | a0001c0002t0007g0209 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.643-1942A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678754 | ||||||
| chr17:4678794
|
G | A | 1 | a0001c0004t0004g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.643-1982C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678794 | ||||||
| chr17:4678888
|
G | A | 15 | a0002c0003t0003g0017a0002c0003t0003g0231a0002c0003t0003g0232others(12): Show | 16 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.643-2076C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678888 | ||||||
| chr17:4679032
|
C | CT | 16 | a0001c0001t0001g0043a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.643-2221dupA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679032 | ||||||
| chr17:4679131
|
A | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(230): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.643-2319T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679131 | ||||||
| chr17:4679272
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.643-2460A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679272 | ||||||
| chr17:4679274
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.643-2462G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679274 | ||||||
| chr17:4679289
|
G | A | 22 | a0001c0001t0007g0207a0001c0001t0007g0208a0001c0001t0007g0218others(19): Show | 24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.643-2477C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679289 | ||||||
| chr17:4679352
|
G | A | 2 | a0001c0001t0002g0256a0001c0001t0002g0260 | 2 | NA18968.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.643-2540C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679352 | ||||||
| chr17:4679529
|
G | A | 3 | a0001c0007t0011g0247a0001c0007t0011g0248a0001c0007t0019g0245 | 3 | HG02145.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.643-2717C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679529 | ||||||
| chr17:4679577
|
T | C | 30 | a0001c0001t0002g0165a0001c0001t0002g0188a0001c0001t0002g0251others(27): Show | 30 | HG00544.hp2 HG01943.hp1 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.643-2765A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679577 | ||||||
| chr17:4679616
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.643-2804T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679616 | ||||||
| chr17:4679656
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.643-2844G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679656 | ||||||
| chr17:4679728
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(213): Show | 238 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.642+2774T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679728 | ||||||
| chr17:4679765
|
T | A | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.642+2737A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679765 | ||||||
| chr17:4679783
|
C | A | 1 | a0001c0001t0001g0043 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.642+2719G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679783 | ||||||
| chr17:4679801
|
T | C | 22 | a0001c0001t0007g0207a0001c0001t0007g0208a0001c0001t0007g0218others(19): Show | 24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.642+2701A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679801 | ||||||
| chr17:4679862
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.642+2640C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679862 | ||||||
| chr17:4680159
|
C | T | 1 | a0001c0013t0015g0007 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.642+2343G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680159 | ||||||
| chr17:4680353
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.642+2149A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680353 | ||||||
| chr17:4680524
|
C | T | 1 | a0001c0004t0004g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.642+1978G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680524 | ||||||
| chr17:4680569
|
C | A | 22 | a0001c0001t0007g0207a0001c0001t0007g0208a0001c0001t0007g0218others(19): Show | 24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.642+1933G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680569 | ||||||
| chr17:4680741
|
G | A | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.642+1761C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680741 | ||||||
| chr17:4680750
|
TCAAACCA others(21): Show |
T | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.642+1724_642+1751d others(30): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680750 | ||||||
| chr17:4680803
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.642+1699A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680803 | ||||||
| chr17:4680920
|
T | C | 22 | a0001c0001t0007g0207a0001c0001t0007g0208a0001c0001t0007g0218others(19): Show | 24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.642+1582A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680920 | ||||||
| chr17:4680936
|
C | G | 30 | a0001c0001t0002g0165a0001c0001t0002g0188a0001c0001t0002g0251others(27): Show | 30 | HG00544.hp2 HG01943.hp1 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.642+1566G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680936 | ||||||
| chr17:4681255
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0249others(4): Show | 10 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.642+1247G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681255 | ||||||
| chr17:4681322
|
A | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.642+1180T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681322 | ||||||
| chr17:4681361
|
A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.642+1141T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681361 | ||||||
| chr17:4681375
|
C | CT | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.642+1126dupA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681375 | ||||||
| chr17:4681527
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0281others(2): Show | 8 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+975G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681527 | ||||||
| chr17:4681539
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.642+963A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681539 | ||||||
| chr17:4681605
|
T | G | 7 | a0001c0001t0001g0049a0001c0001t0001g0123a0001c0001t0001g0283others(4): Show | 7 | HG01109.hp2 HG01168.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.642+897A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681605 | ||||||
| chr17:4681611
|
C | A | 1 | a0001c0002t0008g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.642+891G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681611 | ||||||
| chr17:4681629
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.642+873T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681629 | ||||||
| chr17:4681686
|
G | T | 1 | a0001c0001t0002g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.642+816C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681686 | ||||||
| chr17:4681758
|
C | T | 1 | a0001c0002t0006g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.642+744G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681758 | ||||||
| chr17:4681764
|
C | T | 2 | a0001c0014t0001g0222a0001c0014t0001g0223 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.642+738G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681764 | ||||||
| chr17:4681782
|
G | C | 16 | a0001c0002t0005g0003a0001c0002t0005g0029a0001c0002t0005g0030others(13): Show | 18 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.642+720C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681782 | ||||||
| chr17:4681851
|
T | TA | 4 | a0001c0002t0006g0080a0001c0002t0006g0082a0001c0002t0007g0209others(1): Show | 4 | HG01167.hp2 HG02723.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.642+650_642+651ins others(1): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681851 | ||||||
| chr17:4681852
|
T | A | 5 | a0001c0002t0006g0080a0001c0002t0006g0082a0001c0002t0007g0209others(2): Show | 5 | HG01167.hp2 HG02723.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+650A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681852 | ||||||
| chr17:4681853
|
A | T | 18 | a0001c0001t0001g0084a0001c0002t0005g0003a0001c0002t0005g0029others(15): Show | 20 | HG02055.hp1 HG02055.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.642+649T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681853 | ||||||
| chr17:4682126
|
C | A | 1 | a0001c0001t0001g0133 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.642+376G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4682126 | ||||||
| chr17:4682180
|
G | T | 2 | a0002c0003t0003g0234a0002c0003t0003g0235 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.642+322C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4682180 | ||||||
| chr17:4682275
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.642+227A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4682275 | ||||||
| chr17:4682302
|
G | A | 1 | a0001c0001t0002g0267 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.642+200C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4682302 | ||||||
| chr17:4682476
|
G | A | 1 | a0001c0013t0015g0007 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.642+26C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4682476 | ||||||
| chr17:4682735
|
CAATT | C | 3 | a0001c0001t0007g0207a0001c0001t0007g0208a0001c0001t0007g0218 | 3 | HG01109.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.570+64_570+67delAA others(2): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 4/16 | chr17 | 4682735 | ||||||
| chr17:4682958
|
GA | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
splice_region_variant&intron_variant | LOW | c.421-7delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4682958 | ||||||
| chr17:4683221
|
CTT | C | 12 | a0001c0001t0001g0186a0001c0001t0002g0275a0001c0001t0009g0081others(9): Show | 12 | HG01167.hp2 HG02258.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-271_421-270del others(2): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683221 | ||||||
| chr17:4683221
|
CTTT | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(255): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.421-272_421-270del others(3): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683221 | ||||||
| chr17:4683260
|
A | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(268): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.421-308T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683260 | ||||||
| chr17:4683271
|
A | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.421-319T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683271 | ||||||
| chr17:4683281
|
C | T | 1 | a0001c0006t0001g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.421-329G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683281 | ||||||
| chr17:4683307
|
G | A | 1 | a0001c0002t0006g0005 | 3 | HG02630.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.421-355C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683307 | ||||||
| chr17:4683339
|
G | C | 2 | a0001c0030t0004g0219a0014c0031t0004g0205 | 2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.421-387C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683339 | ||||||
| chr17:4683345
|
C | T | 2 | a0001c0030t0004g0219a0014c0031t0004g0205 | 2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.421-393G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683345 | ||||||
| chr17:4683355
|
A | G | 2 | a0001c0030t0004g0219a0014c0031t0004g0205 | 2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.421-403T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683355 | ||||||
| chr17:4683363
|
A | G | 6 | a0001c0001t0001g0182a0001c0001t0002g0264a0001c0001t0002g0276others(3): Show | 6 | HG00558.hp2 HG00741.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.421-411T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683363 | ||||||
| chr17:4683365
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0281others(2): Show | 8 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-413G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683365 | ||||||
| chr17:4683366
|
G | A | 2 | a0001c0030t0004g0219a0014c0031t0004g0205 | 2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.421-414C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683366 | ||||||
| chr17:4683369
|
C | T | 5 | a0004c0009t0007g0025a0004c0009t0007g0026a0004c0009t0007g0027others(2): Show | 5 | HG02258.hp1 HG02809.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.421-417G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683369 | ||||||
| chr17:4683376
|
A | C | 2 | a0001c0001t0001g0283a0001c0001t0001g0285 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.421-424T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683376 | ||||||
| chr17:4683376
|
A | T | 1 | a0010c0020t0001g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.421-424T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683376 | ||||||
| chr17:4683381
|
T | C | 2 | a0001c0001t0001g0282a0002c0003t0003g0238 | 2 | HG03927.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421-429A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683381 | ||||||
| chr17:4683383
|
A | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(270): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.421-431T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683383 | ||||||
| chr17:4683387
|
A | T | 1 | a0002c0003t0003g0238 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.421-435T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683387 | ||||||
| chr17:4683388
|
T | G | 1 | a0001c0002t0005g0034 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.421-436A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683388 | ||||||
| chr17:4683410
|
C | T | 7 | a0001c0001t0001g0183a0001c0001t0001g0280a0001c0001t0001g0282others(4): Show | 7 | HG00423.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.421-458G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683410 | ||||||
| chr17:4683411
|
G | A | 7 | a0001c0001t0001g0125a0001c0001t0007g0208a0001c0004t0004g0206others(4): Show | 7 | HG02148.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.421-459C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683411 | ||||||
| chr17:4683421
|
T | C | 12 | a0001c0001t0001g0211a0001c0001t0001g0288a0001c0001t0009g0081others(9): Show | 12 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-469A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683421 | ||||||
| chr17:4683422
|
A | G | 39 | a0001c0001t0001g0162a0001c0001t0001g0164a0001c0001t0001g0182others(36): Show | 39 | HG00558.hp2 HG00642.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.421-470T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683422 | ||||||
| chr17:4683422
|
A | T | 3 | a0001c0001t0009g0081a0001c0002t0006g0080a0001c0002t0006g0082 | 3 | HG02622.hp2 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.421-470T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683422 | ||||||
| chr17:4683427
|
A | G | 16 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0281others(13): Show | 20 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.421-475T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683427 | ||||||
| chr17:4683431
|
A | G | 1 | a0001c0001t0010g0053 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.421-479T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683431 | ||||||
| chr17:4683433
|
G | T | 4 | a0002c0003t0003g0233a0002c0003t0003g0236a0002c0003t0003g0241others(1): Show | 4 | HG01515.hp2 HG01517.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-481C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683433 | ||||||
| chr17:4683436
|
G | T | 2 | a0001c0001t0002g0274a0012c0027t0002g0259 | 2 | NA18954.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.421-484C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683436 | ||||||
| chr17:4683442
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.421-490C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683442 | ||||||
| chr17:4683448
|
C | CT | 12 | a0001c0001t0001g0166a0001c0001t0001g0187a0001c0001t0001g0192others(9): Show | 12 | HG01106.hp2 HG01517.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-497_421-496ins others(1): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683448 | ||||||
| chr17:4683455
|
G | A | 9 | a0001c0001t0002g0252a0001c0001t0002g0253a0001c0001t0002g0254others(6): Show | 9 | HG02717.hp2 NA18941.hp2 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.421-503C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683455 | ||||||
| chr17:4683466
|
G | A | 1 | a0001c0002t0008g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.421-514C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683466 | ||||||
| chr17:4683498
|
T | C | 10 | a0001c0001t0001g0066a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG00741.hp1 HG01074.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.421-546A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683498 | ||||||
| chr17:4683507
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.421-555A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683507 | ||||||
| chr17:4683509
|
A | ACGCCTGG others(126): Show |
1 | a0001c0001t0009g0024 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.421-558_421-557ins others(133): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683509 | ||||||
| chr17:4683509
|
A | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(256): Show | 284 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.421-557T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683509 | ||||||
| chr17:4683510
|
C | G | 13 | a0001c0001t0001g0079a0001c0001t0001g0084a0001c0001t0001g0107others(10): Show | 13 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-558G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683510 | ||||||
| chr17:4683510
|
C | T | 90 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(87): Show | 97 | HG00099.hp1 HG00544.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.421-558G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683510 | ||||||
| chr17:4683515
|
A | G | 15 | a0001c0001t0001g0079a0001c0001t0001g0084a0001c0001t0001g0107others(12): Show | 15 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.421-563T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683515 | ||||||
| chr17:4683518
|
T | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(268): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.421-566A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683518 | ||||||
| chr17:4683531
|
C | CTT | 8 | a0001c0001t0002g0252a0001c0001t0002g0253a0001c0001t0002g0254others(5): Show | 8 | NA18941.hp2 NA18956.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-581_421-580dup others(2): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683531 | ||||||
| chr17:4683531
|
C | CTTT | 26 | a0001c0001t0002g0251a0001c0001t0002g0255a0001c0001t0002g0256others(23): Show | 28 | HG00544.hp2 HG01943.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.421-582_421-580dup others(3): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683531 | ||||||
| chr17:4683531
|
C | CTTTT | 20 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0038others(17): Show | 23 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.421-583_421-580dup others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683531 | ||||||
| chr17:4683531
|
C | CTTTTT | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(165): Show | 187 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.421-584_421-580dup others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683531 | ||||||
| chr17:4683531
|
C | CTTTTTT | 19 | a0001c0001t0001g0041a0001c0001t0001g0074a0001c0001t0001g0076others(16): Show | 19 | HG00423.hp1 HG00642.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.421-585_421-580dup others(6): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683531 | ||||||
| chr17:4683531
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0143 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.421-590_421-580dup others(11): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683531 | ||||||
| chr17:4683531
|
CTTT | C | 19 | a0001c0001t0001g0211a0001c0001t0007g0207a0001c0001t0007g0208others(16): Show | 20 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.421-582_421-580del others(3): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683531 | ||||||
| chr17:4683787
|
T | TC | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(268): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.421-836dupG | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683787 | ||||||
| chr17:4683800
|
G | A | 2 | a0006c0008t0004g0213a0006c0008t0004g0220 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.421-848C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683800 | ||||||
| chr17:4683829
|
C | CT | 101 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0015others(98): Show | 107 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.421-878dupA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683829 | ||||||
| chr17:4683829
|
C | CTT | 10 | a0001c0001t0001g0201a0001c0001t0002g0253a0001c0001t0002g0254others(7): Show | 10 | HG01884.hp1 HG02717.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.421-879_421-878dup others(2): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683829 | ||||||
| chr17:4683829
|
CT | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0281a0001c0001t0001g0285others(9): Show | 14 | HG00735.hp2 HG01106.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.421-878delA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683829 | ||||||
| chr17:4683829
|
CTT | C | 21 | a0001c0001t0001g0211a0001c0001t0001g0283a0001c0001t0007g0208others(18): Show | 21 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.421-879_421-878del others(2): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683829 | ||||||
| chr17:4683943
|
A | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.421-991T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683943 | ||||||
| chr17:4684047
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.421-1095T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684047 | ||||||
| chr17:4684060
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 209 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.421-1108G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684060 | ||||||
| chr17:4684114
|
A | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.421-1162T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684114 | ||||||
| chr17:4684165
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.421-1213C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684165 | ||||||
| chr17:4684228
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0048others(6): Show | 12 | HG00408.hp1 HG00673.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-1276G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684228 | ||||||
| chr17:4684282
|
C | T | 5 | a0001c0001t0009g0081a0001c0002t0006g0080a0001c0002t0006g0082others(2): Show | 5 | HG01167.hp2 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.421-1330G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684282 | ||||||
| chr17:4684349
|
A | C | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-1397T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684349 | ||||||
| chr17:4684353
|
T | G | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-1401A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684353 | ||||||
| chr17:4684375
|
A | C | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-1423T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684375 | ||||||
| chr17:4684382
|
C | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.421-1430G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684382 | ||||||
| chr17:4684431
|
A | G | 28 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(25): Show | 28 | HG00544.hp2 HG01943.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.421-1479T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684431 | ||||||
| chr17:4684437
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.421-1485T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684437 | ||||||
| chr17:4684576
|
T | G | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-1624A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684576 | ||||||
| chr17:4684629
|
T | TG | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.421-1678dupC | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684629 | ||||||
| chr17:4684731
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.421-1779C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684731 | ||||||
| chr17:4684783
|
C | G | 54 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0249others(51): Show | 59 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(56): Show |
intron_variant | MODIFIER | c.421-1831G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684783 | ||||||
| chr17:4684881
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.421-1929T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684881 | ||||||
| chr17:4684893
|
G | T | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-1941C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684893 | ||||||
| chr17:4685205
|
G | C | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.421-2253C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685205 | ||||||
| chr17:4685305
|
C | A | 1 | a0002c0003t0003g0240 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.421-2353G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685305 | ||||||
| chr17:4685403
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.421-2451C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685403 | ||||||
| chr17:4685561
|
G | A | 97 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0010others(94): Show | 104 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.421-2609C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685561 | ||||||
| chr17:4685626
|
CA | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.421-2675delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685626 | ||||||
| chr17:4685641
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.421-2689A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685641 | ||||||
| chr17:4685663
|
C | T | 9 | a0001c0002t0005g0229a0001c0002t0005g0230a0001c0002t0006g0005others(6): Show | 11 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.421-2711G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685663 | ||||||
| chr17:4685678
|
A | T | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-2726T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685678 | ||||||
| chr17:4685792
|
T | TAAAAAAA others(1): Show |
6 | a0001c0002t0005g0229a0001c0004t0004g0036a0001c0015t0018g0239others(3): Show | 6 | HG01070.hp2 HG01258.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-2848_421-2841d others(10): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685792 | ||||||
| chr17:4685792
|
T | TAAAAAAA others(2): Show |
46 | a0001c0001t0001g0211a0001c0001t0001g0249a0001c0001t0001g0250others(43): Show | 49 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.421-2849_421-2841d others(11): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685792 | ||||||
| chr17:4685792
|
T | TAAAAAAA others(3): Show |
30 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0281others(27): Show | 33 | HG00544.hp2 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.421-2850_421-2841d others(12): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685792 | ||||||
| chr17:4685792
|
T | TAAAAAAA others(4): Show |
1 | a0011c0024t0002g0263 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.421-2841_421-2840i others(13): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685792 | ||||||
| chr17:4685792
|
T | TAAAAAAA others(6): Show |
2 | a0001c0001t0001g0282a0001c0001t0001g0286 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.421-2841_421-2840i others(15): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685792 | ||||||
| chr17:4685799
|
A | AAAAAAAA others(1): Show |
195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(192): Show | 214 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.421-2848_421-2847i others(10): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685799 | ||||||
| chr17:4685828
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.421-2876T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685828 | ||||||
| chr17:4685849
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0105 | 2 | NA18973.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.421-2897G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685849 | ||||||
| chr17:4685861
|
C | T | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.421-2909G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685861 | ||||||
| chr17:4685899
|
C | T | 1 | a0001c0025t0007g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.421-2947G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685899 | ||||||
| chr17:4685914
|
T | C | 25 | a0001c0002t0005g0229a0001c0002t0005g0230a0001c0002t0006g0005others(22): Show | 28 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.421-2962A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685914 | ||||||
| chr17:4685952
|
C | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.421-3000G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685952 | ||||||
| chr17:4685954
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.421-3002C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685954 | ||||||
| chr17:4686155
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.421-3203G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686155 | ||||||
| chr17:4686251
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-3299A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686251 | ||||||
| chr17:4686252
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-3300G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686252 | ||||||
| chr17:4686254
|
A | C | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-3302T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686254 | ||||||
| chr17:4686366
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.421-3414C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686366 | ||||||
| chr17:4686396
|
C | T | 1 | a0001c0002t0017g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.421-3444G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686396 | ||||||
| chr17:4686513
|
T | TTTTC | 3 | a0001c0001t0002g0264a0001c0001t0002g0276a0001c0001t0002g0277 | 3 | NA18946.hp1 NA18948.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.421-3565_421-3562d others(6): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686513 | ||||||
| chr17:4686580
|
C | T | 17 | a0001c0015t0018g0239a0001c0023t0005g0088a0002c0003t0003g0017others(14): Show | 18 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.421-3628G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686580 | ||||||
| chr17:4686581
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.421-3629C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686581 | ||||||
| chr17:4686587
|
G | A | 12 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0249others(9): Show | 15 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.421-3635C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686587 | ||||||
| chr17:4686660
|
G | A | 1 | a0001c0025t0007g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.421-3708C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686660 | ||||||
| chr17:4686746
|
G | A | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.421-3794C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686746 | ||||||
| chr17:4686793
|
C | T | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.421-3841G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686793 | ||||||
| chr17:4686797
|
C | T | 2 | a0001c0001t0009g0023a0001c0001t0009g0024 | 2 | HG00438.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.421-3845G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686797 | ||||||
| chr17:4686805
|
A | C | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-3853T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686805 | ||||||
| chr17:4686857
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.421-3905G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686857 | ||||||
| chr17:4686879
|
G | A | 5 | a0001c0002t0007g0037a0004c0009t0007g0025a0004c0009t0007g0026others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.421-3927C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686879 | ||||||
| chr17:4686954
|
C | G | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3934G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686954 | ||||||
| chr17:4686955
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3933A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686955 | ||||||
| chr17:4686957
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3931G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686957 | ||||||
| chr17:4686982
|
A | C | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3906T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686982 | ||||||
| chr17:4686984
|
T | A | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3904A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686984 | ||||||
| chr17:4686991
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+3897G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686991 | ||||||
| chr17:4687201
|
C | T | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.420+3687G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687201 | ||||||
| chr17:4687301
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+3587G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687301 | ||||||
| chr17:4687320
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+3568T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687320 | ||||||
| chr17:4687323
|
T | A | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3565A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687323 | ||||||
| chr17:4687340
|
C | G | 2 | a0002c0003t0003g0017a0008c0033t0003g0289 | 3 | HG00099.hp1 HG01261.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.420+3548G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687340 | ||||||
| chr17:4687341
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0116others(1): Show | 4 | HG00741.hp1 HG01074.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+3547C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687341 | ||||||
| chr17:4687374
|
C | G | 13 | a0001c0001t0001g0211a0001c0001t0007g0207a0001c0001t0007g0208others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.420+3514G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687374 | ||||||
| chr17:4687380
|
G | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+3508C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687380 | ||||||
| chr17:4687428
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+3460G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687428 | ||||||
| chr17:4687455
|
C | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+3433G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687455 | ||||||
| chr17:4687498
|
CAAA | C | 45 | a0001c0001t0001g0047a0001c0001t0001g0151a0001c0001t0001g0249others(42): Show | 47 | HG00544.hp2 HG01167.hp2 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.420+3387_420+3389d others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687498 | ||||||
| chr17:4687498
|
CAAAA | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(99): Show | 117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.420+3386_420+3389d others(6): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687498 | ||||||
| chr17:4687498
|
CAAAAA | C | 126 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0010others(123): Show | 134 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.420+3385_420+3389d others(7): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687498 | ||||||
| chr17:4687511
|
A | C | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3377T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687511 | ||||||
| chr17:4687701
|
A | C | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3187T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687701 | ||||||
| chr17:4687761
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+3127A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687761 | ||||||
| chr17:4687812
|
A | C | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3076T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687812 | ||||||
| chr17:4687828
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+3060C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687828 | ||||||
| chr17:4687891
|
A | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+2997T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687891 | ||||||
| chr17:4688044
|
G | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0249others(37): Show | 43 | HG00544.hp2 HG01243.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.420+2844C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688044 | ||||||
| chr17:4688080
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+2808C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688080 | ||||||
| chr17:4688152
|
T | C | 5 | a0001c0007t0011g0247a0001c0007t0011g0248a0001c0007t0016g0246others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+2736A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688152 | ||||||
| chr17:4688184
|
C | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+2704G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688184 | ||||||
| chr17:4688191
|
C | T | 1 | a0001c0002t0007g0209 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.420+2697G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688191 | ||||||
| chr17:4688195
|
C | T | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.420+2693G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688195 | ||||||
| chr17:4688272
|
G | T | 1 | a0001c0001t0009g0185 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.420+2616C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688272 | ||||||
| chr17:4688288
|
C | T | 1 | a0001c0001t0007g0207 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.420+2600G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688288 | ||||||
| chr17:4688291
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+2597A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688291 | ||||||
| chr17:4688352
|
G | A | 3 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0118 | 3 | HG00741.hp1 HG01074.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.420+2536C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688352 | ||||||
| chr17:4688358
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.420+2530T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688358 | ||||||
| chr17:4688489
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+2399C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688489 | ||||||
| chr17:4688501
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0286 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.420+2387C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688501 | ||||||
| chr17:4688558
|
G | A | 18 | a0001c0001t0001g0211a0001c0001t0007g0207a0001c0001t0007g0208others(15): Show | 18 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.420+2330C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688558 | ||||||
| chr17:4688857
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+2031A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688857 | ||||||
| chr17:4689220
|
C | T | 2 | a0001c0002t0005g0229a0001c0002t0005g0230 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.420+1668G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689220 | ||||||
| chr17:4689321
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+1567T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689321 | ||||||
| chr17:4689396
|
G | A | 2 | a0001c0014t0001g0222a0001c0014t0001g0223 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.420+1492C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689396 | ||||||
| chr17:4689436
|
A | G | 3 | a0001c0001t0001g0084a0001c0001t0001g0108a0001c0029t0001g0141 | 3 | HG01891.hp2 HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.420+1452T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689436 | ||||||
| chr17:4689604
|
C | T | 1 | a0002c0003t0003g0238 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.420+1284G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689604 | ||||||
| chr17:4689690
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+1198C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689690 | ||||||
| chr17:4689820
|
G | A | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.420+1068C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689820 | ||||||
| chr17:4689823
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+1065A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689823 | ||||||
| chr17:4689843
|
T | A | 5 | a0001c0007t0011g0247a0001c0007t0011g0248a0001c0007t0016g0246others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+1045A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689843 | ||||||
| chr17:4689894
|
C | T | 2 | a0001c0001t0001g0048a0001c0010t0001g0065 | 2 | HG04228.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.420+994G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689894 | ||||||
| chr17:4690073
|
A | C | 2 | a0001c0013t0015g0007a0004c0017t0007g0021 | 3 | HG02615.hp1 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.420+815T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690073 | ||||||
| chr17:4690231
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+657C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690231 | ||||||
| chr17:4690268
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+620A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690268 | ||||||
| chr17:4690271
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(193): Show | 215 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.420+617C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690271 | ||||||
| chr17:4690289
|
G | C | 1 | a0001c0001t0009g0024 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.420+599C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690289 | ||||||
| chr17:4690307
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.420+581A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690307 | ||||||
| chr17:4690375
|
G | A | 9 | a0001c0002t0005g0229a0001c0002t0005g0230a0001c0002t0006g0005others(6): Show | 11 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.420+513C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690375 | ||||||
| chr17:4690454
|
C | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+434G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690454 | ||||||
| chr17:4690460
|
A | G | 3 | a0006c0008t0004g0213a0006c0008t0004g0214a0006c0008t0004g0220 | 3 | HG02280.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.420+428T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690460 | ||||||
| chr17:4690461
|
C | T | 12 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0249others(9): Show | 15 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.420+427G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690461 | ||||||
| chr17:4690557
|
A | G | 5 | a0001c0002t0007g0037a0004c0009t0007g0025a0004c0009t0007g0026others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+331T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690557 | ||||||
| chr17:4690572
|
A | C | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.420+316T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690572 | ||||||
| chr17:4690583
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.420+305C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690583 | ||||||
| chr17:4690620
|
G | A | 1 | a0003c0005t0001g0158 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.420+268C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690620 | ||||||
| chr17:4690621
|
C | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(274): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.420+267G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690621 | ||||||
| chr17:4690632
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.420+256C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690632 | ||||||
| chr17:4690708
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.420+180A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690708 | ||||||
| chr17:4691026
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.315-33C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 2/16 | chr17 | 4691026 | ||||||
| chr17:4691028
|
G | A | 2 | a0001c0001t0001g0183a0003c0005t0001g0112 | 2 | HG00423.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.315-35C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 2/16 | chr17 | 4691028 | ||||||
| chr17:4691038
|
C | T | 3 | a0003c0005t0001g0169a0003c0005t0001g0184a0003c0005t0001g0190 | 3 | NA18979.hp1 NA18991.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.315-45G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 2/16 | chr17 | 4691038 | ||||||
| chr17:4691552
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-110A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4691552 | ||||||
| chr17:4691642
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-200T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4691642 | ||||||
| chr17:4691670
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(177): Show | 198 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.250-228G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4691670 | ||||||
| chr17:4691673
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-231C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4691673 | ||||||
| chr17:4691881
|
T | A | 2 | a0001c0013t0015g0007a0004c0017t0007g0021 | 3 | HG02615.hp1 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.250-439A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4691881 | ||||||
| chr17:4691907
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0130 | 2 | NA18963.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.250-465G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4691907 | ||||||
| chr17:4692006
|
A | C | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.250-564T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692006 | ||||||
| chr17:4692007
|
A | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(278): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-565T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692007 | ||||||
| chr17:4692008
|
A | T | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.250-566T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692008 | ||||||
| chr17:4692054
|
A | G | 1 | a0001c0006t0001g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.250-612T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692054 | ||||||
| chr17:4692193
|
C | A | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-751G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692193 | ||||||
| chr17:4692222
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-780G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692222 | ||||||
| chr17:4692243
|
G | A | 5 | a0001c0007t0011g0247a0001c0007t0011g0248a0001c0007t0016g0246others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-801C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692243 | ||||||
| chr17:4692264
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.250-822C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692264 | ||||||
| chr17:4692384
|
G | A | 1 | a0001c0004t0004g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.250-942C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692384 | ||||||
| chr17:4692404
|
T | C | 18 | a0001c0001t0001g0211a0001c0001t0007g0207a0001c0001t0007g0208others(15): Show | 18 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.250-962A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692404 | ||||||
| chr17:4692423
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-981A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692423 | ||||||
| chr17:4692446
|
A | G | 1 | a0001c0015t0018g0239 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.250-1004T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692446 | ||||||
| chr17:4692454
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-1012C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692454 | ||||||
| chr17:4692466
|
CA | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(277): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.250-1025delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692466 | ||||||
| chr17:4692631
|
C | G | 1 | a0001c0002t0017g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.250-1189G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692631 | ||||||
| chr17:4692732
|
G | A | 18 | a0001c0001t0001g0211a0001c0001t0007g0207a0001c0001t0007g0208others(15): Show | 18 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.250-1290C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692732 | ||||||
| chr17:4692853
|
T | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0280others(7): Show | 13 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.250-1411A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692853 | ||||||
| chr17:4692860
|
A | G | 2 | a0001c0001t0001g0282a0001c0001t0001g0286 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.250-1418T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692860 | ||||||
| chr17:4692874
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 211 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.250-1432C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692874 | ||||||
| chr17:4692982
|
C | G | 1 | a0001c0004t0004g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.250-1540G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692982 | ||||||
| chr17:4693067
|
T | A | 4 | a0001c0001t0001g0211a0001c0004t0004g0210a0001c0004t0004g0212others(1): Show | 4 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-1625A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693067 | ||||||
| chr17:4693161
|
A | C | 11 | a0001c0002t0005g0229a0001c0002t0005g0230a0001c0002t0006g0005others(8): Show | 13 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.250-1719T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693161 | ||||||
| chr17:4693246
|
C | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.250-1804G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693246 | ||||||
| chr17:4693384
|
T | C | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-1942A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693384 | ||||||
| chr17:4693619
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-2177G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693619 | ||||||
| chr17:4693648
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-2206C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693648 | ||||||
| chr17:4693719
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-2277T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693719 | ||||||
| chr17:4693805
|
C | T | 5 | a0003c0005t0001g0169a0003c0005t0001g0175a0003c0005t0001g0184others(2): Show | 5 | NA18955.hp2 NA18979.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-2363G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693805 | ||||||
| chr17:4693876
|
G | T | 1 | a0001c0001t0002g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.250-2434C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693876 | ||||||
| chr17:4694208
|
G | A | 2 | a0001c0013t0015g0007a0004c0017t0007g0021 | 3 | HG02615.hp1 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.250-2766C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694208 | ||||||
| chr17:4694368
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-2926C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694368 | ||||||
| chr17:4694370
|
G | A | 1 | a0001c0001t0009g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.250-2928C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694370 | ||||||
| chr17:4694390
|
G | A | 4 | a0001c0004t0004g0206a0006c0008t0004g0213a0006c0008t0004g0214others(1): Show | 4 | HG02280.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-2948C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694390 | ||||||
| chr17:4694424
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.250-2982C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694424 | ||||||
| chr17:4694477
|
C | T | 2 | a0001c0001t0002g0256a0001c0001t0002g0260 | 2 | NA18968.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.250-3035G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694477 | ||||||
| chr17:4694497
|
C | CAAAAA | 56 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0066others(53): Show | 61 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.250-3060_250-3056d others(7): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | ||||||
| chr17:4694497
|
C | CAAAAAA | 8 | a0001c0001t0001g0100a0001c0001t0001g0119a0001c0001t0001g0120others(5): Show | 8 | HG00741.hp1 HG02129.hp1 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-3061_250-3056d others(8): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | ||||||
| chr17:4694497
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0071 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.250-3056_250-3055i others(16): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | ||||||
| chr17:4694497
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0001g0012a0001c0001t0001g0058a0001c0001t0001g0173 | 4 | HG02735.hp1 HG03688.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-3056_250-3055i others(17): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | ||||||
| chr17:4694497
|
C | CAAAAAAA others(9): Show |
43 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(40): Show | 48 | HG01074.hp1 HG01099.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.250-3056_250-3055i others(18): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | ||||||
| chr17:4694497
|
C | CAAAAAAA others(10): Show |
109 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(106): Show | 118 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.250-3056_250-3055i others(19): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | ||||||
| chr17:4694497
|
C | CAAAAAAA others(11): Show |
43 | a0001c0001t0001g0008a0001c0001t0001g0045a0001c0001t0001g0048others(40): Show | 44 | HG00408.hp1 HG00408.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.250-3056_250-3055i others(20): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | ||||||
| chr17:4694497
|
C | CAAAAAAA others(12): Show |
5 | a0001c0001t0001g0015a0001c0001t0001g0168a0001c0002t0006g0080others(2): Show | 6 | HG02080.hp1 HG02723.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-3056_250-3055i others(21): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | ||||||
| chr17:4694497
|
C | CAAAAAAA others(13): Show |
4 | a0001c0002t0005g0229a0001c0002t0006g0228a0001c0013t0015g0007others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-3056_250-3055i others(22): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | ||||||
| chr17:4694497
|
C | CAAAAAAA others(14): Show |
6 | a0001c0002t0005g0230a0001c0002t0006g0005a0001c0002t0006g0224others(3): Show | 8 | HG02257.hp1 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-3056_250-3055i others(23): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | ||||||
| chr17:4694497
|
C | CAAAAAAA others(15): Show |
2 | a0001c0002t0006g0221a0001c0002t0006g0225 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.250-3056_250-3055i others(24): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | ||||||
| chr17:4694521
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250-3079C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694521 | ||||||
| chr17:4694592
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 211 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.250-3150C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694592 | ||||||
| chr17:4694628
|
C | A | 28 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(25): Show | 28 | HG00544.hp2 HG01943.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.250-3186G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694628 | ||||||
| chr17:4694659
|
CA | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-3218delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694659 | ||||||
| chr17:4694700
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.250-3258G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694700 | ||||||
| chr17:4694808
|
T | C | 2 | a0001c0004t0004g0035a0001c0004t0004g0036 | 2 | HG00642.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.250-3366A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694808 | ||||||
| chr17:4694894
|
C | T | 51 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0249others(48): Show | 56 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.250-3452G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694894 | ||||||
| chr17:4695062
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.250-3620G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695062 | ||||||
| chr17:4695089
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-3647C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695089 | ||||||
| chr17:4695105
|
G | A | 6 | a0001c0002t0006g0005a0001c0002t0006g0221a0001c0002t0006g0224others(3): Show | 8 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-3663C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695105 | ||||||
| chr17:4695158
|
T | C | 5 | a0001c0002t0007g0037a0004c0009t0007g0025a0004c0009t0007g0026others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-3716A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695158 | ||||||
| chr17:4695174
|
T | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | NA19077.hp1 NA19085.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.250-3732A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695174 | ||||||
| chr17:4695179
|
G | A | 1 | a0002c0003t0003g0238 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.250-3737C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695179 | ||||||
| chr17:4695225
|
G | A | 1 | a0001c0001t0002g0273 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.250-3783C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695225 | ||||||
| chr17:4695298
|
G | A | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-3856C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695298 | ||||||
| chr17:4695325
|
A | AAAATAAA others(1): Show |
280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(277): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.250-3891_250-3884d others(10): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695325 | ||||||
| chr17:4695325
|
A | T | 1 | a0004c0018t0007g0022 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.250-3883T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695325 | ||||||
| chr17:4695398
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-3956G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695398 | ||||||
| chr17:4695595
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.250-4153C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695595 | ||||||
| chr17:4695665
|
CT | C | 3 | a0001c0001t0007g0207a0001c0001t0007g0208a0001c0001t0007g0218 | 3 | HG01109.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.250-4224delA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695665 | ||||||
| chr17:4695666
|
TTA | T | 14 | a0001c0001t0001g0211a0001c0004t0004g0035a0001c0004t0004g0036others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-4226_250-4225d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695666 | ||||||
| chr17:4695667
|
TA | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 216 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.250-4226delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695667 | ||||||
| chr17:4695667
|
TAA | T | 9 | a0001c0001t0001g0069a0001c0001t0001g0109a0001c0001t0002g0253others(6): Show | 9 | HG01515.hp2 HG02257.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-4227_250-4226d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695667 | ||||||
| chr17:4695667
|
TAAA | T | 12 | a0001c0001t0001g0281a0001c0002t0005g0229a0001c0002t0005g0230others(9): Show | 14 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.250-4228_250-4226d others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695667 | ||||||
| chr17:4695667
|
TAAAA | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0249others(7): Show | 13 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.250-4229_250-4226d others(6): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695667 | ||||||
| chr17:4695676
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.250-4234T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695676 | ||||||
| chr17:4695717
|
G | A | 5 | a0001c0002t0007g0037a0004c0009t0007g0025a0004c0009t0007g0026others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-4275C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695717 | ||||||
| chr17:4695811
|
T | A | 2 | a0001c0001t0009g0023a0001c0001t0009g0024 | 2 | HG00438.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.250-4369A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695811 | ||||||
| chr17:4695848
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 5 | NA18982.hp1 NA18985.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-4406C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695848 | ||||||
| chr17:4695956
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-4514G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695956 | ||||||
| chr17:4695957
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-4515T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695957 | ||||||
| chr17:4695969
|
A | G | 2 | a0001c0030t0004g0219a0014c0031t0004g0205 | 2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.250-4527T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695969 | ||||||
| chr17:4696007
|
T | TA | 74 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0211others(71): Show | 79 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.250-4566dupT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696007 | ||||||
| chr17:4696032
|
GA | G | 72 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0211others(69): Show | 77 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.250-4591delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696032 | ||||||
| chr17:4696032
|
GAA | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(203): Show | 226 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.250-4592_250-4591d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696032 | ||||||
| chr17:4696227
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.250-4785C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696227 | ||||||
| chr17:4696276
|
G | A | 5 | a0001c0001t0009g0081a0001c0002t0006g0080a0001c0002t0006g0082others(2): Show | 5 | HG01167.hp2 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-4834C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696276 | ||||||
| chr17:4696280
|
C | A | 1 | a0001c0004t0004g0210 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.250-4838G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696280 | ||||||
| chr17:4696362
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-4920T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696362 | ||||||
| chr17:4696586
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-5144A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696586 | ||||||
| chr17:4696605
|
C | T | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(278): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-5163G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696605 | ||||||
| chr17:4696795
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.250-5353G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696795 | ||||||
| chr17:4696934
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.250-5492G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696934 | ||||||
| chr17:4696985
|
G | C | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-5543C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696985 | ||||||
| chr17:4697215
|
C | CGAGAG | 15 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(12): Show | 16 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.250-5778_250-5774d others(7): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697215 | ||||||
| chr17:4697360
|
A | G | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-5918T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697360 | ||||||
| chr17:4697469
|
G | A | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-6027C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697469 | ||||||
| chr17:4697622
|
G | A | 3 | a0001c0001t0007g0207a0001c0001t0007g0208a0001c0001t0007g0218 | 3 | HG01109.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.250-6180C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697622 | ||||||
| chr17:4697725
|
G | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(252): Show | 277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.249+6138C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697725 | ||||||
| chr17:4697751
|
T | C | 1 | a0001c0002t0005g0003 | 3 | HG02451.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.249+6112A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697751 | ||||||
| chr17:4697813
|
G | C | 58 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0249others(55): Show | 63 | HG00544.hp2 HG00642.hp1 HG01243.hp2 others(60): Show |
intron_variant | MODIFIER | c.249+6050C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697813 | ||||||
| chr17:4697921
|
C | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.249+5942G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697921 | ||||||
| chr17:4697935
|
G | T | 3 | a0006c0008t0004g0213a0006c0008t0004g0214a0006c0008t0004g0220 | 3 | HG02280.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.249+5928C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697935 | ||||||
| chr17:4697991
|
C | T | 1 | a0001c0006t0001g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+5872G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697991 | ||||||
| chr17:4698008
|
G | GCT | 5 | a0001c0007t0011g0247a0001c0007t0011g0248a0001c0007t0016g0246others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+5854_249+5855i others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698008 | ||||||
| chr17:4698008
|
G | GT | 28 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0068others(25): Show | 28 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.249+5854dupA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698008 | ||||||
| chr17:4698008
|
GT | G | 11 | a0001c0001t0001g0079a0001c0001t0001g0107a0001c0001t0001g0108others(8): Show | 11 | HG01891.hp2 HG02723.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+5854delA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698008 | ||||||
| chr17:4698008
|
GTT | G | 15 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(12): Show | 16 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.249+5853_249+5854d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698008 | ||||||
| chr17:4698351
|
C | T | 1 | a0001c0025t0007g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.249+5512G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698351 | ||||||
| chr17:4698359
|
AAGCTGGG others(11): Show |
A | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.249+5486_249+5503d others(20): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698359 | ||||||
| chr17:4698438
|
G | A | 16 | a0001c0015t0018g0239a0002c0003t0003g0017a0002c0003t0003g0231others(13): Show | 17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.249+5425C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698438 | ||||||
| chr17:4698470
|
T | TA | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(183): Show | 204 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.249+5392dupT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698470 | ||||||
| chr17:4698484
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.249+5379C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698484 | ||||||
| chr17:4698639
|
C | CAA | 5 | a0001c0001t0001g0148a0001c0013t0015g0007a0001c0014t0001g0222others(2): Show | 6 | HG02615.hp1 HG02809.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+5222_249+5223d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698639 | ||||||
| chr17:4698639
|
C | CAAA | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(260): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.249+5221_249+5223d others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698639 | ||||||
| chr17:4698639
|
C | CAAAA | 14 | a0001c0001t0001g0108a0001c0001t0001g0199a0001c0001t0002g0256others(11): Show | 14 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+5220_249+5223d others(6): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698639 | ||||||
| chr17:4698653
|
C | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.249+5210G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698653 | ||||||
| chr17:4698727
|
A | ATGT | 26 | a0001c0001t0001g0211a0001c0001t0007g0207a0001c0001t0007g0208others(23): Show | 28 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.249+5133_249+5135d others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698727 | ||||||
| chr17:4698727
|
ATGT | A | 15 | a0001c0002t0008g0085a0001c0002t0008g0086a0001c0002t0008g0089others(12): Show | 15 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.249+5133_249+5135d others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698727 | ||||||
| chr17:4698863
|
A | T | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.249+5000T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698863 | ||||||
| chr17:4699045
|
G | A | 1 | a0001c0007t0011g0247 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.249+4818C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699045 | ||||||
| chr17:4699151
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+4712C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699151 | ||||||
| chr17:4699220
|
A | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 211 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.249+4643T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699220 | ||||||
| chr17:4699260
|
T | C | 5 | a0001c0007t0011g0247a0001c0007t0011g0248a0001c0007t0016g0246others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+4603A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699260 | ||||||
| chr17:4699286
|
A | G | 1 | a0001c0001t0009g0163 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.249+4577T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699286 | ||||||
| chr17:4699396
|
T | A | 2 | a0001c0030t0004g0219a0014c0031t0004g0205 | 2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.249+4467A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699396 | ||||||
| chr17:4699499
|
G | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.249+4364C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699499 | ||||||
| chr17:4699642
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 211 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.249+4221C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699642 | ||||||
| chr17:4699647
|
C | T | 6 | a0001c0001t0001g0162a0001c0002t0007g0037a0004c0009t0007g0025others(3): Show | 6 | HG02258.hp1 HG02615.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+4216G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699647 | ||||||
| chr17:4699790
|
T | C | 1 | a0001c0002t0006g0226 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.249+4073A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699790 | ||||||
| chr17:4699803
|
T | C | 1 | a0001c0001t0009g0160 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.249+4060A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699803 | ||||||
| chr17:4699811
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.249+4052A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699811 | ||||||
| chr17:4699897
|
A | AT | 48 | a0001c0001t0001g0211a0001c0001t0001g0280a0001c0001t0001g0281others(45): Show | 51 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.249+3965dupA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699897 | ||||||
| chr17:4699897
|
A | ATT | 23 | a0001c0001t0001g0196a0001c0001t0002g0253a0001c0001t0002g0254others(20): Show | 25 | HG01175.hp2 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.249+3964_249+3965d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699897 | ||||||
| chr17:4699897
|
A | ATTT | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(130): Show | 150 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.249+3963_249+3965d others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699897 | ||||||
| chr17:4699897
|
A | ATTTT | 45 | a0001c0001t0001g0009a0001c0001t0001g0038a0001c0001t0001g0046others(42): Show | 46 | HG00438.hp1 HG00673.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.249+3962_249+3965d others(6): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699897 | ||||||
| chr17:4699897
|
A | ATTTTT | 12 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0002t0008g0085others(9): Show | 12 | HG02055.hp1 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.249+3961_249+3965d others(7): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699897 | ||||||
| chr17:4699922
|
A | G | 1 | a0001c0004t0004g0210 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.249+3941T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699922 | ||||||
| chr17:4700149
|
C | T | 2 | a0002c0003t0003g0234a0002c0003t0003g0235 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.249+3714G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700149 | ||||||
| chr17:4700352
|
C | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(177): Show | 198 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.249+3511G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700352 | ||||||
| chr17:4700353
|
G | A | 5 | a0001c0007t0011g0247a0001c0007t0011g0248a0001c0007t0016g0246others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+3510C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700353 | ||||||
| chr17:4700410
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.249+3453G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700410 | ||||||
| chr17:4700442
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.249+3421G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700442 | ||||||
| chr17:4700516
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.249+3347A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700516 | ||||||
| chr17:4700735
|
G | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.249+3128C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700735 | ||||||
| chr17:4700755
|
T | C | 2 | a0001c0002t0006g0227a0001c0002t0006g0228 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.249+3108A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700755 | ||||||
| chr17:4700849
|
T | C | 2 | a0001c0001t0001g0146a0010c0020t0001g0147 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.249+3014A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700849 | ||||||
| chr17:4700928
|
C | CA | 24 | a0001c0001t0007g0207a0001c0001t0007g0208a0001c0001t0007g0218others(21): Show | 25 | HG00099.hp1 HG00642.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.249+2934dupT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700928 | ||||||
| chr17:4700928
|
C | CAA | 9 | a0001c0001t0001g0211a0001c0004t0004g0210a0001c0004t0004g0212others(6): Show | 9 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+2933_249+2934d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700928 | ||||||
| chr17:4700928
|
CA | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(182): Show | 204 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.249+2934delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700928 | ||||||
| chr17:4700975
|
A | G | 27 | a0001c0002t0005g0229a0001c0002t0005g0230a0001c0002t0006g0005others(24): Show | 30 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.249+2888T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700975 | ||||||
| chr17:4700992
|
T | TA | 67 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0012others(64): Show | 75 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.249+2870dupT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700992 | ||||||
| chr17:4700992
|
T | TAA | 10 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0192others(7): Show | 10 | HG01106.hp2 HG02258.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.249+2869_249+2870d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700992 | ||||||
| chr17:4700992
|
TA | T | 71 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0058others(68): Show | 75 | HG00099.hp1 HG00544.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.249+2870delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700992 | ||||||
| chr17:4700992
|
TAA | T | 28 | a0001c0001t0001g0211a0001c0001t0001g0249a0001c0001t0002g0251others(25): Show | 30 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.249+2869_249+2870d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700992 | ||||||
| chr17:4700993
|
A | T | 2 | a0002c0003t0003g0231a0002c0003t0003g0232 | 2 | HG02523.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.249+2870T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700993 | ||||||
| chr17:4701202
|
T | C | 79 | a0001c0001t0001g0211a0001c0001t0002g0251a0001c0001t0002g0252others(76): Show | 82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.249+2661A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701202 | ||||||
| chr17:4701307
|
G | A | 9 | a0001c0001t0001g0016a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 10 | HG00597.hp2 HG01192.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+2556C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701307 | ||||||
| chr17:4701324
|
T | TG | 50 | a0001c0001t0001g0211a0001c0001t0007g0207a0001c0001t0007g0208others(47): Show | 53 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.249+2538dupC | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701324 | ||||||
| chr17:4701324
|
T | TGG | 41 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0249others(38): Show | 44 | HG00544.hp2 HG01243.hp2 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.249+2537_249+2538d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701324 | ||||||
| chr17:4701339
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.249+2524T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701339 | ||||||
| chr17:4701490
|
G | A | 11 | a0001c0002t0005g0229a0001c0002t0005g0230a0001c0002t0006g0005others(8): Show | 13 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.249+2373C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701490 | ||||||
| chr17:4701495
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0280others(7): Show | 13 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.249+2368G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701495 | ||||||
| chr17:4701498
|
G | A | 1 | a0001c0002t0005g0034 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.249+2365C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701498 | ||||||
| chr17:4701527
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.249+2336A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701527 | ||||||
| chr17:4701535
|
A | G | 1 | a0001c0010t0001g0065 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.249+2328T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701535 | ||||||
| chr17:4701541
|
T | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0211others(88): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.249+2322A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701541 | ||||||
| chr17:4701543
|
C | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0211others(88): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.249+2320G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701543 | ||||||
| chr17:4701642
|
A | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0048others(7): Show | 13 | HG00408.hp1 HG00673.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.249+2221T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701642 | ||||||
| chr17:4701701
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.249+2162G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701701 | ||||||
| chr17:4701737
|
A | G | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02630.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.249+2126T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701737 | ||||||
| chr17:4701761
|
C | T | 1 | a0004c0017t0007g0021 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.249+2102G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701761 | ||||||
| chr17:4701773
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.249+2090G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701773 | ||||||
| chr17:4701905
|
A | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.249+1958T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701905 | ||||||
| chr17:4702068
|
A | G | 11 | a0001c0002t0005g0229a0001c0002t0005g0230a0001c0002t0006g0005others(8): Show | 13 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.249+1795T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702068 | ||||||
| chr17:4702162
|
T | G | 2 | a0001c0013t0015g0007a0004c0017t0007g0021 | 3 | HG02615.hp1 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.249+1701A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702162 | ||||||
| chr17:4702209
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.249+1654C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702209 | ||||||
| chr17:4702230
|
G | A | 9 | a0001c0001t0001g0016a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 10 | HG00597.hp2 HG01192.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+1633C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702230 | ||||||
| chr17:4702421
|
AAAT | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0280others(7): Show | 13 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.249+1439_249+1441d others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702421 | ||||||
| chr17:4702551
|
C | T | 5 | a0001c0001t0001g0050a0001c0001t0010g0053a0005c0011t0010g0051others(2): Show | 5 | HG01346.hp2 HG02273.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+1312G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702551 | ||||||
| chr17:4702592
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.249+1271A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702592 | ||||||
| chr17:4702675
|
C | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.249+1188G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702675 | ||||||
| chr17:4702964
|
C | G | 19 | a0001c0001t0001g0211a0001c0001t0007g0207a0001c0001t0007g0208others(16): Show | 19 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.249+899G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702964 | ||||||
| chr17:4703100
|
C | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(187): Show | 209 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.249+763G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703100 | ||||||
| chr17:4703125
|
C | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02040.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.249+738G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703125 | ||||||
| chr17:4703142
|
C | T | 10 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 10 | HG00408.hp2 NA18956.hp1 NA18973.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+721G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703142 | ||||||
| chr17:4703303
|
C | T | 5 | a0001c0002t0007g0037a0004c0009t0007g0025a0004c0009t0007g0026others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+560G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703303 | ||||||
| chr17:4703467
|
A | C | 2 | a0001c0004t0004g0035a0001c0004t0004g0036 | 2 | HG00642.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.249+396T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703467 | ||||||
| chr17:4703521
|
C | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.249+342G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703521 | ||||||
| chr17:4703571
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.249+292G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703571 | ||||||
| chr17:4703602
|
GC | G | 4 | a0004c0009t0007g0025a0004c0009t0007g0026a0004c0009t0007g0027others(1): Show | 4 | HG02258.hp1 HG02976.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+260delG | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703602 | ||||||
| chr17:4703814
|
C | T | 2 | a0001c0001t0009g0023a0001c0001t0009g0024 | 2 | HG00438.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.249+49G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703814 |