Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9520 |
|---|---|
| ensemblid | ENSG00000141279.18 |
| hgncid | 7900 |
| symbol | NPEPPS |
| name | aminopeptidase puromycin sensitive |
| refseq_nuc | NM_006310.4 |
| refseq_prot | NP_006301.3 |
| ensembl_nuc | ENST00000322157.9 |
| ensembl_prot | ENSP00000320324.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 47531108 |
| end | 47623276 |
| strand | + |
| ver | v1.2 |
| region | chr17:47531108-47623276 |
| region5000 | chr17:47526108-47628276 |
| regionname0 | NPEPPS_chr17_47531108_47623276 |
| regionname5000 | NPEPPS_chr17_47526108_47628276 |
| 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 | 1/0 | 919 | 336 | 70 | 58 | 155 | 14 | 38 | 121 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0002 | 0/1 | 919 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0003 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0004 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0005 | 0/0 | 919 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0006 | 0/0 | 919 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| 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 | 1/0 | 2760 | 306 | 64 | 50 | 142 | 12 | 37 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| c0002 | 0/0 | 2760 | 13 | 0 | 0 | 13 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| c0003 | 0/0 | 2760 | 11 | 1 | 7 | 0 | 2 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| c0004 | 0/0 | 2760 | 3 | 2 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| c0005 | 0/1 | 2760 | 2 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| c0006 | 0/0 | 2760 | 2 | 2 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| c0007 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| c0008 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| c0009 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| c0010 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| c0011 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1550 | 122 | 28 | 20 | 51 | 6 | 15 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| t0002 | 0/0 | 1553 | 101 | 13 | 20 | 51 | 2 | 15 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| t0003 | 0/0 | 1552 | 75 | 29 | 16 | 23 | 2 | 5 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| t0004 | 0/0 | 1552 | 31 | 1 | 1 | 28 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| t0005 | 0/0 | 1553 | 5 | 0 | 0 | 0 | 2 | 3 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| t0006 | 0/0 | 1553 | 2 | 0 | 1 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| t0007 | 0/0 | 1553 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| t0008 | 0/0 | 1553 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| t0009 | 0/0 | 1553 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| t0010 | 0/0 | 1553 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| t0011 | 0/0 | 1550 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| t0012 | 0/0 | 1552 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| 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 | 2 | 0 | 0 | 0 | 2 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0008 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0267 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| 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 | 1/0 | 2760 | 306 | 64 | 50 | 142 | 12 | 37 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0002 | 0/0 | 2760 | 13 | 0 | 0 | 13 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0003 | 0/0 | 2760 | 11 | 1 | 7 | 0 | 2 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0004 | 0/0 | 2760 | 3 | 2 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0006 | 0/0 | 2760 | 2 | 2 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0011 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0002c0005 | 0/1 | 2760 | 2 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0003c0010 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0004c0007 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0005c0008 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0006c0009 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4309 | 105 | 25 | 19 | 39 | 6 | 15 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0001t0002 | 0/0 | 4312 | 100 | 13 | 20 | 50 | 2 | 15 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0001t0003 | 0/0 | 4311 | 57 | 24 | 7 | 22 | 0 | 4 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0001t0004 | 0/0 | 4311 | 31 | 1 | 1 | 28 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0001t0005 | 0/0 | 4312 | 5 | 0 | 0 | 0 | 2 | 3 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0001t0006 | 0/0 | 4312 | 2 | 0 | 1 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0001t0007 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0001t0008 | 0/0 | 4312 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0001t0009 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0001t0010 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0001t0011 | 0/0 | 4309 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0001t0012 | 0/0 | 4311 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0002t0001 | 0/0 | 4309 | 12 | 0 | 0 | 12 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0002t0003 | 0/0 | 4311 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0003t0003 | 0/0 | 4311 | 11 | 1 | 7 | 0 | 2 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0004t0003 | 0/0 | 4311 | 3 | 2 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0006t0003 | 0/0 | 4311 | 2 | 2 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0001c0011t0001 | 0/0 | 4309 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0002c0005t0001 | 0/1 | 4309 | 2 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0003c0010t0001 | 0/0 | 4309 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0004c0007t0001 | 0/0 | 4309 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0005c0008t0003 | 0/0 | 4311 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| a0006c0009t0002 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | copy fasta | chr17 | 47526108 | 47628276 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0267 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0005g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0007g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0008g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0009g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0010g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0011g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0001t0012g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0003t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0003t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0003t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0003t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0003t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0003t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0003t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0003t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0003t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0003t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0004t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0004t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0004t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0006t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0006t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0001c0011t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0002c0005t0001g0008 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0002c0005t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0003c0010t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0004c0007t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0005c0008t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| a0006c0009t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0003 | g0306 | EUR | GBR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0203 | EUR | GBR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0328 | EUR | GBR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0212 | EUR | FIN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0293 | EUR | FIN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0327 | EUR | FIN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | CHS | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | CHS | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | CHS | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | CHS | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | CHS | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00735 | hp1 | a0001 | c0003 | t0003 | g0302 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0204 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01071 | hp2 | a0002 | c0005 | t0001 | g0020 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01081 | hp2 | a0001 | c0003 | t0003 | g0309 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01099 | hp1 | a0001 | c0003 | t0003 | g0303 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01106 | hp1 | a0001 | c0004 | t0003 | g0060 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01168 | hp2 | a0001 | c0003 | t0003 | g0310 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01169 | hp1 | a0001 | c0003 | t0003 | g0305 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01175 | hp2 | a0001 | c0003 | t0003 | g0301 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0335 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01243 | hp2 | a0001 | c0001 | t0011 | g0285 | AMR | PUR | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0333 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01261 | hp2 | a0001 | c0003 | t0003 | g0308 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0129 | EUR | IBS | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0001 | EUR | IBS | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0001 | EUR | IBS | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | PEL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01975 | hp1 | a0005 | c0008 | t0003 | g0050 | AMR | PEL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PEL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0134 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02055 | hp1 | a0003 | c0010 | t0001 | g0110 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02055 | hp2 | a0001 | c0003 | t0003 | g0300 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02056 | hp2 | a0001 | c0001 | t0012 | g0083 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02080 | hp1 | a0001 | c0001 | t0009 | g0094 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CDX | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | CDX | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02602 | hp1 | a0001 | c0003 | t0003 | g0304 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02717 | hp1 | a0001 | c0011 | t0001 | g0311 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02809 | hp1 | a0001 | c0004 | t0003 | g0059 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02818 | hp1 | a0004 | c0007 | t0001 | g0248 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | ESN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | ESN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | ESN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ESN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0208 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03041 | hp1 | a0001 | c0004 | t0003 | g0080 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0224 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ESN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | ESN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ESN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | MSL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0291 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0048 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | ESN | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | MSL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | STU | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0049 | SAS | PJL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | BEB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | BEB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | BEB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | BEB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | BEB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | STU | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | STU | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | STU | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | YRI | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | YRI | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0292 | EAS | CHB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | CHB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18906 | hp1 | a0001 | c0006 | t0003 | g0340 | AFR | YRI | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | YRI | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18991 | hp1 | a0001 | c0001 | t0010 | g0186 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19007 | hp1 | a0006 | c0009 | t0002 | g0114 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | LWK | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | LWK | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | LWK | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | LWK | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19067 | hp2 | a0001 | c0002 | t0003 | g0266 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | YRI | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | YRI | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ASW | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA20129 | hp2 | a0001 | c0006 | t0003 | g0339 | AFR | ASW | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA20752 | hp1 | a0001 | c0003 | t0003 | g0307 | EUR | TSI | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | GIH | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0207 | SAS | GIH | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | MSL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0338 | AFR | MSL | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | USA | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | USA | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | USA | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | USA | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | LWK | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | LWK | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0005 | t0001 | g0008 | REF | REF | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0267 | REF | REF | NPEPPS_chr17_47526108_47628276 | NPEPPS | chr17 | 47526108 | 47628276 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:47582746
|
C | T | 1 | a0003 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.545C>T | p.Thr182Ile | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/23 | 738/4309 | 545/2760 | 182/919 | chr17 | 47582746 | ||
| chr17:47586188
|
A | G | 1 | a0006 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.890A>G | p.Asn297Ser | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 7/23 | 1083/4309 | 890/2760 | 297/919 | chr17 | 47586188 | ||
| chr17:47596394
|
A | G | 1 | a0005 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.1468A>G | p.Ile490Val | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/23 | 1661/4309 | 1468/2760 | 490/919 | chr17 | 47596394 | ||
| chr17:47604006
|
C | T | 1 | a0004 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1832C>T | p.Pro611Leu | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 16/23 | 2025/4309 | 1832/2760 | 611/919 | chr17 | 47604006 | ||
| chr17:47621777
|
G | C | 1 | a0002 | 2 | HG01071.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.2617G>C | p.Glu873Gln | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 23/23 | 2810/4309 | 2617/2760 | 873/919 | chr17 | 47621777 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:47531345
|
C | T | 1 | a0001c0011 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.45C>T | p.Leu15Leu | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/23 | 238/4309 | 45/2760 | 15/919 | chr17 | 47531345 | ||
| chr17:47531519
|
C | T | 2 | a0001c0003a0001c0006 | 13 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(10): Show |
synonymous_variant | LOW | c.219C>T | p.Asp73Asp | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/23 | 412/4309 | 219/2760 | 73/919 | chr17 | 47531519 | ||
| chr17:47587320
|
A | G | 1 | a0001c0004 | 3 | HG01106.hp1 HG02809.hp1 HG03041.hp1 |
synonymous_variant | LOW | c.1071A>G | p.Gln357Gln | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/23 | 1264/4309 | 1071/2760 | 357/919 | chr17 | 47587320 | ||
| chr17:47592512
|
T | C | 1 | a0001c0003 | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
synonymous_variant | LOW | c.1393T>C | p.Leu465Leu | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/23 | 1586/4309 | 1393/2760 | 465/919 | chr17 | 47592512 | ||
| chr17:47599705
|
C | G | 1 | a0001c0002 | 13 | NA18943.hp2 NA18962.hp2 NA18977.hp1 others(10): Show |
synonymous_variant | LOW | c.1566C>G | p.Ser522Ser | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 14/23 | 1759/4309 | 1566/2760 | 522/919 | chr17 | 47599705 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:47531152
|
C | G | 1 | a0001c0001t0012 | 1 | HG02056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-149C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/23 | 149 | chr17 | 47531152 | |||||
| chr17:47531217
|
G | A | 1 | a0001c0001t0007 | 1 | HG03471.hp2 | 5_prime_UTR_variant | MODIFIER | c.-84G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/23 | 84 | chr17 | 47531217 | |||||
| chr17:47622199
|
T | C | 1 | a0001c0001t0008 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*279T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 23/23 | 279 | chr17 | 47622199 | |||||
| chr17:47622326
|
C | T | 1 | a0001c0001t0011 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*406C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 23/23 | 406 | chr17 | 47622326 | |||||
| chr17:47622425
|
CT | C | 8 | a0001c0001t0003a0001c0001t0004a0001c0001t0012others(5): Show | 107 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*518delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 23/23 | 518 | INFO_REALIGN_3_PRIME | chr17 | 47622425 | ||||
| chr17:47622756
|
T | A | 1 | a0001c0001t0009 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*836T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 23/23 | 836 | chr17 | 47622756 | |||||
| chr17:47622772
|
T | C | 1 | a0001c0001t0006 | 2 | HG00099.hp2 HG00735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*852T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 23/23 | 852 | chr17 | 47622772 | |||||
| chr17:47622863
|
C | T | 1 | a0001c0001t0005 | 5 | HG01515.hp2 HG01517.hp2 HG03017.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*943C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 23/23 | 943 | chr17 | 47622863 | |||||
| chr17:47622907
|
C | T | 1 | a0001c0001t0010 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*987C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 23/23 | 987 | chr17 | 47622907 | |||||
| chr17:47623018
|
C | CCTA | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(13): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1099_*1101dupCTA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 23/23 | 1102 | INFO_REALIGN_3_PRIME | chr17 | 47623018 | ||||
| chr17:47623042
|
C | G | 2 | a0001c0001t0004a0001c0001t0012 | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1122C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 23/23 | 1122 | chr17 | 47623042 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:47531569
|
C | T | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.255+14C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47531569 | ||||||
| chr17:47531731
|
TGGGGCTG others(5): Show |
T | 1 | a0001c0001t0002g0003 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.255+182_255+193del others(12): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47531731 | |||||
| chr17:47531804
|
C | T | 1 | a0001c0001t0007g0338 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.255+249C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47531804 | ||||||
| chr17:47531834
|
C | G | 1 | a0001c0001t0002g0337 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.255+279C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47531834 | ||||||
| chr17:47531875
|
G | C | 1 | a0001c0001t0002g0337 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.255+320G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47531875 | ||||||
| chr17:47531876
|
C | G | 1 | a0001c0001t0002g0337 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.255+321C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47531876 | ||||||
| chr17:47531885
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.255+330C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47531885 | ||||||
| chr17:47531904
|
T | G | 26 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(23): Show | 26 | HG00140.hp2 HG00280.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.255+349T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47531904 | ||||||
| chr17:47532088
|
G | A | 1 | a0001c0001t0002g0029 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.255+533G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47532088 | ||||||
| chr17:47532088
|
G | C | 1 | a0001c0001t0001g0030 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.255+533G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47532088 | ||||||
| chr17:47532088
|
G | T | 1 | a0001c0001t0008g0335 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255+533G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47532088 | ||||||
| chr17:47532104
|
G | T | 1 | a0001c0001t0001g0334 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.255+549G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47532104 | ||||||
| chr17:47532124
|
G | A | 1 | a0001c0001t0002g0031 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.255+569G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47532124 | ||||||
| chr17:47532184
|
C | T | 1 | a0001c0001t0002g0333 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.255+629C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47532184 | ||||||
| chr17:47532349
|
C | T | 2 | a0001c0001t0002g0331a0001c0001t0002g0332 | 2 | HG00423.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.255+794C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47532349 | ||||||
| chr17:47532364
|
C | T | 19 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(16): Show | 19 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.255+809C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47532364 | ||||||
| chr17:47532623
|
C | T | 1 | a0001c0011t0001g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.255+1068C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47532623 | ||||||
| chr17:47532658
|
C | CA | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0081others(80): Show | 83 | HG00438.hp1 HG00544.hp1 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.255+1126dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47532658 | |||||
| chr17:47532658
|
C | CAA | 9 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0034others(6): Show | 9 | HG01109.hp2 HG01358.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+1125_255+1126d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47532658 | |||||
| chr17:47532658
|
CA | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0297others(7): Show | 10 | HG00323.hp1 HG00738.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.255+1126delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47532658 | |||||
| chr17:47532658
|
CAA | C | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+1125_255+1126d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47532658 | |||||
| chr17:47532785
|
C | T | 1 | a0001c0001t0007g0338 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.255+1230C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47532785 | ||||||
| chr17:47532903
|
G | A | 1 | a0006c0009t0002g0114 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.255+1348G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47532903 | ||||||
| chr17:47532978
|
C | G | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.255+1423C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47532978 | ||||||
| chr17:47533281
|
C | T | 1 | a0001c0001t0002g0113 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.255+1726C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47533281 | ||||||
| chr17:47533481
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.255+1926T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47533481 | ||||||
| chr17:47533708
|
G | A | 4 | a0001c0001t0002g0041a0001c0001t0002g0116a0001c0001t0002g0117others(1): Show | 4 | HG01069.hp2 HG01891.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+2153G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47533708 | ||||||
| chr17:47533993
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.255+2438A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47533993 | ||||||
| chr17:47534097
|
CT | C | 6 | a0001c0001t0001g0123a0001c0001t0002g0122a0001c0001t0003g0042others(3): Show | 6 | HG01099.hp2 HG02647.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+2554delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47534097 | |||||
| chr17:47534154
|
C | T | 1 | a0001c0001t0005g0291 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.255+2599C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47534154 | ||||||
| chr17:47534214
|
C | G | 1 | a0001c0001t0002g0290 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.255+2659C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47534214 | ||||||
| chr17:47534214
|
C | T | 1 | a0001c0001t0003g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.255+2659C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47534214 | ||||||
| chr17:47534338
|
T | C | 211 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.255+2783T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47534338 | ||||||
| chr17:47534342
|
G | C | 2 | a0001c0001t0002g0100a0001c0001t0002g0228 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.255+2787G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47534342 | ||||||
| chr17:47534358
|
C | T | 1 | a0001c0001t0001g0330 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.255+2803C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47534358 | ||||||
| chr17:47534454
|
C | T | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289 | 3 | NA18973.hp2 NA19064.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.255+2899C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47534454 | ||||||
| chr17:47534696
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG00423.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.255+3141G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47534696 | ||||||
| chr17:47534956
|
T | G | 1 | a0001c0001t0002g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.255+3401T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47534956 | ||||||
| chr17:47535107
|
G | A | 1 | a0001c0001t0004g0124 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.255+3552G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47535107 | ||||||
| chr17:47535175
|
G | T | 1 | a0001c0001t0003g0099 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.255+3620G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47535175 | ||||||
| chr17:47535201
|
C | T | 13 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0001t0001g0277others(10): Show | 13 | HG01169.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.255+3646C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47535201 | ||||||
| chr17:47535242
|
C | CA | 80 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0106others(77): Show | 80 | HG00099.hp1 HG00423.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.255+3714dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535242 | |||||
| chr17:47535242
|
C | CAA | 36 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0232others(33): Show | 36 | HG00735.hp1 HG00738.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.255+3713_255+3714d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535242 | |||||
| chr17:47535242
|
C | CAAA | 14 | a0001c0001t0003g0032a0001c0001t0003g0047a0001c0001t0003g0048others(11): Show | 14 | HG00544.hp2 HG03471.hp2 HG03492.hp2 others(11): Show |
intron_variant | MODIFIER | c.255+3712_255+3714d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535242 | |||||
| chr17:47535242
|
C | CAAAA | 17 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0045others(14): Show | 17 | HG00438.hp1 HG00558.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.255+3711_255+3714d others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535242 | |||||
| chr17:47535242
|
CA | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(6): Show | 9 | HG00140.hp2 HG01168.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+3714delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535242 | |||||
| chr17:47535242
|
CAAAAAAA others(3): Show |
C | 12 | a0001c0001t0002g0029a0001c0001t0002g0031a0001c0001t0002g0084others(9): Show | 12 | HG01433.hp1 HG02602.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.255+3705_255+3714d others(12): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535242 | |||||
| chr17:47535242
|
CAAAAAAA others(4): Show |
C | 104 | a0001c0001t0002g0003a0001c0001t0002g0041a0001c0001t0002g0085others(101): Show | 106 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.255+3704_255+3714d others(13): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535242 | |||||
| chr17:47535242
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0227 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.255+3703_255+3714d others(14): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535242 | |||||
| chr17:47535279
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.255+3724C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47535279 | ||||||
| chr17:47535419
|
C | T | 2 | a0001c0001t0002g0100a0001c0001t0002g0228 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.255+3864C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47535419 | ||||||
| chr17:47535466
|
G | A | 1 | a0001c0001t0008g0335 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255+3911G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47535466 | ||||||
| chr17:47535476
|
G | A | 16 | a0001c0001t0002g0041a0001c0001t0002g0116a0001c0001t0002g0117others(13): Show | 16 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.255+3921G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47535476 | ||||||
| chr17:47535535
|
G | C | 1 | a0001c0003t0003g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.255+3980G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47535535 | ||||||
| chr17:47535540
|
G | A | 165 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.255+3985G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47535540 | ||||||
| chr17:47535549
|
C | CA | 19 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0030others(16): Show | 19 | HG01358.hp2 HG01993.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.255+4015dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535549 | |||||
| chr17:47535549
|
CA | C | 146 | a0001c0001t0001g0274a0001c0001t0001g0323a0001c0001t0002g0003others(143): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.255+4015delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535549 | |||||
| chr17:47535549
|
CAA | C | 15 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0003g0002others(12): Show | 16 | HG02083.hp1 HG02273.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.255+4014_255+4015d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535549 | |||||
| chr17:47535655
|
T | A | 116 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(113): Show | 118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.255+4100T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47535655 | ||||||
| chr17:47535787
|
TTTATGA | T | 5 | a0001c0001t0002g0122a0001c0001t0002g0172a0001c0001t0002g0173others(2): Show | 5 | HG02083.hp1 NA18945.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+4239_255+4244d others(8): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535787 | |||||
| chr17:47535827
|
G | A | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.255+4272G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47535827 | ||||||
| chr17:47535832
|
C | CT | 31 | a0001c0001t0001g0081a0001c0001t0001g0102a0001c0001t0001g0106others(28): Show | 31 | HG00558.hp2 HG01346.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.255+4299dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535832 | |||||
| chr17:47535832
|
CT | C | 64 | a0001c0001t0001g0254a0001c0001t0002g0031a0001c0001t0002g0084others(61): Show | 65 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.255+4299delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535832 | |||||
| chr17:47535832
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0002g0231a0001c0001t0002g0238 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.255+4289_255+4299d others(13): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47535832 | |||||
| chr17:47535984
|
G | A | 12 | a0001c0001t0003g0002a0001c0001t0003g0098a0001c0001t0003g0099others(9): Show | 13 | HG02615.hp1 HG02717.hp2 HG02897.hp1 others(10): Show |
intron_variant | MODIFIER | c.255+4429G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47535984 | ||||||
| chr17:47536125
|
G | A | 46 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(43): Show | 46 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.255+4570G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536125 | ||||||
| chr17:47536224
|
T | G | 1 | a0001c0001t0002g0168 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.255+4669T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536224 | ||||||
| chr17:47536277
|
G | A | 2 | a0001c0001t0002g0100a0001c0001t0002g0228 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.255+4722G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536277 | ||||||
| chr17:47536373
|
CTGCATAT others(30): Show |
C | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+4819_255+4855d others(39): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536373 | ||||||
| chr17:47536382
|
TTC | T | 109 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0041others(106): Show | 110 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.255+4833_255+4834d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47536382 | |||||
| chr17:47536386
|
CTCT | C | 25 | a0001c0001t0002g0029a0001c0001t0002g0093a0001c0001t0002g0153others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.255+4833_255+4835d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47536386 | |||||
| chr17:47536387
|
TC | T | 14 | a0001c0001t0002g0167a0001c0001t0002g0209a0001c0001t0003g0002others(11): Show | 15 | HG02615.hp1 HG02717.hp2 HG02922.hp2 others(12): Show |
intron_variant | MODIFIER | c.255+4833delC | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536387 | ||||||
| chr17:47536388
|
C | CTTT | 8 | a0001c0003t0003g0300a0001c0003t0003g0302a0001c0003t0003g0303others(5): Show | 8 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+4852_255+4854d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47536388 | |||||
| chr17:47536388
|
CT | C | 70 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(67): Show | 70 | HG00140.hp2 HG00280.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.255+4854delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47536388 | |||||
| chr17:47536388
|
CTT | C | 6 | a0001c0001t0001g0028a0001c0001t0003g0061a0001c0001t0003g0066others(3): Show | 6 | HG01346.hp2 HG01517.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+4853_255+4854d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47536388 | |||||
| chr17:47536390
|
T | C | 1 | a0001c0002t0001g0108 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.255+4835T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536390 | ||||||
| chr17:47536391
|
T | C | 29 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0034others(26): Show | 29 | HG00738.hp1 HG01109.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.255+4836T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536391 | ||||||
| chr17:47536392
|
T | C | 2 | a0001c0001t0003g0061a0001c0001t0003g0066 | 2 | HG01346.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.255+4837T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536392 | ||||||
| chr17:47536431
|
T | C | 17 | a0001c0001t0002g0041a0001c0001t0002g0116a0001c0001t0002g0117others(14): Show | 17 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.255+4876T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536431 | ||||||
| chr17:47536461
|
C | T | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+4906C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536461 | ||||||
| chr17:47536462
|
G | A | 1 | a0001c0001t0002g0293 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.255+4907G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536462 | ||||||
| chr17:47536480
|
C | A | 5 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0307others(2): Show | 5 | HG01081.hp2 HG01175.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+4925C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536480 | ||||||
| chr17:47536480
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.255+4925C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536480 | ||||||
| chr17:47536629
|
T | C | 211 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.255+5074T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536629 | ||||||
| chr17:47536673
|
G | T | 13 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.255+5118G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536673 | ||||||
| chr17:47536693
|
G | A | 3 | a0001c0001t0002g0168a0001c0001t0002g0175a0001c0001t0002g0178 | 3 | HG01993.hp2 HG02273.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.255+5138G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536693 | ||||||
| chr17:47536704
|
C | CT | 46 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(43): Show | 46 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.255+5173dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47536704 | |||||
| chr17:47536704
|
C | CTT | 19 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0021others(16): Show | 19 | HG00140.hp2 HG01071.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.255+5172_255+5173d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47536704 | |||||
| chr17:47536704
|
CT | C | 52 | a0001c0001t0001g0081a0001c0001t0001g0239a0001c0001t0001g0283others(49): Show | 52 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.255+5173delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47536704 | |||||
| chr17:47536704
|
CTTTTTTT others(1): Show |
C | 102 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(99): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.255+5166_255+5173d others(10): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47536704 | |||||
| chr17:47536704
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0003g0119 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.255+5163_255+5173d others(13): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47536704 | |||||
| chr17:47536790
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.255+5235C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47536790 | ||||||
| chr17:47537002
|
C | T | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+5447C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537002 | ||||||
| chr17:47537019
|
T | G | 1 | a0001c0001t0002g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.255+5464T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537019 | ||||||
| chr17:47537162
|
G | GA | 50 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(47): Show | 50 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.255+5617dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47537162 | |||||
| chr17:47537283
|
G | A | 1 | a0001c0001t0002g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.255+5728G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537283 | ||||||
| chr17:47537363
|
C | T | 3 | a0001c0004t0003g0059a0001c0004t0003g0060a0001c0004t0003g0080 | 3 | HG01106.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.255+5808C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537363 | ||||||
| chr17:47537397
|
T | A | 211 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.255+5842T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537397 | ||||||
| chr17:47537553
|
C | T | 13 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.255+5998C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537553 | ||||||
| chr17:47537567
|
CCT | C | 32 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0045others(29): Show | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.255+6013_255+6014d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537567 | ||||||
| chr17:47537609
|
CTTGAACT others(21): Show |
C | 1 | a0001c0001t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.255+6058_255+6085d others(30): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47537609 | |||||
| chr17:47537632
|
C | T | 2 | a0001c0001t0005g0207a0001c0001t0005g0208 | 2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.255+6077C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537632 | ||||||
| chr17:47537678
|
G | T | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6123G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537678 | ||||||
| chr17:47537687
|
C | T | 1 | a0001c0001t0007g0338 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.255+6132C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537687 | ||||||
| chr17:47537701
|
T | A | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6146T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537701 | ||||||
| chr17:47537702
|
A | T | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6147A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537702 | ||||||
| chr17:47537710
|
A | G | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6155A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537710 | ||||||
| chr17:47537715
|
A | C | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6160A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537715 | ||||||
| chr17:47537722
|
C | A | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6167C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537722 | ||||||
| chr17:47537723
|
T | C | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6168T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537723 | ||||||
| chr17:47537724
|
A | T | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6169A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537724 | ||||||
| chr17:47537742
|
T | A | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6187T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537742 | ||||||
| chr17:47537748
|
A | C | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6193A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537748 | ||||||
| chr17:47537753
|
T | G | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6198T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537753 | ||||||
| chr17:47537758
|
T | A | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6203T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537758 | ||||||
| chr17:47537766
|
C | A | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6211C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537766 | ||||||
| chr17:47537767
|
T | C | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6212T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537767 | ||||||
| chr17:47537771
|
C | T | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6216C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537771 | ||||||
| chr17:47537776
|
C | T | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6221C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537776 | ||||||
| chr17:47537779
|
C | T | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6224C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537779 | ||||||
| chr17:47537780
|
A | C | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6225A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537780 | ||||||
| chr17:47537782
|
A | T | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6227A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537782 | ||||||
| chr17:47537788
|
G | T | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6233G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537788 | ||||||
| chr17:47537789
|
G | T | 1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.255+6234G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537789 | ||||||
| chr17:47537790
|
T | A | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6235T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537790 | ||||||
| chr17:47537791
|
T | C | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6236T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537791 | ||||||
| chr17:47537795
|
T | C | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6240T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537795 | ||||||
| chr17:47537803
|
T | A | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6248T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537803 | ||||||
| chr17:47537805
|
T | G | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6250T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537805 | ||||||
| chr17:47537806
|
T | A | 50 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(47): Show | 50 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.255+6251T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537806 | ||||||
| chr17:47537809
|
T | A | 1 | a0001c0001t0001g0255 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.255+6254T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537809 | ||||||
| chr17:47537813
|
T | G | 1 | a0001c0003t0003g0305 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.255+6258T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537813 | ||||||
| chr17:47537827
|
T | C | 339 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(336): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.255+6272T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47537827 | ||||||
| chr17:47538119
|
C | G | 40 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(37): Show | 40 | HG00738.hp1 HG01109.hp2 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.255+6564C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47538119 | ||||||
| chr17:47538150
|
G | GCCAAAGT | 4 | a0001c0001t0003g0042a0001c0001t0003g0119a0001c0001t0003g0120others(1): Show | 4 | HG02647.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+6596_255+6602d others(9): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538150 | |||||
| chr17:47538178
|
C | G | 1 | a0001c0001t0002g0215 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.255+6623C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47538178 | ||||||
| chr17:47538202
|
C | CT | 26 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0102others(23): Show | 26 | HG00673.hp1 HG01099.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.255+6670dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTT | 9 | a0001c0001t0002g0031a0001c0001t0002g0089a0001c0001t0002g0096others(6): Show | 9 | NA18942.hp2 NA18946.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.255+6668_255+6670d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTT | 8 | a0001c0001t0002g0151a0001c0001t0002g0197a0001c0001t0002g0294others(5): Show | 8 | HG00735.hp1 HG00738.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.255+6665_255+6670d others(8): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT | 9 | a0001c0001t0002g0168a0001c0001t0002g0198a0001c0001t0002g0199others(6): Show | 9 | HG00099.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+6664_255+6670d others(9): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0002g0090a0001c0001t0005g0001 | 3 | HG01515.hp2 HG01517.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.255+6661_255+6670d others(12): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0002g0160 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.255+6660_255+6670d others(13): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0200 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.255+6659_255+6670d others(14): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(6): Show |
6 | a0001c0001t0002g0215a0001c0001t0002g0217a0001c0001t0004g0126others(3): Show | 6 | HG00544.hp2 HG01123.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+6658_255+6670d others(15): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(7): Show |
12 | a0001c0001t0002g0159a0001c0001t0002g0169a0001c0001t0004g0046others(9): Show | 12 | HG00741.hp1 HG01515.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.255+6657_255+6670d others(16): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(8): Show |
11 | a0001c0001t0002g0178a0001c0001t0003g0098a0001c0001t0003g0158others(8): Show | 11 | HG00438.hp1 HG01993.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+6656_255+6670d others(17): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(9): Show |
8 | a0001c0001t0002g0118a0001c0001t0002g0153a0001c0001t0003g0152others(5): Show | 8 | HG01346.hp1 HG01891.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+6655_255+6670d others(18): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(10): Show |
7 | a0001c0001t0002g0029a0001c0001t0002g0091a0001c0001t0002g0100others(4): Show | 7 | HG00544.hp1 HG01069.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+6654_255+6670d others(19): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(11): Show |
3 | a0001c0001t0002g0097a0001c0001t0002g0161a0001c0001t0003g0121 | 3 | HG01255.hp2 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.255+6653_255+6670d others(20): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG01361.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.255+6652_255+6670d others(21): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0002g0092a0001c0001t0002g0209 | 2 | HG01192.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.255+6651_255+6670d others(22): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(14): Show |
4 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0213others(1): Show | 4 | HG00438.hp2 HG00642.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+6650_255+6670d others(23): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(15): Show |
3 | a0001c0001t0002g0154a0001c0001t0002g0201a0001c0001t0002g0293 | 3 | HG00323.hp1 HG04228.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.255+6649_255+6670d others(24): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(16): Show |
3 | a0001c0001t0002g0122a0001c0001t0002g0172a0001c0001t0003g0042 | 3 | HG03486.hp1 NA18960.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.255+6648_255+6670d others(25): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0002g0220 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.255+6670_255+6671i others(26): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(18): Show |
2 | a0001c0001t0002g0167a0001c0001t0002g0214 | 2 | HG06807.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.255+6670_255+6671i others(27): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(19): Show |
2 | a0001c0001t0002g0170a0001c0001t0002g0290 | 2 | HG04184.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.255+6670_255+6671i others(28): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(20): Show |
2 | a0001c0001t0002g0219a0001c0001t0002g0332 | 2 | NA18981.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.255+6670_255+6671i others(29): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(21): Show |
1 | a0006c0009t0002g0114 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.255+6670_255+6671i others(30): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(22): Show |
4 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0002g0202others(1): Show | 4 | HG02735.hp2 NA18945.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+6670_255+6671i others(31): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(23): Show |
3 | a0001c0001t0002g0216a0001c0001t0002g0296a0001c0001t0002g0331 | 3 | HG00423.hp2 NA18957.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.255+6670_255+6671i others(32): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(24): Show |
2 | a0001c0001t0002g0210a0001c0001t0008g0335 | 2 | HG01243.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.255+6670_255+6671i others(33): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(25): Show |
2 | a0001c0001t0006g0203a0001c0001t0006g0204 | 2 | HG00099.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.255+6670_255+6671i others(34): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(26): Show |
1 | a0001c0001t0002g0295 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.255+6670_255+6671i others(35): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0002g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.255+6670_255+6671i others(36): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(30): Show |
1 | a0001c0001t0002g0003 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.255+6670_255+6671i others(39): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(31): Show |
1 | a0001c0001t0002g0205 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.255+6670_255+6671i others(40): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(32): Show |
2 | a0001c0001t0002g0175a0001c0001t0002g0206 | 2 | HG02273.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.255+6670_255+6671i others(41): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(33): Show |
1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.255+6670_255+6671i others(42): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
C | CTTTTTTT others(49): Show |
1 | a0001c0001t0002g0171 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.255+6670_255+6671i others(58): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
CTTTT | C | 9 | a0001c0001t0003g0002a0001c0001t0003g0099a0001c0001t0003g0156others(6): Show | 10 | HG00558.hp2 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.255+6667_255+6670d others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
CTTTTTT | C | 43 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(40): Show | 43 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.255+6665_255+6670d others(8): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538202
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.255+6660_255+6670d others(13): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538202 | |||||
| chr17:47538283
|
C | T | 76 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0084others(73): Show | 77 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.255+6728C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47538283 | ||||||
| chr17:47538300
|
C | T | 17 | a0001c0001t0002g0041a0001c0001t0002g0116a0001c0001t0002g0117others(14): Show | 17 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.255+6745C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47538300 | ||||||
| chr17:47538333
|
G | C | 1 | a0001c0001t0002g0179 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.255+6778G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47538333 | ||||||
| chr17:47538377
|
G | GA | 4 | a0001c0001t0001g0103a0001c0001t0001g0123a0001c0001t0001g0233others(1): Show | 4 | HG01099.hp2 HG01934.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+6822_255+6823i others(3): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47538377 | ||||||
| chr17:47538458
|
C | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | NA18942.hp1 NA18945.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+6903C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47538458 | ||||||
| chr17:47538497
|
A | AACC | 3 | a0001c0004t0003g0059a0001c0004t0003g0060a0001c0004t0003g0080 | 3 | HG01106.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.255+6946_255+6948d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538497 | |||||
| chr17:47538499
|
C | T | 40 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(37): Show | 40 | HG00738.hp1 HG01109.hp2 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.255+6944C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47538499 | ||||||
| chr17:47538503
|
C | CGCGCCTA others(7): Show |
2 | a0001c0001t0004g0134a0001c0001t0004g0143 | 2 | HG00544.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.255+6949_255+6962d others(16): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538503 | |||||
| chr17:47538526
|
C | CT | 66 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0081others(63): Show | 66 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.255+6991dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47538526 | |||||
| chr17:47538531
|
T | C | 1 | a0001c0001t0001g0010 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.255+6976T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47538531 | ||||||
| chr17:47538577
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.255+7022C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47538577 | ||||||
| chr17:47538578
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.255+7023G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47538578 | ||||||
| chr17:47538638
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.255+7083T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47538638 | ||||||
| chr17:47538966
|
T | C | 116 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(113): Show | 118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.256-6943T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47538966 | ||||||
| chr17:47539064
|
G | A | 12 | a0001c0001t0003g0002a0001c0001t0003g0098a0001c0001t0003g0099others(9): Show | 13 | HG02615.hp1 HG02717.hp2 HG02897.hp1 others(10): Show |
intron_variant | MODIFIER | c.256-6845G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47539064 | ||||||
| chr17:47539100
|
C | CT | 48 | a0001c0001t0001g0027a0001c0001t0001g0081a0001c0001t0003g0034others(45): Show | 48 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.256-6793dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47539100 | |||||
| chr17:47539153
|
T | C | 13 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0092others(10): Show | 13 | HG01192.hp2 HG02083.hp1 HG03491.hp1 others(10): Show |
intron_variant | MODIFIER | c.256-6756T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47539153 | ||||||
| chr17:47539157
|
ACT | A | 65 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0084others(62): Show | 66 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.256-6749_256-6748d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47539157 | |||||
| chr17:47539290
|
G | T | 1 | a0001c0001t0004g0140 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.256-6619G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47539290 | ||||||
| chr17:47539420
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.256-6489T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47539420 | ||||||
| chr17:47539429
|
A | G | 50 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(47): Show | 50 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.256-6480A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47539429 | ||||||
| chr17:47539498
|
C | A | 1 | a0001c0002t0003g0266 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.256-6411C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47539498 | ||||||
| chr17:47539518
|
A | C | 1 | a0001c0003t0003g0309 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.256-6391A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47539518 | ||||||
| chr17:47539528
|
TG | T | 210 | a0001c0001t0001g0081a0001c0001t0001g0283a0001c0001t0002g0003others(207): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.256-6373delG | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47539528 | |||||
| chr17:47539529
|
G | T | 1 | a0001c0001t0002g0199 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.256-6380G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47539529 | ||||||
| chr17:47540139
|
T | G | 67 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0084others(64): Show | 68 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.256-5770T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47540139 | ||||||
| chr17:47540250
|
A | T | 1 | a0001c0001t0002g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.256-5659A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47540250 | ||||||
| chr17:47540754
|
G | C | 6 | a0001c0001t0003g0098a0001c0001t0003g0152a0001c0001t0003g0158others(3): Show | 6 | HG02897.hp1 HG02922.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.256-5155G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47540754 | ||||||
| chr17:47541235
|
G | T | 1 | a0001c0001t0002g0193 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.256-4674G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47541235 | ||||||
| chr17:47541437
|
C | T | 1 | a0001c0001t0003g0119 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.256-4472C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47541437 | ||||||
| chr17:47541446
|
G | A | 148 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(145): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.256-4463G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47541446 | ||||||
| chr17:47541814
|
A | G | 1 | a0001c0001t0003g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.256-4095A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47541814 | ||||||
| chr17:47541889
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.256-4020G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47541889 | ||||||
| chr17:47542073
|
T | C | 1 | a0001c0001t0002g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.256-3836T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47542073 | ||||||
| chr17:47542075
|
G | A | 2 | a0001c0001t0002g0100a0001c0001t0002g0228 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.256-3834G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47542075 | ||||||
| chr17:47542208
|
G | A | 1 | a0001c0001t0007g0338 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.256-3701G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47542208 | ||||||
| chr17:47542227
|
C | G | 1 | a0001c0001t0004g0045 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.256-3682C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47542227 | ||||||
| chr17:47542337
|
G | A | 5 | a0001c0002t0001g0107a0001c0002t0001g0108a0001c0002t0001g0240others(2): Show | 5 | NA18962.hp2 NA18977.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-3572G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47542337 | ||||||
| chr17:47542423
|
G | A | 1 | a0005c0008t0003g0050 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.256-3486G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47542423 | ||||||
| chr17:47542487
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.256-3422G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47542487 | ||||||
| chr17:47542546
|
C | CA | 9 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0112others(6): Show | 9 | HG01175.hp1 HG01192.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.256-3339dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47542546 | |||||
| chr17:47542546
|
CA | C | 196 | a0001c0001t0001g0016a0001c0001t0001g0081a0001c0001t0001g0263others(193): Show | 198 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.256-3339delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47542546 | |||||
| chr17:47542546
|
CAA | C | 8 | a0001c0001t0002g0086a0001c0001t0002g0166a0001c0001t0002g0167others(5): Show | 8 | HG00099.hp1 HG01256.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.256-3340_256-3339d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47542546 | |||||
| chr17:47542671
|
G | T | 6 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0242others(3): Show | 6 | NA18941.hp1 NA18971.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-3238G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47542671 | ||||||
| chr17:47542883
|
A | G | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.256-3026A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47542883 | ||||||
| chr17:47543062
|
A | G | 1 | a0001c0002t0001g0249 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.256-2847A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543062 | ||||||
| chr17:47543067
|
A | G | 1 | a0001c0002t0001g0249 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.256-2842A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543067 | ||||||
| chr17:47543068
|
T | C | 1 | a0001c0002t0001g0249 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.256-2841T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543068 | ||||||
| chr17:47543069
|
G | A | 1 | a0001c0002t0001g0249 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.256-2840G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543069 | ||||||
| chr17:47543072
|
G | A | 1 | a0001c0002t0001g0249 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.256-2837G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543072 | ||||||
| chr17:47543091
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.256-2818C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543091 | ||||||
| chr17:47543123
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.256-2786G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543123 | ||||||
| chr17:47543131
|
G | A | 2 | a0001c0001t0001g0316a0001c0001t0001g0325 | 2 | HG01433.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.256-2778G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543131 | ||||||
| chr17:47543145
|
C | CA | 9 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0002g0041others(6): Show | 9 | HG01433.hp1 HG02148.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.256-2746dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47543145 | |||||
| chr17:47543199
|
A | G | 1 | a0001c0001t0007g0338 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.256-2710A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543199 | ||||||
| chr17:47543218
|
G | A | 5 | a0001c0001t0003g0002a0001c0001t0003g0099a0001c0001t0003g0156others(2): Show | 6 | HG02615.hp1 HG02717.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.256-2691G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543218 | ||||||
| chr17:47543282
|
C | A | 2 | a0001c0001t0003g0035a0001c0001t0003g0049 | 2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.256-2627C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543282 | ||||||
| chr17:47543313
|
A | AT | 208 | a0001c0001t0001g0081a0001c0001t0001g0314a0001c0001t0002g0003others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.256-2582dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47543313 | |||||
| chr17:47543328
|
A | T | 2 | a0001c0001t0006g0203a0001c0001t0006g0204 | 2 | HG00099.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.256-2581A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543328 | ||||||
| chr17:47543375
|
A | G | 2 | a0001c0001t0001g0322a0001c0001t0001g0324 | 2 | HG01123.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.256-2534A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543375 | ||||||
| chr17:47543483
|
A | AT | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(39): Show | 43 | HG00423.hp1 HG00544.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.256-2403dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47543483 | |||||
| chr17:47543483
|
A | ATT | 31 | a0001c0001t0002g0069a0001c0001t0002g0096a0001c0001t0003g0036others(28): Show | 31 | HG00738.hp1 HG01106.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.256-2404_256-2403d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47543483 | |||||
| chr17:47543483
|
A | ATTT | 15 | a0001c0001t0001g0081a0001c0001t0003g0033a0001c0001t0003g0034others(12): Show | 15 | HG01109.hp2 HG01358.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.256-2405_256-2403d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47543483 | |||||
| chr17:47543558
|
C | T | 47 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0002g0337others(44): Show | 47 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.256-2351C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543558 | ||||||
| chr17:47543640
|
A | G | 1 | a0001c0001t0001g0015 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.256-2269A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543640 | ||||||
| chr17:47543870
|
AGTTT | A | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(17): Show | 20 | HG00323.hp2 HG00642.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.256-2018_256-2015d others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47543870 | |||||
| chr17:47543891
|
GTTTA | G | 97 | a0001c0001t0002g0041a0001c0001t0002g0084a0001c0001t0002g0087others(94): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.256-2002_256-1999d others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47543891 | |||||
| chr17:47543891
|
GTTTATTT others(1): Show |
G | 35 | a0001c0001t0002g0029a0001c0001t0002g0117a0001c0001t0002g0118others(32): Show | 35 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.256-2006_256-1999d others(10): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47543891 | |||||
| chr17:47543891
|
GTTTATTT others(5): Show |
G | 26 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0085others(23): Show | 26 | HG01192.hp2 HG02083.hp1 HG02165.hp2 others(23): Show |
intron_variant | MODIFIER | c.256-2010_256-1999d others(14): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47543891 | |||||
| chr17:47543895
|
A | G | 3 | a0001c0001t0002g0210a0001c0001t0002g0227a0001c0006t0003g0339 | 3 | HG02735.hp2 HG03239.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.256-2014A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543895 | ||||||
| chr17:47543899
|
A | G | 100 | a0001c0001t0002g0041a0001c0001t0002g0084a0001c0001t0002g0087others(97): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.256-2010A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543899 | ||||||
| chr17:47543903
|
A | G | 123 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0084others(120): Show | 125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.256-2006A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543903 | ||||||
| chr17:47543964
|
C | T | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-1945C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47543964 | ||||||
| chr17:47544155
|
A | C | 4 | a0001c0001t0003g0042a0001c0001t0003g0119a0001c0001t0003g0120others(1): Show | 4 | HG02647.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.256-1754A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47544155 | ||||||
| chr17:47544354
|
A | G | 1 | a0001c0001t0002g0175 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.256-1555A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47544354 | ||||||
| chr17:47544356
|
A | T | 1 | a0001c0001t0001g0237 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.256-1553A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47544356 | ||||||
| chr17:47544451
|
G | T | 4 | a0001c0001t0003g0042a0001c0001t0003g0119a0001c0001t0003g0120others(1): Show | 4 | HG02647.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.256-1458G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47544451 | ||||||
| chr17:47544502
|
G | GTATT | 22 | a0001c0001t0001g0011a0001c0001t0001g0229a0001c0001t0001g0242others(19): Show | 22 | HG00280.hp2 HG00423.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.256-1361_256-1358d others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47544502 | |||||
| chr17:47544502
|
GTATT | G | 68 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(65): Show | 68 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.256-1361_256-1358d others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47544502 | |||||
| chr17:47544502
|
GTATTTAT others(1): Show |
G | 116 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0041others(113): Show | 118 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.256-1365_256-1358d others(10): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47544502 | |||||
| chr17:47544502
|
GTATTTAT others(5): Show |
G | 5 | a0001c0001t0002g0029a0001c0001t0002g0206a0001c0001t0002g0215others(2): Show | 5 | HG01123.hp2 HG01346.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-1369_256-1358d others(14): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47544502 | |||||
| chr17:47544502
|
GTATTTAT others(9): Show |
G | 12 | a0001c0001t0002g0154a0001c0001t0002g0213a0001c0001t0003g0077others(9): Show | 12 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.256-1373_256-1358d others(18): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47544502 | |||||
| chr17:47544596
|
G | C | 1 | a0001c0001t0004g0129 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.256-1313G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47544596 | ||||||
| chr17:47544614
|
A | G | 4 | a0001c0001t0002g0177a0001c0001t0002g0187a0001c0001t0002g0192others(1): Show | 4 | HG01106.hp2 HG01496.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.256-1295A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47544614 | ||||||
| chr17:47544711
|
C | CT | 118 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0111others(115): Show | 119 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.256-1178dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 47544711 | |||||
| chr17:47544724
|
T | A | 1 | a0001c0001t0001g0237 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.256-1185T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47544724 | ||||||
| chr17:47544737
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.256-1172G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47544737 | ||||||
| chr17:47544776
|
C | T | 7 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0003g0055others(4): Show | 7 | HG00738.hp1 HG01109.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.256-1133C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47544776 | ||||||
| chr17:47544905
|
A | G | 1 | a0001c0004t0003g0059 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.256-1004A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47544905 | ||||||
| chr17:47544953
|
C | T | 4 | a0001c0001t0003g0042a0001c0001t0003g0119a0001c0001t0003g0120others(1): Show | 4 | HG02647.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.256-956C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47544953 | ||||||
| chr17:47545048
|
C | T | 148 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(145): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.256-861C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47545048 | ||||||
| chr17:47545194
|
A | G | 1 | a0001c0001t0003g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.256-715A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47545194 | ||||||
| chr17:47545195
|
C | T | 1 | a0001c0001t0007g0338 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.256-714C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47545195 | ||||||
| chr17:47545324
|
G | A | 1 | a0001c0001t0002g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.256-585G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47545324 | ||||||
| chr17:47545350
|
A | T | 1 | a0001c0001t0001g0242 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.256-559A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47545350 | ||||||
| chr17:47545539
|
C | G | 1 | a0001c0001t0002g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.256-370C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47545539 | ||||||
| chr17:47545541
|
A | G | 1 | a0001c0002t0003g0266 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.256-368A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47545541 | ||||||
| chr17:47545571
|
C | T | 8 | a0001c0002t0001g0104a0001c0002t0001g0236a0001c0002t0001g0241others(5): Show | 8 | NA18943.hp2 NA18988.hp2 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.256-338C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47545571 | ||||||
| chr17:47545696
|
A | C | 1 | a0004c0007t0001g0248 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.256-213A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47545696 | ||||||
| chr17:47545746
|
G | A | 1 | a0001c0001t0010g0186 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.256-163G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47545746 | ||||||
| chr17:47545796
|
C | T | 4 | a0001c0001t0003g0042a0001c0001t0003g0119a0001c0001t0003g0120others(1): Show | 4 | HG02647.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.256-113C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 1/22 | chr17 | 47545796 | ||||||
| chr17:47546043
|
G | GGTGT | 107 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.340+78_340+81dupTG others(2): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546043 | |||||
| chr17:47546043
|
G | GGTGTGT | 18 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0017others(15): Show | 18 | HG01099.hp2 HG01106.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.340+76_340+81dupTG others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546043 | |||||
| chr17:47546043
|
G | GGTGTGTG others(1): Show |
27 | a0001c0001t0001g0251a0001c0001t0002g0069a0001c0001t0002g0231others(24): Show | 27 | HG00738.hp1 HG01109.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.340+74_340+81dupTG others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546043 | |||||
| chr17:47546043
|
G | GGTGTGTG others(3): Show |
5 | a0001c0001t0001g0239a0001c0001t0001g0268a0001c0001t0003g0040others(2): Show | 5 | HG01993.hp1 HG03130.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+72_340+81dupTG others(8): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546043 | |||||
| chr17:47546043
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0002g0238 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.340+70_340+81dupTG others(10): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546043 | |||||
| chr17:47546043
|
G | GGTGTGTG others(7): Show |
1 | a0001c0001t0003g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.340+68_340+81dupTG others(12): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546043 | |||||
| chr17:47546043
|
G | T | 1 | a0001c0001t0002g0029 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.340+50G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47546043 | ||||||
| chr17:47546043
|
GGTGTGTG others(13): Show |
G | 1 | a0001c0001t0001g0230 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.340+62_340+81delTG others(18): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546043 | |||||
| chr17:47546045
|
T | G | 3 | a0001c0001t0002g0150a0001c0001t0005g0001a0001c0001t0005g0291 | 4 | HG01515.hp2 HG01517.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+52T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47546045 | ||||||
| chr17:47546073
|
T | A | 1 | a0001c0001t0001g0237 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.340+80T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47546073 | ||||||
| chr17:47546073
|
T | TGAGAGA | 5 | a0001c0001t0002g0162a0001c0001t0002g0176a0001c0001t0002g0214others(2): Show | 5 | HG00323.hp1 HG04204.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+95_340+100dupG others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546073 | |||||
| chr17:47546073
|
T | TGAGAGAG others(1): Show |
12 | a0001c0001t0002g0084a0001c0001t0003g0002a0001c0001t0003g0098others(9): Show | 13 | HG02615.hp1 HG02717.hp2 HG02897.hp1 others(10): Show |
intron_variant | MODIFIER | c.340+93_340+100dupG others(7): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546073 | |||||
| chr17:47546073
|
T | TGTGA | 6 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0280others(3): Show | 6 | HG01169.hp2 HG01433.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.340+81_340+82insTG others(2): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546073 | |||||
| chr17:47546073
|
T | TGTGAGA | 10 | a0001c0001t0002g0182a0001c0003t0003g0300a0001c0003t0003g0301others(7): Show | 10 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+81_340+82insTG others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546073 | |||||
| chr17:47546073
|
T | TGTGAGAG others(1): Show |
69 | a0001c0001t0002g0003a0001c0001t0002g0041a0001c0001t0002g0087others(66): Show | 70 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.340+81_340+82insTG others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546073 | |||||
| chr17:47546073
|
T | TGTGAGAG others(3): Show |
3 | a0001c0001t0003g0152a0001c0001t0005g0207a0001c0001t0005g0208 | 3 | HG03017.hp1 HG03516.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.340+81_340+82insTG others(8): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546073 | |||||
| chr17:47546073
|
T | TGTGTGA | 5 | a0001c0001t0003g0042a0001c0001t0003g0119a0001c0001t0003g0120others(2): Show | 5 | HG02647.hp1 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+81_340+82insTG others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546073 | |||||
| chr17:47546073
|
T | TGTGTGAG others(1): Show |
6 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0180others(3): Show | 6 | HG03491.hp1 HG03492.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+81_340+82insTG others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546073 | |||||
| chr17:47546073
|
T | TGTGTGAG others(3): Show |
17 | a0001c0001t0002g0029a0001c0001t0002g0031a0001c0001t0002g0091others(14): Show | 17 | HG00544.hp1 HG02273.hp2 HG02735.hp2 others(14): Show |
intron_variant | MODIFIER | c.340+81_340+82insTG others(8): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546073 | |||||
| chr17:47546073
|
T | TGTGTGTG others(1): Show |
4 | a0001c0001t0003g0039a0001c0001t0003g0051a0001c0001t0003g0076others(1): Show | 4 | NA18985.hp2 NA18998.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+81_340+82insTG others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546073 | |||||
| chr17:47546073
|
T | TGTGTGTG others(3): Show |
2 | a0001c0001t0002g0092a0001c0001t0002g0118 | 2 | HG01192.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.340+81_340+82insTG others(8): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546073 | |||||
| chr17:47546073
|
T | TGTGTGTG others(5): Show |
27 | a0001c0001t0002g0089a0001c0001t0002g0117a0001c0001t0002g0198others(24): Show | 27 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.340+81_340+82insTG others(10): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546073 | |||||
| chr17:47546073
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0004g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.340+81_340+82insTG others(12): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546073 | |||||
| chr17:47546073
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0002g0181 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.340+81_340+82insTG others(12): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47546073 | |||||
| chr17:47546075
|
A | T | 4 | a0001c0001t0001g0245a0001c0001t0001g0334a0001c0001t0003g0078others(1): Show | 4 | HG01891.hp2 HG02523.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+82A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47546075 | ||||||
| chr17:47546076
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.340+83G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47546076 | ||||||
| chr17:47546367
|
A | C | 1 | a0001c0001t0002g0206 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.340+374A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47546367 | ||||||
| chr17:47546379
|
T | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0265 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.340+386T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47546379 | ||||||
| chr17:47546382
|
C | T | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.340+389C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47546382 | ||||||
| chr17:47546515
|
A | C | 1 | a0001c0001t0001g0237 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.340+522A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47546515 | ||||||
| chr17:47546557
|
G | A | 1 | a0001c0001t0001g0330 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.340+564G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47546557 | ||||||
| chr17:47546613
|
A | C | 4 | a0001c0001t0003g0042a0001c0001t0003g0119a0001c0001t0003g0120others(1): Show | 4 | HG02647.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+620A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47546613 | ||||||
| chr17:47546991
|
G | C | 1 | a0001c0001t0001g0243 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.340+998G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47546991 | ||||||
| chr17:47547361
|
T | G | 1 | a0001c0001t0002g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.340+1368T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47547361 | ||||||
| chr17:47547391
|
G | A | 1 | a0001c0001t0001g0298 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.340+1398G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47547391 | ||||||
| chr17:47547440
|
G | C | 1 | a0001c0001t0011g0285 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.340+1447G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47547440 | ||||||
| chr17:47547547
|
G | C | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.340+1554G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47547547 | ||||||
| chr17:47547744
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.340+1751C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47547744 | ||||||
| chr17:47547883
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.340+1890G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47547883 | ||||||
| chr17:47548024
|
T | A | 6 | a0001c0001t0003g0033a0001c0001t0003g0035a0001c0001t0003g0047others(3): Show | 6 | HG01358.hp2 HG01993.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+2031T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47548024 | ||||||
| chr17:47548033
|
T | A | 1 | a0001c0001t0001g0330 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.340+2040T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47548033 | ||||||
| chr17:47548447
|
T | C | 5 | a0001c0002t0001g0107a0001c0002t0001g0108a0001c0002t0001g0240others(2): Show | 5 | NA18962.hp2 NA18977.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+2454T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47548447 | ||||||
| chr17:47548590
|
CT | C | 39 | a0001c0001t0001g0261a0001c0001t0001g0274a0001c0001t0002g0029others(36): Show | 39 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.340+2618delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47548590 | |||||
| chr17:47548590
|
CTT | C | 171 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0031others(168): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.340+2617_340+2618d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47548590 | |||||
| chr17:47548626
|
C | T | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.340+2633C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47548626 | ||||||
| chr17:47548632
|
C | T | 1 | a0001c0001t0003g0120 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.340+2639C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47548632 | ||||||
| chr17:47548636
|
A | C | 211 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.340+2643A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47548636 | ||||||
| chr17:47548645
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.340+2652C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47548645 | ||||||
| chr17:47548681
|
ATTC | A | 4 | a0001c0001t0002g0177a0001c0001t0002g0187a0001c0001t0002g0192others(1): Show | 4 | HG01106.hp2 HG01496.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+2693_340+2695d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47548681 | |||||
| chr17:47548862
|
A | G | 1 | a0001c0002t0001g0108 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.340+2869A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47548862 | ||||||
| chr17:47548916
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027 | 3 | HG00280.hp2 HG01175.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.340+2923G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47548916 | ||||||
| chr17:47548938
|
C | T | 1 | a0001c0001t0004g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.340+2945C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47548938 | ||||||
| chr17:47549029
|
G | A | 217 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.340+3036G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47549029 | ||||||
| chr17:47549126
|
T | G | 3 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0004g0131 | 3 | HG01346.hp1 HG01891.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.340+3133T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47549126 | ||||||
| chr17:47549180
|
T | G | 1 | a0001c0001t0001g0109 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.340+3187T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47549180 | ||||||
| chr17:47549555
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.340+3562G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47549555 | ||||||
| chr17:47549595
|
C | T | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.340+3602C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47549595 | ||||||
| chr17:47549639
|
G | A | 16 | a0001c0001t0001g0244a0001c0001t0001g0274a0001c0001t0001g0297others(13): Show | 16 | NA18943.hp2 NA18946.hp2 NA18962.hp2 others(13): Show |
intron_variant | MODIFIER | c.340+3646G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47549639 | ||||||
| chr17:47549706
|
A | G | 339 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(336): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.340+3713A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47549706 | ||||||
| chr17:47549736
|
G | A | 2 | a0001c0003t0003g0302a0001c0003t0003g0303 | 2 | HG00735.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.340+3743G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47549736 | ||||||
| chr17:47549780
|
C | CA | 36 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0103others(33): Show | 36 | HG00735.hp1 HG00741.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.340+3809dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47549780 | |||||
| chr17:47549883
|
A | G | 1 | a0001c0001t0004g0143 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.340+3890A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47549883 | ||||||
| chr17:47549932
|
AT | A | 37 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0176others(34): Show | 37 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.340+3953delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47549932 | |||||
| chr17:47550035
|
C | T | 2 | a0001c0001t0003g0120a0001c0001t0003g0121 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.340+4042C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47550035 | ||||||
| chr17:47550070
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.340+4077G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47550070 | ||||||
| chr17:47550125
|
A | G | 7 | a0001c0001t0004g0046a0001c0001t0004g0132a0001c0001t0004g0135others(4): Show | 7 | NA18612.hp1 NA18964.hp1 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.340+4132A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47550125 | ||||||
| chr17:47550127
|
G | A | 7 | a0001c0001t0004g0046a0001c0001t0004g0132a0001c0001t0004g0135others(4): Show | 7 | NA18612.hp1 NA18964.hp1 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.340+4134G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47550127 | ||||||
| chr17:47550306
|
G | A | 336 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(333): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.340+4313G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47550306 | ||||||
| chr17:47550327
|
G | C | 165 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.340+4334G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47550327 | ||||||
| chr17:47550329
|
G | GT | 38 | a0001c0001t0001g0282a0001c0001t0002g0117a0001c0001t0002g0118others(35): Show | 38 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.340+4352dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47550329 | |||||
| chr17:47550351
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.340+4358G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47550351 | ||||||
| chr17:47550394
|
G | A | 165 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.340+4401G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47550394 | ||||||
| chr17:47550436
|
G | T | 5 | a0001c0001t0002g0191a0001c0001t0003g0042a0001c0001t0003g0119others(2): Show | 5 | HG02015.hp2 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+4443G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47550436 | ||||||
| chr17:47550631
|
AT | A | 193 | a0001c0001t0001g0081a0001c0001t0001g0317a0001c0001t0001g0319others(190): Show | 195 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.340+4653delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47550631 | |||||
| chr17:47550749
|
C | T | 4 | a0001c0001t0001g0115a0001c0001t0001g0277a0001c0001t0001g0282others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+4756C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47550749 | ||||||
| chr17:47550791
|
T | G | 2 | a0001c0001t0002g0100a0001c0001t0002g0228 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.340+4798T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47550791 | ||||||
| chr17:47550812
|
A | T | 1 | a0001c0001t0002g0093 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.340+4819A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47550812 | ||||||
| chr17:47550878
|
C | T | 1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.340+4885C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47550878 | ||||||
| chr17:47550882
|
C | T | 3 | a0001c0001t0002g0100a0001c0001t0002g0228a0001c0001t0007g0338 | 3 | HG02451.hp1 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.340+4889C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47550882 | ||||||
| chr17:47551101
|
A | G | 1 | a0001c0002t0001g0249 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.340+5108A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47551101 | ||||||
| chr17:47551104
|
T | C | 1 | a0001c0001t0004g0142 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.340+5111T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47551104 | ||||||
| chr17:47551327
|
A | T | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.340+5334A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47551327 | ||||||
| chr17:47551482
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.340+5489T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47551482 | ||||||
| chr17:47551700
|
C | T | 1 | a0001c0001t0002g0197 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.340+5707C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47551700 | ||||||
| chr17:47551701
|
A | G | 217 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.340+5708A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47551701 | ||||||
| chr17:47551723
|
G | C | 1 | a0001c0001t0002g0184 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.340+5730G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47551723 | ||||||
| chr17:47551915
|
G | T | 1 | a0001c0002t0001g0249 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.340+5922G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47551915 | ||||||
| chr17:47551916
|
A | G | 1 | a0001c0002t0001g0249 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.340+5923A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47551916 | ||||||
| chr17:47551966
|
C | CT | 90 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(87): Show | 91 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.340+5987dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47551966 | |||||
| chr17:47551966
|
C | CTT | 12 | a0001c0001t0002g0041a0001c0001t0002g0090a0001c0001t0002g0091others(9): Show | 12 | HG00544.hp1 HG00558.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.340+5986_340+5987d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47551966 | |||||
| chr17:47551980
|
TC | T | 10 | a0001c0001t0003g0002a0001c0001t0003g0042a0001c0001t0003g0099others(7): Show | 11 | HG01169.hp1 HG02615.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.340+5988delC | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47551980 | ||||||
| chr17:47551981
|
C | T | 153 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.340+5988C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47551981 | ||||||
| chr17:47552040
|
G | A | 217 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.340+6047G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47552040 | ||||||
| chr17:47552278
|
A | G | 1 | a0001c0001t0003g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.340+6285A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47552278 | ||||||
| chr17:47552306
|
T | C | 6 | a0001c0001t0001g0312a0001c0001t0001g0316a0001c0001t0001g0318others(3): Show | 6 | HG01074.hp2 HG01109.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+6313T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47552306 | ||||||
| chr17:47552342
|
C | G | 48 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(45): Show | 48 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.340+6349C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47552342 | ||||||
| chr17:47552450
|
T | G | 1 | a0001c0001t0002g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.340+6457T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47552450 | ||||||
| chr17:47552622
|
G | A | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.340+6629G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47552622 | ||||||
| chr17:47552686
|
G | A | 1 | a0001c0001t0004g0133 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.340+6693G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47552686 | ||||||
| chr17:47552748
|
T | G | 1 | a0004c0007t0001g0248 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.340+6755T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47552748 | ||||||
| chr17:47553054
|
A | G | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.340+7061A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47553054 | ||||||
| chr17:47553088
|
T | C | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.340+7095T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47553088 | ||||||
| chr17:47553131
|
C | T | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.340+7138C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47553131 | ||||||
| chr17:47553188
|
G | A | 2 | a0001c0001t0002g0100a0001c0001t0002g0228 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.340+7195G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47553188 | ||||||
| chr17:47553329
|
C | T | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.340+7336C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47553329 | ||||||
| chr17:47553404
|
T | G | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.340+7411T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47553404 | ||||||
| chr17:47553417
|
G | C | 3 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163 | 3 | HG01255.hp2 HG01361.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.340+7424G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47553417 | ||||||
| chr17:47553560
|
A | T | 1 | a0001c0001t0004g0138 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.340+7567A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47553560 | ||||||
| chr17:47553759
|
C | CT | 15 | a0001c0002t0001g0107a0001c0002t0001g0236a0001c0003t0003g0300others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.340+7780dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47553759 | |||||
| chr17:47553761
|
T | C | 3 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0298 | 3 | HG02165.hp1 NA19062.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.340+7768T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47553761 | ||||||
| chr17:47553951
|
C | T | 7 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0169others(4): Show | 7 | HG00544.hp1 HG00558.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+7958C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47553951 | ||||||
| chr17:47554044
|
CT | C | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.340+8064delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47554044 | |||||
| chr17:47554091
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.340+8098A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47554091 | ||||||
| chr17:47554190
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG00423.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.340+8197G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47554190 | ||||||
| chr17:47554206
|
A | G | 1 | a0001c0001t0004g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.340+8213A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47554206 | ||||||
| chr17:47554371
|
T | A | 1 | a0001c0001t0002g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.340+8378T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47554371 | ||||||
| chr17:47554415
|
G | A | 13 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.340+8422G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47554415 | ||||||
| chr17:47554456
|
G | A | 1 | a0001c0001t0005g0291 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.340+8463G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47554456 | ||||||
| chr17:47554597
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.340+8604C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47554597 | ||||||
| chr17:47554598
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.340+8605G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47554598 | ||||||
| chr17:47554692
|
C | T | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.340+8699C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47554692 | ||||||
| chr17:47554717
|
G | A | 2 | a0001c0001t0003g0077a0001c0001t0003g0079 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.340+8724G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47554717 | ||||||
| chr17:47554748
|
A | G | 1 | a0001c0001t0002g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.340+8755A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47554748 | ||||||
| chr17:47555008
|
C | A | 6 | a0001c0001t0003g0098a0001c0001t0003g0152a0001c0001t0003g0158others(3): Show | 6 | HG02897.hp1 HG02922.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+9015C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47555008 | ||||||
| chr17:47555062
|
G | A | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.340+9069G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47555062 | ||||||
| chr17:47555273
|
A | C | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.340+9280A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47555273 | ||||||
| chr17:47555347
|
C | CT | 43 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0027others(40): Show | 43 | HG00280.hp2 HG00738.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.340+9371dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47555347 | |||||
| chr17:47555347
|
CT | C | 163 | a0001c0001t0001g0274a0001c0001t0001g0329a0001c0001t0002g0003others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.340+9371delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47555347 | |||||
| chr17:47555502
|
C | A | 4 | a0001c0001t0002g0089a0001c0001t0002g0096a0001c0001t0002g0184others(1): Show | 4 | NA18942.hp2 NA18946.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+9509C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47555502 | ||||||
| chr17:47555560
|
T | G | 1 | a0001c0001t0007g0338 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.340+9567T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47555560 | ||||||
| chr17:47555566
|
C | T | 1 | a0001c0001t0004g0129 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.340+9573C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47555566 | ||||||
| chr17:47555589
|
T | C | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.340+9596T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47555589 | ||||||
| chr17:47555607
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.340+9614G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47555607 | ||||||
| chr17:47555642
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.340+9649C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47555642 | ||||||
| chr17:47555643
|
G | C | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.340+9650G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47555643 | ||||||
| chr17:47555680
|
G | T | 12 | a0001c0001t0003g0002a0001c0001t0003g0098a0001c0001t0003g0099others(9): Show | 13 | HG02615.hp1 HG02717.hp2 HG02897.hp1 others(10): Show |
intron_variant | MODIFIER | c.340+9687G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47555680 | ||||||
| chr17:47555981
|
C | CT | 9 | a0001c0001t0001g0081a0001c0001t0001g0102a0001c0001t0002g0238others(6): Show | 9 | HG01346.hp1 HG03486.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+10010dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47555981 | |||||
| chr17:47555981
|
CT | C | 22 | a0001c0001t0001g0016a0001c0001t0001g0235a0001c0001t0001g0278others(19): Show | 23 | HG01169.hp2 HG01884.hp2 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.340+10010delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47555981 | |||||
| chr17:47556073
|
CT | C | 64 | a0001c0001t0001g0081a0001c0001t0001g0247a0001c0001t0001g0258others(61): Show | 64 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.340+10101delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47556073 | |||||
| chr17:47556119
|
T | C | 211 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.340+10126T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47556119 | ||||||
| chr17:47556302
|
T | G | 1 | a0001c0001t0004g0138 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.340+10309T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47556302 | ||||||
| chr17:47556578
|
T | C | 1 | a0001c0001t0004g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.340+10585T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47556578 | ||||||
| chr17:47556609
|
C | CG | 11 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0102others(8): Show | 11 | HG01106.hp2 HG01109.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.340+10620dupG | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47556609 | |||||
| chr17:47556639
|
A | G | 5 | a0001c0001t0003g0002a0001c0001t0003g0099a0001c0001t0003g0156others(2): Show | 6 | HG02615.hp1 HG02717.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+10646A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47556639 | ||||||
| chr17:47556647
|
G | A | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.340+10654G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47556647 | ||||||
| chr17:47556668
|
T | C | 211 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.340+10675T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47556668 | ||||||
| chr17:47556717
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.340+10724C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47556717 | ||||||
| chr17:47556733
|
G | C | 4 | a0001c0001t0001g0245a0001c0001t0001g0247a0001c0001t0001g0265others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+10740G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47556733 | ||||||
| chr17:47556772
|
T | C | 1 | a0001c0006t0003g0340 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.340+10779T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47556772 | ||||||
| chr17:47556831
|
A | G | 3 | a0001c0004t0003g0059a0001c0004t0003g0060a0001c0004t0003g0080 | 3 | HG01106.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.340+10838A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47556831 | ||||||
| chr17:47557317
|
A | G | 1 | a0001c0001t0003g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.340+11324A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47557317 | ||||||
| chr17:47557324
|
C | T | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.340+11331C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47557324 | ||||||
| chr17:47557392
|
A | G | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.340+11399A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47557392 | ||||||
| chr17:47557416
|
TGGTCCCA others(495): Show |
T | 18 | a0001c0001t0002g0029a0001c0001t0002g0093a0001c0001t0002g0097others(15): Show | 18 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.340+11424_341-1149 others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47557416 | ||||||
| chr17:47557516
|
A | G | 1 | a0001c0001t0004g0044 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.340+11523A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47557516 | ||||||
| chr17:47557722
|
T | C | 1 | a0001c0001t0003g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.341-11695T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47557722 | ||||||
| chr17:47557764
|
T | C | 1 | a0001c0001t0002g0194 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.341-11653T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47557764 | ||||||
| chr17:47557856
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.341-11561A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47557856 | ||||||
| chr17:47557873
|
C | T | 143 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0041others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.341-11544C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47557873 | ||||||
| chr17:47557936
|
G | GT | 14 | a0001c0001t0001g0005a0001c0001t0001g0261a0001c0001t0001g0314others(11): Show | 14 | HG00280.hp1 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.341-11466dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47557936 | |||||
| chr17:47557959
|
C | T | 1 | a0001c0001t0003g0147 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.341-11458C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47557959 | ||||||
| chr17:47558015
|
C | T | 32 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0045others(29): Show | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.341-11402C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47558015 | ||||||
| chr17:47558020
|
G | A | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.341-11397G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47558020 | ||||||
| chr17:47558169
|
C | G | 1 | a0001c0001t0002g0227 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.341-11248C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47558169 | ||||||
| chr17:47558207
|
A | G | 1 | a0001c0001t0003g0147 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.341-11210A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47558207 | ||||||
| chr17:47558373
|
C | T | 1 | a0001c0003t0003g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.341-11044C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47558373 | ||||||
| chr17:47558419
|
C | T | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.341-10998C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47558419 | ||||||
| chr17:47558437
|
C | G | 1 | a0001c0001t0002g0231 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.341-10980C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47558437 | ||||||
| chr17:47558506
|
T | C | 1 | a0001c0001t0003g0119 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.341-10911T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47558506 | ||||||
| chr17:47558574
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.341-10843C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47558574 | ||||||
| chr17:47558587
|
G | A | 1 | a0001c0001t0002g0087 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.341-10830G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47558587 | ||||||
| chr17:47558596
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.341-10821A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47558596 | ||||||
| chr17:47558774
|
C | T | 2 | a0001c0001t0001g0277a0003c0010t0001g0110 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.341-10643C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47558774 | ||||||
| chr17:47558902
|
C | T | 1 | a0001c0001t0004g0128 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.341-10515C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47558902 | ||||||
| chr17:47558943
|
A | C | 1 | a0001c0001t0002g0231 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.341-10474A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47558943 | ||||||
| chr17:47559037
|
C | G | 1 | a0001c0001t0002g0228 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.341-10380C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47559037 | ||||||
| chr17:47559047
|
GA | G | 81 | a0001c0001t0001g0081a0001c0001t0001g0245a0001c0001t0002g0069others(78): Show | 81 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.341-10354delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47559047 | |||||
| chr17:47559049
|
A | G | 2 | a0001c0001t0003g0077a0001c0001t0003g0079 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.341-10368A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47559049 | ||||||
| chr17:47559180
|
A | G | 1 | a0001c0001t0003g0067 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.341-10237A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47559180 | ||||||
| chr17:47559198
|
C | T | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.341-10219C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47559198 | ||||||
| chr17:47559465
|
C | T | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.341-9952C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47559465 | ||||||
| chr17:47559743
|
C | CTCTTG | 11 | a0001c0001t0001g0010a0001c0001t0002g0159a0001c0001t0002g0160others(8): Show | 11 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.341-9649_341-9645d others(7): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47559743 | |||||
| chr17:47559743
|
CTCTTG | C | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.341-9649_341-9645d others(7): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47559743 | |||||
| chr17:47559759
|
T | C | 1 | a0001c0001t0002g0219 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.341-9658T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47559759 | ||||||
| chr17:47559897
|
A | G | 1 | a0001c0003t0003g0304 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.341-9520A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47559897 | ||||||
| chr17:47559983
|
A | G | 1 | a0001c0001t0007g0338 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.341-9434A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47559983 | ||||||
| chr17:47560040
|
T | C | 4 | a0001c0001t0001g0111a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | HG01169.hp2 HG03579.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-9377T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47560040 | ||||||
| chr17:47560390
|
A | G | 1 | a0001c0001t0002g0090 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.341-9027A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47560390 | ||||||
| chr17:47560475
|
C | A | 1 | a0001c0001t0002g0333 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.341-8942C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47560475 | ||||||
| chr17:47560707
|
A | G | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.341-8710A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47560707 | ||||||
| chr17:47560901
|
G | C | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.341-8516G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47560901 | ||||||
| chr17:47560935
|
G | A | 1 | a0001c0001t0003g0047 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.341-8482G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47560935 | ||||||
| chr17:47560989
|
G | T | 1 | a0001c0001t0002g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.341-8428G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47560989 | ||||||
| chr17:47561092
|
T | A | 1 | a0001c0001t0001g0286 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.341-8325T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47561092 | ||||||
| chr17:47561101
|
T | C | 1 | a0001c0001t0002g0293 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.341-8316T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47561101 | ||||||
| chr17:47561143
|
T | C | 2 | a0001c0001t0002g0117a0001c0001t0002g0118 | 2 | HG01891.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.341-8274T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47561143 | ||||||
| chr17:47561278
|
C | T | 1 | a0001c0001t0007g0338 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.341-8139C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47561278 | ||||||
| chr17:47561346
|
C | CA | 151 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0023others(148): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.341-8048dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47561346 | |||||
| chr17:47561346
|
C | CAA | 9 | a0001c0001t0002g0151a0001c0001t0002g0166a0001c0001t0002g0169others(6): Show | 9 | HG01243.hp1 HG01433.hp1 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.341-8049_341-8048d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47561346 | |||||
| chr17:47561346
|
CA | C | 6 | a0001c0001t0001g0258a0001c0001t0001g0329a0001c0001t0003g0032others(3): Show | 6 | HG01168.hp1 HG02523.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-8048delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47561346 | |||||
| chr17:47561394
|
C | T | 163 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.341-8023C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47561394 | ||||||
| chr17:47561681
|
G | A | 13 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.341-7736G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47561681 | ||||||
| chr17:47561708
|
A | C | 1 | a0001c0001t0008g0335 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.341-7709A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47561708 | ||||||
| chr17:47561789
|
C | T | 1 | a0001c0001t0003g0052 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.341-7628C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47561789 | ||||||
| chr17:47562061
|
T | A | 1 | a0001c0001t0002g0205 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.341-7356T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47562061 | ||||||
| chr17:47562141
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.341-7276C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47562141 | ||||||
| chr17:47562268
|
C | T | 4 | a0001c0001t0005g0001a0001c0001t0005g0207a0001c0001t0005g0208others(1): Show | 5 | HG01515.hp2 HG01517.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-7149C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47562268 | ||||||
| chr17:47562308
|
G | C | 1 | a0001c0001t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.341-7109G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47562308 | ||||||
| chr17:47562406
|
T | G | 1 | a0001c0001t0001g0330 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.341-7011T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47562406 | ||||||
| chr17:47562607
|
A | AGT | 41 | a0001c0001t0001g0011a0001c0001t0001g0081a0001c0001t0001g0319others(38): Show | 41 | HG00280.hp2 HG00738.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.341-6785_341-6784d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47562607 | |||||
| chr17:47562607
|
A | AGTGT | 7 | a0001c0001t0001g0106a0001c0001t0001g0255a0001c0001t0001g0261others(4): Show | 7 | HG02056.hp1 HG02615.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.341-6787_341-6784d others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47562607 | |||||
| chr17:47562607
|
A | T | 2 | a0001c0001t0003g0077a0001c0001t0003g0079 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.341-6810A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47562607 | ||||||
| chr17:47562607
|
AGT | A | 158 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(155): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.341-6785_341-6784d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47562607 | |||||
| chr17:47562607
|
AGTGT | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026 | 3 | HG01256.hp2 HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.341-6787_341-6784d others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47562607 | |||||
| chr17:47562630
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.341-6787G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47562630 | ||||||
| chr17:47562632
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.341-6785G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47562632 | ||||||
| chr17:47562632
|
GTA | G | 5 | a0001c0001t0002g0210a0001c0001t0002g0227a0001c0001t0003g0042others(2): Show | 5 | HG00438.hp1 HG02735.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-6781_341-6780d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47562632 | |||||
| chr17:47562784
|
G | C | 1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.341-6633G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47562784 | ||||||
| chr17:47562785
|
T | TAA | 35 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0045others(32): Show | 35 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.341-6621_341-6620d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47562785 | |||||
| chr17:47562785
|
T | TAAA | 124 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(121): Show | 126 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.341-6622_341-6620d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47562785 | |||||
| chr17:47563034
|
G | GT | 10 | a0001c0001t0002g0041a0001c0001t0002g0093a0001c0001t0002g0116others(7): Show | 10 | HG01069.hp2 HG01891.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.341-6379dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47563034 | |||||
| chr17:47563039
|
G | T | 211 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.341-6378G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47563039 | ||||||
| chr17:47563041
|
T | A | 32 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0045others(29): Show | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.341-6376T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47563041 | ||||||
| chr17:47563145
|
C | T | 1 | a0001c0001t0003g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.341-6272C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47563145 | ||||||
| chr17:47563404
|
C | T | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.341-6013C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47563404 | ||||||
| chr17:47563428
|
T | C | 1 | a0001c0001t0003g0052 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.341-5989T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47563428 | ||||||
| chr17:47563798
|
T | C | 1 | a0001c0001t0002g0209 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.341-5619T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47563798 | ||||||
| chr17:47563865
|
C | T | 1 | a0001c0001t0002g0168 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.341-5552C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47563865 | ||||||
| chr17:47563978
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.341-5439G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47563978 | ||||||
| chr17:47564083
|
C | T | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.341-5334C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47564083 | ||||||
| chr17:47564162
|
C | T | 211 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.341-5255C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47564162 | ||||||
| chr17:47564377
|
G | A | 163 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.341-5040G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47564377 | ||||||
| chr17:47564459
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.341-4958C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47564459 | ||||||
| chr17:47564825
|
T | G | 65 | a0001c0001t0001g0030a0001c0001t0001g0103a0001c0001t0001g0109others(62): Show | 65 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.341-4592T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47564825 | ||||||
| chr17:47565237
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.341-4180G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47565237 | ||||||
| chr17:47565369
|
C | T | 1 | a0001c0001t0003g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.341-4048C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47565369 | ||||||
| chr17:47565505
|
C | CA | 31 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0019others(28): Show | 31 | HG00673.hp2 HG00735.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.341-3890dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47565505 | |||||
| chr17:47565505
|
CA | C | 143 | a0001c0001t0001g0102a0001c0001t0001g0232a0001c0001t0002g0003others(140): Show | 145 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.341-3890delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47565505 | |||||
| chr17:47565819
|
C | CA | 8 | a0001c0001t0001g0081a0001c0001t0001g0272a0001c0001t0002g0089others(5): Show | 8 | HG06807.hp1 NA18942.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.341-3584dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47565819 | |||||
| chr17:47565858
|
A | C | 1 | a0001c0001t0007g0338 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.341-3559A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47565858 | ||||||
| chr17:47566151
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.341-3266G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47566151 | ||||||
| chr17:47566151
|
G | T | 1 | a0001c0001t0004g0132 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.341-3266G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47566151 | ||||||
| chr17:47566240
|
A | T | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.341-3177A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47566240 | ||||||
| chr17:47566278
|
C | A | 1 | a0001c0006t0003g0339 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.341-3139C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47566278 | ||||||
| chr17:47566505
|
G | GT | 12 | a0001c0001t0001g0005a0001c0001t0001g0237a0001c0001t0001g0277others(9): Show | 12 | HG00738.hp2 HG01099.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.341-2897dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47566505 | |||||
| chr17:47566505
|
GTTT | G | 39 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(36): Show | 39 | HG00738.hp1 HG01261.hp1 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.341-2899_341-2897d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47566505 | |||||
| chr17:47566586
|
C | T | 32 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0045others(29): Show | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.341-2831C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47566586 | ||||||
| chr17:47567015
|
G | A | 2 | a0001c0001t0003g0120a0001c0001t0003g0121 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.341-2402G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47567015 | ||||||
| chr17:47567092
|
A | C | 3 | a0001c0004t0003g0059a0001c0004t0003g0060a0001c0004t0003g0080 | 3 | HG01106.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.341-2325A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47567092 | ||||||
| chr17:47567363
|
A | G | 1 | a0001c0001t0003g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.341-2054A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47567363 | ||||||
| chr17:47567440
|
C | T | 1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.341-1977C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47567440 | ||||||
| chr17:47567525
|
C | T | 13 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.341-1892C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47567525 | ||||||
| chr17:47567839
|
T | G | 3 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0280 | 3 | HG01169.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.341-1578T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47567839 | ||||||
| chr17:47567842
|
C | G | 1 | a0001c0001t0002g0171 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.341-1575C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47567842 | ||||||
| chr17:47568150
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.341-1267C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47568150 | ||||||
| chr17:47568206
|
C | T | 2 | a0001c0001t0002g0154a0001c0001t0002g0213 | 2 | HG00438.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.341-1211C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47568206 | ||||||
| chr17:47568219
|
A | C | 1 | a0001c0001t0002g0217 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.341-1198A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47568219 | ||||||
| chr17:47568338
|
G | A | 5 | a0001c0001t0003g0039a0001c0001t0003g0051a0001c0001t0003g0052others(2): Show | 5 | HG02040.hp2 NA18985.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-1079G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47568338 | ||||||
| chr17:47568581
|
GTCTC | G | 148 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(145): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.341-834_341-831del others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 47568581 | |||||
| chr17:47568590
|
CA | C | 148 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(145): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.341-826delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47568590 | ||||||
| chr17:47568685
|
C | T | 1 | a0001c0001t0004g0129 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.341-732C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47568685 | ||||||
| chr17:47568819
|
C | A | 1 | a0001c0006t0003g0339 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.341-598C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47568819 | ||||||
| chr17:47568843
|
C | T | 1 | a0001c0001t0003g0225 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.341-574C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47568843 | ||||||
| chr17:47568891
|
G | T | 2 | a0001c0001t0003g0120a0001c0001t0003g0121 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.341-526G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47568891 | ||||||
| chr17:47568947
|
G | A | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.341-470G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47568947 | ||||||
| chr17:47569149
|
T | C | 2 | a0001c0001t0003g0077a0001c0001t0003g0079 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.341-268T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47569149 | ||||||
| chr17:47569187
|
G | A | 2 | a0001c0001t0002g0100a0001c0001t0002g0228 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.341-230G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47569187 | ||||||
| chr17:47569211
|
T | C | 1 | a0001c0001t0003g0048 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.341-206T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47569211 | ||||||
| chr17:47569235
|
A | C | 1 | a0001c0006t0003g0339 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.341-182A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 2/22 | chr17 | 47569235 | ||||||
| chr17:47569699
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.418+205C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47569699 | ||||||
| chr17:47569701
|
T | C | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.418+207T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47569701 | ||||||
| chr17:47569815
|
C | T | 1 | a0001c0001t0003g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.418+321C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47569815 | ||||||
| chr17:47570631
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.418+1137G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47570631 | ||||||
| chr17:47570866
|
T | G | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.418+1372T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47570866 | ||||||
| chr17:47571064
|
T | A | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.418+1570T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47571064 | ||||||
| chr17:47571080
|
A | C | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.418+1586A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47571080 | ||||||
| chr17:47571373
|
T | C | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.418+1879T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47571373 | ||||||
| chr17:47571514
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.418+2020C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47571514 | ||||||
| chr17:47571570
|
T | C | 1 | a0001c0001t0002g0090 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.418+2076T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47571570 | ||||||
| chr17:47571574
|
T | C | 1 | a0001c0004t0003g0059 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.418+2080T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47571574 | ||||||
| chr17:47571616
|
G | C | 1 | a0001c0001t0002g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.418+2122G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47571616 | ||||||
| chr17:47571640
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.418+2146C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47571640 | ||||||
| chr17:47571672
|
C | T | 3 | a0001c0004t0003g0059a0001c0004t0003g0060a0001c0004t0003g0080 | 3 | HG01106.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.418+2178C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47571672 | ||||||
| chr17:47571992
|
C | T | 1 | a0001c0001t0002g0219 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.418+2498C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47571992 | ||||||
| chr17:47572031
|
T | C | 1 | a0001c0001t0002g0333 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.418+2537T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47572031 | ||||||
| chr17:47572042
|
C | CA | 148 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(145): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.418+2549dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47572042 | |||||
| chr17:47572078
|
G | C | 2 | a0001c0001t0004g0137a0001c0001t0004g0140 | 2 | NA19065.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.418+2584G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47572078 | ||||||
| chr17:47572079
|
G | A | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.418+2585G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47572079 | ||||||
| chr17:47572284
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.418+2790G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47572284 | ||||||
| chr17:47572328
|
C | A | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.418+2834C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47572328 | ||||||
| chr17:47572478
|
T | TA | 116 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(113): Show | 118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.418+2994dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47572478 | |||||
| chr17:47572616
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.418+3122G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47572616 | ||||||
| chr17:47572830
|
T | C | 211 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.418+3336T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47572830 | ||||||
| chr17:47573055
|
C | T | 2 | a0001c0001t0003g0120a0001c0001t0003g0121 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.418+3561C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47573055 | ||||||
| chr17:47573058
|
G | T | 1 | a0001c0001t0002g0003 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.418+3564G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47573058 | ||||||
| chr17:47573098
|
C | T | 1 | a0001c0001t0003g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+3604C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47573098 | ||||||
| chr17:47573390
|
C | G | 48 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(45): Show | 48 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.418+3896C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47573390 | ||||||
| chr17:47573585
|
C | T | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.418+4091C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47573585 | ||||||
| chr17:47573602
|
A | C | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289 | 3 | NA18973.hp2 NA19064.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.418+4108A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47573602 | ||||||
| chr17:47573690
|
C | T | 148 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(145): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.418+4196C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47573690 | ||||||
| chr17:47573851
|
T | C | 1 | a0001c0001t0003g0068 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.418+4357T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47573851 | ||||||
| chr17:47573943
|
CTG | C | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.418+4452_418+4453d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47573943 | |||||
| chr17:47574051
|
T | TAGAAAAT others(426): Show |
2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.418+4575_418+4576i others(435): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47574051 | |||||
| chr17:47574051
|
T | TAGAAAAT others(429): Show |
1 | a0001c0001t0002g0216 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.418+4575_418+4576i others(438): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47574051 | |||||
| chr17:47574051
|
T | TAGAAAAT others(430): Show |
1 | a0001c0001t0002g0209 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.418+4575_418+4576i others(439): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47574051 | |||||
| chr17:47574051
|
T | TAGAAAAT others(431): Show |
1 | a0001c0001t0002g0092 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.418+4575_418+4576i others(440): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47574051 | |||||
| chr17:47574051
|
T | TAGAAAAT others(435): Show |
1 | a0001c0001t0002g0202 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.418+4575_418+4576i others(444): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47574051 | |||||
| chr17:47574108
|
C | T | 1 | a0001c0001t0003g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.418+4614C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47574108 | ||||||
| chr17:47574420
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.418+4926A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47574420 | ||||||
| chr17:47574695
|
A | C | 1 | a0001c0001t0002g0180 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.419-4695A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47574695 | ||||||
| chr17:47574988
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.419-4402T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47574988 | ||||||
| chr17:47575428
|
TAAC | T | 41 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0002g0095others(38): Show | 41 | HG00738.hp1 HG01109.hp2 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.419-3959_419-3957d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47575428 | |||||
| chr17:47575580
|
A | AATT | 21 | a0001c0001t0001g0022a0001c0001t0001g0030a0001c0001t0001g0105others(18): Show | 21 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.419-3773_419-3771d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47575580 | |||||
| chr17:47575580
|
A | AATTATT | 7 | a0001c0001t0001g0109a0001c0001t0002g0166a0001c0001t0002g0191others(4): Show | 7 | HG01109.hp2 HG02015.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.419-3776_419-3771d others(8): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47575580 | |||||
| chr17:47575580
|
A | AATTATTA others(2): Show |
23 | a0001c0001t0001g0081a0001c0001t0003g0034a0001c0001t0003g0036others(20): Show | 23 | HG00738.hp1 HG01261.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-3779_419-3771d others(11): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47575580 | |||||
| chr17:47575580
|
A | AATTATTA others(5): Show |
14 | a0001c0001t0002g0069a0001c0001t0003g0032a0001c0001t0003g0033others(11): Show | 14 | HG01358.hp2 HG01993.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.419-3782_419-3771d others(14): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47575580 | |||||
| chr17:47575580
|
A | AATTATTA others(8): Show |
2 | a0001c0001t0003g0035a0001c0001t0003g0037 | 2 | HG03688.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.419-3785_419-3771d others(17): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47575580 | |||||
| chr17:47575580
|
AATT | A | 56 | a0001c0001t0001g0106a0001c0001t0001g0255a0001c0001t0001g0261others(53): Show | 57 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.419-3773_419-3771d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47575580 | |||||
| chr17:47575580
|
AATTATT | A | 19 | a0001c0001t0001g0325a0001c0001t0004g0126a0001c0001t0004g0155others(16): Show | 19 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.419-3776_419-3771d others(8): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47575580 | |||||
| chr17:47575580
|
AATTATTA others(2): Show |
A | 3 | a0001c0001t0001g0004a0001c0001t0002g0231a0001c0001t0002g0238 | 3 | HG02965.hp2 HG03540.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.419-3779_419-3771d others(11): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47575580 | |||||
| chr17:47575580
|
AATTATTA others(5): Show |
A | 1 | a0001c0002t0001g0253 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.419-3782_419-3771d others(14): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47575580 | |||||
| chr17:47575586
|
T | A | 1 | a0001c0001t0002g0205 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.419-3804T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47575586 | ||||||
| chr17:47575644
|
G | A | 1 | a0001c0001t0004g0139 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.419-3746G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47575644 | ||||||
| chr17:47575678
|
C | G | 1 | a0001c0001t0001g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.419-3712C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47575678 | ||||||
| chr17:47575712
|
C | T | 2 | a0001c0001t0002g0231a0001c0001t0002g0238 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.419-3678C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47575712 | ||||||
| chr17:47575715
|
C | T | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.419-3675C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47575715 | ||||||
| chr17:47575844
|
G | A | 1 | a0001c0001t0003g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.419-3546G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47575844 | ||||||
| chr17:47575925
|
T | G | 211 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.419-3465T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47575925 | ||||||
| chr17:47575936
|
TG | T | 13 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0092others(10): Show | 13 | HG01192.hp2 HG02083.hp1 HG03491.hp1 others(10): Show |
intron_variant | MODIFIER | c.419-3453delG | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47575936 | ||||||
| chr17:47575998
|
A | T | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.419-3392A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47575998 | ||||||
| chr17:47576203
|
C | T | 163 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.419-3187C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47576203 | ||||||
| chr17:47576417
|
G | A | 6 | a0001c0001t0003g0098a0001c0001t0003g0152a0001c0001t0003g0158others(3): Show | 6 | HG02897.hp1 HG02922.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.419-2973G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47576417 | ||||||
| chr17:47576449
|
A | G | 1 | a0001c0001t0001g0329 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.419-2941A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47576449 | ||||||
| chr17:47576453
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.419-2937C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47576453 | ||||||
| chr17:47576555
|
T | A | 211 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.419-2835T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47576555 | ||||||
| chr17:47576664
|
A | G | 1 | a0001c0001t0005g0207 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.419-2726A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47576664 | ||||||
| chr17:47576818
|
G | A | 1 | a0001c0001t0002g0333 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.419-2572G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47576818 | ||||||
| chr17:47576876
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.419-2514A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47576876 | ||||||
| chr17:47577036
|
G | T | 1 | a0001c0001t0001g0313 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.419-2354G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47577036 | ||||||
| chr17:47577260
|
A | C | 1 | a0001c0001t0001g0280 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.419-2130A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47577260 | ||||||
| chr17:47577260
|
A | T | 2 | a0001c0001t0003g0120a0001c0001t0003g0121 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.419-2130A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47577260 | ||||||
| chr17:47577414
|
A | G | 1 | a0001c0001t0004g0129 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.419-1976A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47577414 | ||||||
| chr17:47577552
|
T | C | 1 | a0001c0001t0002g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.419-1838T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47577552 | ||||||
| chr17:47577577
|
T | G | 1 | a0001c0001t0002g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.419-1813T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47577577 | ||||||
| chr17:47577647
|
A | G | 67 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0084others(64): Show | 68 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.419-1743A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47577647 | ||||||
| chr17:47578082
|
G | A | 1 | a0001c0001t0003g0063 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.419-1308G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47578082 | ||||||
| chr17:47578123
|
AC | A | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.419-1264delC | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47578123 | |||||
| chr17:47578216
|
AAGAG | A | 144 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(141): Show | 146 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.419-1170_419-1167d others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 47578216 | |||||
| chr17:47578217
|
AGAG | A | 3 | a0001c0001t0002g0154a0001c0001t0002g0170a0001c0001t0002g0296 | 3 | HG04184.hp2 NA18957.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.419-1172_419-1170d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47578217 | ||||||
| chr17:47578521
|
A | T | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.419-869A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47578521 | ||||||
| chr17:47578934
|
T | A | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.419-456T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47578934 | ||||||
| chr17:47578936
|
A | T | 1 | a0001c0001t0001g0235 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.419-454A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47578936 | ||||||
| chr17:47579066
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.419-324C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47579066 | ||||||
| chr17:47579222
|
C | T | 1 | a0001c0001t0002g0331 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.419-168C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 3/22 | chr17 | 47579222 | ||||||
| chr17:47579930
|
C | CGT | 17 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0025others(14): Show | 17 | HG00558.hp2 HG01169.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.540+452_540+453dup others(2): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 47579930 | |||||
| chr17:47579930
|
C | CGTGT | 5 | a0001c0001t0002g0091a0001c0001t0002g0169a0001c0001t0002g0231others(2): Show | 5 | HG00544.hp1 HG02965.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+450_540+453dup others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 47579930 | |||||
| chr17:47579930
|
C | CGTGTGTG others(3): Show |
1 | a0001c0006t0003g0340 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.540+444_540+453dup others(10): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 47579930 | |||||
| chr17:47579930
|
CGT | C | 123 | a0001c0001t0001g0115a0001c0001t0001g0282a0001c0001t0002g0003others(120): Show | 124 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(121): Show |
intron_variant | MODIFIER | c.540+452_540+453del others(2): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 47579930 | |||||
| chr17:47579930
|
CGTGT | C | 8 | a0001c0001t0001g0330a0001c0001t0002g0170a0001c0003t0003g0302others(5): Show | 8 | HG00099.hp1 HG00735.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.540+450_540+453del others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 47579930 | |||||
| chr17:47579930
|
CGTGTGT | C | 5 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0123others(2): Show | 5 | HG01099.hp2 HG01934.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+448_540+453del others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 47579930 | |||||
| chr17:47579930
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0002g0212 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.540+440_540+453del others(14): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 47579930 | |||||
| chr17:47579988
|
T | C | 1 | a0001c0001t0002g0093 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.540+477T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | chr17 | 47579988 | ||||||
| chr17:47580216
|
C | T | 39 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(36): Show | 39 | HG00140.hp2 HG00280.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.540+705C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | chr17 | 47580216 | ||||||
| chr17:47580353
|
C | G | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.540+842C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | chr17 | 47580353 | ||||||
| chr17:47580357
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(1): Show | 4 | HG00280.hp2 HG01175.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+846T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | chr17 | 47580357 | ||||||
| chr17:47580477
|
C | T | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.540+966C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | chr17 | 47580477 | ||||||
| chr17:47580760
|
G | T | 32 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0045others(29): Show | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.540+1249G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | chr17 | 47580760 | ||||||
| chr17:47580786
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.540+1275G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | chr17 | 47580786 | ||||||
| chr17:47581188
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.541-1554G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | chr17 | 47581188 | ||||||
| chr17:47581237
|
C | A | 1 | a0001c0001t0004g0139 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.541-1505C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | chr17 | 47581237 | ||||||
| chr17:47581525
|
A | T | 1 | a0001c0001t0003g0058 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.541-1217A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | chr17 | 47581525 | ||||||
| chr17:47581683
|
G | GGTTT | 139 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(136): Show | 141 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.541-1034_541-1031d others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 47581683 | |||||
| chr17:47581683
|
G | GGTTTGTT others(1): Show |
12 | a0001c0001t0002g0097a0001c0001t0002g0217a0001c0003t0003g0301others(9): Show | 12 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.541-1038_541-1031d others(10): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 47581683 | |||||
| chr17:47581683
|
G | GGTTTGTT others(5): Show |
1 | a0001c0003t0003g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.541-1042_541-1031d others(14): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 47581683 | |||||
| chr17:47581795
|
G | C | 103 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(100): Show | 104 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.541-947G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | chr17 | 47581795 | ||||||
| chr17:47582492
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.541-250G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 4/22 | chr17 | 47582492 | ||||||
| chr17:47582871
|
T | C | 4 | a0001c0001t0002g0089a0001c0001t0002g0096a0001c0001t0002g0184others(1): Show | 4 | NA18942.hp2 NA18946.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+22T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47582871 | ||||||
| chr17:47583322
|
C | A | 2 | a0001c0001t0002g0100a0001c0001t0002g0228 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.648+473C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47583322 | ||||||
| chr17:47583521
|
T | G | 163 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.648+672T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47583521 | ||||||
| chr17:47583640
|
T | C | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.648+791T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47583640 | ||||||
| chr17:47583923
|
T | TA | 163 | a0001c0001t0001g0109a0001c0001t0001g0256a0001c0001t0001g0257others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.648+1087dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 47583923 | |||||
| chr17:47584134
|
T | C | 3 | a0001c0001t0002g0214a0001c0001t0002g0290a0001c0001t0009g0094 | 3 | HG02080.hp1 NA18973.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.648+1285T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47584134 | ||||||
| chr17:47584220
|
C | CG | 96 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0041others(93): Show | 98 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.649-1275dupG | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 47584220 | |||||
| chr17:47584226
|
A | G | 20 | a0001c0001t0002g0029a0001c0001t0002g0093a0001c0001t0002g0153others(17): Show | 20 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.649-1274A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47584226 | ||||||
| chr17:47584227
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0003g0065 | 2 | HG02683.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.649-1273A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47584227 | ||||||
| chr17:47584414
|
G | C | 1 | a0001c0002t0001g0104 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.649-1086G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47584414 | ||||||
| chr17:47584507
|
A | C | 1 | a0001c0001t0001g0271 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.649-993A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47584507 | ||||||
| chr17:47584616
|
G | T | 3 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0298 | 3 | HG02165.hp1 NA19062.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.649-884G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47584616 | ||||||
| chr17:47584947
|
C | T | 4 | a0001c0001t0003g0098a0001c0001t0003g0158a0001c0001t0003g0224others(1): Show | 4 | HG02897.hp1 HG03041.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-553C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47584947 | ||||||
| chr17:47584974
|
C | T | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.649-526C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47584974 | ||||||
| chr17:47585015
|
G | T | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.649-485G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47585015 | ||||||
| chr17:47585017
|
T | C | 216 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(213): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.649-483T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47585017 | ||||||
| chr17:47585107
|
G | A | 1 | a0001c0001t0003g0225 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.649-393G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47585107 | ||||||
| chr17:47585480
|
CT | C | 48 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(45): Show | 48 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.649-12delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 47585480 | |||||
| chr17:47585488
|
T | A | 1 | a0001c0001t0001g0286 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.649-12T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 5/22 | chr17 | 47585488 | ||||||
| chr17:47585806
|
G | A | 1 | a0001c0001t0003g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.849+106G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 6/22 | chr17 | 47585806 | ||||||
| chr17:47586014
|
G | A | 3 | a0001c0001t0002g0100a0001c0001t0002g0228a0001c0001t0007g0338 | 3 | HG02451.hp1 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.850-134G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 6/22 | chr17 | 47586014 | ||||||
| chr17:47586101
|
T | C | 1 | a0001c0001t0003g0119 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.850-47T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 6/22 | chr17 | 47586101 | ||||||
| chr17:47586314
|
G | GTA | 44 | a0001c0001t0001g0004a0001c0001t0001g0111a0001c0001t0001g0284others(41): Show | 44 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.947-31_947-30dupAT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr17 | 47586314 | |||||
| chr17:47586336
|
C | A | 40 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(37): Show | 40 | HG00738.hp1 HG01109.hp2 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.947-29C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 7/22 | chr17 | 47586336 | ||||||
| chr17:47586546
|
T | G | 11 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(8): Show | 11 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.980+148T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 8/22 | chr17 | 47586546 | ||||||
| chr17:47587025
|
G | A | 1 | a0001c0001t0003g0119 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.981-205G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 8/22 | chr17 | 47587025 | ||||||
| chr17:47587202
|
T | C | 2 | a0001c0001t0003g0077a0001c0001t0003g0079 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.981-28T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 8/22 | chr17 | 47587202 | ||||||
| chr17:47587207
|
C | CT | 48 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0002g0154others(45): Show | 48 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(45): Show |
splice_region_variant&intron_variant | LOW | c.981-9dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr17 | 47587207 | |||||
| chr17:47587351
|
AATATTTT others(13): Show |
A | 32 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0045others(29): Show | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1095+14_1095+33del others(20): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr17 | 47587351 | |||||
| chr17:47587436
|
C | G | 1 | a0001c0001t0002g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1095+92C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47587436 | ||||||
| chr17:47587495
|
A | G | 217 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1095+151A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47587495 | ||||||
| chr17:47587571
|
A | G | 2 | a0001c0001t0001g0326a0001c0001t0003g0079 | 2 | HG01074.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1095+227A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47587571 | ||||||
| chr17:47587811
|
A | T | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1095+467A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47587811 | ||||||
| chr17:47587885
|
T | C | 1 | a0001c0011t0001g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1095+541T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47587885 | ||||||
| chr17:47588086
|
G | A | 3 | a0001c0001t0002g0031a0001c0001t0002g0179a0001c0001t0002g0196 | 3 | NA18961.hp1 NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1095+742G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47588086 | ||||||
| chr17:47588564
|
C | CA | 6 | a0001c0001t0002g0029a0001c0001t0002g0122a0001c0001t0002g0172others(3): Show | 6 | HG02083.hp1 NA18945.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1095+1233dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr17 | 47588564 | |||||
| chr17:47588621
|
A | T | 1 | a0001c0001t0001g0005 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1095+1277A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47588621 | ||||||
| chr17:47588934
|
T | C | 2 | a0001c0001t0002g0069a0001c0001t0003g0074 | 2 | NA18963.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1095+1590T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47588934 | ||||||
| chr17:47588973
|
A | G | 1 | a0001c0001t0001g0321 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1095+1629A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47588973 | ||||||
| chr17:47588991
|
A | T | 2 | a0001c0001t0002g0231a0001c0001t0002g0238 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1095+1647A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47588991 | ||||||
| chr17:47589227
|
A | T | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1096-1490A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47589227 | ||||||
| chr17:47589531
|
T | C | 1 | a0001c0001t0002g0091 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1096-1186T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47589531 | ||||||
| chr17:47589632
|
T | C | 8 | a0001c0001t0002g0031a0001c0001t0002g0089a0001c0001t0002g0096others(5): Show | 8 | NA18942.hp2 NA18946.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.1096-1085T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47589632 | ||||||
| chr17:47590048
|
G | A | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1096-669G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47590048 | ||||||
| chr17:47590069
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1096-648G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47590069 | ||||||
| chr17:47590184
|
G | A | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1096-533G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47590184 | ||||||
| chr17:47590289
|
C | T | 1 | a0001c0001t0003g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1096-428C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47590289 | ||||||
| chr17:47590456
|
CA | C | 163 | a0001c0001t0001g0123a0001c0001t0002g0003a0001c0001t0002g0029others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1096-247delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr17 | 47590456 | |||||
| chr17:47590597
|
G | A | 1 | a0001c0001t0008g0335 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1096-120G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 9/22 | chr17 | 47590597 | ||||||
| chr17:47591007
|
A | T | 49 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(46): Show | 49 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.1260+126A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 10/22 | chr17 | 47591007 | ||||||
| chr17:47591098
|
G | A | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1260+217G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 10/22 | chr17 | 47591098 | ||||||
| chr17:47591142
|
C | T | 2 | a0001c0001t0003g0120a0001c0001t0003g0121 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1260+261C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 10/22 | chr17 | 47591142 | ||||||
| chr17:47591143
|
A | G | 212 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(209): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1260+262A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 10/22 | chr17 | 47591143 | ||||||
| chr17:47591335
|
C | T | 1 | a0001c0001t0002g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1260+454C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 10/22 | chr17 | 47591335 | ||||||
| chr17:47591394
|
A | T | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1260+513A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 10/22 | chr17 | 47591394 | ||||||
| chr17:47591518
|
C | T | 1 | a0001c0001t0002g0333 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1261-438C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 10/22 | chr17 | 47591518 | ||||||
| chr17:47591655
|
A | G | 116 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(113): Show | 118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1261-301A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 10/22 | chr17 | 47591655 | ||||||
| chr17:47592062
|
T | TA | 210 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(207): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1365+11dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr17 | 47592062 | |||||
| chr17:47592158
|
A | C | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1365+98A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 11/22 | chr17 | 47592158 | ||||||
| chr17:47592257
|
G | A | 1 | a0001c0001t0002g0217 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1365+197G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 11/22 | chr17 | 47592257 | ||||||
| chr17:47592269
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1365+209G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 11/22 | chr17 | 47592269 | ||||||
| chr17:47592452
|
C | T | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1366-33C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 11/22 | chr17 | 47592452 | ||||||
| chr17:47592598
|
C | G | 48 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(45): Show | 48 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.1426+53C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47592598 | ||||||
| chr17:47592818
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1426+273G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47592818 | ||||||
| chr17:47592893
|
A | G | 1 | a0001c0001t0003g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1426+348A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47592893 | ||||||
| chr17:47592946
|
G | A | 148 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(145): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1426+401G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47592946 | ||||||
| chr17:47593489
|
G | A | 30 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0034others(27): Show | 30 | HG00738.hp1 HG01109.hp2 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.1426+944G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47593489 | ||||||
| chr17:47593628
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1426+1083T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47593628 | ||||||
| chr17:47594115
|
A | T | 1 | a0001c0001t0001g0233 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1426+1570A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47594115 | ||||||
| chr17:47594140
|
G | A | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1426+1595G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47594140 | ||||||
| chr17:47594346
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1426+1801C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47594346 | ||||||
| chr17:47594412
|
CT | C | 186 | a0001c0001t0001g0081a0001c0001t0001g0317a0001c0001t0002g0003others(183): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1426+1882delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 47594412 | |||||
| chr17:47594419
|
T | G | 1 | a0001c0001t0002g0333 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1426+1874T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47594419 | ||||||
| chr17:47594440
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0002g0217 | 2 | HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1426+1895C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47594440 | ||||||
| chr17:47594456
|
G | A | 1 | a0001c0001t0002g0332 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1427-1897G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47594456 | ||||||
| chr17:47594496
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1427-1857C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47594496 | ||||||
| chr17:47594503
|
C | T | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1427-1850C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47594503 | ||||||
| chr17:47594586
|
T | TTTATG | 4 | a0001c0001t0001g0245a0001c0003t0003g0300a0001c0003t0003g0306others(1): Show | 4 | HG00099.hp1 HG01081.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1427-1763_1427-176 others(9): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 47594586 | |||||
| chr17:47594586
|
T | TTTATGTT others(3): Show |
3 | a0001c0001t0003g0042a0001c0003t0003g0302a0001c0003t0003g0303 | 3 | HG00735.hp1 HG01099.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1427-1763_1427-176 others(14): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 47594586 | |||||
| chr17:47594586
|
TTTATTTT others(3): Show |
T | 1 | a0001c0001t0003g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1427-1762_1427-175 others(14): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 47594586 | |||||
| chr17:47594591
|
T | G | 14 | a0001c0001t0001g0245a0001c0001t0003g0042a0001c0001t0003g0077others(11): Show | 14 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1427-1762T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47594591 | ||||||
| chr17:47594591
|
T | TTTATG | 79 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(76): Show | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1427-1712_1427-170 others(9): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 47594591 | |||||
| chr17:47594591
|
T | TTTATGTT others(3): Show |
39 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0025others(36): Show | 39 | HG00558.hp2 HG01071.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1427-1717_1427-170 others(14): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 47594591 | |||||
| chr17:47594591
|
T | TTTATGTT others(8): Show |
10 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0023others(7): Show | 10 | HG01175.hp1 HG02647.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1427-1722_1427-170 others(19): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 47594591 | |||||
| chr17:47594591
|
T | TTTATGTT others(13): Show |
3 | a0001c0001t0001g0016a0001c0001t0003g0064a0001c0001t0004g0138 | 3 | HG01993.hp1 HG03017.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1427-1727_1427-170 others(24): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 47594591 | |||||
| chr17:47594591
|
TTTATG | T | 22 | a0001c0001t0001g0237a0001c0001t0001g0242a0001c0001t0001g0250others(19): Show | 23 | HG00738.hp2 HG01255.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.1427-1712_1427-170 others(9): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 47594591 | |||||
| chr17:47594591
|
TTTATGTT others(3): Show |
T | 65 | a0001c0001t0001g0284a0001c0001t0002g0003a0001c0001t0002g0031others(62): Show | 66 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1427-1717_1427-170 others(14): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 47594591 | |||||
| chr17:47594591
|
TTTATGTT others(8): Show |
T | 40 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0093others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.1427-1722_1427-170 others(19): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 47594591 | |||||
| chr17:47594629
|
A | ATGTTATG others(16): Show |
1 | a0001c0001t0007g0338 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1427-1708_1427-170 others(27): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 47594629 | |||||
| chr17:47594663
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1427-1690C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47594663 | ||||||
| chr17:47594725
|
C | T | 4 | a0001c0001t0001g0103a0001c0001t0001g0123a0001c0001t0001g0233others(1): Show | 4 | HG01099.hp2 HG01934.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1427-1628C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47594725 | ||||||
| chr17:47594834
|
G | T | 148 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(145): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1427-1519G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47594834 | ||||||
| chr17:47595016
|
C | T | 1 | a0001c0001t0002g0332 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1427-1337C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47595016 | ||||||
| chr17:47595094
|
C | T | 1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1427-1259C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47595094 | ||||||
| chr17:47595142
|
G | C | 1 | a0001c0006t0003g0339 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1427-1211G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47595142 | ||||||
| chr17:47595150
|
C | T | 1 | a0001c0001t0004g0044 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1427-1203C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47595150 | ||||||
| chr17:47595166
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1427-1187G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47595166 | ||||||
| chr17:47595467
|
C | G | 48 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(45): Show | 48 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.1427-886C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47595467 | ||||||
| chr17:47595480
|
C | G | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1427-873C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47595480 | ||||||
| chr17:47595711
|
G | A | 3 | a0001c0002t0001g0107a0001c0002t0001g0240a0001c0002t0001g0253 | 3 | NA18977.hp1 NA18983.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1427-642G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47595711 | ||||||
| chr17:47595748
|
C | T | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1427-605C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47595748 | ||||||
| chr17:47595981
|
C | CA | 43 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(40): Show | 43 | HG00323.hp1 HG00673.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.1427-347dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 47595981 | |||||
| chr17:47595981
|
CA | C | 59 | a0001c0001t0001g0297a0001c0001t0002g0190a0001c0001t0002g0214others(56): Show | 60 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1427-347delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 47595981 | |||||
| chr17:47596010
|
A | T | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1427-343A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47596010 | ||||||
| chr17:47596069
|
C | T | 2 | a0001c0001t0003g0120a0001c0001t0003g0121 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1427-284C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47596069 | ||||||
| chr17:47596287
|
A | C | 13 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1427-66A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 12/22 | chr17 | 47596287 | ||||||
| chr17:47596813
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1536+351C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47596813 | ||||||
| chr17:47596819
|
G | A | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1536+357G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47596819 | ||||||
| chr17:47596972
|
C | T | 32 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0045others(29): Show | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1536+510C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47596972 | ||||||
| chr17:47596985
|
T | C | 6 | a0001c0001t0003g0065a0001c0001t0003g0120a0001c0001t0003g0121others(3): Show | 6 | HG01106.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1536+523T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47596985 | ||||||
| chr17:47597047
|
C | CA | 204 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1536+600dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 47597047 | |||||
| chr17:47597167
|
TTATAA | T | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1536+709_1536+713d others(7): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 47597167 | |||||
| chr17:47597321
|
A | T | 217 | a0001c0001t0001g0081a0001c0001t0002g0003a0001c0001t0002g0029others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1536+859A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47597321 | ||||||
| chr17:47597429
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1536+967C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47597429 | ||||||
| chr17:47597632
|
G | A | 116 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(113): Show | 118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1536+1170G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47597632 | ||||||
| chr17:47598316
|
T | TA | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1537-1352dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 47598316 | |||||
| chr17:47598415
|
G | A | 148 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(145): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1537-1261G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47598415 | ||||||
| chr17:47598419
|
T | C | 2 | a0001c0001t0004g0138a0001c0001t0004g0142 | 2 | NA18983.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1537-1257T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47598419 | ||||||
| chr17:47599031
|
G | A | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1537-645G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47599031 | ||||||
| chr17:47599137
|
C | T | 8 | a0001c0002t0001g0104a0001c0002t0001g0236a0001c0002t0001g0241others(5): Show | 8 | NA18943.hp2 NA18988.hp2 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.1537-539C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47599137 | ||||||
| chr17:47599151
|
A | G | 1 | a0001c0001t0002g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1537-525A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47599151 | ||||||
| chr17:47599160
|
G | C | 163 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1537-516G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47599160 | ||||||
| chr17:47599303
|
A | G | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1537-373A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47599303 | ||||||
| chr17:47599348
|
A | G | 13 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1537-328A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47599348 | ||||||
| chr17:47599384
|
T | A | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1537-292T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47599384 | ||||||
| chr17:47599394
|
C | T | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1537-282C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47599394 | ||||||
| chr17:47599638
|
G | T | 1 | a0001c0001t0002g0206 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1537-38G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 13/22 | chr17 | 47599638 | ||||||
| chr17:47599826
|
CT | C | 161 | a0001c0001t0001g0234a0001c0001t0002g0003a0001c0001t0002g0029others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1600+99delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr17 | 47599826 | |||||
| chr17:47600142
|
T | A | 6 | a0001c0001t0004g0044a0001c0001t0004g0126a0001c0001t0004g0128others(3): Show | 6 | HG00438.hp1 NA18941.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.1600+403T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 14/22 | chr17 | 47600142 | ||||||
| chr17:47600385
|
G | A | 1 | a0001c0001t0003g0078 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1600+646G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 14/22 | chr17 | 47600385 | ||||||
| chr17:47600693
|
C | G | 1 | a0001c0001t0004g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1601-915C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 14/22 | chr17 | 47600693 | ||||||
| chr17:47600727
|
A | T | 1 | a0001c0001t0003g0099 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1601-881A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 14/22 | chr17 | 47600727 | ||||||
| chr17:47600869
|
C | G | 1 | a0001c0001t0002g0162 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1601-739C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 14/22 | chr17 | 47600869 | ||||||
| chr17:47601042
|
G | A | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1601-566G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 14/22 | chr17 | 47601042 | ||||||
| chr17:47601121
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1601-487G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 14/22 | chr17 | 47601121 | ||||||
| chr17:47601136
|
G | A | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1601-472G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 14/22 | chr17 | 47601136 | ||||||
| chr17:47601213
|
C | T | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1601-395C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 14/22 | chr17 | 47601213 | ||||||
| chr17:47601288
|
T | G | 2 | a0001c0001t0003g0120a0001c0001t0003g0121 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1601-320T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 14/22 | chr17 | 47601288 | ||||||
| chr17:47601450
|
T | C | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1601-158T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 14/22 | chr17 | 47601450 | ||||||
| chr17:47601463
|
A | G | 1 | a0001c0001t0004g0139 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1601-145A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 14/22 | chr17 | 47601463 | ||||||
| chr17:47601973
|
GA | G | 10 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0175others(7): Show | 10 | HG00673.hp1 HG01106.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1740+238delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr17 | 47601973 | |||||
| chr17:47602127
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1740+380A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47602127 | ||||||
| chr17:47602317
|
T | C | 1 | a0001c0001t0001g0244 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1740+570T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47602317 | ||||||
| chr17:47602330
|
T | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0256 | 2 | NA18960.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1740+583T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47602330 | ||||||
| chr17:47602331
|
A | T | 3 | a0001c0001t0001g0255a0001c0001t0002g0101a0001c0001t0002g0206 | 3 | HG01884.hp2 HG03139.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1740+584A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47602331 | ||||||
| chr17:47602498
|
C | T | 1 | a0001c0001t0003g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1740+751C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47602498 | ||||||
| chr17:47602569
|
C | T | 2 | a0001c0001t0003g0152a0001c0001t0003g0225 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1740+822C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47602569 | ||||||
| chr17:47602637
|
C | CA | 30 | a0001c0001t0001g0030a0001c0001t0001g0081a0001c0001t0001g0102others(27): Show | 30 | HG00423.hp1 HG01109.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1740+909dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr17 | 47602637 | |||||
| chr17:47602637
|
CA | C | 30 | a0001c0001t0001g0283a0001c0001t0002g0003a0001c0001t0003g0074others(27): Show | 30 | HG00544.hp2 HG00558.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.1740+909delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr17 | 47602637 | |||||
| chr17:47602747
|
C | A | 12 | a0001c0001t0003g0002a0001c0001t0003g0098a0001c0001t0003g0099others(9): Show | 13 | HG02615.hp1 HG02717.hp2 HG02897.hp1 others(10): Show |
intron_variant | MODIFIER | c.1740+1000C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47602747 | ||||||
| chr17:47602789
|
A | G | 1 | a0001c0001t0002g0238 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1740+1042A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47602789 | ||||||
| chr17:47602820
|
T | A | 1 | a0001c0001t0002g0212 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1740+1073T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47602820 | ||||||
| chr17:47603102
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1741-813C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47603102 | ||||||
| chr17:47603138
|
C | T | 1 | a0001c0001t0004g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1741-777C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47603138 | ||||||
| chr17:47603181
|
C | G | 1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1741-734C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47603181 | ||||||
| chr17:47603187
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1741-728G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47603187 | ||||||
| chr17:47603243
|
C | A | 11 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1741-672C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47603243 | ||||||
| chr17:47603424
|
A | C | 1 | a0001c0001t0002g0212 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1741-491A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 15/22 | chr17 | 47603424 | ||||||
| chr17:47604195
|
T | G | 1 | a0001c0001t0002g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1875+146T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 16/22 | chr17 | 47604195 | ||||||
| chr17:47604248
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1875+199G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 16/22 | chr17 | 47604248 | ||||||
| chr17:47604774
|
G | T | 1 | a0001c0001t0001g0244 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1876-559G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 16/22 | chr17 | 47604774 | ||||||
| chr17:47604878
|
G | A | 1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1876-455G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 16/22 | chr17 | 47604878 | ||||||
| chr17:47605759
|
G | T | 32 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0045others(29): Show | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2095+207G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47605759 | ||||||
| chr17:47606436
|
T | C | 2 | a0001c0001t0002g0100a0001c0001t0002g0228 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2095+884T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47606436 | ||||||
| chr17:47606461
|
C | CT | 39 | a0001c0001t0001g0024a0001c0001t0001g0258a0001c0001t0001g0323others(36): Show | 39 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.2095+922dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47606461 | |||||
| chr17:47606461
|
CT | C | 49 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(46): Show | 49 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.2095+922delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47606461 | |||||
| chr17:47606518
|
C | T | 48 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(45): Show | 48 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.2095+966C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47606518 | ||||||
| chr17:47606744
|
A | AGCTTCTA others(20): Show |
336 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(333): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.2095+1192_2095+119 others(31): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47606744 | ||||||
| chr17:47606760
|
A | G | 1 | a0001c0001t0002g0116 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2095+1208A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47606760 | ||||||
| chr17:47607113
|
A | G | 1 | a0001c0001t0004g0138 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2095+1561A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47607113 | ||||||
| chr17:47607285
|
T | C | 32 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0045others(29): Show | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2095+1733T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47607285 | ||||||
| chr17:47607741
|
A | C | 1 | a0001c0001t0002g0172 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2095+2189A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47607741 | ||||||
| chr17:47608022
|
G | T | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2095+2470G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47608022 | ||||||
| chr17:47608318
|
G | C | 1 | a0001c0001t0001g0016 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2095+2766G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47608318 | ||||||
| chr17:47608371
|
C | T | 4 | a0001c0001t0004g0126a0001c0001t0004g0128a0001c0001t0004g0145others(1): Show | 4 | NA18941.hp2 NA18969.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2095+2819C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47608371 | ||||||
| chr17:47608448
|
C | T | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2095+2896C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47608448 | ||||||
| chr17:47608453
|
C | CA | 109 | a0001c0001t0001g0030a0001c0001t0001g0284a0001c0001t0002g0003others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.2095+2922dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47608453 | |||||
| chr17:47608453
|
C | CAA | 15 | a0001c0001t0002g0087a0001c0001t0002g0095a0001c0001t0002g0189others(12): Show | 16 | HG02145.hp1 HG02615.hp1 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.2095+2921_2095+292 others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47608453 | |||||
| chr17:47608453
|
CA | C | 9 | a0001c0001t0001g0026a0001c0001t0001g0123a0001c0001t0001g0239others(6): Show | 9 | HG00323.hp2 HG01099.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.2095+2922delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47608453 | |||||
| chr17:47608498
|
C | T | 1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2095+2946C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47608498 | ||||||
| chr17:47608512
|
A | C | 1 | a0001c0002t0003g0266 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2095+2960A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47608512 | ||||||
| chr17:47608633
|
G | C | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2095+3081G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47608633 | ||||||
| chr17:47608649
|
A | C | 3 | a0001c0001t0002g0168a0001c0001t0002g0178a0001c0001t0002g0221 | 3 | HG01993.hp2 HG02273.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2095+3097A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47608649 | ||||||
| chr17:47608650
|
G | A | 116 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(113): Show | 118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2095+3098G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47608650 | ||||||
| chr17:47608760
|
A | G | 38 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0033others(35): Show | 38 | HG00738.hp1 HG01109.hp2 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.2095+3208A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47608760 | ||||||
| chr17:47609012
|
G | A | 3 | a0001c0004t0003g0059a0001c0004t0003g0060a0001c0004t0003g0080 | 3 | HG01106.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2096-3448G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47609012 | ||||||
| chr17:47609047
|
TGAGA | T | 48 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(45): Show | 48 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.2096-3408_2096-340 others(8): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47609047 | |||||
| chr17:47609053
|
A | T | 1 | a0001c0002t0003g0266 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2096-3407A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47609053 | ||||||
| chr17:47609428
|
A | C | 1 | a0001c0001t0002g0154 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2096-3032A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47609428 | ||||||
| chr17:47609461
|
G | C | 1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2096-2999G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47609461 | ||||||
| chr17:47609671
|
C | A | 1 | a0001c0001t0002g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2096-2789C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47609671 | ||||||
| chr17:47609801
|
T | G | 1 | a0001c0001t0001g0005 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2096-2659T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47609801 | ||||||
| chr17:47610181
|
A | C | 8 | a0001c0001t0001g0115a0001c0001t0001g0277a0001c0001t0001g0282others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2096-2279A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47610181 | ||||||
| chr17:47610304
|
GC | G | 5 | a0001c0001t0002g0206a0001c0001t0005g0001a0001c0001t0005g0207others(2): Show | 6 | HG01515.hp2 HG01517.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.2096-2154delC | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47610304 | |||||
| chr17:47610347
|
A | G | 336 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(333): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.2096-2113A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47610347 | ||||||
| chr17:47610393
|
T | TG | 3 | a0001c0001t0003g0039a0001c0001t0003g0051a0001c0001t0003g0056 | 3 | HG01261.hp1 NA18985.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2096-2067_2096-206 others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47610393 | ||||||
| chr17:47610394
|
T | G | 46 | a0001c0001t0001g0007a0001c0001t0001g0081a0001c0001t0001g0316others(43): Show | 46 | HG00738.hp1 HG01109.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.2096-2066T>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47610394 | ||||||
| chr17:47610396
|
G | T | 16 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0034others(13): Show | 16 | HG02056.hp1 NA18944.hp2 NA18963.hp2 others(13): Show |
intron_variant | MODIFIER | c.2096-2064G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47610396 | ||||||
| chr17:47610400
|
G | C | 1 | a0001c0001t0003g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2096-2060G>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47610400 | ||||||
| chr17:47610400
|
G | T | 2 | a0001c0006t0003g0339a0001c0006t0003g0340 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2096-2060G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47610400 | ||||||
| chr17:47610401
|
G | A | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.2096-2059G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47610401 | ||||||
| chr17:47610532
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0010 | 2 | HG03927.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2096-1928C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47610532 | ||||||
| chr17:47610629
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0330 | 2 | NA18944.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.2096-1831G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47610629 | ||||||
| chr17:47610661
|
C | T | 5 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0004t0003g0059others(2): Show | 5 | HG01106.hp1 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2096-1799C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47610661 | ||||||
| chr17:47610845
|
C | CT | 54 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0030others(51): Show | 54 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.2096-1589dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47610845 | |||||
| chr17:47610845
|
C | CTT | 35 | a0001c0001t0001g0237a0001c0001t0001g0271a0001c0001t0001g0288others(32): Show | 35 | HG00673.hp2 HG00738.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.2096-1590_2096-158 others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47610845 | |||||
| chr17:47610845
|
C | CTTT | 14 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0038others(11): Show | 14 | HG01109.hp2 HG01261.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.2096-1591_2096-158 others(7): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47610845 | |||||
| chr17:47610845
|
C | CTTTT | 8 | a0001c0001t0001g0081a0001c0001t0003g0037a0001c0001t0003g0053others(5): Show | 8 | HG02083.hp2 HG02559.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.2096-1592_2096-158 others(8): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47610845 | |||||
| chr17:47610845
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0003g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2096-1600_2096-158 others(16): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47610845 | |||||
| chr17:47610845
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0119 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2096-1602_2096-158 others(18): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47610845 | |||||
| chr17:47610845
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0002g0089a0001c0001t0002g0096a0001c0001t0002g0195 | 3 | NA18942.hp2 NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2096-1598_2096-158 others(14): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47610845 | |||||
| chr17:47610845
|
CTTTTTTT others(4): Show |
C | 156 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.2096-1599_2096-158 others(15): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47610845 | |||||
| chr17:47610845
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0002g0192a0001c0001t0002g0202 | 2 | HG01106.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.2096-1600_2096-158 others(16): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47610845 | |||||
| chr17:47611094
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2096-1366C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47611094 | ||||||
| chr17:47611172
|
G | A | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2096-1288G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47611172 | ||||||
| chr17:47611362
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2096-1098A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47611362 | ||||||
| chr17:47611458
|
C | CA | 129 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(126): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.2096-986dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr17 | 47611458 | |||||
| chr17:47611472
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2096-988A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47611472 | ||||||
| chr17:47611483
|
G | T | 2 | a0001c0001t0002g0210a0001c0001t0002g0227 | 2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.2096-977G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47611483 | ||||||
| chr17:47611491
|
C | G | 5 | a0001c0001t0001g0106a0001c0001t0001g0255a0001c0001t0001g0261others(2): Show | 5 | HG02615.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2096-969C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47611491 | ||||||
| chr17:47611963
|
A | G | 1 | a0001c0001t0003g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2096-497A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 17/22 | chr17 | 47611963 | ||||||
| chr17:47612663
|
CT | C | 118 | a0001c0001t0001g0321a0001c0001t0002g0003a0001c0001t0002g0029others(115): Show | 120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.2238+79delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr17 | 47612663 | |||||
| chr17:47612985
|
A | T | 163 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2238+383A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 18/22 | chr17 | 47612985 | ||||||
| chr17:47613031
|
G | A | 1 | a0001c0001t0002g0332 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2238+429G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 18/22 | chr17 | 47613031 | ||||||
| chr17:47613257
|
C | CT | 26 | a0001c0001t0001g0004a0001c0001t0001g0109a0001c0001t0001g0243others(23): Show | 26 | HG00673.hp2 HG00735.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.2239-388dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr17 | 47613257 | |||||
| chr17:47613257
|
CTTTT | C | 29 | a0001c0001t0004g0044a0001c0001t0004g0045a0001c0001t0004g0046others(26): Show | 29 | HG00438.hp1 HG00544.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2239-391_2239-388d others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr17 | 47613257 | |||||
| chr17:47613279
|
T | C | 2 | a0001c0001t0003g0040a0001c0001t0003g0121 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2239-390T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 18/22 | chr17 | 47613279 | ||||||
| chr17:47613279
|
T | TC | 48 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0002g0069others(45): Show | 48 | HG00738.hp1 HG01099.hp2 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.2239-390_2239-389i others(3): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 18/22 | chr17 | 47613279 | ||||||
| chr17:47613424
|
G | A | 4 | a0001c0001t0002g0090a0001c0001t0002g0214a0001c0001t0002g0219others(1): Show | 4 | HG02080.hp2 NA18973.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.2239-245G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 18/22 | chr17 | 47613424 | ||||||
| chr17:47613557
|
G | A | 1 | a0001c0001t0002g0003 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2239-112G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 18/22 | chr17 | 47613557 | ||||||
| chr17:47613586
|
A | G | 1 | a0001c0001t0003g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2239-83A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 18/22 | chr17 | 47613586 | ||||||
| chr17:47613744
|
G | T | 1 | a0001c0001t0002g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2295+19G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47613744 | ||||||
| chr17:47613822
|
A | G | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2295+97A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47613822 | ||||||
| chr17:47613882
|
C | A | 1 | a0001c0001t0001g0006 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2295+157C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47613882 | ||||||
| chr17:47613886
|
ATATGT | A | 12 | a0001c0001t0003g0002a0001c0001t0003g0098a0001c0001t0003g0099others(9): Show | 13 | HG02615.hp1 HG02717.hp2 HG02897.hp1 others(10): Show |
intron_variant | MODIFIER | c.2295+165_2295+169d others(7): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47613886 | |||||
| chr17:47613893
|
ATATCAGT others(2): Show |
A | 49 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(46): Show | 49 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.2295+178_2295+186d others(11): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47613893 | |||||
| chr17:47613979
|
A | AT | 6 | a0001c0001t0001g0260a0001c0001t0001g0271a0001c0001t0001g0334others(3): Show | 6 | HG00673.hp2 HG02145.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2295+268dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47613979 | |||||
| chr17:47613981
|
T | TA | 32 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0045others(29): Show | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2295+256_2295+257i others(3): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47613981 | ||||||
| chr17:47613982
|
T | A | 19 | a0001c0001t0002g0041a0001c0001t0002g0116a0001c0001t0002g0117others(16): Show | 19 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.2295+257T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47613982 | ||||||
| chr17:47614127
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2295+402G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47614127 | ||||||
| chr17:47614158
|
GAGA | G | 3 | a0001c0001t0002g0206a0001c0006t0003g0339a0001c0006t0003g0340 | 3 | HG03669.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2295+436_2295+438d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47614158 | |||||
| chr17:47614318
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2295+593C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47614318 | ||||||
| chr17:47614526
|
C | G | 2 | a0001c0003t0003g0302a0001c0003t0003g0303 | 2 | HG00735.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.2295+801C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47614526 | ||||||
| chr17:47614705
|
C | G | 5 | a0001c0002t0001g0107a0001c0002t0001g0108a0001c0002t0001g0240others(2): Show | 5 | NA18962.hp2 NA18977.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.2295+980C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47614705 | ||||||
| chr17:47614871
|
C | A | 1 | a0001c0001t0004g0148 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2295+1146C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47614871 | ||||||
| chr17:47615013
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2295+1288T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47615013 | ||||||
| chr17:47615026
|
C | T | 1 | a0001c0001t0002g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2295+1301C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47615026 | ||||||
| chr17:47615068
|
T | A | 2 | a0001c0001t0002g0194a0001c0001t0002g0205 | 2 | HG03834.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2295+1343T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47615068 | ||||||
| chr17:47615073
|
C | CT | 7 | a0001c0001t0001g0250a0001c0001t0001g0252a0001c0001t0001g0279others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2295+1371dupT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47615073 | |||||
| chr17:47615073
|
C | CTTT | 45 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0002g0238others(42): Show | 45 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.2295+1369_2295+137 others(7): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47615073 | |||||
| chr17:47615073
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2295+1348C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47615073 | ||||||
| chr17:47615073
|
CT | C | 7 | a0001c0001t0001g0232a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01496.hp2 NA18942.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.2295+1371delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47615073 | |||||
| chr17:47615073
|
CTTTTTTT others(2): Show |
C | 159 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.2295+1363_2295+137 others(13): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47615073 | |||||
| chr17:47615073
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0002g0333a0001c0001t0003g0222 | 2 | HG01256.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2295+1362_2295+137 others(14): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47615073 | |||||
| chr17:47615102
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2295+1377G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47615102 | ||||||
| chr17:47615163
|
TGCCTCCC others(25): Show |
T | 1 | a0001c0001t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2295+1446_2295+147 others(36): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47615163 | |||||
| chr17:47615490
|
A | C | 4 | a0001c0001t0002g0041a0001c0001t0002g0116a0001c0001t0002g0117others(1): Show | 4 | HG01069.hp2 HG01891.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.2295+1765A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47615490 | ||||||
| chr17:47615533
|
C | T | 3 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0298 | 3 | HG02165.hp1 NA19062.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2295+1808C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47615533 | ||||||
| chr17:47615569
|
A | T | 1 | a0001c0001t0002g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2295+1844A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47615569 | ||||||
| chr17:47615651
|
A | G | 1 | a0001c0001t0001g0320 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2295+1926A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47615651 | ||||||
| chr17:47616131
|
A | G | 116 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(113): Show | 118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2296-2219A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47616131 | ||||||
| chr17:47616249
|
C | T | 49 | a0001c0001t0001g0081a0001c0001t0002g0069a0001c0001t0003g0032others(46): Show | 49 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.2296-2101C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47616249 | ||||||
| chr17:47616251
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2296-2099G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47616251 | ||||||
| chr17:47616552
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2296-1798C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47616552 | ||||||
| chr17:47616746
|
T | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2296-1604T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47616746 | ||||||
| chr17:47616784
|
CA | C | 56 | a0001c0001t0001g0081a0001c0001t0001g0115a0001c0001t0001g0247others(53): Show | 56 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.2296-1550delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47616784 | |||||
| chr17:47616865
|
GA | G | 14 | a0001c0001t0001g0330a0001c0003t0003g0300a0001c0003t0003g0301others(11): Show | 14 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.2296-1473delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47616865 | |||||
| chr17:47616882
|
C | T | 13 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.2296-1468C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47616882 | ||||||
| chr17:47617031
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2296-1319A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47617031 | ||||||
| chr17:47617496
|
C | CAT | 4 | a0001c0001t0002g0097a0001c0001t0002g0175a0001c0001t0003g0042others(1): Show | 4 | HG02273.hp2 HG02486.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2296-839_2296-838d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47617496 | |||||
| chr17:47617509
|
A | ATT | 12 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0154others(9): Show | 12 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.2296-840_2296-839i others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47617509 | |||||
| chr17:47617511
|
A | ATT | 134 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(131): Show | 136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.2296-834_2296-833d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47617511 | |||||
| chr17:47617511
|
A | ATTT | 13 | a0001c0003t0003g0300a0001c0003t0003g0301a0001c0003t0003g0302others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.2296-835_2296-833d others(5): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47617511 | |||||
| chr17:47617511
|
A | T | 13 | a0001c0001t0001g0004a0001c0001t0002g0090a0001c0001t0002g0091others(10): Show | 13 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.2296-839A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47617511 | ||||||
| chr17:47617614
|
G | GTAAT | 163 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2296-734_2296-733i others(6): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47617614 | |||||
| chr17:47617744
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0005g0001a0001c0001t0005g0207others(2): Show | 6 | HG01515.hp2 HG01517.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.2296-606A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47617744 | ||||||
| chr17:47617876
|
AT | A | 163 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2296-464delT | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr17 | 47617876 | |||||
| chr17:47618022
|
C | A | 1 | a0001c0001t0002g0165 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2296-328C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47618022 | ||||||
| chr17:47618054
|
T | C | 1 | a0001c0001t0002g0093 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2296-296T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47618054 | ||||||
| chr17:47618245
|
A | C | 13 | a0001c0001t0002g0029a0001c0001t0002g0090a0001c0001t0002g0153others(10): Show | 13 | HG00423.hp2 HG00438.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.2296-105A>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47618245 | ||||||
| chr17:47618343
|
C | A | 1 | a0001c0001t0002g0183 | 1 | HG01358.hp1 | splice_region_variant&intron_variant | LOW | c.2296-7C>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 19/22 | chr17 | 47618343 | ||||||
| chr17:47618466
|
C | T | 162 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(159): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.2403+9C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 20/22 | chr17 | 47618466 | ||||||
| chr17:47618476
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2403+19T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 20/22 | chr17 | 47618476 | ||||||
| chr17:47618548
|
T | C | 116 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(113): Show | 118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2403+91T>C | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 20/22 | chr17 | 47618548 | ||||||
| chr17:47619998
|
C | T | 3 | a0001c0004t0003g0059a0001c0004t0003g0060a0001c0004t0003g0080 | 3 | HG01106.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2607+214C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47619998 | ||||||
| chr17:47620006
|
G | A | 1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2607+222G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47620006 | ||||||
| chr17:47620068
|
G | T | 2 | a0001c0001t0006g0203a0001c0001t0006g0204 | 2 | HG00099.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.2607+284G>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47620068 | ||||||
| chr17:47620138
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2607+354C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47620138 | ||||||
| chr17:47620139
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG00423.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2607+355G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47620139 | ||||||
| chr17:47620182
|
C | T | 1 | a0001c0001t0002g0195 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2607+398C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47620182 | ||||||
| chr17:47620183
|
C | G | 161 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.2607+399C>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47620183 | ||||||
| chr17:47620201
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2607+417G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47620201 | ||||||
| chr17:47620214
|
C | CA | 78 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0018others(75): Show | 79 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.2607+452dupA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr17 | 47620214 | |||||
| chr17:47620214
|
C | CAA | 8 | a0001c0001t0003g0042a0001c0001t0003g0119a0001c0001t0004g0045others(5): Show | 8 | HG00735.hp1 HG03486.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.2607+451_2607+452d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr17 | 47620214 | |||||
| chr17:47620274
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2607+490A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47620274 | ||||||
| chr17:47620569
|
A | G | 1 | a0001c0001t0002g0100 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2607+785A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47620569 | ||||||
| chr17:47620570
|
A | T | 1 | a0001c0001t0002g0100 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2607+786A>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47620570 | ||||||
| chr17:47620809
|
G | A | 163 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2608-959G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47620809 | ||||||
| chr17:47620855
|
C | T | 1 | a0001c0003t0003g0308 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2608-913C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47620855 | ||||||
| chr17:47621117
|
G | A | 65 | a0001c0001t0002g0003a0001c0001t0002g0031a0001c0001t0002g0084others(62): Show | 66 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2608-651G>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47621117 | ||||||
| chr17:47621135
|
C | T | 1 | a0001c0001t0012g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2608-633C>T | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47621135 | ||||||
| chr17:47621146
|
A | G | 1 | a0001c0001t0002g0296 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2608-622A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47621146 | ||||||
| chr17:47621180
|
CA | C | 290 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.2608-568delA | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr17 | 47621180 | |||||
| chr17:47621180
|
CAA | C | 7 | a0001c0001t0001g0265a0001c0001t0001g0281a0001c0001t0001g0283others(4): Show | 7 | HG00323.hp2 HG01069.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2608-569_2608-568d others(4): Show |
NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr17 | 47621180 | |||||
| chr17:47621259
|
A | G | 2 | a0001c0001t0003g0042a0001c0001t0003g0119 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2608-509A>G | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47621259 | ||||||
| chr17:47621543
|
T | A | 1 | a0001c0001t0001g0284 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2608-225T>A | NPEPPS | ENSG00000141279.18 | transcript | ENST00000322157.9 | protein_coding | 22/22 | chr17 | 47621543 |