Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23198 |
|---|---|
| ensemblid | ENSG00000068878.15 |
| hgncid | 20635 |
| symbol | PSME4 |
| name | proteasome activator subunit 4 |
| refseq_nuc | NM_014614.3 |
| refseq_prot | NP_055429.2 |
| ensembl_nuc | ENST00000404125.6 |
| ensembl_prot | ENSP00000384211.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 53864069 |
| end | 53970993 |
| strand | - |
| ver | v1.2 |
| region | chr2:53864069-53970993 |
| region5000 | chr2:53859069-53975993 |
| regionname0 | PSME4_chr2_53864069_53970993 |
| regionname5000 | PSME4_chr2_53859069_53975993 |
| 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 | 1843 | 172 | 63 | 32 | 47 | 11 | 18 | 34 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002 | 0/1 | 1843 | 130 | 15 | 18 | 72 | 3 | 21 | 55 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0003 | 0/0 | 1843 | 57 | 6 | 4 | 47 | 0 | 0 | 39 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0004 | 0/0 | 1843 | 8 | 0 | 6 | 1 | 0 | 1 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0005 | 0/0 | 1843 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0006 | 0/0 | 1843 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0007 | 0/0 | 1843 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0008 | 0/0 | 1843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0009 | 0/0 | 1843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0010 | 0/0 | 1843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0011 | 0/0 | 1843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0012 | 0/0 | 1843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0013 | 0/0 | 1843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0014 | 0/0 | 1843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0015 | 0/0 | 1843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0016 | 0/0 | 1843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0017 | 0/0 | 1843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| 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 | 5532 | 72 | 26 | 19 | 7 | 6 | 13 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0002 | 0/0 | 5532 | 62 | 6 | 0 | 46 | 2 | 8 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0003 | 0/1 | 5532 | 59 | 6 | 16 | 24 | 1 | 11 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0004 | 0/0 | 5532 | 57 | 6 | 4 | 47 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0005 | 0/0 | 5532 | 46 | 1 | 4 | 37 | 2 | 2 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0006 | 0/0 | 5532 | 35 | 23 | 5 | 3 | 3 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0007 | 0/0 | 5532 | 8 | 6 | 1 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0008 | 0/0 | 5532 | 8 | 0 | 6 | 1 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0009 | 0/0 | 5532 | 7 | 6 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0010 | 0/0 | 5532 | 3 | 3 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0011 | 0/0 | 5532 | 3 | 2 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0012 | 0/0 | 5532 | 2 | 2 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0013 | 0/0 | 5532 | 2 | 0 | 0 | 2 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0014 | 0/0 | 5532 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0015 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0016 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0017 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0018 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0019 | 0/0 | 5532 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0020 | 0/0 | 5532 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0021 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0022 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0023 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0024 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0025 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0026 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0027 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0028 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0029 | 0/0 | 5532 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0030 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0031 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0032 | 0/0 | 5532 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| c0033 | 0/0 | 5532 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1719 | 197 | 44 | 37 | 87 | 8 | 20 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0002 | 0/1 | 1717 | 125 | 17 | 20 | 66 | 3 | 18 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0003 | 0/0 | 1719 | 33 | 21 | 6 | 3 | 2 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0004 | 0/0 | 1718 | 7 | 0 | 0 | 7 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0005 | 0/0 | 1719 | 4 | 4 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0006 | 0/0 | 1718 | 4 | 4 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0007 | 0/0 | 1720 | 3 | 0 | 0 | 3 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0008 | 0/0 | 1717 | 2 | 0 | 0 | 2 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0009 | 0/0 | 1719 | 2 | 0 | 0 | 2 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0010 | 0/0 | 1717 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0011 | 0/0 | 1717 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0012 | 0/0 | 1718 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0013 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0014 | 0/0 | 1719 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0015 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| t0016 | 0/0 | 1718 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| 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 | 2 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0203 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| 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 | 5532 | 72 | 26 | 19 | 7 | 6 | 13 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0005 | 0/0 | 5532 | 46 | 1 | 4 | 37 | 2 | 2 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0006 | 0/0 | 5532 | 35 | 23 | 5 | 3 | 3 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0007 | 0/0 | 5532 | 8 | 6 | 1 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0009 | 0/0 | 5532 | 7 | 6 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0017 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0018 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0019 | 0/0 | 5532 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0022 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0002 | 0/0 | 5532 | 62 | 6 | 0 | 46 | 2 | 8 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0003 | 0/1 | 5532 | 59 | 6 | 16 | 24 | 1 | 11 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0010 | 0/0 | 5532 | 3 | 3 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0015 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0020 | 0/0 | 5532 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0021 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0029 | 0/0 | 5532 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0032 | 0/0 | 5532 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0033 | 0/0 | 5532 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0003c0004 | 0/0 | 5532 | 57 | 6 | 4 | 47 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0004c0008 | 0/0 | 5532 | 8 | 0 | 6 | 1 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0005c0011 | 0/0 | 5532 | 3 | 2 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0006c0013 | 0/0 | 5532 | 2 | 0 | 0 | 2 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0007c0012 | 0/0 | 5532 | 2 | 2 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0008c0030 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0009c0027 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0010c0026 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0011c0023 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0012c0024 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0013c0025 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0014c0016 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0015c0028 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0016c0014 | 0/0 | 5532 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0017c0031 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 7250 | 69 | 24 | 19 | 6 | 6 | 13 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0001t0003 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0001t0007 | 0/0 | 7251 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0001t0012 | 0/0 | 7249 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0005t0001 | 0/0 | 7250 | 43 | 1 | 4 | 34 | 2 | 2 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0005t0007 | 0/0 | 7251 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0005t0009 | 0/0 | 7250 | 2 | 0 | 0 | 2 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0006t0003 | 0/0 | 7250 | 29 | 18 | 5 | 3 | 2 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0006t0005 | 0/0 | 7250 | 4 | 4 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0006t0014 | 0/0 | 7250 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0006t0015 | 0/0 | 7251 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0007t0001 | 0/0 | 7250 | 4 | 2 | 1 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0007t0006 | 0/0 | 7249 | 4 | 4 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0009t0001 | 0/0 | 7250 | 6 | 5 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0009t0013 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0017t0001 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0018t0001 | 0/0 | 7250 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0019t0001 | 0/0 | 7250 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0001c0022t0016 | 0/0 | 7249 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0002t0001 | 0/0 | 7250 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0002t0002 | 0/0 | 7248 | 56 | 6 | 0 | 41 | 2 | 7 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0002t0004 | 0/0 | 7249 | 5 | 0 | 0 | 5 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0003t0001 | 0/0 | 7250 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0003t0002 | 0/1 | 7248 | 53 | 5 | 16 | 21 | 1 | 9 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0003t0004 | 0/0 | 7249 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0003t0008 | 0/0 | 7248 | 2 | 0 | 0 | 2 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0003t0010 | 0/0 | 7248 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0003t0011 | 0/0 | 7248 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0010t0002 | 0/0 | 7248 | 3 | 3 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0015t0002 | 0/0 | 7248 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0020t0002 | 0/0 | 7248 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0021t0002 | 0/0 | 7248 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0029t0002 | 0/0 | 7248 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0032t0004 | 0/0 | 7249 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0002c0033t0002 | 0/0 | 7248 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0003c0004t0001 | 0/0 | 7250 | 55 | 6 | 3 | 46 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0003c0004t0003 | 0/0 | 7250 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0003c0004t0007 | 0/0 | 7251 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0004c0008t0001 | 0/0 | 7250 | 8 | 0 | 6 | 1 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0005c0011t0001 | 0/0 | 7250 | 2 | 2 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0005c0011t0002 | 0/0 | 7248 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0006c0013t0002 | 0/0 | 7248 | 2 | 0 | 0 | 2 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0007c0012t0002 | 0/0 | 7248 | 2 | 2 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0008c0030t0002 | 0/0 | 7248 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0009c0027t0003 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0010c0026t0001 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0011c0023t0003 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0012c0024t0001 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0013c0025t0001 | 0/0 | 7250 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0014c0016t0001 | 0/0 | 7250 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0015c0028t0001 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0016c0014t0002 | 0/0 | 7248 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| a0017c0031t0002 | 0/0 | 7248 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | copy fasta | chr2 | 53859069 | 53975993 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0203 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0001t0012g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0007g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0009g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0005t0009g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0003g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0005g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0014g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0006t0015g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0007t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0007t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0007t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0007t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0007t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0007t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0007t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0007t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0009t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0009t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0009t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0009t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0009t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0009t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0009t0013g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0017t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0018t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0019t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0001c0022t0016g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0008g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0008g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0010g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0003t0011g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0010t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0010t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0010t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0015t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0020t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0021t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0029t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0032t0004g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0002c0033t0002g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0003c0004t0007g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0004c0008t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0004c0008t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0004c0008t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0004c0008t0001g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0004c0008t0001g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0004c0008t0001g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0004c0008t0001g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0004c0008t0001g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0005c0011t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0005c0011t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0005c0011t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0006c0013t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0006c0013t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0007c0012t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0007c0012t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0008c0030t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0009c0027t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0010c0026t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0011c0023t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0012c0024t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0013c0025t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0014c0016t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0015c0028t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0016c0014t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| a0017c0031t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0295 | EUR | GBR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00099 | hp2 | a0001 | c0006 | t0014 | g0164 | EUR | GBR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | FIN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0090 | EUR | FIN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0089 | EUR | FIN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0273 | EUR | FIN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00408 | hp1 | a0001 | c0005 | t0001 | g0373 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00408 | hp2 | a0002 | c0003 | t0002 | g0113 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00423 | hp1 | a0001 | c0005 | t0001 | g0348 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00438 | hp1 | a0002 | c0003 | t0002 | g0132 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00438 | hp2 | a0003 | c0004 | t0001 | g0288 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00544 | hp2 | a0003 | c0004 | t0001 | g0252 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00558 | hp1 | a0002 | c0003 | t0002 | g0075 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00558 | hp2 | a0003 | c0004 | t0001 | g0183 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00597 | hp1 | a0001 | c0005 | t0001 | g0326 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00609 | hp1 | a0001 | c0005 | t0001 | g0349 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00621 | hp1 | a0001 | c0005 | t0007 | g0331 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00621 | hp2 | a0002 | c0002 | t0004 | g0121 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00733 | hp2 | a0002 | c0003 | t0002 | g0145 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00735 | hp1 | a0002 | c0003 | t0002 | g0105 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00735 | hp2 | a0003 | c0004 | t0001 | g0290 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG00738 | hp2 | a0001 | c0006 | t0003 | g0161 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01069 | hp1 | a0001 | c0022 | t0016 | g0111 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01069 | hp2 | a0002 | c0003 | t0002 | g0134 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01070 | hp2 | a0004 | c0008 | t0001 | g0378 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01071 | hp2 | a0002 | c0003 | t0002 | g0135 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01074 | hp1 | a0001 | c0009 | t0001 | g0370 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01074 | hp2 | a0013 | c0025 | t0001 | g0259 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01081 | hp2 | a0001 | c0007 | t0001 | g0015 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01099 | hp2 | a0001 | c0006 | t0003 | g0027 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01106 | hp1 | a0001 | c0006 | t0003 | g0030 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01106 | hp2 | a0002 | c0003 | t0002 | g0108 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01109 | hp1 | a0003 | c0004 | t0003 | g0219 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01109 | hp2 | a0004 | c0008 | t0001 | g0381 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01167 | hp1 | a0002 | c0003 | t0002 | g0138 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01167 | hp2 | a0001 | c0006 | t0003 | g0156 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01168 | hp2 | a0002 | c0003 | t0002 | g0146 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01169 | hp2 | a0002 | c0003 | t0002 | g0147 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01175 | hp1 | a0002 | c0003 | t0002 | g0133 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01175 | hp2 | a0001 | c0005 | t0001 | g0313 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01192 | hp2 | a0002 | c0003 | t0002 | g0020 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01243 | hp1 | a0005 | c0011 | t0002 | g0363 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01243 | hp2 | a0001 | c0005 | t0001 | g0182 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01255 | hp1 | a0002 | c0015 | t0002 | g0359 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01256 | hp1 | a0004 | c0008 | t0001 | g0380 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01256 | hp2 | a0002 | c0003 | t0002 | g0149 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01257 | hp1 | a0004 | c0008 | t0001 | g0382 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01257 | hp2 | a0002 | c0003 | t0002 | g0136 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01261 | hp1 | a0017 | c0031 | t0002 | g0021 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01346 | hp2 | a0001 | c0006 | t0003 | g0029 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01358 | hp1 | a0001 | c0005 | t0001 | g0315 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01496 | hp2 | a0001 | c0018 | t0001 | g0226 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01515 | hp1 | a0002 | c0003 | t0002 | g0152 | EUR | IBS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01515 | hp2 | a0001 | c0005 | t0001 | g0316 | EUR | IBS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01516 | hp2 | a0001 | c0006 | t0003 | g0026 | EUR | IBS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01517 | hp2 | a0001 | c0005 | t0001 | g0318 | EUR | IBS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01884 | hp1 | a0001 | c0006 | t0003 | g0266 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01884 | hp2 | a0003 | c0004 | t0001 | g0253 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01891 | hp1 | a0009 | c0027 | t0003 | g0162 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01891 | hp2 | a0005 | c0011 | t0001 | g0362 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01928 | hp1 | a0004 | c0008 | t0001 | g0379 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01928 | hp2 | a0002 | c0003 | t0002 | g0148 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01943 | hp1 | a0003 | c0004 | t0001 | g0258 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01943 | hp2 | a0002 | c0021 | t0002 | g0110 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01952 | hp2 | a0002 | c0003 | t0002 | g0109 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01978 | hp1 | a0002 | c0003 | t0002 | g0139 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01978 | hp2 | a0014 | c0016 | t0001 | g0339 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02004 | hp1 | a0004 | c0008 | t0001 | g0376 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02004 | hp2 | a0003 | c0004 | t0001 | g0260 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0355 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02015 | hp2 | a0003 | c0004 | t0001 | g0249 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02027 | hp2 | a0003 | c0004 | t0001 | g0033 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02040 | hp1 | a0001 | c0005 | t0001 | g0372 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02056 | hp2 | a0001 | c0005 | t0001 | g0342 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02083 | hp2 | a0002 | c0003 | t0002 | g0128 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02129 | hp1 | a0001 | c0005 | t0001 | g0329 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02132 | hp1 | a0003 | c0004 | t0001 | g0300 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02132 | hp2 | a0001 | c0005 | t0001 | g0321 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02145 | hp1 | a0001 | c0006 | t0005 | g0004 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | CDX | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02155 | hp2 | a0002 | c0003 | t0002 | g0066 | EAS | CDX | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02257 | hp2 | a0001 | c0006 | t0003 | g0172 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02258 | hp2 | a0001 | c0006 | t0003 | g0218 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02280 | hp1 | a0003 | c0004 | t0001 | g0247 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02280 | hp2 | a0001 | c0006 | t0003 | g0175 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02293 | hp1 | a0001 | c0005 | t0001 | g0333 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02451 | hp1 | a0001 | c0007 | t0001 | g0179 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02523 | hp1 | a0003 | c0004 | t0001 | g0256 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02523 | hp2 | a0002 | c0002 | t0004 | g0096 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02572 | hp1 | a0002 | c0010 | t0002 | g0018 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02572 | hp2 | a0003 | c0004 | t0001 | g0042 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02602 | hp1 | a0002 | c0003 | t0011 | g0009 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0084 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02615 | hp1 | a0001 | c0006 | t0003 | g0176 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0356 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0085 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02622 | hp2 | a0003 | c0004 | t0001 | g0245 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02630 | hp2 | a0001 | c0006 | t0003 | g0171 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02647 | hp1 | a0003 | c0004 | t0001 | g0192 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02647 | hp2 | a0001 | c0006 | t0003 | g0371 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02683 | hp1 | a0001 | c0007 | t0001 | g0017 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02683 | hp2 | a0001 | c0005 | t0001 | g0319 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0131 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02717 | hp1 | a0001 | c0009 | t0001 | g0367 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02717 | hp2 | a0008 | c0030 | t0002 | g0310 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02735 | hp1 | a0004 | c0008 | t0001 | g0383 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02735 | hp2 | a0002 | c0003 | t0002 | g0024 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02738 | hp1 | a0001 | c0019 | t0001 | g0037 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02809 | hp1 | a0002 | c0003 | t0010 | g0006 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0357 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02818 | hp1 | a0001 | c0009 | t0001 | g0369 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02818 | hp2 | a0007 | c0012 | t0002 | g0062 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02886 | hp1 | a0001 | c0005 | t0001 | g0322 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02886 | hp2 | a0001 | c0006 | t0003 | g0157 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02895 | hp1 | a0001 | c0006 | t0003 | g0158 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0119 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02896 | hp2 | a0001 | c0006 | t0003 | g0168 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0086 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02922 | hp2 | a0002 | c0010 | t0002 | g0056 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02965 | hp2 | a0001 | c0007 | t0006 | g0196 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02970 | hp1 | a0002 | c0003 | t0002 | g0055 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02970 | hp2 | a0001 | c0006 | t0003 | g0031 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02976 | hp2 | a0001 | c0006 | t0005 | g0003 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03017 | hp2 | a0002 | c0029 | t0002 | g0307 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03041 | hp2 | a0002 | c0003 | t0002 | g0049 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03098 | hp1 | a0010 | c0026 | t0001 | g0013 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03098 | hp2 | a0001 | c0017 | t0001 | g0309 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03130 | hp2 | a0007 | c0012 | t0002 | g0058 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03139 | hp1 | a0001 | c0009 | t0001 | g0366 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03139 | hp2 | a0001 | c0007 | t0001 | g0361 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03195 | hp1 | a0001 | c0006 | t0015 | g0169 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0358 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03209 | hp1 | a0001 | c0007 | t0006 | g0197 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03225 | hp2 | a0001 | c0007 | t0006 | g0014 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03239 | hp1 | a0002 | c0003 | t0002 | g0060 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03453 | hp1 | a0005 | c0011 | t0001 | g0364 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03486 | hp1 | a0001 | c0006 | t0003 | g0174 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03490 | hp1 | a0002 | c0003 | t0002 | g0079 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03516 | hp1 | a0001 | c0001 | t0012 | g0041 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03516 | hp2 | a0001 | c0009 | t0001 | g0360 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03540 | hp2 | a0015 | c0028 | t0001 | g0368 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03579 | hp1 | a0012 | c0024 | t0001 | g0312 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03579 | hp2 | a0002 | c0003 | t0002 | g0074 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0142 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03704 | hp1 | a0001 | c0006 | t0003 | g0160 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03710 | hp1 | a0002 | c0003 | t0002 | g0144 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03710 | hp2 | a0002 | c0003 | t0002 | g0137 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03831 | hp1 | a0001 | c0005 | t0001 | g0353 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0154 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03834 | hp1 | a0002 | c0003 | t0002 | g0011 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0153 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03927 | hp1 | a0002 | c0003 | t0002 | g0112 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0232 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03942 | hp1 | a0002 | c0033 | t0002 | g0375 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03942 | hp2 | a0002 | c0003 | t0001 | g0080 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG04115 | hp1 | a0002 | c0003 | t0002 | g0106 | SAS | STU | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0151 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | STU | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG04199 | hp2 | a0002 | c0003 | t0002 | g0127 | SAS | STU | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | STU | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0141 | SAS | STU | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18522 | hp1 | a0001 | c0009 | t0001 | g0365 | AFR | YRI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | YRI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | CHB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18612 | hp2 | a0001 | c0005 | t0001 | g0332 | EAS | CHB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18747 | hp1 | a0001 | c0005 | t0001 | g0324 | EAS | CHB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18747 | hp2 | a0003 | c0004 | t0001 | g0195 | EAS | CHB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18906 | hp2 | a0001 | c0006 | t0003 | g0155 | AFR | YRI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18940 | hp1 | a0001 | c0005 | t0001 | g0351 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18940 | hp2 | a0003 | c0004 | t0001 | g0291 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18941 | hp2 | a0001 | c0005 | t0001 | g0320 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18943 | hp1 | a0001 | c0005 | t0001 | g0347 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18943 | hp2 | a0002 | c0003 | t0008 | g0008 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18945 | hp1 | a0003 | c0004 | t0001 | g0268 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18948 | hp1 | a0002 | c0003 | t0002 | g0297 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18948 | hp2 | a0003 | c0004 | t0001 | g0202 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18950 | hp1 | a0001 | c0005 | t0001 | g0327 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18950 | hp2 | a0002 | c0003 | t0002 | g0299 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18951 | hp2 | a0001 | c0006 | t0003 | g0166 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18952 | hp1 | a0003 | c0004 | t0001 | g0201 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18952 | hp2 | a0002 | c0020 | t0002 | g0222 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18953 | hp1 | a0003 | c0004 | t0001 | g0285 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18953 | hp2 | a0001 | c0005 | t0001 | g0346 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18954 | hp2 | a0004 | c0008 | t0001 | g0377 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18959 | hp2 | a0003 | c0004 | t0001 | g0257 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18961 | hp2 | a0001 | c0001 | t0007 | g0224 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18962 | hp1 | a0003 | c0004 | t0001 | g0246 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18963 | hp1 | a0003 | c0004 | t0007 | g0287 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18963 | hp2 | a0001 | c0005 | t0001 | g0325 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18964 | hp1 | a0001 | c0005 | t0001 | g0330 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18964 | hp2 | a0003 | c0004 | t0001 | g0286 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18965 | hp1 | a0003 | c0004 | t0001 | g0039 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18967 | hp1 | a0002 | c0003 | t0002 | g0019 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18967 | hp2 | a0003 | c0004 | t0001 | g0289 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18968 | hp2 | a0001 | c0005 | t0009 | g0220 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18969 | hp1 | a0001 | c0005 | t0001 | g0317 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18969 | hp2 | a0003 | c0004 | t0001 | g0274 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18970 | hp1 | a0002 | c0003 | t0002 | g0071 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18971 | hp2 | a0001 | c0005 | t0009 | g0221 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18972 | hp1 | a0003 | c0004 | t0001 | g0200 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18973 | hp1 | a0001 | c0006 | t0003 | g0163 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18973 | hp2 | a0003 | c0004 | t0001 | g0194 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18975 | hp2 | a0001 | c0006 | t0003 | g0165 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18978 | hp2 | a0003 | c0004 | t0001 | g0304 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18981 | hp1 | a0002 | c0003 | t0002 | g0114 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18981 | hp2 | a0003 | c0004 | t0001 | g0301 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18982 | hp1 | a0002 | c0003 | t0002 | g0076 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18983 | hp1 | a0001 | c0005 | t0001 | g0343 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18983 | hp2 | a0003 | c0004 | t0001 | g0264 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18984 | hp1 | a0002 | c0003 | t0002 | g0070 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18986 | hp2 | a0001 | c0005 | t0001 | g0334 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18988 | hp1 | a0016 | c0014 | t0002 | g0067 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18989 | hp1 | a0003 | c0004 | t0001 | g0303 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18990 | hp2 | a0003 | c0004 | t0001 | g0248 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18991 | hp1 | a0002 | c0003 | t0002 | g0016 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18991 | hp2 | a0002 | c0032 | t0004 | g0374 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18994 | hp1 | a0003 | c0004 | t0001 | g0034 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18994 | hp2 | a0001 | c0005 | t0001 | g0345 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18995 | hp1 | a0003 | c0004 | t0001 | g0298 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18995 | hp2 | a0002 | c0003 | t0002 | g0072 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18999 | hp1 | a0003 | c0004 | t0001 | g0254 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19000 | hp1 | a0001 | c0005 | t0001 | g0311 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19000 | hp2 | a0002 | c0003 | t0002 | g0104 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19001 | hp1 | a0002 | c0002 | t0004 | g0048 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19001 | hp2 | a0003 | c0004 | t0001 | g0040 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19002 | hp1 | a0006 | c0013 | t0002 | g0046 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19002 | hp2 | a0001 | c0005 | t0001 | g0341 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19003 | hp2 | a0002 | c0003 | t0002 | g0081 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19004 | hp1 | a0003 | c0004 | t0001 | g0265 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19004 | hp2 | a0001 | c0005 | t0001 | g0328 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19006 | hp1 | a0006 | c0013 | t0002 | g0073 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19006 | hp2 | a0003 | c0004 | t0001 | g0306 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19009 | hp1 | a0003 | c0004 | t0001 | g0262 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19009 | hp2 | a0001 | c0005 | t0001 | g0338 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19011 | hp1 | a0003 | c0004 | t0001 | g0302 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19030 | hp1 | a0001 | c0006 | t0003 | g0167 | AFR | LWK | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19043 | hp1 | a0002 | c0003 | t0002 | g0059 | AFR | LWK | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19043 | hp2 | a0001 | c0006 | t0003 | g0177 | AFR | LWK | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19055 | hp1 | a0002 | c0003 | t0004 | g0340 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19056 | hp1 | a0003 | c0004 | t0001 | g0269 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19057 | hp1 | a0003 | c0004 | t0001 | g0250 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19057 | hp2 | a0001 | c0005 | t0001 | g0337 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19058 | hp2 | a0003 | c0004 | t0001 | g0283 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19062 | hp1 | a0001 | c0005 | t0001 | g0354 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19063 | hp1 | a0003 | c0004 | t0001 | g0263 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19065 | hp2 | a0001 | c0005 | t0001 | g0335 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19066 | hp1 | a0001 | c0005 | t0001 | g0344 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19067 | hp1 | a0002 | c0003 | t0002 | g0107 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19067 | hp2 | a0002 | c0002 | t0004 | g0123 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19070 | hp1 | a0003 | c0004 | t0001 | g0261 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19070 | hp2 | a0002 | c0003 | t0002 | g0052 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19072 | hp1 | a0002 | c0002 | t0004 | g0064 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19072 | hp2 | a0003 | c0004 | t0001 | g0271 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19075 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19075 | hp2 | a0003 | c0004 | t0001 | g0208 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19077 | hp1 | a0003 | c0004 | t0001 | g0193 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19079 | hp2 | a0001 | c0005 | t0001 | g0352 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19080 | hp2 | a0001 | c0005 | t0001 | g0323 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19085 | hp1 | a0003 | c0004 | t0001 | g0207 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19085 | hp2 | a0002 | c0003 | t0008 | g0007 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19086 | hp1 | a0002 | c0003 | t0002 | g0069 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19086 | hp2 | a0003 | c0004 | t0001 | g0284 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19087 | hp1 | a0001 | c0005 | t0001 | g0314 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19088 | hp1 | a0003 | c0004 | t0001 | g0251 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19088 | hp2 | a0002 | c0003 | t0002 | g0057 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19091 | hp1 | a0001 | c0005 | t0001 | g0336 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19091 | hp2 | a0002 | c0003 | t0002 | g0061 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA19240 | hp2 | a0001 | c0006 | t0003 | g0159 | AFR | YRI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ASW | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA20129 | hp2 | a0001 | c0006 | t0005 | g0002 | AFR | ASW | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA20805 | hp2 | a0001 | c0006 | t0003 | g0025 | EUR | TSI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG01123 | hp2 | a0002 | c0003 | t0002 | g0150 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02109 | hp1 | a0001 | c0006 | t0005 | g0005 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0255 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02486 | hp1 | a0011 | c0023 | t0003 | g0028 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02559 | hp1 | a0001 | c0006 | t0003 | g0178 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG02559 | hp2 | a0001 | c0007 | t0006 | g0012 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG03471 | hp2 | a0002 | c0010 | t0002 | g0051 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG06807 | hp1 | a0002 | c0003 | t0002 | g0078 | AFR | USA | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| HG06807 | hp2 | a0001 | c0006 | t0003 | g0170 | AFR | USA | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18955 | hp1 | a0003 | c0004 | t0001 | g0032 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA18955 | hp2 | a0001 | c0005 | t0001 | g0350 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | USA | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| NA20300 | hp2 | a0001 | c0009 | t0013 | g0292 | AFR | USA | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0002 | g0077 | REF | REF | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0203 | REF | REF | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53869391
|
T | C | 1 | a0007 | 2 | HG02818.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.5248A>G | p.Thr1750Ala | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/47 | 5457/7250 | 5248/5532 | 1750/1843 | chr2 | 53869391 | ||
| chr2:53892888
|
A | T | 7 | a0002a0005a0006others(4): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
missense_variant | MODERATE | c.4111T>A | p.Ser1371Thr | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/47 | 4320/7250 | 4111/5532 | 1371/1843 | chr2 | 53892888 | ||
| chr2:53904110
|
T | A | 1 | a0006 | 2 | NA19002.hp1 NA19006.hp1 |
missense_variant | MODERATE | c.2990A>T | p.Tyr997Phe | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/47 | 3199/7250 | 2990/5532 | 997/1843 | chr2 | 53904110 | ||
| chr2:53906849
|
T | C | 1 | a0013 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.2804A>G | p.His935Arg | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 25/47 | 3013/7250 | 2804/5532 | 935/1843 | chr2 | 53906849 | ||
| chr2:53908331
|
T | C | 1 | a0011 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2773A>G | p.Met925Val | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/47 | 2982/7250 | 2773/5532 | 925/1843 | chr2 | 53908331 | ||
| chr2:53908553
|
T | C | 1 | a0012 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.2642A>G | p.Asp881Gly | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 23/47 | 2851/7250 | 2642/5532 | 881/1843 | chr2 | 53908553 | ||
| chr2:53908799
|
T | C | 2 | a0003a0013 | 58 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(55): Show |
missense_variant | MODERATE | c.2614A>G | p.Ile872Val | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 22/47 | 2823/7250 | 2614/5532 | 872/1843 | chr2 | 53908799 | ||
| chr2:53919155
|
T | C | 1 | a0010 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.2512A>G | p.Asn838Asp | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/47 | 2721/7250 | 2512/5532 | 838/1843 | chr2 | 53919155 | ||
| chr2:53920941
|
C | T | 1 | a0014 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.2210G>A | p.Cys737Tyr | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 18/47 | 2419/7250 | 2210/5532 | 737/1843 | chr2 | 53920941 | ||
| chr2:53920978
|
G | A | 1 | a0009 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.2173C>T | p.Leu725Phe | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 18/47 | 2382/7250 | 2173/5532 | 725/1843 | chr2 | 53920978 | ||
| chr2:53931953
|
T | C | 1 | a0015 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1198A>G | p.Ile400Val | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/47 | 1407/7250 | 1198/5532 | 400/1843 | chr2 | 53931953 | ||
| chr2:53936137
|
A | T | 1 | a0016 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.784T>A | p.Leu262Met | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/47 | 993/7250 | 784/5532 | 262/1843 | chr2 | 53936137 | ||
| chr2:53937391
|
T | C | 2 | a0005a0008 | 4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.695A>G | p.Lys232Arg | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 5/47 | 904/7250 | 695/5532 | 232/1843 | chr2 | 53937391 | ||
| chr2:53948527
|
G | A | 1 | a0008 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.394C>T | p.Leu132Phe | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/47 | 603/7250 | 394/5532 | 132/1843 | chr2 | 53948527 | ||
| chr2:53949279
|
T | C | 1 | a0017 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.247A>G | p.Ile83Val | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/47 | 456/7250 | 247/5532 | 83/1843 | chr2 | 53949279 | ||
| chr2:53970692
|
C | A | 1 | a0004 | 8 | HG01070.hp2 HG01109.hp2 HG01256.hp1 others(5): Show |
missense_variant | MODERATE | c.93G>T | p.Glu31Asp | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/47 | 302/7250 | 93/5532 | 31/1843 | chr2 | 53970692 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53866122
|
G | A | 1 | a0002c0021 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.5499C>T | p.Thr1833Thr | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 46/47 | 5708/7250 | 5499/5532 | 1833/1843 | chr2 | 53866122 | ||
| chr2:53866819
|
G | A | 3 | a0001c0006a0009c0027a0011c0023 | 37 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(34): Show |
synonymous_variant | LOW | c.5325C>T | p.Tyr1775Tyr | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 45/47 | 5534/7250 | 5325/5532 | 1775/1843 | chr2 | 53866819 | ||
| chr2:53887962
|
A | T | 1 | a0001c0019 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.4416T>A | p.Leu1472Leu | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 39/47 | 4625/7250 | 4416/5532 | 1472/1843 | chr2 | 53887962 | ||
| chr2:53888767
|
A | G | 16 | a0001c0022a0002c0002a0002c0003others(13): Show | 141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
synonymous_variant | LOW | c.4342T>C | p.Leu1448Leu | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/47 | 4551/7250 | 4342/5532 | 1448/1843 | chr2 | 53888767 | ||
| chr2:53893683
|
G | A | 23 | a0001c0005a0001c0006a0001c0009others(20): Show | 240 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
synonymous_variant | LOW | c.4029C>T | p.Cys1343Cys | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/47 | 4238/7250 | 4029/5532 | 1343/1843 | chr2 | 53893683 | ||
| chr2:53898342
|
A | G | 1 | a0002c0010 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.3435T>C | p.Asn1145Asn | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 30/47 | 3644/7250 | 3435/5532 | 1145/1843 | chr2 | 53898342 | ||
| chr2:53899904
|
C | T | 25 | a0001c0005a0001c0006a0001c0007others(22): Show | 249 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(246): Show |
synonymous_variant | LOW | c.3399G>A | p.Gln1133Gln | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/47 | 3608/7250 | 3399/5532 | 1133/1843 | chr2 | 53899904 | ||
| chr2:53906607
|
T | C | 8 | a0001c0022a0002c0003a0002c0021others(5): Show | 68 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
synonymous_variant | LOW | c.2934A>G | p.Ser978Ser | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/47 | 3143/7250 | 2934/5532 | 978/1843 | chr2 | 53906607 | ||
| chr2:53919177
|
C | T | 1 | a0001c0018 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.2490G>A | p.Pro830Pro | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/47 | 2699/7250 | 2490/5532 | 830/1843 | chr2 | 53919177 | ||
| chr2:53923100
|
A | G | 4 | a0001c0005a0001c0017a0004c0008others(1): Show | 56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
synonymous_variant | LOW | c.1927T>C | p.Leu643Leu | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 16/47 | 2136/7250 | 1927/5532 | 643/1843 | chr2 | 53923100 | ||
| chr2:53931945
|
C | T | 2 | a0005c0011a0008c0030 | 4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
synonymous_variant | LOW | c.1206G>A | p.Gln402Gln | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/47 | 1415/7250 | 1206/5532 | 402/1843 | chr2 | 53931945 | ||
| chr2:53931969
|
T | C | 1 | a0002c0029 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1182A>G | p.Thr394Thr | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/47 | 1391/7250 | 1182/5532 | 394/1843 | chr2 | 53931969 | ||
| chr2:53936108
|
A | G | 1 | a0002c0015 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.813T>C | p.Asp271Asp | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/47 | 1022/7250 | 813/5532 | 271/1843 | chr2 | 53936108 | ||
| chr2:53970599
|
G | A | 1 | a0002c0033 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.186C>T | p.Ala62Ala | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/47 | 395/7250 | 186/5532 | 62/1843 | chr2 | 53970599 | ||
| chr2:53970599
|
G | C | 1 | a0002c0032 | 1 | NA18991.hp2 | synonymous_variant | LOW | c.186C>G | p.Ala62Ala | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/47 | 395/7250 | 186/5532 | 62/1843 | chr2 | 53970599 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53864127
|
A | G | 1 | a0001c0006t0014 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1451T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1962 | chr2 | 53864127 | |||||
| chr2:53864317
|
C | T | 1 | a0001c0009t0013 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1261G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1772 | chr2 | 53864317 | |||||
| chr2:53864433
|
G | GA | 5 | a0001c0001t0007a0001c0005t0007a0001c0006t0015others(2): Show | 8 | HG00621.hp1 HG02559.hp2 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1144dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1655 | chr2 | 53864433 | |||||
| chr2:53864433
|
GA | G | 19 | a0001c0001t0012a0001c0022t0016a0002c0002t0002others(16): Show | 131 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1144delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1655 | chr2 | 53864433 | |||||
| chr2:53864551
|
C | T | 21 | a0001c0022t0016a0002c0002t0002a0002c0002t0004others(18): Show | 137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1027G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1538 | chr2 | 53864551 | |||||
| chr2:53864567
|
T | C | 1 | a0001c0005t0009 | 2 | NA18968.hp2 NA18971.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1011A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1522 | chr2 | 53864567 | |||||
| chr2:53864611
|
T | C | 8 | a0001c0001t0003a0001c0006t0003a0001c0006t0005others(5): Show | 39 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*967A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1478 | chr2 | 53864611 | |||||
| chr2:53864638
|
ACT | A | 1 | a0001c0007t0006 | 4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*938_*939delAG | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1449 | chr2 | 53864638 | |||||
| chr2:53864748
|
T | A | 21 | a0001c0022t0016a0002c0002t0002a0002c0002t0004others(18): Show | 137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*830A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1341 | chr2 | 53864748 | |||||
| chr2:53865348
|
CA | C | 20 | a0002c0002t0002a0002c0002t0004a0002c0003t0002others(17): Show | 136 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*229delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 740 | chr2 | 53865348 | |||||
| chr2:53970806
|
A | C | 1 | a0002c0003t0011 | 1 | HG02602.hp1 | 5_prime_UTR_variant | MODIFIER | c.-22T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/47 | 22 | chr2 | 53970806 | |||||
| chr2:53970857
|
C | T | 1 | a0002c0003t0008 | 2 | NA18943.hp2 NA19085.hp2 |
5_prime_UTR_variant | MODIFIER | c.-73G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/47 | 73 | chr2 | 53970857 | |||||
| chr2:53970962
|
C | G | 2 | a0001c0006t0005a0002c0003t0010 | 5 | HG02109.hp1 HG02145.hp1 HG02809.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-178G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/47 | 178 | chr2 | 53970962 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53865614
|
A | G | 1 | a0010c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.*5-41T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 46/46 | chr2 | 53865614 | ||||||
| chr2:53865847
|
C | T | 244 | a0001c0001t0003g0204a0001c0005t0001g0182a0001c0005t0001g0311others(241): Show | 244 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.*4+238G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 46/46 | chr2 | 53865847 | ||||||
| chr2:53866286
|
T | C | 2 | a0001c0007t0001g0361a0010c0026t0001g0013 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5398-63A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 45/46 | chr2 | 53866286 | ||||||
| chr2:53866361
|
A | G | 2 | a0001c0006t0003g0027a0001c0006t0003g0030 | 2 | HG01099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.5398-138T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 45/46 | chr2 | 53866361 | ||||||
| chr2:53866731
|
T | C | 3 | a0001c0006t0003g0172a0001c0006t0003g0175a0001c0006t0003g0371 | 3 | HG02257.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.5397+16A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 45/46 | chr2 | 53866731 | ||||||
| chr2:53866908
|
A | C | 1 | a0001c0005t0001g0322 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5264-28T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53866908 | ||||||
| chr2:53866918
|
A | G | 1 | a0003c0004t0001g0194 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.5264-38T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53866918 | ||||||
| chr2:53866933
|
T | C | 2 | a0001c0007t0001g0361a0010c0026t0001g0013 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5264-53A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53866933 | ||||||
| chr2:53867106
|
C | T | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5264-226G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867106 | ||||||
| chr2:53867147
|
C | A | 37 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(34): Show | 37 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.5264-267G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867147 | ||||||
| chr2:53867178
|
G | A | 4 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(1): Show | 4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5264-298C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867178 | ||||||
| chr2:53867230
|
C | G | 3 | a0001c0006t0003g0163a0001c0006t0003g0165a0001c0006t0003g0166 | 3 | NA18951.hp2 NA18973.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.5264-350G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867230 | ||||||
| chr2:53867284
|
G | C | 245 | a0001c0001t0003g0204a0001c0005t0001g0182a0001c0005t0001g0311others(242): Show | 245 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.5264-404C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867284 | ||||||
| chr2:53867312
|
T | C | 14 | a0001c0001t0001g0173a0001c0001t0001g0180a0001c0001t0001g0198others(11): Show | 14 | HG02451.hp2 HG02486.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.5264-432A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867312 | ||||||
| chr2:53867320
|
C | T | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5264-440G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867320 | ||||||
| chr2:53867326
|
G | A | 1 | a0002c0003t0001g0080 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5264-446C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867326 | ||||||
| chr2:53867395
|
G | T | 1 | a0001c0006t0003g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5264-515C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867395 | ||||||
| chr2:53867500
|
AG | A | 61 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(58): Show | 61 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.5264-621delC | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867500 | ||||||
| chr2:53867501
|
G | GA | 4 | a0002c0003t0002g0146a0002c0032t0004g0374a0005c0011t0002g0363others(1): Show | 4 | HG01168.hp2 HG01243.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.5264-622_5264-621i others(3): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867501 | ||||||
| chr2:53867501
|
G | GAA | 43 | a0002c0003t0002g0011a0002c0003t0002g0016a0002c0003t0002g0020others(40): Show | 43 | HG00408.hp2 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.5264-622_5264-621i others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867501 | ||||||
| chr2:53867501
|
G | GAAA | 21 | a0001c0022t0016g0111a0002c0003t0002g0049a0002c0003t0002g0052others(18): Show | 21 | HG00438.hp1 HG00558.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.5264-622_5264-621i others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867501 | ||||||
| chr2:53867502
|
G | A | 74 | a0001c0022t0016g0111a0002c0002t0002g0120a0002c0003t0002g0011others(71): Show | 74 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.5264-622C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867502 | ||||||
| chr2:53867502
|
G | GA | 73 | a0001c0001t0001g0211a0001c0001t0001g0241a0001c0005t0001g0311others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.5264-623dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867502 | ||||||
| chr2:53867526
|
A | G | 141 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.5264-646T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867526 | ||||||
| chr2:53867646
|
G | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5264-766C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867646 | ||||||
| chr2:53867648
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5264-768G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867648 | ||||||
| chr2:53867651
|
T | C | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5264-771A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867651 | ||||||
| chr2:53867669
|
C | CA | 38 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0305others(35): Show | 38 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.5264-790dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867669 | ||||||
| chr2:53867669
|
CA | C | 69 | a0001c0001t0001g0205a0001c0001t0001g0239a0001c0005t0001g0182others(66): Show | 69 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.5264-790delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867669 | ||||||
| chr2:53867669
|
CAAA | C | 67 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(64): Show | 67 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.5264-792_5264-790d others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867669 | ||||||
| chr2:53867669
|
CAAAA | C | 67 | a0001c0022t0016g0111a0002c0003t0002g0011a0002c0003t0002g0016others(64): Show | 67 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.5264-793_5264-790d others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867669 | ||||||
| chr2:53867887
|
A | G | 1 | a0003c0004t0001g0255 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5264-1007T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867887 | ||||||
| chr2:53868151
|
A | G | 1 | a0001c0006t0014g0164 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5263+1225T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868151 | ||||||
| chr2:53868180
|
G | T | 66 | a0002c0003t0002g0011a0002c0003t0002g0016a0002c0003t0002g0019others(63): Show | 66 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.5263+1196C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868180 | ||||||
| chr2:53868227
|
T | C | 1 | a0002c0002t0002g0141 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5263+1149A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868227 | ||||||
| chr2:53868313
|
G | A | 37 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(34): Show | 37 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.5263+1063C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868313 | ||||||
| chr2:53868345
|
G | T | 1 | a0003c0004t0001g0251 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.5263+1031C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868345 | ||||||
| chr2:53868357
|
C | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0235a0001c0001t0001g0308 | 3 | HG01261.hp2 HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.5263+1019G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868357 | ||||||
| chr2:53868456
|
AAATATAT others(100): Show |
A | 66 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.5263+813_5263+919d others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868456 | ||||||
| chr2:53868476
|
A | AT | 69 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.5263+899dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868476 | ||||||
| chr2:53868482
|
A | AAT | 15 | a0001c0001t0001g0276a0001c0006t0003g0031a0001c0006t0003g0155others(12): Show | 15 | HG01167.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.5263+892_5263+893d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868482 | ||||||
| chr2:53868482
|
AAT | A | 5 | a0001c0001t0001g0035a0001c0007t0001g0015a0001c0007t0001g0017others(2): Show | 5 | HG01081.hp2 HG02451.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.5263+892_5263+893d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868482 | ||||||
| chr2:53868486
|
TATATATA others(62): Show |
T | 135 | a0001c0022t0016g0111a0002c0002t0002g0022a0002c0002t0002g0023others(132): Show | 135 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.5263+821_5263+889d others(71): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868486 | ||||||
| chr2:53868488
|
TATATATA others(60): Show |
T | 1 | a0002c0002t0002g0125 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.5263+821_5263+887d others(69): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868488 | ||||||
| chr2:53868497
|
G | GATATATA others(27): Show |
1 | a0001c0006t0003g0172 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5263+845_5263+878d others(36): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868497 | ||||||
| chr2:53868509
|
A | AAAATATA others(26): Show |
32 | a0001c0001t0003g0204a0001c0006t0003g0025a0001c0006t0003g0026others(29): Show | 32 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.5263+834_5263+866d others(35): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868509 | ||||||
| chr2:53868509
|
A | AAAATATA others(60): Show |
1 | a0001c0006t0003g0175 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5263+866_5263+867i others(69): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868509 | ||||||
| chr2:53868526
|
TATATAAT others(22): Show |
T | 1 | a0017c0031t0002g0021 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.5263+821_5263+849d others(31): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868526 | ||||||
| chr2:53868542
|
T | TA | 15 | a0001c0006t0005g0002a0001c0006t0005g0004a0003c0004t0001g0040others(12): Show | 15 | HG02132.hp1 HG02145.hp1 NA18959.hp2 others(12): Show |
intron_variant | MODIFIER | c.5263+833dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868542 | ||||||
| chr2:53868542
|
T | TAAAATAT others(61): Show |
1 | a0001c0006t0003g0371 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5263+833_5263+834i others(70): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868542 | ||||||
| chr2:53868564
|
A | AATATATA others(26): Show |
1 | a0009c0027t0003g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5263+811_5263+812i others(35): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868564 | ||||||
| chr2:53868572
|
T | A | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5263+804A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868572 | ||||||
| chr2:53868575
|
TA | T | 7 | a0001c0001t0001g0053a0001c0001t0001g0181a0001c0001t0001g0240others(4): Show | 7 | HG01243.hp1 HG01255.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.5263+800delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868575 | ||||||
| chr2:53868576
|
A | AAATATAT others(25): Show |
2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5263+799_5263+800i others(34): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868576 | ||||||
| chr2:53868583
|
A | AT | 5 | a0002c0002t0002g0043a0002c0002t0002g0054a0002c0002t0002g0089others(2): Show | 5 | HG00280.hp2 HG00323.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.5263+792dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868583 | ||||||
| chr2:53868589
|
AAT | A | 3 | a0001c0001t0003g0204a0001c0006t0003g0161a0001c0006t0003g0178 | 3 | HG00738.hp2 HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.5263+785_5263+786d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868589 | ||||||
| chr2:53868614
|
C | A | 136 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(133): Show | 136 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.5263+762G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868614 | ||||||
| chr2:53868868
|
T | C | 1 | a0003c0004t0003g0219 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5263+508A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868868 | ||||||
| chr2:53869121
|
C | T | 1 | a0002c0003t0002g0057 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.5263+255G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53869121 | ||||||
| chr2:53869186
|
A | T | 4 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179others(1): Show | 4 | HG01081.hp2 HG02451.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.5263+190T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53869186 | ||||||
| chr2:53869600
|
AG | A | 6 | a0001c0001t0001g0053a0001c0001t0001g0181a0001c0001t0001g0191others(3): Show | 6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.5101-63delC | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53869600 | ||||||
| chr2:53869602
|
G | C | 1 | a0003c0004t0001g0268 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.5101-64C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53869602 | ||||||
| chr2:53869933
|
A | G | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5101-395T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53869933 | ||||||
| chr2:53869975
|
C | T | 67 | a0002c0003t0002g0011a0002c0003t0002g0016a0002c0003t0002g0019others(64): Show | 67 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.5101-437G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53869975 | ||||||
| chr2:53870028
|
C | T | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5101-490G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870028 | ||||||
| chr2:53870115
|
G | A | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5101-577C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870115 | ||||||
| chr2:53870246
|
C | T | 107 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(104): Show | 107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.5101-708G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870246 | ||||||
| chr2:53870373
|
G | GT | 29 | a0001c0001t0001g0038a0001c0001t0001g0053a0001c0001t0001g0181others(26): Show | 29 | HG00609.hp2 HG01081.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.5101-836dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870373 | ||||||
| chr2:53870373
|
GT | G | 150 | a0001c0001t0001g0185a0001c0001t0001g0273a0001c0005t0001g0314others(147): Show | 150 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.5101-836delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870373 | ||||||
| chr2:53870373
|
GTT | G | 63 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.5101-837_5101-836d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870373 | ||||||
| chr2:53870436
|
C | T | 1 | a0002c0003t0002g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5101-898G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870436 | ||||||
| chr2:53870437
|
A | G | 1 | a0002c0003t0002g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5101-899T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870437 | ||||||
| chr2:53870438
|
G | A | 1 | a0002c0003t0002g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5101-900C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870438 | ||||||
| chr2:53870440
|
C | A | 1 | a0002c0003t0002g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5101-902G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870440 | ||||||
| chr2:53870536
|
A | AT | 6 | a0001c0001t0001g0241a0001c0001t0001g0280a0002c0015t0002g0359others(3): Show | 6 | HG01255.hp1 HG03486.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.5101-999dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870536 | ||||||
| chr2:53870604
|
C | T | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5101-1066G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870604 | ||||||
| chr2:53870908
|
T | A | 2 | a0001c0001t0001g0267a0005c0011t0001g0362 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.5101-1370A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870908 | ||||||
| chr2:53870913
|
G | A | 1 | a0002c0002t0004g0048 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.5101-1375C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870913 | ||||||
| chr2:53871094
|
C | T | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.5101-1556G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871094 | ||||||
| chr2:53871296
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5101-1758C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871296 | ||||||
| chr2:53871314
|
G | A | 8 | a0004c0008t0001g0376a0004c0008t0001g0377a0004c0008t0001g0378others(5): Show | 8 | HG01070.hp2 HG01109.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.5101-1776C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871314 | ||||||
| chr2:53871315
|
A | C | 1 | a0002c0002t0002g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5101-1777T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871315 | ||||||
| chr2:53871383
|
T | TG | 4 | a0001c0001t0001g0035a0001c0001t0001g0223a0001c0001t0001g0230others(1): Show | 4 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.5101-1846dupC | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871383 | ||||||
| chr2:53871402
|
C | T | 136 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(133): Show | 136 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.5101-1864G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871402 | ||||||
| chr2:53871408
|
C | A | 2 | a0003c0004t0001g0201a0003c0004t0001g0271 | 2 | NA18952.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.5101-1870G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871408 | ||||||
| chr2:53871446
|
G | C | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5101-1908C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871446 | ||||||
| chr2:53871503
|
C | T | 2 | a0005c0011t0002g0363a0008c0030t0002g0310 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.5101-1965G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871503 | ||||||
| chr2:53871518
|
T | C | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5101-1980A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871518 | ||||||
| chr2:53871546
|
G | A | 6 | a0001c0001t0001g0053a0001c0001t0001g0181a0001c0001t0001g0191others(3): Show | 6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.5101-2008C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871546 | ||||||
| chr2:53871592
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5101-2054A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871592 | ||||||
| chr2:53871595
|
T | C | 1 | a0002c0002t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5101-2057A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871595 | ||||||
| chr2:53871671
|
C | A | 4 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(1): Show | 4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5101-2133G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871671 | ||||||
| chr2:53871731
|
T | C | 2 | a0002c0002t0002g0141a0002c0002t0002g0142 | 2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.5101-2193A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871731 | ||||||
| chr2:53871785
|
G | A | 66 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.5101-2247C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871785 | ||||||
| chr2:53871984
|
C | A | 141 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.5100+2355G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871984 | ||||||
| chr2:53872022
|
A | AG | 13 | a0001c0006t0003g0167a0002c0002t0002g0044a0002c0002t0004g0064others(10): Show | 13 | HG01106.hp2 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.5100+2316dupC | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872022 | ||||||
| chr2:53872107
|
G | A | 1 | a0002c0003t0002g0020 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5100+2232C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872107 | ||||||
| chr2:53872150
|
T | C | 2 | a0003c0004t0001g0033a0003c0004t0001g0256 | 2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.5100+2189A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872150 | ||||||
| chr2:53872283
|
G | A | 1 | a0001c0005t0001g0322 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5100+2056C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872283 | ||||||
| chr2:53872585
|
C | CA | 66 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(63): Show | 66 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.5100+1753dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872585 | ||||||
| chr2:53872599
|
C | T | 2 | a0001c0007t0006g0012a0001c0007t0006g0014 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.5100+1740G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872599 | ||||||
| chr2:53872695
|
T | C | 5 | a0003c0004t0001g0286a0003c0004t0001g0298a0003c0004t0001g0302others(2): Show | 5 | NA18963.hp1 NA18964.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.5100+1644A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872695 | ||||||
| chr2:53872741
|
C | CA | 62 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(59): Show | 62 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.5100+1597dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | ||||||
| chr2:53872741
|
C | CAA | 16 | a0001c0001t0001g0173a0001c0001t0001g0198a0001c0001t0001g0199others(13): Show | 16 | HG01884.hp2 HG01891.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.5100+1596_5100+159 others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | ||||||
| chr2:53872741
|
CA | C | 9 | a0001c0001t0001g0231a0001c0001t0001g0242a0001c0001t0001g0244others(6): Show | 9 | HG02258.hp2 HG03017.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.5100+1597delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | ||||||
| chr2:53872741
|
CAA | C | 100 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(97): Show | 100 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.5100+1596_5100+159 others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | ||||||
| chr2:53872741
|
CAAA | C | 60 | a0001c0006t0003g0158a0001c0006t0003g0161a0001c0006t0003g0172others(57): Show | 60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.5100+1595_5100+159 others(7): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | ||||||
| chr2:53872741
|
CAAAA | C | 8 | a0002c0003t0002g0024a0002c0003t0002g0049a0002c0003t0002g0077others(5): Show | 8 | HG00408.hp2 HG01168.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.5100+1594_5100+159 others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | ||||||
| chr2:53872741
|
CAAAAAAA others(3): Show |
C | 66 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.5100+1588_5100+159 others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | ||||||
| chr2:53872741
|
CAAAAAAA others(4): Show |
C | 1 | a0004c0008t0001g0383 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5100+1587_5100+159 others(15): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | ||||||
| chr2:53872741
|
CAAAAAAA others(8): Show |
C | 4 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(1): Show | 4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5100+1583_5100+159 others(19): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | ||||||
| chr2:53872813
|
G | A | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5100+1526C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872813 | ||||||
| chr2:53872896
|
T | TA | 9 | a0001c0001t0001g0267a0001c0005t0001g0354a0001c0006t0003g0025others(6): Show | 9 | HG01099.hp2 HG01106.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.5100+1442dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872896 | ||||||
| chr2:53872896
|
TA | T | 138 | a0001c0001t0001g0231a0001c0007t0001g0361a0002c0002t0002g0022others(135): Show | 138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.5100+1442delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872896 | ||||||
| chr2:53873023
|
G | T | 136 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(133): Show | 136 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.5100+1316C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873023 | ||||||
| chr2:53873175
|
A | C | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5100+1164T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873175 | ||||||
| chr2:53873238
|
C | CA | 69 | a0002c0003t0002g0011a0002c0003t0002g0016a0002c0003t0002g0019others(66): Show | 69 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.5100+1100dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | ||||||
| chr2:53873238
|
C | CAA | 66 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(63): Show | 66 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.5100+1099_5100+110 others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | ||||||
| chr2:53873238
|
C | CAAAAAAA others(7): Show |
4 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(1): Show | 4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5100+1100_5100+110 others(18): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | ||||||
| chr2:53873238
|
C | CAAAAAAA others(8): Show |
14 | a0001c0006t0003g0031a0001c0006t0003g0155a0001c0006t0003g0156others(11): Show | 14 | HG00738.hp2 HG01167.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.5100+1100_5100+110 others(19): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | ||||||
| chr2:53873238
|
C | CAAAAAAA others(9): Show |
70 | a0001c0005t0001g0182a0001c0005t0001g0313a0001c0005t0001g0314others(67): Show | 70 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.5100+1100_5100+110 others(20): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | ||||||
| chr2:53873238
|
C | CAAAAAAA others(10): Show |
9 | a0001c0001t0003g0204a0001c0005t0001g0311a0001c0005t0001g0319others(6): Show | 9 | HG00621.hp1 HG02145.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.5100+1100_5100+110 others(21): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | ||||||
| chr2:53873238
|
C | CAAAAAAA others(11): Show |
7 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(4): Show | 7 | HG01099.hp2 HG01106.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.5100+1100_5100+110 others(22): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | ||||||
| chr2:53873238
|
C | CAAAAAAA others(12): Show |
2 | a0001c0006t0003g0175a0001c0006t0003g0371 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.5100+1100_5100+110 others(23): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | ||||||
| chr2:53873238
|
C | CAAAAAAA others(13): Show |
1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5100+1100_5100+110 others(24): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | ||||||
| chr2:53873243
|
A | AAAAAAAA others(10): Show |
1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5100+1095_5100+109 others(21): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873243 | ||||||
| chr2:53873247
|
A | AAAAAAAA others(11): Show |
1 | a0004c0008t0001g0381 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5100+1091_5100+109 others(22): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873247 | ||||||
| chr2:53873247
|
A | AAAAAAAA others(10): Show |
1 | a0004c0008t0001g0378 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.5100+1091_5100+109 others(21): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873247 | ||||||
| chr2:53873247
|
A | AAAAAAAA others(9): Show |
2 | a0004c0008t0001g0380a0004c0008t0001g0383 | 2 | HG01256.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.5100+1091_5100+109 others(20): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873247 | ||||||
| chr2:53873248
|
G | A | 5 | a0004c0008t0001g0378a0004c0008t0001g0380a0004c0008t0001g0381others(2): Show | 5 | HG01070.hp2 HG01109.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.5100+1091C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873248 | ||||||
| chr2:53873249
|
A | G | 1 | a0008c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5100+1090T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873249 | ||||||
| chr2:53873254
|
A | T | 1 | a0002c0002t0004g0121 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.5100+1085T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873254 | ||||||
| chr2:53873352
|
G | A | 6 | a0001c0001t0001g0053a0001c0001t0001g0181a0001c0001t0001g0191others(3): Show | 6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.5100+987C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873352 | ||||||
| chr2:53873502
|
C | T | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5100+837G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873502 | ||||||
| chr2:53873525
|
G | A | 1 | a0004c0008t0001g0378 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.5100+814C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873525 | ||||||
| chr2:53873937
|
CAT | C | 4 | a0001c0001t0001g0180a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG02630.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.5100+400_5100+401d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873937 | ||||||
| chr2:53874267
|
C | T | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5100+72G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53874267 | ||||||
| chr2:53874635
|
C | T | 38 | a0001c0001t0003g0204a0001c0006t0003g0025a0001c0006t0003g0026others(35): Show | 38 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.4945-141G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53874635 | ||||||
| chr2:53874731
|
G | T | 2 | a0002c0010t0002g0018a0002c0010t0002g0056 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.4945-237C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53874731 | ||||||
| chr2:53874762
|
T | C | 4 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(1): Show | 4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4945-268A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53874762 | ||||||
| chr2:53874820
|
C | A | 136 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(133): Show | 136 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.4945-326G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53874820 | ||||||
| chr2:53874839
|
G | A | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4945-345C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53874839 | ||||||
| chr2:53874996
|
C | T | 4 | a0001c0001t0001g0053a0001c0001t0001g0181a0001c0001t0001g0240others(1): Show | 4 | HG01255.hp2 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.4945-502G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53874996 | ||||||
| chr2:53875233
|
G | C | 1 | a0001c0001t0003g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4944+394C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53875233 | ||||||
| chr2:53875273
|
G | A | 1 | a0002c0033t0002g0375 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4944+354C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53875273 | ||||||
| chr2:53875854
|
T | C | 69 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.4816-99A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53875854 | ||||||
| chr2:53875947
|
T | G | 2 | a0001c0006t0003g0168a0001c0006t0003g0171 | 2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.4816-192A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53875947 | ||||||
| chr2:53875953
|
C | A | 1 | a0002c0002t0002g0356 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4816-198G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53875953 | ||||||
| chr2:53876065
|
G | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4816-310C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876065 | ||||||
| chr2:53876128
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0241 | 2 | HG01255.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4816-373G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876128 | ||||||
| chr2:53876430
|
C | T | 2 | a0001c0007t0001g0361a0010c0026t0001g0013 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4816-675G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876430 | ||||||
| chr2:53876508
|
T | C | 2 | a0002c0003t0002g0060a0002c0003t0002g0079 | 2 | HG03239.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.4816-753A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876508 | ||||||
| chr2:53876533
|
AAG | A | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4816-780_4816-779d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876533 | ||||||
| chr2:53876545
|
C | T | 1 | a0002c0003t0010g0006 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4816-790G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876545 | ||||||
| chr2:53876583
|
T | TTA | 33 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(30): Show | 33 | HG00099.hp2 HG00738.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.4816-830_4816-829d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876583 | ||||||
| chr2:53876583
|
T | TTATA | 7 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(4): Show | 7 | HG01167.hp2 HG02258.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4816-832_4816-829d others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876583 | ||||||
| chr2:53876642
|
A | G | 4 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(1): Show | 4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4816-887T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876642 | ||||||
| chr2:53876713
|
A | ACTTTT | 6 | a0002c0002t0002g0044a0002c0002t0002g0065a0002c0002t0002g0099others(3): Show | 6 | HG02056.hp1 NA18971.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.4816-959_4816-958i others(7): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876713 | ||||||
| chr2:53876713
|
A | ATCCTTTT others(16): Show |
1 | a0015c0028t0001g0368 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4816-959_4816-958i others(25): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876713 | ||||||
| chr2:53876716
|
C | CT | 60 | a0001c0001t0001g0243a0001c0001t0001g0267a0001c0001t0003g0204others(57): Show | 60 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.4816-962dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTT | 7 | a0002c0002t0002g0047a0002c0002t0002g0119a0002c0003t0002g0057others(4): Show | 7 | HG01168.hp2 HG02895.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.4816-967_4816-962d others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT | 106 | a0001c0005t0009g0220a0001c0005t0009g0221a0002c0002t0002g0023others(103): Show | 106 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.4816-968_4816-962d others(9): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(1): Show |
17 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(14): Show | 17 | HG00408.hp2 HG01069.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.4816-969_4816-962d others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(4): Show |
1 | a0014c0016t0001g0339 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4816-972_4816-962d others(13): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(5): Show |
2 | a0001c0005t0001g0349a0001c0009t0001g0369 | 2 | HG00609.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4816-973_4816-962d others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(9): Show |
1 | a0001c0007t0006g0196 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4816-977_4816-962d others(18): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(10): Show |
2 | a0001c0007t0006g0012a0001c0007t0006g0014 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4816-978_4816-962d others(19): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(11): Show |
1 | a0001c0007t0006g0197 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4816-979_4816-962d others(20): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(13): Show |
5 | a0001c0005t0001g0333a0001c0005t0001g0334a0001c0005t0001g0337others(2): Show | 5 | HG02293.hp1 NA18955.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.4816-981_4816-962d others(22): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(14): Show |
5 | a0001c0005t0001g0313a0001c0005t0001g0314a0001c0005t0001g0328others(2): Show | 5 | HG01175.hp2 HG01257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.4816-962_4816-961i others(23): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(15): Show |
18 | a0001c0005t0001g0311a0001c0005t0001g0319a0001c0005t0001g0325others(15): Show | 18 | HG01074.hp1 HG01928.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.4816-962_4816-961i others(24): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(16): Show |
11 | a0001c0005t0001g0316a0001c0005t0001g0317a0001c0005t0001g0318others(8): Show | 11 | HG00597.hp1 HG01256.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.4816-962_4816-961i others(25): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(17): Show |
5 | a0001c0005t0001g0332a0001c0005t0001g0345a0001c0005t0001g0348others(2): Show | 5 | HG00423.hp1 HG01070.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.4816-962_4816-961i others(26): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(18): Show |
2 | a0001c0005t0001g0329a0001c0005t0001g0373 | 2 | HG00408.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.4816-962_4816-961i others(27): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(19): Show |
1 | a0001c0005t0001g0182 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4816-962_4816-961i others(28): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(20): Show |
1 | a0001c0005t0001g0336 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4816-962_4816-961i others(29): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(22): Show |
2 | a0001c0005t0001g0315a0001c0005t0001g0323 | 2 | HG01358.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.4816-962_4816-961i others(31): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(23): Show |
2 | a0001c0005t0001g0351a0001c0005t0007g0331 | 2 | HG00621.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.4816-962_4816-961i others(32): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(24): Show |
1 | a0001c0005t0001g0342 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4816-962_4816-961i others(33): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(27): Show |
1 | a0001c0005t0001g0324 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4816-962_4816-961i others(36): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | CTTTTTTT others(32): Show |
1 | a0001c0005t0001g0321 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4816-962_4816-961i others(41): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
C | T | 9 | a0002c0002t0002g0044a0002c0002t0002g0065a0002c0002t0002g0098others(6): Show | 9 | HG02056.hp1 HG03540.hp2 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.4816-961G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876716
|
CTT | C | 36 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(33): Show | 36 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.4816-963_4816-962d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | ||||||
| chr2:53876752
|
G | A | 1 | a0002c0002t0002g0357 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4816-997C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876752 | ||||||
| chr2:53876767
|
G | GGAGT | 108 | a0001c0001t0001g0279a0001c0001t0003g0204a0001c0005t0001g0182others(105): Show | 108 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.4816-1016_4816-101 others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876767 | ||||||
| chr2:53877004
|
T | C | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4816-1249A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877004 | ||||||
| chr2:53877181
|
C | T | 249 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(246): Show | 249 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.4816-1426G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877181 | ||||||
| chr2:53877247
|
C | CA | 65 | a0001c0001t0001g0038a0001c0001t0001g0173a0001c0001t0001g0198others(62): Show | 65 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.4816-1493dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877247 | ||||||
| chr2:53877247
|
CA | C | 16 | a0001c0001t0001g0205a0001c0001t0001g0229a0001c0005t0001g0320others(13): Show | 16 | HG00438.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.4816-1493delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877247 | ||||||
| chr2:53877271
|
T | A | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4816-1516A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877271 | ||||||
| chr2:53877291
|
A | C | 1 | a0001c0005t0001g0326 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4816-1536T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877291 | ||||||
| chr2:53877291
|
A | G | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4816-1536T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877291 | ||||||
| chr2:53877365
|
A | G | 8 | a0002c0002t0002g0044a0002c0002t0002g0065a0002c0002t0002g0098others(5): Show | 8 | HG02056.hp1 NA18971.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.4816-1610T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877365 | ||||||
| chr2:53877478
|
T | C | 68 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(65): Show | 68 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.4816-1723A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877478 | ||||||
| chr2:53877509
|
TA | T | 59 | a0002c0003t0001g0080a0003c0004t0001g0032a0003c0004t0001g0033others(56): Show | 59 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.4816-1755delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877509 | ||||||
| chr2:53877585
|
T | G | 4 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(1): Show | 4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4816-1830A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877585 | ||||||
| chr2:53877591
|
A | G | 65 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(62): Show | 65 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.4816-1836T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877591 | ||||||
| chr2:53877594
|
T | A | 244 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(241): Show | 244 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.4816-1839A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877594 | ||||||
| chr2:53877763
|
T | G | 1 | a0001c0006t0003g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4816-2008A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877763 | ||||||
| chr2:53878071
|
A | G | 1 | a0002c0002t0002g0082 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4816-2316T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878071 | ||||||
| chr2:53878270
|
C | T | 2 | a0001c0005t0001g0315a0001c0005t0001g0319 | 2 | HG01358.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.4816-2515G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878270 | ||||||
| chr2:53878340
|
A | G | 246 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(243): Show | 246 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.4816-2585T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878340 | ||||||
| chr2:53878341
|
T | C | 5 | a0001c0006t0003g0167a0001c0006t0003g0168a0001c0006t0003g0170others(2): Show | 5 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.4816-2586A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878341 | ||||||
| chr2:53878353
|
G | A | 38 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(35): Show | 38 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.4816-2598C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878353 | ||||||
| chr2:53878366
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4816-2611C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878366 | ||||||
| chr2:53878372
|
T | C | 1 | a0001c0005t0001g0330 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.4816-2617A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878372 | ||||||
| chr2:53878389
|
T | C | 1 | a0002c0003t0002g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4816-2634A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878389 | ||||||
| chr2:53878398
|
T | C | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | NA18968.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.4816-2643A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878398 | ||||||
| chr2:53878460
|
A | T | 1 | a0003c0004t0001g0252 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4816-2705T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878460 | ||||||
| chr2:53878461
|
C | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4816-2706G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878461 | ||||||
| chr2:53878477
|
C | T | 6 | a0001c0001t0001g0053a0001c0001t0001g0181a0001c0001t0001g0191others(3): Show | 6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4816-2722G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878477 | ||||||
| chr2:53878642
|
G | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4816-2887C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878642 | ||||||
| chr2:53878648
|
C | T | 11 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(8): Show | 11 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.4816-2893G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878648 | ||||||
| chr2:53878683
|
C | T | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4816-2928G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878683 | ||||||
| chr2:53878748
|
G | C | 1 | a0010c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4816-2993C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878748 | ||||||
| chr2:53878819
|
A | G | 3 | a0005c0011t0001g0364a0005c0011t0002g0363a0008c0030t0002g0310 | 3 | HG01243.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4816-3064T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878819 | ||||||
| chr2:53878873
|
C | A | 138 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(135): Show | 138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.4816-3118G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878873 | ||||||
| chr2:53878911
|
G | A | 1 | a0002c0002t0002g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4816-3156C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878911 | ||||||
| chr2:53878912
|
C | T | 1 | a0003c0004t0003g0219 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4816-3157G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878912 | ||||||
| chr2:53878989
|
G | T | 3 | a0002c0003t0002g0016a0002c0003t0002g0057a0002c0003t0002g0072 | 3 | NA18991.hp1 NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.4816-3234C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878989 | ||||||
| chr2:53879037
|
C | T | 1 | a0001c0005t0001g0342 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4816-3282G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879037 | ||||||
| chr2:53879080
|
T | C | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4816-3325A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879080 | ||||||
| chr2:53879091
|
G | A | 4 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(1): Show | 4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4816-3336C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879091 | ||||||
| chr2:53879094
|
C | T | 1 | a0002c0003t0002g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4816-3339G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879094 | ||||||
| chr2:53879139
|
G | T | 1 | a0001c0006t0003g0163 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.4816-3384C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879139 | ||||||
| chr2:53879508
|
T | C | 3 | a0001c0006t0003g0172a0001c0006t0003g0175a0001c0006t0003g0371 | 3 | HG02257.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.4816-3753A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879508 | ||||||
| chr2:53879589
|
G | A | 11 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(8): Show | 11 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.4816-3834C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879589 | ||||||
| chr2:53879671
|
C | T | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4816-3916G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879671 | ||||||
| chr2:53879679
|
G | A | 1 | a0003c0004t0001g0284 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.4816-3924C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879679 | ||||||
| chr2:53879716
|
C | T | 1 | a0001c0006t0003g0026 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4816-3961G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879716 | ||||||
| chr2:53879739
|
C | A | 1 | a0001c0005t0001g0335 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.4816-3984G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879739 | ||||||
| chr2:53879771
|
C | T | 55 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.4816-4016G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879771 | ||||||
| chr2:53879801
|
C | CA | 22 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0223others(19): Show | 22 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.4816-4047dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879801 | ||||||
| chr2:53879801
|
C | CAAAAAA | 122 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(119): Show | 122 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.4816-4052_4816-404 others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879801 | ||||||
| chr2:53879801
|
C | CAAAAAAA | 12 | a0002c0002t0002g0045a0002c0002t0002g0098a0002c0002t0002g0117others(9): Show | 12 | HG01515.hp1 HG02027.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4816-4053_4816-404 others(11): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879801 | ||||||
| chr2:53879801
|
CA | C | 70 | a0001c0001t0001g0173a0001c0005t0001g0182a0001c0005t0001g0314others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.4816-4047delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879801 | ||||||
| chr2:53879845
|
T | C | 1 | a0002c0002t0002g0357 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4816-4090A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879845 | ||||||
| chr2:53879879
|
C | A | 4 | a0003c0004t0001g0262a0003c0004t0001g0263a0003c0004t0001g0264others(1): Show | 4 | NA18983.hp2 NA19004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.4816-4124G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879879 | ||||||
| chr2:53879986
|
C | T | 14 | a0001c0001t0001g0173a0001c0001t0001g0180a0001c0001t0001g0198others(11): Show | 14 | HG02451.hp2 HG02486.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.4816-4231G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879986 | ||||||
| chr2:53880009
|
T | C | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.4816-4254A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880009 | ||||||
| chr2:53880120
|
A | T | 1 | a0010c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4816-4365T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880120 | ||||||
| chr2:53880199
|
A | G | 140 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.4816-4444T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880199 | ||||||
| chr2:53880332
|
C | T | 2 | a0002c0003t0002g0138a0002c0003t0002g0147 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4816-4577G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880332 | ||||||
| chr2:53880508
|
C | T | 1 | a0004c0008t0001g0381 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4816-4753G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880508 | ||||||
| chr2:53880750
|
G | C | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4815+4940C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880750 | ||||||
| chr2:53880756
|
C | A | 2 | a0002c0003t0002g0060a0002c0003t0002g0079 | 2 | HG03239.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.4815+4934G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880756 | ||||||
| chr2:53880806
|
T | C | 14 | a0001c0001t0001g0173a0001c0001t0001g0180a0001c0001t0001g0198others(11): Show | 14 | HG02451.hp2 HG02486.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.4815+4884A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880806 | ||||||
| chr2:53881000
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | NA18968.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.4815+4690C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881000 | ||||||
| chr2:53881030
|
G | C | 4 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(1): Show | 4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4815+4660C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881030 | ||||||
| chr2:53881145
|
G | C | 2 | a0001c0006t0003g0174a0001c0006t0003g0218 | 2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4815+4545C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881145 | ||||||
| chr2:53881185
|
TATAAG | T | 3 | a0005c0011t0001g0364a0005c0011t0002g0363a0008c0030t0002g0310 | 3 | HG01243.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4815+4500_4815+450 others(9): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881185 | ||||||
| chr2:53881320
|
T | G | 378 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0035others(375): Show | 379 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.4815+4370A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881320 | ||||||
| chr2:53881497
|
T | C | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.4815+4193A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881497 | ||||||
| chr2:53881586
|
A | ACCTGTCA others(3): Show |
2 | a0002c0002t0002g0086a0002c0002t0002g0119 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4815+4094_4815+410 others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881586 | ||||||
| chr2:53881602
|
A | AT | 13 | a0001c0001t0001g0173a0001c0001t0001g0198a0001c0001t0001g0199others(10): Show | 13 | HG02451.hp2 HG02486.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.4815+4087dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881602 | ||||||
| chr2:53881602
|
A | T | 1 | a0002c0002t0002g0043 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4815+4088T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881602 | ||||||
| chr2:53881646
|
C | T | 61 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(58): Show | 61 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.4815+4044G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881646 | ||||||
| chr2:53882102
|
A | G | 106 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(103): Show | 106 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4815+3588T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882102 | ||||||
| chr2:53882213
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0235a0001c0001t0001g0308 | 3 | HG01261.hp2 HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.4815+3477C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882213 | ||||||
| chr2:53882314
|
C | A | 181 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(178): Show | 181 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.4815+3376G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882314 | ||||||
| chr2:53882319
|
T | C | 10 | a0001c0001t0001g0036a0001c0001t0001g0189a0001c0001t0001g0190others(7): Show | 10 | HG00733.hp1 HG01069.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.4815+3371A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882319 | ||||||
| chr2:53882357
|
T | A | 14 | a0001c0001t0001g0173a0001c0001t0001g0180a0001c0001t0001g0198others(11): Show | 14 | HG02451.hp2 HG02486.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.4815+3333A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882357 | ||||||
| chr2:53882493
|
C | G | 6 | a0001c0009t0001g0360a0001c0009t0001g0366a0001c0009t0001g0367others(3): Show | 6 | HG01074.hp1 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.4815+3197G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882493 | ||||||
| chr2:53882562
|
G | A | 5 | a0002c0003t0002g0020a0002c0003t0002g0077a0002c0003t0002g0078others(2): Show | 5 | HG01106.hp2 HG01192.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.4815+3128C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882562 | ||||||
| chr2:53882580
|
A | G | 1 | a0003c0004t0001g0247 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4815+3110T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882580 | ||||||
| chr2:53882861
|
G | A | 4 | a0001c0001t0001g0180a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG02630.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.4815+2829C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882861 | ||||||
| chr2:53882900
|
C | CA | 10 | a0001c0007t0001g0179a0001c0007t0001g0361a0001c0009t0001g0360others(7): Show | 10 | HG01074.hp1 HG02451.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.4815+2789dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882900 | ||||||
| chr2:53882900
|
C | CAA | 55 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.4815+2788_4815+278 others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882900 | ||||||
| chr2:53882908
|
AAT | A | 21 | a0002c0003t0002g0060a0002c0003t0002g0069a0002c0003t0002g0079others(18): Show | 21 | HG00408.hp2 HG00438.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.4815+2780_4815+278 others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882908 | ||||||
| chr2:53882909
|
AT | A | 54 | a0002c0002t0002g0082a0002c0002t0002g0356a0002c0002t0002g0358others(51): Show | 54 | HG00558.hp1 HG00733.hp2 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.4815+2780delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882909 | ||||||
| chr2:53882910
|
T | A | 140 | a0001c0001t0003g0204a0001c0005t0001g0182a0001c0005t0001g0311others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.4815+2780A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882910 | ||||||
| chr2:53882914
|
T | A | 137 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(134): Show | 137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.4815+2776A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882914 | ||||||
| chr2:53882988
|
A | G | 1 | a0001c0005t0001g0372 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4815+2702T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882988 | ||||||
| chr2:53883333
|
C | A | 2 | a0001c0007t0001g0361a0010c0026t0001g0013 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4815+2357G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53883333 | ||||||
| chr2:53883442
|
G | C | 59 | a0002c0003t0001g0080a0003c0004t0001g0032a0003c0004t0001g0033others(56): Show | 59 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.4815+2248C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53883442 | ||||||
| chr2:53883455
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0277 | 2 | HG01346.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.4815+2235C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53883455 | ||||||
| chr2:53883654
|
A | T | 1 | a0002c0002t0002g0088 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.4815+2036T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53883654 | ||||||
| chr2:53883746
|
CT | C | 38 | a0001c0005t0001g0182a0001c0006t0003g0025a0001c0006t0003g0026others(35): Show | 38 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.4815+1943delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53883746 | ||||||
| chr2:53883898
|
T | A | 1 | a0003c0004t0001g0271 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4815+1792A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53883898 | ||||||
| chr2:53884121
|
A | G | 3 | a0001c0006t0003g0161a0001c0006t0003g0178a0001c0006t0003g0266 | 3 | HG00738.hp2 HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.4815+1569T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53884121 | ||||||
| chr2:53884171
|
T | C | 1 | a0001c0005t0001g0338 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4815+1519A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53884171 | ||||||
| chr2:53884223
|
T | C | 8 | a0001c0001t0001g0206a0001c0001t0001g0225a0001c0001t0001g0227others(5): Show | 8 | HG00597.hp2 HG00609.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.4815+1467A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53884223 | ||||||
| chr2:53884312
|
G | A | 8 | a0004c0008t0001g0376a0004c0008t0001g0377a0004c0008t0001g0378others(5): Show | 8 | HG01070.hp2 HG01109.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.4815+1378C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53884312 | ||||||
| chr2:53884314
|
G | A | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4815+1376C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53884314 | ||||||
| chr2:53885475
|
T | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0277 | 2 | HG01346.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.4815+215A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53885475 | ||||||
| chr2:53885599
|
C | T | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4815+91G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53885599 | ||||||
| chr2:53885827
|
C | T | 1 | a0002c0002t0002g0141 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4730-52G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53885827 | ||||||
| chr2:53885916
|
A | G | 2 | a0002c0003t0002g0138a0002c0003t0002g0147 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4730-141T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53885916 | ||||||
| chr2:53885927
|
A | G | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4730-152T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53885927 | ||||||
| chr2:53885975
|
T | C | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4730-200A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53885975 | ||||||
| chr2:53886067
|
T | C | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.4730-292A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886067 | ||||||
| chr2:53886162
|
C | G | 3 | a0002c0003t0002g0016a0002c0003t0002g0057a0002c0003t0002g0072 | 3 | NA18991.hp1 NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.4730-387G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886162 | ||||||
| chr2:53886233
|
C | A | 1 | a0002c0003t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4730-458G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886233 | ||||||
| chr2:53886304
|
G | A | 1 | a0003c0004t0001g0265 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4730-529C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886304 | ||||||
| chr2:53886335
|
G | A | 1 | a0002c0003t0002g0137 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4730-560C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886335 | ||||||
| chr2:53886531
|
T | C | 1 | a0002c0003t0002g0152 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4729+728A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886531 | ||||||
| chr2:53886676
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.4729+583A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886676 | ||||||
| chr2:53886703
|
A | G | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4729+556T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886703 | ||||||
| chr2:53886765
|
G | A | 1 | a0007c0012t0002g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4729+494C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886765 | ||||||
| chr2:53886782
|
A | G | 1 | a0002c0003t0002g0136 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4729+477T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886782 | ||||||
| chr2:53886828
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4729+431T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886828 | ||||||
| chr2:53886829
|
C | G | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4729+430G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886829 | ||||||
| chr2:53886831
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4729+428C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886831 | ||||||
| chr2:53886835
|
A | G | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.4729+424T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886835 | ||||||
| chr2:53887005
|
A | G | 1 | a0002c0002t0002g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4729+254T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53887005 | ||||||
| chr2:53887078
|
T | C | 1 | a0007c0012t0002g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4729+181A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53887078 | ||||||
| chr2:53887084
|
T | C | 139 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(136): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.4729+175A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53887084 | ||||||
| chr2:53887493
|
G | C | 1 | a0001c0005t0001g0333 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.4521-26C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 39/46 | chr2 | 53887493 | ||||||
| chr2:53887611
|
C | A | 1 | a0001c0001t0001g0242 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4521-144G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 39/46 | chr2 | 53887611 | ||||||
| chr2:53887625
|
G | A | 67 | a0002c0002t0004g0123a0002c0003t0002g0011a0002c0003t0002g0016others(64): Show | 67 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.4521-158C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 39/46 | chr2 | 53887625 | ||||||
| chr2:53887727
|
T | C | 55 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.4520+131A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 39/46 | chr2 | 53887727 | ||||||
| chr2:53887802
|
T | A | 3 | a0001c0001t0003g0204a0001c0006t0005g0003a0001c0006t0005g0005 | 3 | HG02109.hp1 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4520+56A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 39/46 | chr2 | 53887802 | ||||||
| chr2:53887830
|
G | A | 139 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(136): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.4520+28C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 39/46 | chr2 | 53887830 | ||||||
| chr2:53888208
|
TGAAA | T | 6 | a0001c0007t0001g0361a0001c0007t0006g0012a0001c0007t0006g0014others(3): Show | 6 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.4389-223_4389-220d others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/46 | chr2 | 53888208 | ||||||
| chr2:53888260
|
A | G | 6 | a0001c0007t0001g0361a0001c0007t0006g0012a0001c0007t0006g0014others(3): Show | 6 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.4389-271T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/46 | chr2 | 53888260 | ||||||
| chr2:53888540
|
C | T | 2 | a0003c0004t0001g0192a0003c0004t0001g0245 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.4388+181G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/46 | chr2 | 53888540 | ||||||
| chr2:53888638
|
G | A | 2 | a0001c0005t0001g0372a0001c0005t0001g0373 | 2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.4388+83C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/46 | chr2 | 53888638 | ||||||
| chr2:53888676
|
C | T | 38 | a0001c0001t0003g0204a0001c0006t0003g0025a0001c0006t0003g0026others(35): Show | 38 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.4388+45G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/46 | chr2 | 53888676 | ||||||
| chr2:53888693
|
A | G | 1 | a0002c0003t0002g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4388+28T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/46 | chr2 | 53888693 | ||||||
| chr2:53888708
|
T | A | 64 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(61): Show | 64 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.4388+13A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/46 | chr2 | 53888708 | ||||||
| chr2:53888866
|
C | T | 141 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.4297-54G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53888866 | ||||||
| chr2:53888893
|
T | A | 2 | a0002c0002t0002g0086a0002c0002t0002g0119 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4297-81A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53888893 | ||||||
| chr2:53889095
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4297-283G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889095 | ||||||
| chr2:53889150
|
C | T | 38 | a0001c0001t0003g0204a0001c0006t0003g0025a0001c0006t0003g0026others(35): Show | 38 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.4297-338G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889150 | ||||||
| chr2:53889164
|
C | A | 1 | a0002c0002t0002g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4297-352G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889164 | ||||||
| chr2:53889212
|
T | C | 246 | a0001c0001t0003g0204a0001c0005t0001g0182a0001c0005t0001g0311others(243): Show | 246 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.4297-400A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889212 | ||||||
| chr2:53889326
|
C | T | 16 | a0002c0003t0002g0019a0002c0003t0002g0069a0002c0003t0002g0105others(13): Show | 16 | HG00438.hp1 HG00735.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.4297-514G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889326 | ||||||
| chr2:53889352
|
G | C | 2 | a0001c0006t0003g0174a0001c0006t0003g0218 | 2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4297-540C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889352 | ||||||
| chr2:53889387
|
T | C | 1 | a0003c0004t0001g0256 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4297-575A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889387 | ||||||
| chr2:53889544
|
T | A | 1 | a0003c0004t0001g0261 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.4296+560A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889544 | ||||||
| chr2:53889663
|
A | C | 141 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.4296+441T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889663 | ||||||
| chr2:53889701
|
T | C | 2 | a0003c0004t0001g0193a0003c0004t0001g0251 | 2 | NA19077.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.4296+403A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889701 | ||||||
| chr2:53890006
|
A | G | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4296+98T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53890006 | ||||||
| chr2:53890023
|
T | C | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4296+81A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53890023 | ||||||
| chr2:53890058
|
A | T | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4296+46T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53890058 | ||||||
| chr2:53890624
|
C | A | 1 | a0001c0001t0001g0231 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4192-416G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53890624 | ||||||
| chr2:53890760
|
G | C | 1 | a0002c0002t0002g0099 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.4192-552C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53890760 | ||||||
| chr2:53890780
|
A | AACTTC | 6 | a0001c0001t0001g0053a0001c0001t0001g0181a0001c0001t0001g0191others(3): Show | 6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4192-573_4192-572i others(7): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53890780 | ||||||
| chr2:53890807
|
C | T | 6 | a0001c0007t0001g0361a0001c0007t0006g0012a0001c0007t0006g0014others(3): Show | 6 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.4192-599G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53890807 | ||||||
| chr2:53891014
|
A | G | 259 | a0001c0001t0001g0053a0001c0001t0001g0181a0001c0001t0001g0191others(256): Show | 259 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.4192-806T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891014 | ||||||
| chr2:53891025
|
T | TA | 55 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.4192-818dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891025 | ||||||
| chr2:53891092
|
C | T | 3 | a0001c0001t0003g0204a0001c0006t0005g0003a0001c0006t0005g0005 | 3 | HG02109.hp1 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4192-884G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891092 | ||||||
| chr2:53891253
|
G | A | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4192-1045C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891253 | ||||||
| chr2:53891552
|
A | AT | 38 | a0001c0001t0003g0204a0001c0006t0003g0025a0001c0006t0003g0026others(35): Show | 38 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.4191+1255dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891552 | ||||||
| chr2:53891552
|
AT | A | 140 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.4191+1255delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891552 | ||||||
| chr2:53891778
|
C | G | 5 | a0001c0006t0003g0167a0001c0006t0003g0168a0001c0006t0003g0170others(2): Show | 5 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.4191+1030G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891778 | ||||||
| chr2:53891782
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4191+1026C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891782 | ||||||
| chr2:53891858
|
CA | C | 240 | a0001c0001t0001g0212a0001c0001t0003g0204a0001c0005t0001g0182others(237): Show | 240 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.4191+949delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891858 | ||||||
| chr2:53891866
|
A | G | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4191+942T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891866 | ||||||
| chr2:53891906
|
T | C | 140 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.4191+902A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891906 | ||||||
| chr2:53891920
|
G | A | 140 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.4191+888C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891920 | ||||||
| chr2:53891923
|
G | C | 4 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(1): Show | 4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4191+885C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891923 | ||||||
| chr2:53891924
|
G | C | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4191+884C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891924 | ||||||
| chr2:53892215
|
C | T | 1 | a0001c0005t0001g0330 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.4191+593G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53892215 | ||||||
| chr2:53892311
|
G | C | 1 | a0002c0003t0002g0113 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4191+497C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53892311 | ||||||
| chr2:53892434
|
C | A | 103 | a0001c0001t0003g0204a0001c0005t0001g0182a0001c0005t0001g0311others(100): Show | 103 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.4191+374G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53892434 | ||||||
| chr2:53892559
|
C | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0004a0003c0004t0003g0219 | 3 | HG01109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4191+249G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53892559 | ||||||
| chr2:53892563
|
T | C | 63 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(60): Show | 63 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.4191+245A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53892563 | ||||||
| chr2:53892576
|
A | T | 63 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(60): Show | 63 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.4191+232T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53892576 | ||||||
| chr2:53892733
|
T | C | 9 | a0002c0003t0002g0024a0002c0003t0002g0136a0002c0003t0002g0137others(6): Show | 9 | HG00733.hp2 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.4191+75A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53892733 | ||||||
| chr2:53893048
|
G | A | 62 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(59): Show | 62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.4039-88C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893048 | ||||||
| chr2:53893067
|
A | G | 140 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.4039-107T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893067 | ||||||
| chr2:53893135
|
T | C | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4039-175A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893135 | ||||||
| chr2:53893238
|
AT | A | 258 | a0001c0001t0001g0053a0001c0001t0001g0181a0001c0001t0001g0191others(255): Show | 258 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.4039-279delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893238 | ||||||
| chr2:53893257
|
C | T | 63 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(60): Show | 63 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.4039-297G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893257 | ||||||
| chr2:53893360
|
G | T | 257 | a0001c0001t0001g0053a0001c0001t0001g0181a0001c0001t0001g0191others(254): Show | 257 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.4038+314C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893360 | ||||||
| chr2:53893454
|
C | T | 140 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.4038+220G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893454 | ||||||
| chr2:53893621
|
G | A | 1 | a0003c0004t0001g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4038+53C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893621 | ||||||
| chr2:53893831
|
G | A | 1 | a0002c0003t0002g0297 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3913-32C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53893831 | ||||||
| chr2:53893964
|
C | T | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3913-165G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53893964 | ||||||
| chr2:53894016
|
G | A | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3913-217C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894016 | ||||||
| chr2:53894255
|
C | A | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3913-456G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894255 | ||||||
| chr2:53894307
|
T | C | 3 | a0001c0001t0003g0204a0001c0006t0005g0003a0001c0006t0005g0005 | 3 | HG02109.hp1 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3913-508A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894307 | ||||||
| chr2:53894365
|
C | T | 7 | a0001c0007t0001g0361a0001c0007t0006g0012a0001c0007t0006g0014others(4): Show | 7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3913-566G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894365 | ||||||
| chr2:53894435
|
C | T | 11 | a0001c0006t0003g0031a0001c0006t0003g0155a0001c0006t0003g0156others(8): Show | 11 | HG01167.hp2 HG01891.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3912+572G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894435 | ||||||
| chr2:53894516
|
C | CCTGCCTC others(98): Show |
6 | a0001c0001t0001g0053a0001c0001t0001g0181a0001c0001t0001g0191others(3): Show | 6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3912+386_3912+490d others(107): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894516 | ||||||
| chr2:53894633
|
C | G | 2 | a0003c0004t0001g0202a0003c0004t0001g0208 | 2 | NA18948.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.3912+374G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894633 | ||||||
| chr2:53894696
|
C | A | 3 | a0001c0006t0003g0172a0001c0006t0003g0175a0001c0006t0003g0371 | 3 | HG02257.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3912+311G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894696 | ||||||
| chr2:53894769
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0278 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3912+238C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894769 | ||||||
| chr2:53894819
|
T | C | 9 | a0002c0003t0002g0024a0002c0003t0002g0136a0002c0003t0002g0137others(6): Show | 9 | HG00733.hp2 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.3912+188A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894819 | ||||||
| chr2:53894823
|
C | A | 37 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(34): Show | 37 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.3912+184G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894823 | ||||||
| chr2:53895106
|
C | T | 1 | a0003c0004t0001g0248 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3843-30G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 33/46 | chr2 | 53895106 | ||||||
| chr2:53895296
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3843-220C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 33/46 | chr2 | 53895296 | ||||||
| chr2:53895488
|
C | T | 66 | a0002c0003t0002g0011a0002c0003t0002g0016a0002c0003t0002g0019others(63): Show | 66 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.3842+95G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 33/46 | chr2 | 53895488 | ||||||
| chr2:53895509
|
C | T | 68 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(65): Show | 68 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.3842+74G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 33/46 | chr2 | 53895509 | ||||||
| chr2:53895529
|
T | C | 1 | a0002c0003t0011g0009 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3842+54A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 33/46 | chr2 | 53895529 | ||||||
| chr2:53895819
|
A | G | 341 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0173others(338): Show | 341 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.3689-83T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53895819 | ||||||
| chr2:53895832
|
C | T | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3689-96G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53895832 | ||||||
| chr2:53895847
|
C | T | 138 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(135): Show | 138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.3689-111G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53895847 | ||||||
| chr2:53895943
|
A | T | 1 | a0001c0005t0001g0373 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3689-207T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53895943 | ||||||
| chr2:53896072
|
AT | A | 7 | a0001c0007t0001g0361a0001c0007t0006g0012a0001c0007t0006g0014others(4): Show | 7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3689-337delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53896072 | ||||||
| chr2:53896175
|
C | T | 3 | a0002c0003t0002g0016a0002c0003t0002g0057a0002c0003t0002g0072 | 3 | NA18991.hp1 NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3689-439G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53896175 | ||||||
| chr2:53896211
|
A | G | 7 | a0001c0005t0001g0332a0001c0005t0001g0336a0001c0005t0001g0343others(4): Show | 7 | HG00423.hp1 HG00609.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.3689-475T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53896211 | ||||||
| chr2:53896387
|
C | T | 139 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(136): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.3688+417G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53896387 | ||||||
| chr2:53896639
|
T | A | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3688+165A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53896639 | ||||||
| chr2:53896683
|
T | A | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3688+121A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53896683 | ||||||
| chr2:53896721
|
T | A | 1 | a0002c0002t0002g0118 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3688+83A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53896721 | ||||||
| chr2:53897023
|
T | A | 1 | a0002c0002t0002g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3607-138A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897023 | ||||||
| chr2:53897167
|
G | GT | 134 | a0001c0001t0001g0035a0001c0001t0001g0189a0001c0001t0001g0216others(131): Show | 134 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.3607-283dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897167 | ||||||
| chr2:53897167
|
G | GTT | 69 | a0001c0005t0001g0182a0001c0005t0001g0313a0001c0005t0001g0314others(66): Show | 69 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.3607-284_3607-283d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897167 | ||||||
| chr2:53897167
|
G | GTTT | 9 | a0001c0005t0001g0311a0001c0005t0001g0333a0001c0005t0001g0342others(6): Show | 9 | HG00621.hp1 HG01074.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.3607-285_3607-283d others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897167 | ||||||
| chr2:53897167
|
G | T | 1 | a0001c0005t0001g0330 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3607-282C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897167 | ||||||
| chr2:53897167
|
GT | G | 32 | a0001c0001t0001g0212a0001c0001t0001g0278a0001c0006t0003g0025others(29): Show | 32 | HG00099.hp2 HG00738.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.3607-283delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897167 | ||||||
| chr2:53897167
|
GTT | G | 7 | a0001c0006t0003g0168a0001c0006t0003g0172a0001c0006t0003g0175others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.3607-284_3607-283d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897167 | ||||||
| chr2:53897174
|
T | TG | 4 | a0005c0011t0001g0362a0005c0011t0001g0364a0005c0011t0002g0363others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3607-290_3607-289i others(3): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897174 | ||||||
| chr2:53897177
|
T | G | 1 | a0001c0001t0001g0272 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3607-292A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897177 | ||||||
| chr2:53897258
|
C | T | 1 | a0001c0006t0003g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3607-373G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897258 | ||||||
| chr2:53897277
|
C | T | 1 | a0002c0002t0002g0097 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3607-392G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897277 | ||||||
| chr2:53897336
|
A | G | 3 | a0002c0003t0002g0016a0002c0003t0002g0057a0002c0003t0002g0072 | 3 | NA18991.hp1 NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3607-451T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897336 | ||||||
| chr2:53897555
|
G | A | 1 | a0002c0003t0002g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3606+315C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897555 | ||||||
| chr2:53897654
|
T | C | 140 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.3606+216A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897654 | ||||||
| chr2:53897710
|
G | C | 7 | a0001c0007t0001g0361a0001c0007t0006g0012a0001c0007t0006g0014others(4): Show | 7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3606+160C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897710 | ||||||
| chr2:53897764
|
T | C | 65 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(62): Show | 65 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.3606+106A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897764 | ||||||
| chr2:53898121
|
T | C | 188 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(185): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.3477-122A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 30/46 | chr2 | 53898121 | ||||||
| chr2:53898358
|
T | C | 139 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(136): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
splice_region_variant&intron_variant | LOW | c.3423-4A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898358 | ||||||
| chr2:53898387
|
T | C | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3423-33A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898387 | ||||||
| chr2:53898412
|
A | G | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3423-58T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898412 | ||||||
| chr2:53898468
|
C | T | 2 | a0007c0012t0002g0058a0007c0012t0002g0062 | 2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3423-114G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898468 | ||||||
| chr2:53898543
|
C | T | 1 | a0002c0002t0001g0232 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3423-189G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898543 | ||||||
| chr2:53898547
|
T | G | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3423-193A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898547 | ||||||
| chr2:53898633
|
G | GCA | 15 | a0001c0001t0001g0036a0001c0001t0001g0189a0001c0001t0001g0190others(12): Show | 15 | HG00733.hp1 HG01069.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.3423-281_3423-280d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | ||||||
| chr2:53898633
|
G | GCACACAC others(5): Show |
1 | a0001c0001t0003g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3423-291_3423-280d others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | ||||||
| chr2:53898633
|
G | GTA | 58 | a0001c0005t0001g0311a0001c0006t0003g0027a0001c0006t0003g0161others(55): Show | 58 | HG00423.hp2 HG00544.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.3423-280_3423-279i others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | ||||||
| chr2:53898633
|
G | GTACA | 14 | a0001c0006t0003g0031a0001c0006t0003g0155a0001c0006t0003g0156others(11): Show | 14 | HG01167.hp2 HG01891.hp1 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.3423-280_3423-279i others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | ||||||
| chr2:53898633
|
GCA | G | 77 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(74): Show | 77 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.3423-281_3423-280d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | ||||||
| chr2:53898633
|
GCACA | G | 65 | a0001c0005t0001g0321a0001c0005t0001g0325a0001c0005t0001g0327others(62): Show | 65 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.3423-283_3423-280d others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | ||||||
| chr2:53898633
|
GCACACA | G | 4 | a0001c0006t0005g0004a0002c0002t0004g0096a0002c0003t0002g0145others(1): Show | 4 | HG00733.hp2 HG02015.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3423-285_3423-280d others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | ||||||
| chr2:53898633
|
GCACACAC others(1): Show |
G | 3 | a0001c0005t0001g0317a0001c0005t0001g0326a0001c0006t0005g0002 | 3 | HG00597.hp1 NA18969.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3423-287_3423-280d others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | ||||||
| chr2:53898633
|
GCACACAC others(3): Show |
G | 2 | a0001c0009t0001g0369a0010c0026t0001g0013 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3423-289_3423-280d others(12): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | ||||||
| chr2:53898634
|
C | T | 82 | a0001c0005t0001g0313a0001c0005t0001g0314a0001c0005t0001g0315others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.3423-280G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898634 | ||||||
| chr2:53898636
|
C | T | 64 | a0001c0005t0001g0323a0001c0005t0001g0324a0001c0005t0001g0338others(61): Show | 64 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.3423-282G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898636 | ||||||
| chr2:53898638
|
C | T | 12 | a0001c0005t0001g0321a0001c0005t0001g0325a0001c0005t0001g0327others(9): Show | 12 | HG00609.hp1 HG00621.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.3423-284G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898638 | ||||||
| chr2:53898640
|
C | T | 3 | a0001c0006t0005g0004a0002c0002t0004g0096a0002c0003t0002g0145 | 3 | HG00733.hp2 HG02145.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.3423-286G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898640 | ||||||
| chr2:53898642
|
C | T | 3 | a0001c0005t0001g0317a0001c0005t0001g0326a0001c0006t0005g0002 | 3 | HG00597.hp1 NA18969.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3423-288G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898642 | ||||||
| chr2:53898644
|
C | T | 1 | a0001c0009t0001g0369 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3423-290G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898644 | ||||||
| chr2:53898702
|
T | C | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3423-348A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898702 | ||||||
| chr2:53898713
|
A | T | 1 | a0001c0006t0015g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3423-359T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898713 | ||||||
| chr2:53898931
|
C | A | 139 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(136): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.3423-577G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898931 | ||||||
| chr2:53899037
|
G | GA | 61 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(58): Show | 61 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.3423-684dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53899037 | ||||||
| chr2:53899127
|
C | T | 2 | a0001c0006t0005g0003a0001c0006t0005g0005 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3422+754G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53899127 | ||||||
| chr2:53899168
|
G | A | 138 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(135): Show | 138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.3422+713C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53899168 | ||||||
| chr2:53899581
|
C | G | 249 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(246): Show | 249 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.3422+300G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53899581 | ||||||
| chr2:53899622
|
C | A | 239 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(236): Show | 239 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.3422+259G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53899622 | ||||||
| chr2:53900183
|
AG | A | 3 | a0002c0002t0002g0085a0002c0002t0002g0086a0002c0002t0002g0119 | 3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3286-167delC | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900183 | ||||||
| chr2:53900330
|
G | A | 1 | a0001c0017t0001g0309 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3286-313C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900330 | ||||||
| chr2:53900389
|
G | GTC | 3 | a0002c0003t0002g0145a0002c0003t0011g0009a0002c0033t0002g0375 | 3 | HG00733.hp2 HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.3286-374_3286-373d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900389 | ||||||
| chr2:53900399
|
C | CA | 7 | a0001c0005t0001g0314a0002c0002t0002g0118a0002c0002t0002g0122others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.3286-383dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900399 | ||||||
| chr2:53900583
|
C | T | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3286-566G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900583 | ||||||
| chr2:53900592
|
G | C | 55 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.3286-575C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900592 | ||||||
| chr2:53900617
|
G | C | 102 | a0001c0001t0003g0204a0001c0005t0001g0182a0001c0005t0001g0311others(99): Show | 102 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.3286-600C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900617 | ||||||
| chr2:53900686
|
T | G | 1 | a0001c0001t0001g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3285+664A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900686 | ||||||
| chr2:53900883
|
C | A | 41 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(38): Show | 41 | HG00099.hp2 HG01074.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.3285+467G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900883 | ||||||
| chr2:53901098
|
T | C | 253 | a0001c0001t0003g0204a0001c0005t0001g0182a0001c0005t0001g0311others(250): Show | 253 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.3285+252A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53901098 | ||||||
| chr2:53901177
|
A | G | 1 | a0003c0004t0001g0032 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3285+173T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53901177 | ||||||
| chr2:53901182
|
T | C | 66 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(63): Show | 66 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.3285+168A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53901182 | ||||||
| chr2:53901572
|
A | T | 3 | a0001c0006t0003g0161a0001c0006t0003g0178a0001c0006t0003g0266 | 3 | HG00738.hp2 HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3076-13T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53901572 | ||||||
| chr2:53902046
|
G | A | 2 | a0001c0006t0003g0174a0001c0006t0003g0218 | 2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3076-487C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902046 | ||||||
| chr2:53902301
|
G | A | 1 | a0001c0005t0001g0182 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3076-742C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902301 | ||||||
| chr2:53902345
|
T | C | 141 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.3076-786A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902345 | ||||||
| chr2:53902420
|
A | C | 3 | a0001c0005t0001g0334a0001c0005t0001g0341a0001c0005t0001g0350 | 3 | NA18955.hp2 NA18986.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.3076-861T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902420 | ||||||
| chr2:53902457
|
A | G | 3 | a0005c0011t0001g0362a0005c0011t0001g0364a0005c0011t0002g0363 | 3 | HG01243.hp1 HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3076-898T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902457 | ||||||
| chr2:53902477
|
T | G | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.3076-918A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902477 | ||||||
| chr2:53902631
|
C | T | 7 | a0001c0001t0001g0206a0001c0001t0001g0225a0001c0001t0001g0227others(4): Show | 7 | HG00597.hp2 HG00609.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.3076-1072G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902631 | ||||||
| chr2:53902683
|
G | A | 14 | a0001c0006t0003g0031a0001c0006t0003g0155a0001c0006t0003g0156others(11): Show | 14 | HG00738.hp2 HG01167.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.3076-1124C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902683 | ||||||
| chr2:53902702
|
G | A | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3076-1143C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902702 | ||||||
| chr2:53903015
|
G | A | 7 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(4): Show | 7 | HG00738.hp1 HG01123.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.3075+1010C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903015 | ||||||
| chr2:53903126
|
C | G | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3075+899G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903126 | ||||||
| chr2:53903238
|
A | AC | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3075+786dupG | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903238 | ||||||
| chr2:53903395
|
G | A | 139 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(136): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.3075+630C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903395 | ||||||
| chr2:53903495
|
G | T | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3075+530C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903495 | ||||||
| chr2:53903670
|
G | A | 7 | a0001c0007t0001g0361a0001c0007t0006g0012a0001c0007t0006g0014others(4): Show | 7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3075+355C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903670 | ||||||
| chr2:53903698
|
A | C | 44 | a0001c0001t0003g0204a0001c0006t0003g0025a0001c0006t0003g0026others(41): Show | 44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.3075+327T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903698 | ||||||
| chr2:53903699
|
C | T | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.3075+326G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903699 | ||||||
| chr2:53903748
|
T | A | 1 | a0002c0003t0010g0006 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3075+277A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903748 | ||||||
| chr2:53903761
|
C | G | 1 | a0001c0005t0001g0338 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3075+264G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903761 | ||||||
| chr2:53903867
|
A | AT | 23 | a0002c0003t0001g0080a0002c0003t0002g0019a0002c0003t0002g0060others(20): Show | 23 | HG00408.hp2 HG00438.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.3075+157dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903867 | ||||||
| chr2:53903869
|
T | TA | 44 | a0001c0001t0003g0204a0001c0006t0003g0025a0001c0006t0003g0026others(41): Show | 44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.3075+155dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903869 | ||||||
| chr2:53903869
|
TA | T | 55 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.3075+155delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903869 | ||||||
| chr2:53903870
|
A | T | 1 | a0003c0004t0001g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3075+155T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903870 | ||||||
| chr2:53903877
|
A | AT | 113 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(110): Show | 113 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.3075+147_3075+148i others(3): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903877 | ||||||
| chr2:53903877
|
A | T | 23 | a0002c0003t0001g0080a0002c0003t0002g0019a0002c0003t0002g0060others(20): Show | 23 | HG00408.hp2 HG00438.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.3075+148T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903877 | ||||||
| chr2:53903956
|
C | T | 44 | a0001c0001t0003g0204a0001c0006t0003g0025a0001c0006t0003g0026others(41): Show | 44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.3075+69G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903956 | ||||||
| chr2:53903957
|
G | A | 1 | a0007c0012t0002g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3075+68C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903957 | ||||||
| chr2:53904017
|
C | T | 56 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(53): Show | 56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
splice_region_variant&intron_variant | LOW | c.3075+8G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53904017 | ||||||
| chr2:53904342
|
T | C | 1 | a0001c0009t0001g0369 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2944-186A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904342 | ||||||
| chr2:53904358
|
C | A | 139 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(136): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2944-202G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904358 | ||||||
| chr2:53904409
|
T | C | 11 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(8): Show | 11 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.2944-253A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904409 | ||||||
| chr2:53904478
|
G | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0004a0003c0004t0003g0219 | 3 | HG01109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2944-322C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904478 | ||||||
| chr2:53904559
|
T | C | 140 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2944-403A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904559 | ||||||
| chr2:53904575
|
C | A | 44 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(41): Show | 44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.2944-419G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904575 | ||||||
| chr2:53904620
|
C | CATATTTT others(22): Show |
1 | a0002c0003t0002g0113 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2944-493_2944-465d others(31): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904620 | ||||||
| chr2:53904644
|
T | A | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2944-488A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904644 | ||||||
| chr2:53904715
|
G | A | 1 | a0001c0005t0001g0343 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2944-559C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904715 | ||||||
| chr2:53904763
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2944-607A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904763 | ||||||
| chr2:53904770
|
C | T | 1 | a0002c0002t0002g0093 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2944-614G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904770 | ||||||
| chr2:53904858
|
C | T | 1 | a0001c0005t0001g0333 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2944-702G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904858 | ||||||
| chr2:53904896
|
G | A | 1 | a0003c0004t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2944-740C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904896 | ||||||
| chr2:53904898
|
G | A | 1 | a0001c0005t0001g0335 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2944-742C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904898 | ||||||
| chr2:53904910
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2944-754G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904910 | ||||||
| chr2:53905032
|
T | C | 3 | a0001c0005t0001g0316a0001c0005t0001g0318a0001c0005t0001g0353 | 3 | HG01515.hp2 HG01517.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2944-876A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905032 | ||||||
| chr2:53905038
|
T | C | 8 | a0002c0002t0002g0050a0002c0002t0002g0083a0002c0002t0002g0094others(5): Show | 8 | HG00423.hp2 HG02015.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.2944-882A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905038 | ||||||
| chr2:53905044
|
G | GT | 11 | a0001c0001t0001g0035a0001c0001t0001g0185a0001c0001t0001g0240others(8): Show | 11 | HG00738.hp1 HG01175.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.2944-889dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905044 | ||||||
| chr2:53905136
|
C | T | 140 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2944-980G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905136 | ||||||
| chr2:53905197
|
T | C | 1 | a0003c0004t0001g0252 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2944-1041A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905197 | ||||||
| chr2:53905257
|
C | T | 1 | a0001c0019t0001g0037 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2944-1101G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905257 | ||||||
| chr2:53905403
|
T | C | 140 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2943+1195A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905403 | ||||||
| chr2:53905499
|
G | A | 2 | a0002c0002t0002g0054a0002c0002t0002g0091 | 2 | HG02155.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.2943+1099C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905499 | ||||||
| chr2:53905600
|
G | A | 9 | a0002c0003t0002g0024a0002c0003t0002g0136a0002c0003t0002g0137others(6): Show | 9 | HG00733.hp2 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.2943+998C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905600 | ||||||
| chr2:53905721
|
G | A | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2943+877C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905721 | ||||||
| chr2:53905795
|
TA | T | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2943+802delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905795 | ||||||
| chr2:53906027
|
T | A | 61 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(58): Show | 61 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.2943+571A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53906027 | ||||||
| chr2:53906080
|
A | C | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2943+518T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53906080 | ||||||
| chr2:53906203
|
G | A | 1 | a0001c0005t0001g0341 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2943+395C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53906203 | ||||||
| chr2:53906501
|
G | A | 44 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(41): Show | 44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.2943+97C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53906501 | ||||||
| chr2:53906953
|
G | T | 5 | a0001c0022t0016g0111a0002c0003t0002g0060a0002c0003t0002g0079others(2): Show | 5 | HG01069.hp1 HG01515.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2785-85C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53906953 | ||||||
| chr2:53907023
|
A | G | 1 | a0001c0005t0001g0320 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2785-155T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907023 | ||||||
| chr2:53907025
|
A | G | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2785-157T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907025 | ||||||
| chr2:53907028
|
A | AAT | 141 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.2785-162_2785-161d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907028 | ||||||
| chr2:53907036
|
C | CTTAA | 141 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.2785-172_2785-169d others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907036 | ||||||
| chr2:53907560
|
C | T | 1 | a0002c0029t0002g0307 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2785-692G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907560 | ||||||
| chr2:53907801
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2784+519C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907801 | ||||||
| chr2:53907867
|
T | A | 243 | a0001c0001t0003g0204a0001c0005t0001g0182a0001c0005t0001g0311others(240): Show | 243 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.2784+453A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907867 | ||||||
| chr2:53907915
|
C | T | 243 | a0001c0001t0003g0204a0001c0005t0001g0182a0001c0005t0001g0311others(240): Show | 243 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.2784+405G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907915 | ||||||
| chr2:53908172
|
C | T | 1 | a0003c0004t0001g0261 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2784+148G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53908172 | ||||||
| chr2:53908292
|
G | C | 140 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2784+28C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53908292 | ||||||
| chr2:53908472
|
G | A | 2 | a0004c0008t0001g0376a0004c0008t0001g0379 | 2 | HG01928.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.2685+38C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 23/46 | chr2 | 53908472 | ||||||
| chr2:53908628
|
G | A | 1 | a0001c0005t0001g0323 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2630-63C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 22/46 | chr2 | 53908628 | ||||||
| chr2:53908967
|
A | T | 8 | a0001c0006t0015g0169a0001c0007t0001g0361a0001c0007t0006g0012others(5): Show | 8 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.2573-127T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53908967 | ||||||
| chr2:53909017
|
A | G | 1 | a0003c0004t0001g0042 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2573-177T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909017 | ||||||
| chr2:53909030
|
G | A | 1 | a0007c0012t0002g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2573-190C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909030 | ||||||
| chr2:53909042
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2573-202A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909042 | ||||||
| chr2:53909124
|
A | G | 1 | a0001c0005t0001g0333 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2573-284T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909124 | ||||||
| chr2:53909195
|
A | G | 1 | a0001c0005t0001g0373 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2573-355T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909195 | ||||||
| chr2:53909291
|
C | T | 1 | a0005c0011t0002g0363 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2573-451G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909291 | ||||||
| chr2:53909322
|
T | C | 3 | a0002c0003t0002g0016a0002c0003t0002g0057a0002c0003t0002g0072 | 3 | NA18991.hp1 NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2573-482A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909322 | ||||||
| chr2:53909378
|
C | A | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2573-538G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909378 | ||||||
| chr2:53909404
|
T | C | 1 | a0002c0002t0002g0023 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2573-564A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909404 | ||||||
| chr2:53909419
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2573-579G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909419 | ||||||
| chr2:53909577
|
T | C | 57 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(54): Show | 57 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2572+498A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909577 | ||||||
| chr2:53909708
|
C | T | 1 | a0001c0007t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2572+367G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909708 | ||||||
| chr2:53909714
|
C | T | 13 | a0003c0004t0001g0040a0003c0004t0001g0257a0003c0004t0001g0274others(10): Show | 13 | HG02132.hp1 NA18959.hp2 NA18963.hp1 others(10): Show |
intron_variant | MODIFIER | c.2572+361G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909714 | ||||||
| chr2:53909726
|
C | T | 1 | a0003c0004t0001g0183 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2572+349G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909726 | ||||||
| chr2:53909999
|
A | G | 66 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(63): Show | 66 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.2572+76T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909999 | ||||||
| chr2:53910270
|
G | C | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2517-140C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53910270 | ||||||
| chr2:53910398
|
A | T | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2517-268T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53910398 | ||||||
| chr2:53910689
|
C | A | 3 | a0001c0006t0003g0172a0001c0006t0003g0175a0001c0006t0003g0371 | 3 | HG02257.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2517-559G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53910689 | ||||||
| chr2:53910879
|
G | C | 1 | a0002c0003t0002g0112 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2517-749C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53910879 | ||||||
| chr2:53911113
|
T | C | 7 | a0001c0007t0001g0361a0001c0007t0006g0012a0001c0007t0006g0014others(4): Show | 7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2517-983A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911113 | ||||||
| chr2:53911305
|
G | T | 241 | a0001c0001t0001g0173a0001c0001t0003g0204a0001c0005t0001g0182others(238): Show | 241 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.2517-1175C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911305 | ||||||
| chr2:53911499
|
C | T | 1 | a0003c0004t0001g0033 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2517-1369G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911499 | ||||||
| chr2:53911500
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2517-1370C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911500 | ||||||
| chr2:53911596
|
G | A | 1 | a0005c0011t0002g0363 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2517-1466C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911596 | ||||||
| chr2:53911739
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2517-1609T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911739 | ||||||
| chr2:53911801
|
A | T | 8 | a0001c0001t0001g0173a0001c0006t0003g0155a0001c0006t0003g0156others(5): Show | 8 | HG01167.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2517-1671T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911801 | ||||||
| chr2:53911857
|
G | C | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2517-1727C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911857 | ||||||
| chr2:53911880
|
T | C | 140 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2517-1750A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911880 | ||||||
| chr2:53911962
|
G | A | 1 | a0014c0016t0001g0339 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2517-1832C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911962 | ||||||
| chr2:53912014
|
G | C | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2517-1884C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53912014 | ||||||
| chr2:53912221
|
T | C | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2517-2091A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53912221 | ||||||
| chr2:53912313
|
G | A | 2 | a0002c0003t0002g0109a0002c0003t0002g0133 | 2 | HG01175.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.2517-2183C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53912313 | ||||||
| chr2:53912422
|
T | C | 65 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(62): Show | 65 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.2517-2292A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53912422 | ||||||
| chr2:53912525
|
A | G | 2 | a0001c0009t0001g0369a0015c0028t0001g0368 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2517-2395T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53912525 | ||||||
| chr2:53912676
|
A | G | 2 | a0007c0012t0002g0058a0007c0012t0002g0062 | 2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2517-2546T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53912676 | ||||||
| chr2:53912758
|
A | G | 262 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0001t0001g0181others(259): Show | 262 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.2517-2628T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53912758 | ||||||
| chr2:53913053
|
T | C | 7 | a0001c0007t0001g0361a0001c0007t0006g0012a0001c0007t0006g0014others(4): Show | 7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2517-2923A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53913053 | ||||||
| chr2:53913331
|
C | T | 1 | a0001c0006t0015g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2517-3201G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53913331 | ||||||
| chr2:53913347
|
A | T | 5 | a0001c0009t0001g0360a0001c0009t0001g0366a0001c0009t0001g0367others(2): Show | 5 | HG02717.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2517-3217T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53913347 | ||||||
| chr2:53913438
|
C | G | 55 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2517-3308G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53913438 | ||||||
| chr2:53913474
|
T | C | 1 | a0002c0003t0002g0112 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2517-3344A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53913474 | ||||||
| chr2:53913711
|
C | A | 8 | a0002c0002t0002g0050a0002c0002t0002g0083a0002c0002t0002g0094others(5): Show | 8 | HG00423.hp2 HG02015.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.2517-3581G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53913711 | ||||||
| chr2:53914248
|
T | C | 1 | a0001c0009t0001g0360 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2517-4118A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914248 | ||||||
| chr2:53914355
|
G | A | 68 | a0002c0002t0001g0232a0002c0002t0002g0022a0002c0002t0002g0023others(65): Show | 68 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.2517-4225C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914355 | ||||||
| chr2:53914441
|
T | C | 1 | a0002c0010t0002g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2517-4311A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914441 | ||||||
| chr2:53914500
|
G | C | 46 | a0001c0001t0001g0173a0001c0001t0003g0204a0001c0006t0003g0025others(43): Show | 46 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.2517-4370C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914500 | ||||||
| chr2:53914609
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0235a0001c0001t0001g0308 | 3 | HG01261.hp2 HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2517-4479C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914609 | ||||||
| chr2:53914621
|
G | A | 1 | a0001c0017t0001g0309 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2517-4491C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914621 | ||||||
| chr2:53914693
|
C | A | 55 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2516+4458G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914693 | ||||||
| chr2:53914774
|
G | A | 3 | a0001c0005t0001g0316a0001c0005t0001g0318a0001c0005t0001g0353 | 3 | HG01515.hp2 HG01517.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2516+4377C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914774 | ||||||
| chr2:53914791
|
G | C | 2 | a0001c0005t0001g0334a0001c0005t0001g0350 | 2 | NA18955.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2516+4360C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914791 | ||||||
| chr2:53914824
|
T | A | 2 | a0001c0007t0001g0017a0001c0007t0001g0179 | 2 | HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2516+4327A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914824 | ||||||
| chr2:53914893
|
T | C | 46 | a0001c0001t0001g0173a0001c0001t0003g0204a0001c0006t0003g0025others(43): Show | 46 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.2516+4258A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914893 | ||||||
| chr2:53915216
|
A | C | 1 | a0002c0003t0002g0152 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2516+3935T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915216 | ||||||
| chr2:53915267
|
C | T | 56 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(53): Show | 56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2516+3884G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915267 | ||||||
| chr2:53915276
|
A | C | 1 | a0001c0006t0003g0218 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2516+3875T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915276 | ||||||
| chr2:53915313
|
C | T | 2 | a0001c0007t0001g0361a0012c0024t0001g0312 | 2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2516+3838G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915313 | ||||||
| chr2:53915542
|
T | C | 140 | a0001c0022t0016g0111a0002c0002t0001g0232a0002c0002t0002g0022others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2516+3609A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915542 | ||||||
| chr2:53915553
|
T | G | 1 | a0002c0003t0002g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2516+3598A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915553 | ||||||
| chr2:53915572
|
T | C | 2 | a0002c0002t0002g0356a0002c0002t0002g0358 | 2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2516+3579A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915572 | ||||||
| chr2:53915687
|
G | A | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2516+3464C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915687 | ||||||
| chr2:53915760
|
T | G | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2516+3391A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915760 | ||||||
| chr2:53915803
|
G | A | 1 | a0003c0004t0001g0247 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2516+3348C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915803 | ||||||
| chr2:53915806
|
C | G | 1 | a0002c0015t0002g0359 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2516+3345G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915806 | ||||||
| chr2:53915890
|
G | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0239 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2516+3261C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915890 | ||||||
| chr2:53915958
|
C | G | 1 | a0003c0004t0001g0201 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2516+3193G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915958 | ||||||
| chr2:53915992
|
T | G | 3 | a0001c0006t0003g0031a0001c0006t0003g0176a0001c0006t0003g0177 | 3 | HG02615.hp1 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2516+3159A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915992 | ||||||
| chr2:53916008
|
G | C | 5 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(2): Show | 5 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2516+3143C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916008 | ||||||
| chr2:53916027
|
A | G | 2 | a0002c0002t0002g0355a0002c0029t0002g0307 | 2 | HG02015.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2516+3124T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916027 | ||||||
| chr2:53916084
|
T | A | 4 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(1): Show | 4 | HG00099.hp1 HG01081.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.2516+3067A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916084 | ||||||
| chr2:53916185
|
C | T | 46 | a0001c0001t0001g0173a0001c0001t0003g0204a0001c0006t0003g0025others(43): Show | 46 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.2516+2966G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916185 | ||||||
| chr2:53916198
|
G | A | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2516+2953C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916198 | ||||||
| chr2:53916241
|
C | CA | 11 | a0001c0001t0001g0223a0001c0001t0001g0237a0001c0001t0001g0243others(8): Show | 11 | HG00408.hp1 HG01070.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.2516+2909dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916241 | ||||||
| chr2:53916241
|
C | CAA | 294 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0035others(291): Show | 295 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.2516+2908_2516+290 others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916241 | ||||||
| chr2:53916241
|
C | CAAA | 74 | a0001c0001t0001g0038a0001c0001t0001g0173a0001c0001t0001g0184others(71): Show | 74 | HG00099.hp2 HG00609.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.2516+2907_2516+290 others(7): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916241 | ||||||
| chr2:53916271
|
T | C | 4 | a0001c0005t0001g0321a0001c0005t0001g0324a0001c0005t0001g0338others(1): Show | 4 | HG00621.hp1 HG02132.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.2516+2880A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916271 | ||||||
| chr2:53916294
|
G | C | 1 | a0002c0003t0002g0019 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2516+2857C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916294 | ||||||
| chr2:53916378
|
A | G | 1 | a0003c0004t0001g0208 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2516+2773T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916378 | ||||||
| chr2:53916431
|
C | T | 63 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.2516+2720G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916431 | ||||||
| chr2:53916493
|
T | C | 24 | a0001c0022t0016g0111a0002c0003t0001g0080a0002c0003t0002g0019others(21): Show | 24 | HG00408.hp2 HG00438.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.2516+2658A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916493 | ||||||
| chr2:53916649
|
A | G | 51 | a0003c0004t0001g0032a0003c0004t0001g0033a0003c0004t0001g0034others(48): Show | 51 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.2516+2502T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916649 | ||||||
| chr2:53916745
|
A | T | 1 | a0001c0006t0015g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2516+2406T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916745 | ||||||
| chr2:53916913
|
C | G | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2516+2238G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916913 | ||||||
| chr2:53917057
|
TTAAG | T | 139 | a0001c0022t0016g0111a0002c0002t0002g0022a0002c0002t0002g0023others(136): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2516+2090_2516+209 others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917057 | ||||||
| chr2:53917131
|
T | G | 2 | a0001c0005t0001g0315a0001c0005t0001g0319 | 2 | HG01358.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.2516+2020A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917131 | ||||||
| chr2:53917277
|
C | T | 4 | a0003c0004t0001g0262a0003c0004t0001g0263a0003c0004t0001g0264others(1): Show | 4 | NA18983.hp2 NA19004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2516+1874G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917277 | ||||||
| chr2:53917307
|
T | C | 1 | a0002c0015t0002g0359 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2516+1844A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917307 | ||||||
| chr2:53917311
|
T | C | 72 | a0001c0022t0016g0111a0002c0003t0001g0080a0002c0003t0002g0011others(69): Show | 72 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.2516+1840A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917311 | ||||||
| chr2:53917375
|
T | C | 7 | a0001c0005t0001g0332a0001c0005t0001g0336a0001c0005t0001g0343others(4): Show | 7 | HG00423.hp1 HG00609.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.2516+1776A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917375 | ||||||
| chr2:53917395
|
A | G | 68 | a0001c0022t0016g0111a0002c0003t0001g0080a0002c0003t0002g0011others(65): Show | 68 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2516+1756T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917395 | ||||||
| chr2:53917609
|
C | T | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2516+1542G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917609 | ||||||
| chr2:53917682
|
T | C | 46 | a0001c0001t0001g0173a0001c0001t0003g0204a0001c0006t0003g0025others(43): Show | 46 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.2516+1469A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917682 | ||||||
| chr2:53917695
|
A | C | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2516+1456T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917695 | ||||||
| chr2:53917944
|
A | C | 4 | a0001c0001t0001g0180a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG02630.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2516+1207T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917944 | ||||||
| chr2:53917945
|
T | C | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2516+1206A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917945 | ||||||
| chr2:53918030
|
T | G | 2 | a0002c0003t0002g0059a0002c0003t0002g0074 | 2 | HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2516+1121A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918030 | ||||||
| chr2:53918182
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2516+969C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918182 | ||||||
| chr2:53918226
|
G | A | 56 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(53): Show | 56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2516+925C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918226 | ||||||
| chr2:53918499
|
G | A | 68 | a0001c0022t0016g0111a0002c0003t0001g0080a0002c0003t0002g0011others(65): Show | 68 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2516+652C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918499 | ||||||
| chr2:53918624
|
T | C | 140 | a0001c0022t0016g0111a0002c0002t0002g0022a0002c0002t0002g0023others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2516+527A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918624 | ||||||
| chr2:53918682
|
G | A | 2 | a0002c0002t0002g0356a0002c0002t0002g0358 | 2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2516+469C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918682 | ||||||
| chr2:53918780
|
A | T | 7 | a0001c0007t0001g0361a0001c0007t0006g0012a0001c0007t0006g0014others(4): Show | 7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2516+371T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918780 | ||||||
| chr2:53918819
|
C | T | 2 | a0001c0005t0001g0326a0001c0005t0001g0345 | 2 | HG00597.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.2516+332G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918819 | ||||||
| chr2:53918823
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0282 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2516+328G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918823 | ||||||
| chr2:53919037
|
T | G | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2516+114A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53919037 | ||||||
| chr2:53919041
|
A | G | 1 | a0005c0011t0002g0363 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2516+110T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53919041 | ||||||
| chr2:53919330
|
G | A | 1 | a0002c0003t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2421-84C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919330 | ||||||
| chr2:53919390
|
A | G | 5 | a0002c0003t0002g0049a0002c0003t0002g0055a0002c0003t0002g0059others(2): Show | 5 | HG02809.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2421-144T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919390 | ||||||
| chr2:53919489
|
T | G | 1 | a0002c0002t0002g0085 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2421-243A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919489 | ||||||
| chr2:53919583
|
T | C | 3 | a0001c0006t0005g0002a0001c0006t0005g0004a0003c0004t0003g0219 | 3 | HG01109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2421-337A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919583 | ||||||
| chr2:53919628
|
G | A | 1 | a0001c0006t0003g0218 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2421-382C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919628 | ||||||
| chr2:53919638
|
C | T | 8 | a0004c0008t0001g0376a0004c0008t0001g0377a0004c0008t0001g0378others(5): Show | 8 | HG01070.hp2 HG01109.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2421-392G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919638 | ||||||
| chr2:53919658
|
A | G | 2 | a0001c0005t0001g0317a0001c0005t0001g0329 | 2 | HG02129.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.2421-412T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919658 | ||||||
| chr2:53919816
|
G | GA | 57 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(54): Show | 57 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2420+376dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919816 | ||||||
| chr2:53919925
|
A | G | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2420+268T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919925 | ||||||
| chr2:53920043
|
CA | C | 3 | a0002c0002t0002g0043a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG00280.hp2 HG00323.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.2420+149delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53920043 | ||||||
| chr2:53920101
|
G | A | 1 | a0002c0002t0001g0232 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2420+92C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53920101 | ||||||
| chr2:53920680
|
G | C | 139 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(136): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2262+209C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 18/46 | chr2 | 53920680 | ||||||
| chr2:53920769
|
A | G | 2 | a0002c0003t0002g0059a0002c0003t0002g0074 | 2 | HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2262+120T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 18/46 | chr2 | 53920769 | ||||||
| chr2:53920784
|
T | A | 4 | a0005c0011t0001g0362a0005c0011t0001g0364a0005c0011t0002g0363others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2262+105A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 18/46 | chr2 | 53920784 | ||||||
| chr2:53921173
|
G | C | 5 | a0002c0003t0002g0020a0002c0003t0002g0077a0002c0003t0002g0078others(2): Show | 5 | HG01106.hp2 HG01192.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.2047-69C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921173 | ||||||
| chr2:53921194
|
C | A | 242 | a0001c0001t0001g0173a0001c0001t0003g0204a0001c0005t0001g0182others(239): Show | 242 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.2047-90G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921194 | ||||||
| chr2:53921270
|
G | A | 249 | a0001c0001t0001g0173a0001c0001t0003g0204a0001c0005t0001g0182others(246): Show | 249 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.2047-166C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921270 | ||||||
| chr2:53921491
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2047-387G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921491 | ||||||
| chr2:53921574
|
G | C | 58 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(55): Show | 58 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2047-470C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921574 | ||||||
| chr2:53921595
|
G | A | 64 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.2047-491C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921595 | ||||||
| chr2:53921628
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2047-524C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921628 | ||||||
| chr2:53921640
|
G | A | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2047-536C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921640 | ||||||
| chr2:53921644
|
G | A | 2 | a0001c0001t0001g0272a0001c0001t0001g0273 | 2 | HG00323.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2047-540C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921644 | ||||||
| chr2:53921676
|
G | A | 1 | a0002c0003t0002g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2047-572C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921676 | ||||||
| chr2:53921677
|
G | A | 138 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(135): Show | 138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.2047-573C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921677 | ||||||
| chr2:53921683
|
A | T | 4 | a0001c0005t0001g0321a0001c0005t0001g0324a0001c0005t0001g0338others(1): Show | 4 | HG00621.hp1 HG02132.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-579T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921683 | ||||||
| chr2:53921699
|
T | A | 2 | a0002c0002t0002g0063a0002c0002t0002g0095 | 2 | NA18954.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2047-595A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921699 | ||||||
| chr2:53921753
|
A | G | 1 | a0002c0003t0002g0132 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2047-649T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921753 | ||||||
| chr2:53921783
|
G | C | 71 | a0002c0003t0001g0080a0002c0003t0002g0011a0002c0003t0002g0016others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.2047-679C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921783 | ||||||
| chr2:53921842
|
T | C | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2046+675A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921842 | ||||||
| chr2:53921854
|
C | G | 58 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0313others(55): Show | 58 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2046+663G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921854 | ||||||
| chr2:53921867
|
C | CAAAAAAA others(4): Show |
3 | a0002c0002t0002g0095a0002c0002t0004g0064a0002c0003t0002g0149 | 3 | HG01256.hp2 NA19056.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.2046+649_2046+650i others(13): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921867 | ||||||
| chr2:53921867
|
C | CAAAAAAA others(5): Show |
131 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(128): Show | 131 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.2046+649_2046+650i others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921867 | ||||||
| chr2:53921867
|
C | CAAAAAAA others(6): Show |
4 | a0002c0002t0002g0097a0002c0002t0002g0154a0002c0003t0004g0340others(1): Show | 4 | HG02602.hp1 HG03831.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+649_2046+650i others(15): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921867 | ||||||
| chr2:53921949
|
G | A | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2046+568C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921949 | ||||||
| chr2:53922022
|
A | G | 1 | a0003c0004t0001g0301 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2046+495T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922022 | ||||||
| chr2:53922055
|
C | A | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2046+462G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922055 | ||||||
| chr2:53922108
|
T | C | 67 | a0002c0003t0001g0080a0002c0003t0002g0011a0002c0003t0002g0016others(64): Show | 67 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2046+409A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922108 | ||||||
| chr2:53922131
|
C | A | 4 | a0001c0005t0001g0321a0001c0005t0001g0324a0001c0005t0001g0338others(1): Show | 4 | HG00621.hp1 HG02132.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+386G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922131 | ||||||
| chr2:53922172
|
A | AAAAAG | 4 | a0001c0001t0003g0204a0001c0006t0005g0003a0001c0006t0005g0005others(1): Show | 4 | HG02109.hp1 HG02976.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+340_2046+344d others(7): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922172 | ||||||
| chr2:53922235
|
A | G | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2046+282T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922235 | ||||||
| chr2:53922248
|
T | G | 140 | a0001c0022t0016g0111a0002c0002t0002g0022a0002c0002t0002g0023others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2046+269A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922248 | ||||||
| chr2:53922486
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2046+31A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922486 | ||||||
| chr2:53922729
|
C | T | 1 | a0001c0001t0003g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1979-145G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 16/46 | chr2 | 53922729 | ||||||
| chr2:53922805
|
TC | T | 44 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(41): Show | 44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1979-222delG | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 16/46 | chr2 | 53922805 | ||||||
| chr2:53922868
|
A | C | 2 | a0001c0005t0001g0372a0001c0005t0001g0373 | 2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1978+181T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 16/46 | chr2 | 53922868 | ||||||
| chr2:53922897
|
G | A | 2 | a0001c0006t0003g0031a0001c0006t0003g0177 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1978+152C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 16/46 | chr2 | 53922897 | ||||||
| chr2:53922942
|
A | T | 64 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1978+107T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 16/46 | chr2 | 53922942 | ||||||
| chr2:53922969
|
T | C | 1 | a0004c0008t0001g0382 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1978+80A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 16/46 | chr2 | 53922969 | ||||||
| chr2:53923214
|
A | T | 3 | a0002c0002t0002g0085a0002c0002t0002g0086a0002c0002t0002g0119 | 3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1909-96T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 15/46 | chr2 | 53923214 | ||||||
| chr2:53923281
|
G | A | 1 | a0001c0018t0001g0226 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1908+40C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 15/46 | chr2 | 53923281 | ||||||
| chr2:53923293
|
A | G | 3 | a0003c0004t0001g0183a0003c0004t0001g0195a0003c0004t0001g0261 | 3 | HG00558.hp2 NA18747.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1908+28T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 15/46 | chr2 | 53923293 | ||||||
| chr2:53923301
|
G | C | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1908+20C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 15/46 | chr2 | 53923301 | ||||||
| chr2:53923549
|
G | A | 6 | a0001c0001t0001g0053a0001c0001t0001g0181a0001c0001t0001g0191others(3): Show | 6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1810-130C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923549 | ||||||
| chr2:53923723
|
G | C | 2 | a0001c0001t0001g0272a0001c0001t0001g0273 | 2 | HG00323.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1810-304C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923723 | ||||||
| chr2:53923867
|
G | A | 136 | a0001c0022t0016g0111a0002c0002t0002g0022a0002c0002t0002g0023others(133): Show | 136 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1810-448C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923867 | ||||||
| chr2:53923913
|
C | CA | 69 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0180others(66): Show | 70 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1810-495dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | ||||||
| chr2:53923913
|
C | CAA | 21 | a0001c0001t0001g0038a0001c0001t0001g0215a0001c0006t0003g0030others(18): Show | 21 | HG00438.hp2 HG00735.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1810-496_1810-495d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | ||||||
| chr2:53923913
|
CAAAAAAA others(2): Show |
C | 31 | a0001c0005t0001g0182a0001c0005t0001g0311a0001c0005t0001g0316others(28): Show | 31 | HG00597.hp1 HG01081.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1810-503_1810-495d others(11): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | ||||||
| chr2:53923913
|
CAAAAAAA others(3): Show |
C | 26 | a0001c0005t0001g0313a0001c0005t0001g0314a0001c0005t0001g0315others(23): Show | 26 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.1810-504_1810-495d others(12): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | ||||||
| chr2:53923913
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0185 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1810-505_1810-495d others(13): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | ||||||
| chr2:53923913
|
CAAAAAAA others(5): Show |
C | 7 | a0001c0007t0001g0361a0001c0007t0006g0012a0001c0007t0006g0014others(4): Show | 7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1810-506_1810-495d others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | ||||||
| chr2:53923913
|
CAAAAAAA others(10): Show |
C | 69 | a0001c0009t0013g0292a0002c0002t0002g0022a0002c0002t0002g0023others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1810-511_1810-495d others(19): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | ||||||
| chr2:53923913
|
CAAAAAAA others(11): Show |
C | 72 | a0001c0022t0016g0111a0002c0003t0001g0080a0002c0003t0002g0011others(69): Show | 72 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1810-512_1810-495d others(20): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | ||||||
| chr2:53923925
|
A | C | 2 | a0001c0005t0001g0372a0001c0005t0001g0373 | 2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1810-506T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923925 | ||||||
| chr2:53924037
|
T | C | 5 | a0002c0003t0002g0049a0002c0003t0002g0055a0002c0003t0002g0059others(2): Show | 5 | HG02809.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1810-618A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924037 | ||||||
| chr2:53924395
|
A | G | 3 | a0002c0002t0002g0116a0002c0002t0002g0120a0002c0002t0002g0140 | 3 | HG02027.hp1 NA18990.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1810-976T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924395 | ||||||
| chr2:53924540
|
A | C | 4 | a0002c0003t0002g0070a0002c0003t0002g0071a0002c0003t0002g0081others(1): Show | 4 | NA18970.hp1 NA18984.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809+999T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924540 | ||||||
| chr2:53924551
|
G | T | 1 | a0004c0008t0001g0376 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1809+988C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924551 | ||||||
| chr2:53924570
|
A | G | 1 | a0002c0002t0002g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1809+969T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924570 | ||||||
| chr2:53924649
|
G | A | 1 | a0002c0002t0002g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1809+890C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924649 | ||||||
| chr2:53924791
|
T | C | 6 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(3): Show | 6 | HG01099.hp2 HG01106.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1809+748A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924791 | ||||||
| chr2:53924976
|
T | C | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1809+563A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924976 | ||||||
| chr2:53925281
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1809+258A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53925281 | ||||||
| chr2:53925305
|
T | C | 3 | a0001c0006t0003g0026a0001c0006t0003g0027a0001c0006t0003g0030 | 3 | HG01099.hp2 HG01106.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1809+234A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53925305 | ||||||
| chr2:53925361
|
C | T | 1 | a0001c0006t0003g0159 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1809+178G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53925361 | ||||||
| chr2:53925392
|
T | G | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1809+147A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53925392 | ||||||
| chr2:53925426
|
T | C | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | NA18968.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1809+113A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53925426 | ||||||
| chr2:53925448
|
C | T | 2 | a0002c0003t0002g0060a0002c0003t0002g0079 | 2 | HG03239.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1809+91G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53925448 | ||||||
| chr2:53925468
|
T | C | 1 | a0001c0001t0001g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1809+71A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53925468 | ||||||
| chr2:53925790
|
T | C | 141 | a0001c0001t0001g0225a0001c0022t0016g0111a0002c0002t0002g0022others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1659-101A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 13/46 | chr2 | 53925790 | ||||||
| chr2:53925822
|
G | C | 1 | a0001c0005t0001g0373 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1659-133C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 13/46 | chr2 | 53925822 | ||||||
| chr2:53925843
|
G | A | 8 | a0002c0002t0002g0050a0002c0002t0002g0083a0002c0002t0002g0094others(5): Show | 8 | HG00423.hp2 HG02015.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1658+116C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 13/46 | chr2 | 53925843 | ||||||
| chr2:53926044
|
G | C | 6 | a0001c0001t0001g0053a0001c0001t0001g0181a0001c0001t0001g0191others(3): Show | 6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1594-21C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926044 | ||||||
| chr2:53926147
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0223a0001c0001t0001g0230others(2): Show | 5 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1594-124T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926147 | ||||||
| chr2:53926193
|
A | G | 2 | a0002c0010t0002g0018a0002c0010t0002g0056 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1594-170T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926193 | ||||||
| chr2:53926204
|
T | C | 73 | a0001c0001t0001g0225a0001c0022t0016g0111a0002c0003t0001g0080others(70): Show | 73 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1594-181A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926204 | ||||||
| chr2:53926230
|
A | T | 3 | a0001c0005t0001g0316a0001c0005t0001g0318a0001c0005t0001g0353 | 3 | HG01515.hp2 HG01517.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1594-207T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926230 | ||||||
| chr2:53926402
|
T | TG | 45 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(42): Show | 45 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.1594-380dupC | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926402 | ||||||
| chr2:53926416
|
G | A | 13 | a0001c0001t0001g0180a0001c0001t0001g0198a0001c0001t0001g0199others(10): Show | 13 | HG02486.hp2 HG02630.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.1594-393C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926416 | ||||||
| chr2:53926440
|
G | A | 1 | a0002c0010t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1594-417C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926440 | ||||||
| chr2:53926545
|
T | G | 141 | a0001c0001t0001g0225a0001c0022t0016g0111a0002c0002t0002g0022others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1594-522A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926545 | ||||||
| chr2:53926705
|
G | A | 9 | a0001c0001t0001g0036a0001c0001t0001g0189a0001c0001t0001g0190others(6): Show | 9 | HG00733.hp1 HG01261.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1594-682C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926705 | ||||||
| chr2:53926707
|
C | T | 141 | a0001c0001t0001g0225a0001c0022t0016g0111a0002c0002t0002g0022others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1594-684G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926707 | ||||||
| chr2:53926716
|
G | A | 2 | a0003c0004t0001g0192a0003c0004t0001g0245 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1593+678C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926716 | ||||||
| chr2:53926743
|
C | T | 42 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(39): Show | 42 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1593+651G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926743 | ||||||
| chr2:53926770
|
C | T | 1 | a0010c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1593+624G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926770 | ||||||
| chr2:53926835
|
A | G | 141 | a0001c0001t0001g0225a0001c0022t0016g0111a0002c0002t0002g0022others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1593+559T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926835 | ||||||
| chr2:53926923
|
A | C | 1 | a0002c0003t0002g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1593+471T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926923 | ||||||
| chr2:53926979
|
A | C | 1 | a0001c0009t0001g0370 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1593+415T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926979 | ||||||
| chr2:53926982
|
AG | A | 138 | a0001c0001t0001g0225a0001c0022t0016g0111a0002c0002t0002g0022others(135): Show | 138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1593+411delC | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926982 | ||||||
| chr2:53926983
|
G | A | 2 | a0002c0003t0002g0136a0002c0003t0002g0150 | 2 | HG01123.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1593+411C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926983 | ||||||
| chr2:53927038
|
AAAATCTT others(8): Show |
A | 2 | a0003c0004t0001g0192a0003c0004t0001g0245 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1593+341_1593+355d others(17): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53927038 | ||||||
| chr2:53927043
|
C | T | 1 | a0002c0003t0002g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1593+351G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53927043 | ||||||
| chr2:53927050
|
C | A | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1593+344G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53927050 | ||||||
| chr2:53927097
|
T | C | 1 | a0002c0002t0002g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1593+297A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53927097 | ||||||
| chr2:53927118
|
T | C | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0270 | 3 | HG03209.hp2 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1593+276A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53927118 | ||||||
| chr2:53927575
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1504-92A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 11/46 | chr2 | 53927575 | ||||||
| chr2:53927793
|
G | A | 2 | a0001c0007t0006g0012a0001c0007t0006g0014 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1504-310C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 11/46 | chr2 | 53927793 | ||||||
| chr2:53927906
|
C | T | 1 | a0002c0003t0002g0020 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1503+211G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 11/46 | chr2 | 53927906 | ||||||
| chr2:53928051
|
T | TGTGACTG others(7): Show |
6 | a0002c0002t0002g0050a0002c0002t0002g0083a0002c0002t0002g0094others(3): Show | 6 | HG00423.hp2 HG02083.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1503+65_1503+66ins others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 11/46 | chr2 | 53928051 | ||||||
| chr2:53928052
|
T | A | 6 | a0002c0002t0002g0050a0002c0002t0002g0083a0002c0002t0002g0094others(3): Show | 6 | HG00423.hp2 HG02083.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1503+65A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 11/46 | chr2 | 53928052 | ||||||
| chr2:53928103
|
A | G | 143 | a0001c0001t0001g0225a0001c0005t0001g0320a0001c0022t0016g0111others(140): Show | 143 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1503+14T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 11/46 | chr2 | 53928103 | ||||||
| chr2:53928520
|
T | TCA | 244 | a0001c0001t0001g0173a0001c0001t0001g0225a0001c0005t0001g0182others(241): Show | 244 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.1317-218_1317-217i others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53928520 | ||||||
| chr2:53928901
|
C | G | 2 | a0001c0006t0005g0003a0001c0006t0005g0005 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1317-598G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53928901 | ||||||
| chr2:53928958
|
G | A | 13 | a0003c0004t0001g0040a0003c0004t0001g0257a0003c0004t0001g0274others(10): Show | 13 | HG02132.hp1 NA18959.hp2 NA18963.hp1 others(10): Show |
intron_variant | MODIFIER | c.1317-655C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53928958 | ||||||
| chr2:53929038
|
T | C | 1 | a0002c0003t0002g0133 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1317-735A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53929038 | ||||||
| chr2:53929074
|
G | C | 1 | a0002c0002t0002g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1317-771C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53929074 | ||||||
| chr2:53929165
|
C | CA | 264 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0001t0001g0181others(261): Show | 264 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1317-863dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53929165 | ||||||
| chr2:53929186
|
T | A | 1 | a0007c0012t0002g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1317-883A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53929186 | ||||||
| chr2:53929454
|
G | A | 1 | a0002c0010t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1317-1151C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53929454 | ||||||
| chr2:53929804
|
G | A | 11 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(8): Show | 11 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1317-1501C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53929804 | ||||||
| chr2:53930030
|
TAATA | T | 4 | a0005c0011t0001g0362a0005c0011t0001g0364a0005c0011t0002g0363others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317-1731_1317-172 others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930030 | ||||||
| chr2:53930131
|
G | A | 2 | a0002c0003t0002g0104a0002c0003t0002g0113 | 2 | HG00408.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1316+1704C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930131 | ||||||
| chr2:53930148
|
A | C | 1 | a0002c0002t0004g0064 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1316+1687T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930148 | ||||||
| chr2:53930329
|
A | G | 2 | a0002c0002t0002g0122a0002c0002t0004g0123 | 2 | NA18975.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1316+1506T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930329 | ||||||
| chr2:53930430
|
G | A | 3 | a0001c0006t0003g0163a0001c0006t0003g0165a0001c0006t0003g0166 | 3 | NA18951.hp2 NA18973.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1316+1405C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930430 | ||||||
| chr2:53930631
|
G | C | 1 | a0002c0002t0002g0355 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1316+1204C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930631 | ||||||
| chr2:53930679
|
C | G | 1 | a0002c0002t0002g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1316+1156G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930679 | ||||||
| chr2:53930688
|
T | G | 1 | a0001c0009t0001g0370 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1316+1147A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930688 | ||||||
| chr2:53930698
|
G | C | 1 | a0002c0003t0002g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1316+1137C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930698 | ||||||
| chr2:53930767
|
G | A | 141 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0022t0016g0111others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1316+1068C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930767 | ||||||
| chr2:53930830
|
A | G | 1 | a0001c0001t0001g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1316+1005T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930830 | ||||||
| chr2:53931105
|
C | T | 1 | a0002c0003t0002g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1316+730G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931105 | ||||||
| chr2:53931108
|
T | C | 3 | a0001c0005t0001g0334a0001c0005t0001g0341a0001c0005t0001g0350 | 3 | NA18955.hp2 NA18986.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1316+727A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931108 | ||||||
| chr2:53931214
|
T | A | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1316+621A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931214 | ||||||
| chr2:53931330
|
C | G | 1 | a0002c0015t0002g0359 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1316+505G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931330 | ||||||
| chr2:53931429
|
A | G | 2 | a0001c0006t0005g0003a0001c0006t0005g0005 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1316+406T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931429 | ||||||
| chr2:53931548
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1316+287C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931548 | ||||||
| chr2:53931707
|
C | T | 1 | a0001c0007t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1316+128G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931707 | ||||||
| chr2:53931820
|
C | T | 139 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0022t0016g0111others(136): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1316+15G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931820 | ||||||
| chr2:53932174
|
T | A | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1051-74A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 9/46 | chr2 | 53932174 | ||||||
| chr2:53932196
|
A | G | 1 | a0002c0015t0002g0359 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1051-96T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 9/46 | chr2 | 53932196 | ||||||
| chr2:53932335
|
T | A | 1 | a0002c0003t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1051-235A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 9/46 | chr2 | 53932335 | ||||||
| chr2:53932477
|
T | A | 6 | a0003c0004t0001g0040a0003c0004t0001g0257a0003c0004t0001g0274others(3): Show | 6 | NA18959.hp2 NA18969.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050+191A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 9/46 | chr2 | 53932477 | ||||||
| chr2:53932635
|
C | T | 2 | a0002c0003t0002g0109a0002c0003t0002g0133 | 2 | HG01175.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1050+33G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 9/46 | chr2 | 53932635 | ||||||
| chr2:53932770
|
T | C | 1 | a0002c0002t0002g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.958-10A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53932770 | ||||||
| chr2:53932850
|
A | G | 1 | a0002c0003t0002g0069 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.958-90T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53932850 | ||||||
| chr2:53932862
|
G | A | 99 | a0001c0001t0001g0173a0001c0005t0001g0311a0001c0005t0001g0313others(96): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.958-102C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53932862 | ||||||
| chr2:53932922
|
T | C | 55 | a0001c0005t0001g0311a0001c0005t0001g0313a0001c0005t0001g0314others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.958-162A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53932922 | ||||||
| chr2:53933024
|
A | G | 1 | a0010c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.958-264T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933024 | ||||||
| chr2:53933145
|
A | G | 101 | a0001c0001t0001g0173a0001c0005t0001g0311a0001c0005t0001g0313others(98): Show | 101 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.958-385T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933145 | ||||||
| chr2:53933303
|
G | A | 9 | a0002c0003t0002g0024a0002c0003t0002g0136a0002c0003t0002g0144others(6): Show | 9 | HG00733.hp2 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.958-543C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933303 | ||||||
| chr2:53933308
|
G | A | 44 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(41): Show | 44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.958-548C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933308 | ||||||
| chr2:53933375
|
C | CA | 12 | a0001c0001t0001g0038a0001c0001t0001g0188a0001c0001t0001g0206others(9): Show | 12 | HG00597.hp2 HG01346.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.958-616dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAA | 10 | a0001c0001t0001g0180a0001c0001t0001g0199a0001c0001t0001g0205others(7): Show | 10 | HG01243.hp2 HG02896.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.958-618_958-616dup others(3): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA | 9 | a0001c0001t0001g0267a0001c0006t0003g0163a0001c0006t0003g0167others(6): Show | 9 | HG01109.hp1 HG01884.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.958-622_958-616dup others(7): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(1): Show |
13 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.958-623_958-616dup others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(2): Show |
23 | a0001c0001t0001g0191a0001c0006t0003g0030a0001c0006t0003g0031others(20): Show | 23 | HG00099.hp2 HG00558.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.958-624_958-616dup others(9): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(3): Show |
6 | a0001c0006t0003g0155a0001c0006t0003g0157a0001c0009t0001g0369others(3): Show | 6 | HG01891.hp1 HG02004.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.958-625_958-616dup others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(4): Show |
4 | a0001c0001t0001g0241a0001c0006t0003g0172a0001c0007t0006g0014others(1): Show | 4 | HG02257.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.958-626_958-616dup others(11): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(5): Show |
5 | a0001c0001t0001g0181a0001c0001t0001g0240a0001c0007t0001g0361others(2): Show | 5 | HG01255.hp2 HG02559.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.958-627_958-616dup others(12): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(6): Show |
11 | a0003c0004t0001g0039a0003c0004t0001g0193a0003c0004t0001g0200others(8): Show | 11 | HG01884.hp2 HG02622.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.958-628_958-616dup others(13): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(7): Show |
8 | a0003c0004t0001g0042a0003c0004t0001g0192a0003c0004t0001g0247others(5): Show | 8 | HG02280.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.958-629_958-616dup others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(8): Show |
5 | a0003c0004t0001g0040a0003c0004t0001g0255a0003c0004t0001g0257others(2): Show | 5 | HG02109.hp2 NA18959.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.958-630_958-616dup others(15): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(9): Show |
1 | a0003c0004t0001g0306 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.958-631_958-616dup others(16): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(11): Show |
1 | a0003c0004t0001g0271 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-633_958-616dup others(18): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(13): Show |
1 | a0003c0004t0001g0303 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.958-635_958-616dup others(20): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(14): Show |
4 | a0003c0004t0001g0033a0003c0004t0001g0256a0003c0004t0001g0302others(1): Show | 4 | HG02027.hp2 HG02523.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.958-636_958-616dup others(21): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(15): Show |
1 | a0003c0004t0001g0301 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.958-637_958-616dup others(22): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(17): Show |
3 | a0001c0001t0001g0242a0003c0004t0001g0195a0003c0004t0001g0286 | 3 | HG03225.hp1 NA18747.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.958-639_958-616dup others(24): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(18): Show |
3 | a0003c0004t0001g0249a0003c0004t0001g0298a0003c0004t0001g0300 | 3 | HG02015.hp2 HG02132.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.958-640_958-616dup others(25): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(19): Show |
1 | a0003c0004t0001g0288 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.958-641_958-616dup others(26): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(21): Show |
1 | a0003c0004t0001g0248 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.958-643_958-616dup others(28): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(25): Show |
1 | a0003c0004t0001g0258 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.958-616_958-615ins others(32): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(28): Show |
1 | a0013c0025t0001g0259 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.958-616_958-615ins others(35): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(32): Show |
1 | a0003c0004t0001g0290 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.958-616_958-615ins others(39): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
C | CAAAAAAA others(33): Show |
1 | a0003c0004t0001g0261 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.958-616_958-615ins others(40): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
CA | C | 23 | a0001c0001t0001g0036a0001c0001t0001g0190a0001c0001t0001g0234others(20): Show | 23 | HG00423.hp1 HG00733.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.958-616delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
CAA | C | 39 | a0001c0005t0001g0315a0001c0005t0001g0316a0001c0005t0001g0318others(36): Show | 39 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.958-617_958-616del others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
CAAAAAAA others(2): Show |
C | 15 | a0002c0002t0002g0047a0002c0002t0002g0099a0002c0002t0002g0100others(12): Show | 15 | HG03831.hp2 HG04199.hp2 HG04228.hp2 others(12): Show |
intron_variant | MODIFIER | c.958-624_958-616del others(9): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
CAAAAAAA others(3): Show |
C | 132 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0022t0016g0111others(129): Show | 132 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.958-625_958-616del others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0006t0005g0002a0001c0006t0005g0004a0002c0003t0002g0149 | 3 | HG01256.hp2 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.958-626_958-616del others(11): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933375
|
CAAAAAAA others(5): Show |
C | 1 | a0010c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.958-627_958-616del others(12): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | ||||||
| chr2:53933443
|
A | T | 61 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0022t0016g0111others(58): Show | 61 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.958-683T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933443 | ||||||
| chr2:53933541
|
G | A | 4 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(1): Show | 4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.958-781C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933541 | ||||||
| chr2:53933630
|
T | C | 142 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0022t0016g0111others(139): Show | 142 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.958-870A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933630 | ||||||
| chr2:53933681
|
C | T | 140 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0022t0016g0111others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.958-921G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933681 | ||||||
| chr2:53933686
|
T | C | 56 | a0001c0005t0001g0311a0001c0005t0001g0313a0001c0005t0001g0314others(53): Show | 56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.957+919A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933686 | ||||||
| chr2:53933912
|
G | C | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.957+693C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933912 | ||||||
| chr2:53933913
|
G | T | 141 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0022t0016g0111others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.957+692C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933913 | ||||||
| chr2:53933922
|
A | T | 4 | a0001c0005t0001g0321a0001c0005t0001g0324a0001c0005t0001g0338others(1): Show | 4 | HG00621.hp1 HG02132.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.957+683T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933922 | ||||||
| chr2:53933972
|
A | C | 11 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(8): Show | 11 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.957+633T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933972 | ||||||
| chr2:53934061
|
A | G | 3 | a0002c0002t0002g0356a0002c0002t0002g0358a0012c0024t0001g0312 | 3 | HG02615.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.957+544T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53934061 | ||||||
| chr2:53934226
|
T | C | 43 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(40): Show | 43 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.957+379A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53934226 | ||||||
| chr2:53934307
|
G | T | 1 | a0003c0004t0001g0208 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.957+298C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53934307 | ||||||
| chr2:53934368
|
T | C | 1 | a0003c0004t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.957+237A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53934368 | ||||||
| chr2:53934748
|
G | T | 138 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0022t0016g0111others(135): Show | 138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.835-21C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53934748 | ||||||
| chr2:53934795
|
C | T | 1 | a0001c0005t0001g0313 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.835-68G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53934795 | ||||||
| chr2:53934829
|
T | C | 1 | a0001c0001t0007g0224 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.835-102A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53934829 | ||||||
| chr2:53934875
|
C | T | 1 | a0002c0015t0002g0359 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.835-148G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53934875 | ||||||
| chr2:53934885
|
C | T | 240 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0001t0001g0225others(237): Show | 240 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.835-158G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53934885 | ||||||
| chr2:53934939
|
G | C | 44 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(41): Show | 44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.835-212C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53934939 | ||||||
| chr2:53935003
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.835-276C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935003 | ||||||
| chr2:53935088
|
T | TCCTGAGC others(3): Show |
1 | a0002c0003t0002g0019 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.835-371_835-362dup others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935088 | ||||||
| chr2:53935226
|
T | C | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.835-499A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935226 | ||||||
| chr2:53935317
|
A | T | 253 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0001t0001g0225others(250): Show | 253 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.835-590T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935317 | ||||||
| chr2:53935324
|
G | C | 1 | a0001c0006t0003g0371 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.835-597C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935324 | ||||||
| chr2:53935358
|
C | A | 1 | a0003c0004t0001g0201 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.835-631G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935358 | ||||||
| chr2:53935718
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0223a0001c0001t0001g0230others(1): Show | 4 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+369A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935718 | ||||||
| chr2:53935874
|
G | A | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.834+213C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935874 | ||||||
| chr2:53935897
|
G | GT | 57 | a0001c0005t0001g0313a0001c0005t0001g0314a0001c0005t0001g0315others(54): Show | 57 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.834+189dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935897 | ||||||
| chr2:53936036
|
G | A | 2 | a0002c0002t0002g0101a0002c0002t0002g0126 | 2 | NA19011.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.834+51C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53936036 | ||||||
| chr2:53936212
|
A | T | 1 | a0002c0003t0002g0128 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.760-51T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 6/46 | chr2 | 53936212 | ||||||
| chr2:53936382
|
A | G | 1 | a0002c0003t0002g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.760-221T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 6/46 | chr2 | 53936382 | ||||||
| chr2:53936587
|
C | CAAATA | 142 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0022t0016g0111others(139): Show | 142 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.759+172_759+176dup others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 6/46 | chr2 | 53936587 | ||||||
| chr2:53936709
|
G | A | 2 | a0002c0003t0002g0136a0002c0003t0002g0150 | 2 | HG01123.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.759+55C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 6/46 | chr2 | 53936709 | ||||||
| chr2:53936747
|
G | C | 1 | a0001c0022t0016g0111 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.759+17C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 6/46 | chr2 | 53936747 | ||||||
| chr2:53936931
|
C | T | 3 | a0002c0003t0002g0077a0002c0003t0002g0078a0002c0003t0002g0108 | 3 | HG01106.hp2 HG06807.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.696-104G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 5/46 | chr2 | 53936931 | ||||||
| chr2:53937169
|
T | C | 1 | a0016c0014t0002g0067 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.695+222A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 5/46 | chr2 | 53937169 | ||||||
| chr2:53937236
|
G | A | 39 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(36): Show | 39 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.695+155C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 5/46 | chr2 | 53937236 | ||||||
| chr2:53937382
|
C | T | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.695+9G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 5/46 | chr2 | 53937382 | ||||||
| chr2:53937645
|
T | C | 1 | a0001c0005t0001g0343 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.546-105A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53937645 | ||||||
| chr2:53937711
|
G | T | 197 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0005t0001g0311others(194): Show | 197 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.546-171C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53937711 | ||||||
| chr2:53937724
|
G | A | 1 | a0002c0010t0002g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.546-184C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53937724 | ||||||
| chr2:53937925
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.546-385C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53937925 | ||||||
| chr2:53938163
|
C | G | 1 | a0001c0007t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.546-623G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938163 | ||||||
| chr2:53938474
|
C | CT | 7 | a0001c0001t0001g0180a0001c0001t0001g0214a0001c0001t0001g0215others(4): Show | 7 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.546-935dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938474 | ||||||
| chr2:53938474
|
CT | C | 12 | a0001c0006t0003g0156a0001c0007t0001g0179a0002c0002t0002g0045others(9): Show | 12 | HG01167.hp2 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.546-935delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938474 | ||||||
| chr2:53938510
|
G | C | 1 | a0001c0001t0001g0209 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.546-970C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938510 | ||||||
| chr2:53938546
|
G | C | 1 | a0004c0008t0001g0382 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.546-1006C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938546 | ||||||
| chr2:53938572
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.546-1032C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938572 | ||||||
| chr2:53938635
|
A | G | 103 | a0001c0001t0001g0173a0001c0005t0001g0311a0001c0005t0001g0313others(100): Show | 103 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.546-1095T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938635 | ||||||
| chr2:53938709
|
G | T | 236 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0001t0001g0225others(233): Show | 236 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.546-1169C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938709 | ||||||
| chr2:53938769
|
C | A | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.545+1187G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938769 | ||||||
| chr2:53938795
|
T | G | 1 | a0001c0001t0001g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.545+1161A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938795 | ||||||
| chr2:53938832
|
T | C | 7 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179others(4): Show | 7 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+1124A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938832 | ||||||
| chr2:53938846
|
G | C | 5 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(2): Show | 5 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.545+1110C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938846 | ||||||
| chr2:53938855
|
G | A | 133 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0022t0016g0111others(130): Show | 133 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.545+1101C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938855 | ||||||
| chr2:53939045
|
A | C | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.545+911T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939045 | ||||||
| chr2:53939184
|
C | T | 56 | a0001c0005t0001g0311a0001c0005t0001g0313a0001c0005t0001g0314others(53): Show | 56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.545+772G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939184 | ||||||
| chr2:53939206
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.545+750G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939206 | ||||||
| chr2:53939265
|
C | A | 1 | a0001c0001t0001g0282 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.545+691G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939265 | ||||||
| chr2:53939488
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.545+468C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939488 | ||||||
| chr2:53939526
|
G | A | 64 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.545+430C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939526 | ||||||
| chr2:53939534
|
C | T | 4 | a0002c0003t0002g0077a0002c0003t0002g0078a0002c0003t0002g0108others(1): Show | 4 | HG01106.hp2 HG01261.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+422G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939534 | ||||||
| chr2:53939616
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.545+340C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939616 | ||||||
| chr2:53939663
|
A | G | 4 | a0002c0003t0002g0077a0002c0003t0002g0078a0002c0003t0002g0108others(1): Show | 4 | HG01106.hp2 HG01261.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+293T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939663 | ||||||
| chr2:53939756
|
G | A | 1 | a0008c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.545+200C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939756 | ||||||
| chr2:53940091
|
C | T | 3 | a0001c0001t0001g0180a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | HG02630.hp1 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.501-91G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940091 | ||||||
| chr2:53940461
|
T | C | 2 | a0001c0006t0005g0003a0001c0006t0005g0005 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.501-461A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940461 | ||||||
| chr2:53940467
|
C | T | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.501-467G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940467 | ||||||
| chr2:53940636
|
T | C | 12 | a0002c0002t0002g0023a0002c0002t0002g0043a0002c0002t0002g0054others(9): Show | 12 | HG00280.hp2 HG00323.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.501-636A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940636 | ||||||
| chr2:53940672
|
G | A | 70 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0022t0016g0111others(67): Show | 70 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.501-672C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940672 | ||||||
| chr2:53940832
|
C | T | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.501-832G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940832 | ||||||
| chr2:53940862
|
T | A | 1 | a0001c0019t0001g0037 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.501-862A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940862 | ||||||
| chr2:53940865
|
T | C | 2 | a0006c0013t0002g0046a0006c0013t0002g0073 | 2 | NA19002.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.501-865A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940865 | ||||||
| chr2:53940867
|
T | C | 240 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0001t0001g0225others(237): Show | 240 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.501-867A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940867 | ||||||
| chr2:53940875
|
A | AATATATA others(39): Show |
19 | a0002c0002t0002g0054a0002c0002t0002g0063a0002c0002t0002g0086others(16): Show | 19 | HG00621.hp2 HG02027.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.501-921_501-876dup others(46): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940875 | ||||||
| chr2:53940875
|
A | AATATATA others(58): Show |
1 | a0002c0003t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.501-876_501-875ins others(65): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940875 | ||||||
| chr2:53940875
|
A | AATATATA others(60): Show |
11 | a0001c0001t0001g0053a0002c0003t0002g0011a0002c0003t0002g0052others(8): Show | 11 | HG02809.hp1 HG02818.hp2 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.501-876_501-875ins others(67): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940875 | ||||||
| chr2:53940875
|
A | AATATATA others(129): Show |
1 | a0002c0003t0002g0019 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.501-876_501-875ins others(136): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940875 | ||||||
| chr2:53940896
|
A | AATATATA others(171): Show |
1 | a0002c0003t0002g0079 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.501-897_501-896ins others(178): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940896 | ||||||
| chr2:53940896
|
A | AATATATA others(127): Show |
2 | a0002c0003t0002g0109a0002c0003t0002g0133 | 2 | HG01175.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.501-897_501-896ins others(134): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940896 | ||||||
| chr2:53940896
|
A | AATATATA others(83): Show |
2 | a0002c0003t0002g0070a0016c0014t0002g0067 | 2 | NA18984.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.501-897_501-896ins others(90): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940896 | ||||||
| chr2:53940896
|
A | AATATATA others(129): Show |
1 | a0002c0003t0002g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.501-897_501-896ins others(136): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940896 | ||||||
| chr2:53940896
|
A | AATATATA others(150): Show |
1 | a0002c0021t0002g0110 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.501-897_501-896ins others(157): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940896 | ||||||
| chr2:53940896
|
A | AATATATA others(131): Show |
1 | a0002c0003t0002g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.501-897_501-896ins others(138): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940896 | ||||||
| chr2:53940896
|
AATATATA others(16): Show |
A | 4 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG00738.hp1 HG01123.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-919_501-897del others(23): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940896 | ||||||
| chr2:53940914
|
T | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0213a0001c0001t0001g0214 | 3 | HG01361.hp2 HG01952.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.501-914A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940914 | ||||||
| chr2:53940917
|
A | AAT | 155 | a0001c0001t0001g0173a0001c0001t0001g0180a0001c0001t0001g0181others(152): Show | 155 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.501-919_501-918dup others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940917 | ||||||
| chr2:53940917
|
A | AATATATA others(62): Show |
4 | a0002c0003t0002g0024a0002c0003t0002g0136a0002c0003t0002g0146others(1): Show | 4 | HG01123.hp2 HG01168.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-918_501-917ins others(69): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940917 | ||||||
| chr2:53940917
|
AAT | A | 47 | a0001c0001t0001g0225a0001c0006t0003g0155a0001c0006t0003g0156others(44): Show | 47 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.501-919_501-918del others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940917 | ||||||
| chr2:53940917
|
AATATATA others(30): Show |
A | 3 | a0005c0011t0001g0362a0005c0011t0001g0364a0005c0011t0002g0363 | 3 | HG01243.hp1 HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.501-954_501-918del others(37): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940917 | ||||||
| chr2:53940919
|
T | TATATATA others(37): Show |
5 | a0002c0003t0002g0020a0002c0003t0002g0077a0002c0003t0002g0078others(2): Show | 5 | HG01106.hp2 HG01192.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-920_501-919ins others(44): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940919 | ||||||
| chr2:53940919
|
T | TATATATA others(101): Show |
1 | a0002c0002t0002g0357 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.501-920_501-919ins others(108): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940919 | ||||||
| chr2:53940921
|
TATATATA others(24): Show |
T | 1 | a0001c0006t0003g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.501-952_501-922del others(31): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940921 | ||||||
| chr2:53940923
|
TATATAAT others(10): Show |
T | 2 | a0001c0001t0001g0205a0001c0001t0001g0239 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.501-940_501-924del others(17): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940923 | ||||||
| chr2:53940927
|
TAATACAT others(6): Show |
T | 1 | a0001c0001t0001g0214 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.501-940_501-928del others(13): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940927 | ||||||
| chr2:53940928
|
A | AT | 8 | a0002c0003t0002g0070a0002c0003t0002g0079a0002c0003t0002g0104others(5): Show | 8 | HG01175.hp1 HG01943.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.501-929_501-928ins others(1): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940928 | ||||||
| chr2:53940928
|
A | ATAATACA others(61): Show |
2 | a0002c0002t0002g0099a0002c0002t0002g0131 | 2 | HG02698.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.501-929_501-928ins others(68): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940928 | ||||||
| chr2:53940932
|
C | CATATTTA others(102): Show |
1 | a0002c0003t0002g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.501-933_501-932ins others(109): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940932 | ||||||
| chr2:53940934
|
T | TATTTAAA others(92): Show |
1 | a0002c0003t0002g0081 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.501-935_501-934ins others(99): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940934 | ||||||
| chr2:53940936
|
T | TTTAA | 4 | a0001c0001t0001g0053a0002c0003t0002g0019a0002c0003t0002g0136others(1): Show | 4 | HG01168.hp2 HG01257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-937_501-936ins others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940936 | ||||||
| chr2:53940936
|
T | TTTAAATA others(92): Show |
1 | a0002c0003t0002g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.501-937_501-936ins others(99): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940936 | ||||||
| chr2:53940936
|
TATAAATA others(9): Show |
T | 1 | a0001c0001t0001g0184 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.501-952_501-937del others(16): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940936 | ||||||
| chr2:53940937
|
A | T | 114 | a0001c0001t0001g0213a0001c0001t0001g0225a0001c0006t0003g0155others(111): Show | 114 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.501-937T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940937 | ||||||
| chr2:53940938
|
TAAATATA others(7): Show |
T | 1 | a0001c0001t0001g0213 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.501-952_501-939del others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940938 | ||||||
| chr2:53940940
|
A | AAT | 16 | a0002c0002t0002g0054a0002c0002t0002g0063a0002c0002t0002g0086others(13): Show | 16 | HG02027.hp1 HG02155.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.501-942_501-941dup others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940940 | ||||||
| chr2:53940940
|
A | AATATATA others(88): Show |
1 | a0002c0003t0002g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.501-941_501-940ins others(95): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940940 | ||||||
| chr2:53940940
|
A | C | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.501-940T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940940 | ||||||
| chr2:53940940
|
A | T | 7 | a0001c0001t0001g0053a0002c0003t0002g0019a0002c0003t0002g0066others(4): Show | 7 | HG00733.hp2 HG01168.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.501-940T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940940 | ||||||
| chr2:53940940
|
AATATATA others(9): Show |
A | 1 | a0008c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.501-956_501-941del others(16): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940940 | ||||||
| chr2:53940940
|
AATATATA others(15): Show |
A | 2 | a0001c0005t0001g0314a0001c0005t0009g0221 | 2 | NA18971.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.501-962_501-941del others(22): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940940 | ||||||
| chr2:53940940
|
AATATATA others(17): Show |
A | 55 | a0001c0005t0001g0311a0001c0005t0001g0313a0001c0005t0001g0315others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.501-964_501-941del others(24): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940940 | ||||||
| chr2:53940942
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.501-942A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940942 | ||||||
| chr2:53940942
|
T | TATATATA others(57): Show |
7 | a0002c0002t0002g0047a0002c0002t0002g0082a0002c0002t0002g0092others(4): Show | 7 | HG02040.hp2 HG02523.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-943_501-942ins others(64): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940942 | ||||||
| chr2:53940942
|
TATATATA others(3): Show |
T | 21 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(18): Show | 21 | HG01074.hp1 HG01099.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.501-952_501-943del others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940942 | ||||||
| chr2:53940944
|
T | TATATAAT others(166): Show |
1 | a0001c0022t0016g0111 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.501-945_501-944ins others(173): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | ||||||
| chr2:53940944
|
T | TATATAAT others(78): Show |
1 | a0002c0003t0002g0016 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.501-945_501-944ins others(85): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | ||||||
| chr2:53940944
|
T | TATATAAT others(170): Show |
1 | a0002c0003t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.501-945_501-944ins others(177): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | ||||||
| chr2:53940944
|
T | TATATAAT others(172): Show |
1 | a0002c0003t0002g0152 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.501-945_501-944ins others(179): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | ||||||
| chr2:53940944
|
T | TATATAAT others(55): Show |
6 | a0002c0002t0002g0065a0002c0002t0002g0068a0002c0002t0002g0093others(3): Show | 6 | NA18971.hp1 NA18986.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-945_501-944ins others(62): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | ||||||
| chr2:53940944
|
T | TATATAAT others(151): Show |
1 | a0002c0003t0002g0299 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.501-945_501-944ins others(158): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | ||||||
| chr2:53940944
|
T | TATATATA others(82): Show |
1 | a0002c0003t0002g0071 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.501-945_501-944ins others(89): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | ||||||
| chr2:53940944
|
TATATATA others(1): Show |
T | 5 | a0001c0006t0005g0003a0001c0006t0005g0005a0001c0006t0014g0164others(2): Show | 5 | HG00099.hp2 HG02109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-952_501-945del others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | ||||||
| chr2:53940946
|
T | TATAATAC others(53): Show |
1 | a0002c0002t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.501-947_501-946ins others(60): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940946 | ||||||
| chr2:53940946
|
T | TATATATA others(82): Show |
1 | a0001c0001t0001g0225 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.501-947_501-946ins others(89): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940946 | ||||||
| chr2:53940946
|
TATATAC | T | 3 | a0001c0006t0003g0172a0001c0006t0003g0175a0001c0006t0003g0266 | 3 | HG01884.hp1 HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.501-952_501-947del others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940946 | ||||||
| chr2:53940947
|
A | T | 1 | a0001c0001t0001g0214 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.501-947T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940947 | ||||||
| chr2:53940948
|
T | TA | 14 | a0002c0002t0002g0022a0002c0002t0002g0050a0002c0002t0002g0083others(11): Show | 14 | HG00423.hp2 HG01255.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.501-949dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | ||||||
| chr2:53940948
|
T | TAATACAT others(17): Show |
2 | a0002c0002t0002g0043a0002c0002t0002g0084 | 2 | HG02602.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.501-949_501-948ins others(24): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | ||||||
| chr2:53940948
|
T | TAATACAT others(51): Show |
2 | a0002c0002t0002g0097a0002c0002t0002g0143 | 2 | HG02056.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.501-949_501-948ins others(58): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | ||||||
| chr2:53940948
|
T | TAATACAT others(166): Show |
1 | a0002c0003t0002g0069 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.501-949_501-948ins others(173): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | ||||||
| chr2:53940948
|
T | TAATACAT others(145): Show |
1 | a0002c0003t0001g0080 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.501-949_501-948ins others(152): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | ||||||
| chr2:53940948
|
T | TAATACAT others(147): Show |
1 | a0002c0003t0002g0132 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.501-949_501-948ins others(154): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | ||||||
| chr2:53940948
|
T | TAATACAT others(147): Show |
1 | a0002c0003t0002g0112 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.501-949_501-948ins others(154): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | ||||||
| chr2:53940948
|
T | TATA | 5 | a0002c0003t0002g0020a0002c0003t0002g0077a0002c0003t0002g0078others(2): Show | 5 | HG01106.hp2 HG01192.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-951_501-949dup others(3): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | ||||||
| chr2:53940948
|
T | TATATA | 5 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(2): Show | 5 | HG01167.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-949_501-948ins others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | ||||||
| chr2:53940948
|
T | TATATAAT others(78): Show |
2 | a0002c0003t0002g0137a0002c0003t0002g0144 | 2 | HG03710.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.501-949_501-948ins others(85): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | ||||||
| chr2:53940948
|
T | TATATAAT others(124): Show |
1 | a0002c0003t0002g0113 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.501-949_501-948ins others(131): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | ||||||
| chr2:53940948
|
T | TATATAAT others(84): Show |
1 | a0002c0033t0002g0375 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.501-949_501-948ins others(91): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | ||||||
| chr2:53940948
|
TATAC | T | 8 | a0001c0006t0003g0161a0001c0006t0003g0178a0001c0006t0003g0371others(5): Show | 8 | HG00738.hp2 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.501-952_501-949del others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | ||||||
| chr2:53940949
|
A | AATACATA others(72): Show |
2 | a0002c0003t0002g0057a0002c0003t0002g0072 | 2 | NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.501-950_501-949ins others(79): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940949 | ||||||
| chr2:53940949
|
A | AATACATA others(47): Show |
6 | a0002c0002t0002g0023a0002c0002t0002g0085a0002c0002t0002g0088others(3): Show | 6 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-950_501-949ins others(54): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940949 | ||||||
| chr2:53940949
|
A | AATACATA others(143): Show |
1 | a0002c0003t0002g0297 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.501-950_501-949ins others(150): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940949 | ||||||
| chr2:53940949
|
A | ATATAATA others(74): Show |
2 | a0002c0003t0002g0049a0002c0003t0004g0340 | 2 | HG03041.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.501-950_501-949ins others(81): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940949 | ||||||
| chr2:53940949
|
A | ATATAATA others(76): Show |
2 | a0006c0013t0002g0046a0006c0013t0002g0073 | 2 | NA19002.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.501-950_501-949ins others(83): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940949 | ||||||
| chr2:53940949
|
A | ATATAATA others(120): Show |
5 | a0002c0003t0002g0105a0002c0003t0002g0134a0002c0003t0002g0135others(2): Show | 5 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.501-950_501-949ins others(127): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940949 | ||||||
| chr2:53940949
|
A | ATATATAA others(76): Show |
1 | a0002c0003t0002g0107 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.501-950_501-949ins others(83): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940949 | ||||||
| chr2:53940950
|
T | TATAATAC others(76): Show |
2 | a0002c0003t0002g0075a0002c0003t0002g0114 | 2 | HG00558.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.501-951_501-950ins others(83): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940950 | ||||||
| chr2:53940950
|
T | TATAATAC others(78): Show |
2 | a0002c0003t0002g0128a0007c0012t0002g0058 | 2 | HG02083.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501-951_501-950ins others(85): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940950 | ||||||
| chr2:53940950
|
T | TATAATAC others(122): Show |
2 | a0002c0003t0002g0139a0002c0003t0002g0148 | 2 | HG01928.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.501-951_501-950ins others(129): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940950 | ||||||
| chr2:53940950
|
T | TATAATAC others(76): Show |
1 | a0002c0003t0002g0149 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.501-951_501-950ins others(83): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940950 | ||||||
| chr2:53940950
|
T | TATAATAC others(82): Show |
1 | a0002c0003t0011g0009 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.501-951_501-950ins others(89): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940950 | ||||||
| chr2:53940950
|
TAC | T | 8 | a0001c0006t0003g0167a0001c0006t0003g0168a0001c0006t0003g0170others(5): Show | 8 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.501-952_501-951del others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940950 | ||||||
| chr2:53940952
|
C | A | 19 | a0002c0002t0002g0023a0002c0002t0002g0085a0002c0002t0002g0088others(16): Show | 19 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.501-952G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
C | CATATATA others(7): Show |
1 | a0001c0001t0001g0243 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.501-966_501-953dup others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
C | CATATTT | 14 | a0001c0001t0001g0189a0001c0001t0001g0234a0001c0001t0001g0235others(11): Show | 14 | HG00438.hp2 HG00733.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.501-953_501-952ins others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
C | CATATTTA others(11): Show |
1 | a0001c0007t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.501-953_501-952ins others(18): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
C | CATATTTA others(48): Show |
1 | a0002c0015t0002g0359 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.501-953_501-952ins others(55): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
C | CATATTTA others(54): Show |
1 | a0002c0002t0002g0102 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.501-953_501-952ins others(61): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
C | CATATTTA others(56): Show |
1 | a0002c0002t0002g0045 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.501-953_501-952ins others(63): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
C | CATATTTA others(1): Show |
21 | a0001c0001t0001g0231a0001c0001t0001g0236a0001c0001t0001g0237others(18): Show | 21 | HG00558.hp2 HG01346.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.501-953_501-952ins others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
C | CATATTTA others(3): Show |
3 | a0003c0004t0001g0253a0003c0004t0001g0291a0003c0004t0001g0301 | 3 | HG01884.hp2 NA18940.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.501-953_501-952ins others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
C | CATATTTA others(7): Show |
1 | a0003c0004t0001g0252 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.501-953_501-952ins others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
C | CATATTTA others(9): Show |
2 | a0001c0001t0001g0036a0001c0001t0001g0190 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.501-953_501-952ins others(16): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
C | CATATTTT others(7): Show |
1 | a0001c0001t0001g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.501-953_501-952ins others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
C | T | 71 | a0001c0001t0001g0214a0001c0001t0001g0225a0001c0022t0016g0111others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.501-952G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
CAT | C | 8 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0188others(5): Show | 8 | HG00738.hp1 HG01358.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.501-954_501-953del others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
CATAT | C | 5 | a0001c0001t0001g0191a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 5 | HG02976.hp1 HG03209.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.501-956_501-953del others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940952
|
CATATAT | C | 3 | a0001c0001t0001g0181a0001c0001t0001g0242a0001c0009t0013g0292 | 3 | HG01255.hp2 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.501-958_501-953del others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | ||||||
| chr2:53940953
|
A | ATATT | 18 | a0001c0001t0001g0223a0001c0001t0001g0230a0001c0001t0001g0276others(15): Show | 18 | HG01070.hp1 HG01071.hp1 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.501-954_501-953ins others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940953 | ||||||
| chr2:53940953
|
A | T | 1 | a0001c0001t0001g0184 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.501-953T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940953 | ||||||
| chr2:53940954
|
T | C | 8 | a0002c0002t0002g0140a0002c0002t0002g0141a0002c0002t0002g0142others(5): Show | 8 | HG00621.hp2 HG01123.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.501-954A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940954 | ||||||
| chr2:53940954
|
T | TACATATT others(3): Show |
2 | a0002c0003t0002g0052a0002c0003t0002g0061 | 2 | NA19070.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.501-955_501-954ins others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940954 | ||||||
| chr2:53940954
|
T | TATACATA others(5): Show |
3 | a0002c0003t0002g0127a0002c0003t0010g0006a0007c0012t0002g0062 | 3 | HG02809.hp1 HG02818.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.501-955_501-954ins others(12): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940954 | ||||||
| chr2:53940954
|
T | TATTTAA | 5 | a0002c0002t0002g0086a0002c0002t0002g0091a0002c0002t0002g0119others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.501-955_501-954ins others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940954 | ||||||
| chr2:53940954
|
T | TATTTAAA others(44): Show |
1 | a0002c0002t0002g0083 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.501-955_501-954ins others(51): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940954 | ||||||
| chr2:53940955
|
A | ACATATT | 3 | a0002c0003t0002g0011a0002c0003t0002g0024a0002c0003t0002g0055 | 3 | HG02735.hp2 HG02970.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.501-956_501-955ins others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940955 | ||||||
| chr2:53940955
|
A | ATT | 22 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(19): Show | 23 | HG00597.hp2 HG00609.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.501-956_501-955ins others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940955 | ||||||
| chr2:53940955
|
A | ATTTAAAT others(40): Show |
1 | a0002c0002t0002g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.501-956_501-955ins others(47): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940955 | ||||||
| chr2:53940956
|
T | C | 6 | a0001c0006t0003g0167a0001c0006t0003g0168a0001c0006t0003g0170others(3): Show | 6 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-956A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940956 | ||||||
| chr2:53940956
|
T | TTTAA | 14 | a0001c0001t0001g0053a0001c0007t0001g0015a0002c0002t0002g0022others(11): Show | 14 | HG01081.hp2 HG01106.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.501-957_501-956ins others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940956 | ||||||
| chr2:53940956
|
T | TTTAAATA others(42): Show |
8 | a0002c0002t0002g0050a0002c0002t0002g0094a0002c0002t0002g0103others(5): Show | 8 | HG00423.hp2 HG02129.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.501-957_501-956ins others(49): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940956 | ||||||
| chr2:53940957
|
A | T | 35 | a0001c0001t0001g0035a0001c0001t0001g0180a0001c0001t0001g0187others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.501-957T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940957 | ||||||
| chr2:53940958
|
T | A | 4 | a0002c0002t0002g0153a0002c0003t0002g0011a0002c0003t0002g0024others(1): Show | 4 | HG02735.hp2 HG02970.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-958A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940958 | ||||||
| chr2:53940958
|
T | C | 9 | a0001c0006t0003g0161a0001c0006t0003g0178a0001c0006t0003g0371others(6): Show | 9 | HG00738.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.501-958A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940958 | ||||||
| chr2:53940958
|
T | TTTAA | 7 | a0002c0002t0002g0140a0002c0002t0002g0141a0002c0002t0002g0142others(4): Show | 7 | HG00621.hp2 HG01123.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.501-959_501-958ins others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940958 | ||||||
| chr2:53940959
|
A | T | 6 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0188others(3): Show | 6 | HG00738.hp1 HG01358.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-959T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940959 | ||||||
| chr2:53940960
|
T | A | 22 | a0001c0001t0001g0205a0001c0001t0001g0239a0001c0006t0003g0155others(19): Show | 22 | HG01167.hp2 HG01168.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.501-960A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940960 | ||||||
| chr2:53940960
|
T | C | 5 | a0001c0006t0003g0172a0001c0006t0003g0175a0001c0006t0003g0266others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.501-960A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940960 | ||||||
| chr2:53940961
|
A | T | 10 | a0001c0001t0001g0191a0001c0001t0001g0198a0001c0001t0001g0199others(7): Show | 10 | HG02630.hp2 HG02896.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.501-961T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940961 | ||||||
| chr2:53940962
|
T | A | 1 | a0010c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.501-962A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940962 | ||||||
| chr2:53940962
|
T | C | 5 | a0001c0006t0005g0003a0001c0006t0005g0005a0001c0006t0014g0164others(2): Show | 5 | HG00099.hp2 HG02109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-962A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940962 | ||||||
| chr2:53940963
|
A | T | 11 | a0001c0001t0001g0181a0001c0001t0001g0242a0001c0006t0003g0161others(8): Show | 11 | HG00738.hp2 HG01255.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.501-963T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940963 | ||||||
| chr2:53940964
|
T | A | 6 | a0001c0006t0003g0167a0001c0006t0003g0168a0001c0006t0003g0170others(3): Show | 6 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-964A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940964 | ||||||
| chr2:53940964
|
T | C | 22 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(19): Show | 22 | HG01074.hp1 HG01099.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.501-964A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940964 | ||||||
| chr2:53940965
|
A | T | 6 | a0001c0001t0001g0240a0001c0006t0003g0172a0001c0006t0003g0175others(3): Show | 6 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-965T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940965 | ||||||
| chr2:53940966
|
T | A | 9 | a0001c0006t0003g0161a0001c0006t0003g0178a0001c0006t0003g0371others(6): Show | 9 | HG00738.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.501-966A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940966 | ||||||
| chr2:53940966
|
T | TAATACAT others(41): Show |
1 | a0002c0002t0002g0022 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.501-967_501-966ins others(48): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940966 | ||||||
| chr2:53940967
|
A | T | 5 | a0001c0006t0005g0003a0001c0006t0005g0005a0001c0006t0014g0164others(2): Show | 5 | HG00099.hp2 HG02109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-967T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940967 | ||||||
| chr2:53940968
|
T | A | 5 | a0001c0006t0003g0172a0001c0006t0003g0175a0001c0006t0003g0266others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.501-968A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940968 | ||||||
| chr2:53940968
|
T | TATAATAC others(30): Show |
3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.501-969_501-968ins others(37): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940968 | ||||||
| chr2:53940969
|
A | T | 22 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(19): Show | 22 | HG01074.hp1 HG01099.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.501-969T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940969 | ||||||
| chr2:53940969
|
AT | A | 3 | a0005c0011t0001g0362a0005c0011t0001g0364a0005c0011t0002g0363 | 3 | HG01243.hp1 HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.501-970delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940969 | ||||||
| chr2:53940970
|
T | A | 5 | a0001c0006t0005g0003a0001c0006t0005g0005a0001c0006t0014g0164others(2): Show | 5 | HG00099.hp2 HG02109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-970A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940970 | ||||||
| chr2:53940970
|
T | C | 1 | a0008c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.501-970A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940970 | ||||||
| chr2:53940972
|
T | A | 22 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(19): Show | 22 | HG01074.hp1 HG01099.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.501-972A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940972 | ||||||
| chr2:53940972
|
T | C | 7 | a0001c0001t0001g0205a0001c0001t0001g0239a0002c0003t0002g0020others(4): Show | 7 | HG01106.hp2 HG01192.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-972A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940972 | ||||||
| chr2:53940972
|
T | TACATATT others(3): Show |
6 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(3): Show | 6 | HG01167.hp2 HG02602.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-973_501-972ins others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940972 | ||||||
| chr2:53940974
|
T | A | 2 | a0002c0002t0002g0101a0002c0002t0002g0126 | 2 | NA19011.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.501-974A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940974 | ||||||
| chr2:53940974
|
T | C | 4 | a0002c0002t0002g0043a0005c0011t0001g0362a0005c0011t0001g0364others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-974A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940974 | ||||||
| chr2:53940975
|
A | T | 1 | a0008c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.501-975T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940975 | ||||||
| chr2:53940976
|
T | C | 2 | a0001c0005t0001g0314a0001c0005t0009g0221 | 2 | NA18971.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.501-976A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940976 | ||||||
| chr2:53940977
|
A | T | 7 | a0001c0001t0001g0205a0001c0001t0001g0239a0002c0003t0002g0020others(4): Show | 7 | HG01106.hp2 HG01192.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-977T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940977 | ||||||
| chr2:53940978
|
T | A | 1 | a0008c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.501-978A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940978 | ||||||
| chr2:53940978
|
T | C | 55 | a0001c0005t0001g0311a0001c0005t0001g0313a0001c0005t0001g0315others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.501-978A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940978 | ||||||
| chr2:53940979
|
A | T | 1 | a0002c0002t0002g0043 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.501-979T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940979 | ||||||
| chr2:53940980
|
T | A | 5 | a0002c0003t0002g0020a0002c0003t0002g0077a0002c0003t0002g0078others(2): Show | 5 | HG01106.hp2 HG01192.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-980A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940980 | ||||||
| chr2:53940981
|
A | T | 2 | a0001c0005t0001g0314a0001c0005t0009g0221 | 2 | NA18971.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.501-981T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940981 | ||||||
| chr2:53940982
|
T | A | 4 | a0002c0002t0002g0043a0005c0011t0001g0362a0005c0011t0001g0364others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-982A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940982 | ||||||
| chr2:53940983
|
A | T | 55 | a0001c0005t0001g0311a0001c0005t0001g0313a0001c0005t0001g0315others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.501-983T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940983 | ||||||
| chr2:53940986
|
T | TACATATT others(3): Show |
2 | a0002c0002t0002g0101a0002c0002t0002g0126 | 2 | NA19011.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.501-987_501-986ins others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940986 | ||||||
| chr2:53940994
|
T | C | 7 | a0002c0002t0002g0044a0002c0002t0002g0065a0002c0002t0002g0098others(4): Show | 7 | HG02056.hp1 NA18971.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-994A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940994 | ||||||
| chr2:53940997
|
A | G | 6 | a0002c0003t0002g0019a0002c0003t0002g0069a0002c0003t0002g0109others(3): Show | 6 | HG00438.hp1 HG01175.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-997T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940997 | ||||||
| chr2:53940998
|
T | A | 6 | a0002c0003t0002g0019a0002c0003t0002g0069a0002c0003t0002g0109others(3): Show | 6 | HG00438.hp1 HG01175.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-998A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940998 | ||||||
| chr2:53940998
|
T | TGA | 16 | a0001c0022t0016g0111a0002c0003t0001g0080a0002c0003t0002g0060others(13): Show | 16 | HG00408.hp2 HG00735.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.501-999_501-998ins others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940998 | ||||||
| chr2:53940999
|
A | G | 1 | a0002c0003t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.501-999T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940999 | ||||||
| chr2:53941098
|
T | C | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.501-1098A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941098 | ||||||
| chr2:53941175
|
A | G | 137 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0022t0016g0111others(134): Show | 137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.501-1175T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941175 | ||||||
| chr2:53941354
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.501-1354A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941354 | ||||||
| chr2:53941468
|
C | T | 1 | a0002c0002t0004g0121 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.501-1468G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941468 | ||||||
| chr2:53941477
|
C | T | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.501-1477G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941477 | ||||||
| chr2:53941512
|
G | C | 2 | a0001c0006t0005g0003a0001c0006t0005g0005 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.501-1512C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941512 | ||||||
| chr2:53941744
|
A | G | 54 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(51): Show | 54 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.501-1744T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941744 | ||||||
| chr2:53941772
|
A | G | 1 | a0002c0010t0002g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.501-1772T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941772 | ||||||
| chr2:53941988
|
G | A | 1 | a0002c0002t0002g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.501-1988C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941988 | ||||||
| chr2:53942199
|
C | G | 1 | a0002c0003t0002g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.501-2199G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942199 | ||||||
| chr2:53942253
|
G | T | 1 | a0002c0002t0001g0232 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.501-2253C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942253 | ||||||
| chr2:53942367
|
G | GT | 6 | a0001c0001t0001g0212a0002c0003t0002g0052a0002c0003t0002g0075others(3): Show | 6 | HG00558.hp1 HG02965.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-2368dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942367 | ||||||
| chr2:53942379
|
A | T | 90 | a0001c0001t0001g0053a0001c0001t0001g0180a0001c0001t0001g0198others(87): Show | 90 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.501-2379T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942379 | ||||||
| chr2:53942483
|
G | A | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.501-2483C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942483 | ||||||
| chr2:53942567
|
T | C | 7 | a0001c0001t0001g0181a0001c0001t0001g0191a0001c0001t0001g0217others(4): Show | 7 | HG01255.hp2 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-2567A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942567 | ||||||
| chr2:53942653
|
G | A | 2 | a0001c0005t0001g0334a0001c0005t0001g0350 | 2 | NA18955.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.501-2653C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942653 | ||||||
| chr2:53942812
|
C | G | 4 | a0005c0011t0001g0362a0005c0011t0001g0364a0005c0011t0002g0363others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-2812G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942812 | ||||||
| chr2:53942898
|
G | T | 135 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0022t0016g0111others(132): Show | 135 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.501-2898C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942898 | ||||||
| chr2:53943093
|
T | C | 63 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.501-3093A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943093 | ||||||
| chr2:53943095
|
T | C | 1 | a0001c0006t0003g0157 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.501-3095A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943095 | ||||||
| chr2:53943146
|
G | A | 1 | a0001c0005t0001g0315 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.501-3146C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943146 | ||||||
| chr2:53943202
|
A | G | 54 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(51): Show | 54 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.501-3202T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943202 | ||||||
| chr2:53943295
|
C | T | 2 | a0001c0005t0001g0315a0001c0005t0001g0319 | 2 | HG01358.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.501-3295G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943295 | ||||||
| chr2:53943321
|
T | A | 2 | a0001c0005t0001g0311a0001c0005t0001g0335 | 2 | NA19000.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.501-3321A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943321 | ||||||
| chr2:53943333
|
C | G | 252 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0001t0001g0225others(249): Show | 252 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.501-3333G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943333 | ||||||
| chr2:53943359
|
T | C | 6 | a0003c0004t0001g0042a0003c0004t0001g0192a0003c0004t0001g0245others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-3359A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943359 | ||||||
| chr2:53943513
|
C | G | 2 | a0001c0001t0001g0001a0001c0019t0001g0037 | 3 | HG01168.hp1 HG01169.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.501-3513G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943513 | ||||||
| chr2:53943750
|
A | G | 250 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0001t0001g0225others(247): Show | 250 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.501-3750T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943750 | ||||||
| chr2:53943764
|
C | T | 5 | a0002c0003t0002g0019a0002c0003t0002g0069a0002c0003t0002g0132others(2): Show | 5 | HG00438.hp1 NA18948.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.501-3764G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943764 | ||||||
| chr2:53943846
|
C | CA | 12 | a0001c0001t0001g0038a0001c0005t0001g0311a0001c0005t0001g0314others(9): Show | 12 | HG02738.hp2 HG03831.hp2 NA18959.hp2 others(9): Show |
intron_variant | MODIFIER | c.501-3847dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943846 | ||||||
| chr2:53943846
|
CA | C | 48 | a0001c0001t0001g0010a0001c0001t0001g0173a0001c0001t0001g0212others(45): Show | 48 | HG00323.hp1 HG00621.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.501-3847delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943846 | ||||||
| chr2:53943846
|
CAAA | C | 68 | a0001c0001t0001g0225a0001c0007t0001g0015a0001c0007t0001g0017others(65): Show | 68 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.501-3849_501-3847d others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943846 | ||||||
| chr2:53943846
|
CAAAA | C | 7 | a0001c0001t0001g0053a0002c0003t0002g0049a0002c0003t0002g0055others(4): Show | 7 | HG01167.hp1 HG02809.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-3850_501-3847d others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943846 | ||||||
| chr2:53943956
|
G | T | 251 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0001t0001g0225others(248): Show | 251 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.501-3956C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943956 | ||||||
| chr2:53944010
|
C | T | 1 | a0005c0011t0001g0364 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.501-4010G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944010 | ||||||
| chr2:53944068
|
T | G | 2 | a0003c0004t0001g0033a0003c0004t0001g0256 | 2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.501-4068A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944068 | ||||||
| chr2:53944163
|
AT | A | 7 | a0001c0005t0001g0336a0001c0006t0005g0002a0001c0006t0005g0004others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-4164delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944163 | ||||||
| chr2:53944388
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.500+4033C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944388 | ||||||
| chr2:53944516
|
A | C | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.500+3905T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944516 | ||||||
| chr2:53944530
|
C | G | 1 | a0009c0027t0003g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.500+3891G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944530 | ||||||
| chr2:53944593
|
T | C | 1 | a0001c0009t0001g0369 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.500+3828A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944593 | ||||||
| chr2:53944759
|
T | C | 1 | a0001c0007t0006g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.500+3662A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944759 | ||||||
| chr2:53945080
|
T | C | 3 | a0002c0002t0002g0085a0002c0002t0002g0086a0002c0002t0002g0119 | 3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.500+3341A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945080 | ||||||
| chr2:53945334
|
G | A | 1 | a0005c0011t0002g0363 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.500+3087C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945334 | ||||||
| chr2:53945359
|
C | G | 9 | a0001c0001t0001g0036a0001c0001t0001g0189a0001c0001t0001g0190others(6): Show | 9 | HG00733.hp1 HG01261.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.500+3062G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945359 | ||||||
| chr2:53945372
|
ACTT | A | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.500+3046_500+3048d others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945372 | ||||||
| chr2:53945512
|
A | C | 1 | a0005c0011t0001g0362 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.500+2909T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945512 | ||||||
| chr2:53945548
|
G | T | 2 | a0006c0013t0002g0046a0006c0013t0002g0073 | 2 | NA19002.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.500+2873C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945548 | ||||||
| chr2:53945733
|
T | C | 6 | a0002c0002t0002g0023a0002c0002t0002g0063a0002c0002t0002g0087others(3): Show | 6 | NA18954.hp1 NA18975.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.500+2688A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945733 | ||||||
| chr2:53945754
|
T | C | 1 | a0002c0003t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.500+2667A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945754 | ||||||
| chr2:53945755
|
A | C | 1 | a0008c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.500+2666T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945755 | ||||||
| chr2:53945855
|
T | G | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.500+2566A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945855 | ||||||
| chr2:53945930
|
G | C | 60 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.500+2491C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945930 | ||||||
| chr2:53946087
|
A | C | 2 | a0001c0006t0005g0003a0001c0006t0005g0005 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.500+2334T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53946087 | ||||||
| chr2:53946396
|
T | C | 2 | a0002c0003t0002g0134a0002c0003t0002g0135 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.500+2025A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53946396 | ||||||
| chr2:53946438
|
G | C | 1 | a0002c0002t0001g0232 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.500+1983C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53946438 | ||||||
| chr2:53946569
|
T | A | 251 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0005t0001g0311others(248): Show | 251 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.500+1852A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53946569 | ||||||
| chr2:53946866
|
A | C | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.500+1555T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53946866 | ||||||
| chr2:53946904
|
C | A | 10 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0205others(7): Show | 10 | HG01243.hp2 HG02486.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.500+1517G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53946904 | ||||||
| chr2:53947121
|
A | G | 56 | a0001c0005t0001g0311a0001c0005t0001g0313a0001c0005t0001g0314others(53): Show | 56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.500+1300T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947121 | ||||||
| chr2:53947248
|
A | T | 1 | a0002c0002t0004g0048 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.500+1173T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947248 | ||||||
| chr2:53947290
|
A | G | 3 | a0002c0002t0002g0116a0002c0002t0002g0120a0002c0002t0002g0140 | 3 | HG02027.hp1 NA18990.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.500+1131T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947290 | ||||||
| chr2:53947556
|
A | G | 48 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(45): Show | 48 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.500+865T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947556 | ||||||
| chr2:53947619
|
C | T | 250 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0005t0001g0311others(247): Show | 250 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.500+802G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947619 | ||||||
| chr2:53947704
|
T | TCAAAACA others(3): Show |
248 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0005t0001g0311others(245): Show | 248 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.500+707_500+716dup others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947704 | ||||||
| chr2:53947711
|
A | AAAACAAA others(3): Show |
2 | a0001c0007t0001g0361a0012c0024t0001g0312 | 2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.500+709_500+710ins others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947711 | ||||||
| chr2:53947926
|
G | A | 1 | a0002c0002t0002g0047 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.500+495C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947926 | ||||||
| chr2:53947992
|
A | G | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.500+429T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947992 | ||||||
| chr2:53948303
|
T | C | 24 | a0001c0022t0016g0111a0002c0003t0001g0080a0002c0003t0002g0019others(21): Show | 24 | HG00408.hp2 HG00438.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.500+118A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53948303 | ||||||
| chr2:53948309
|
C | T | 5 | a0001c0001t0001g0181a0001c0001t0001g0191a0001c0001t0001g0240others(2): Show | 5 | HG01255.hp2 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.500+112G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53948309 | ||||||
| chr2:53948369
|
C | A | 2 | a0003c0004t0001g0032a0003c0004t0001g0268 | 2 | NA18945.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.500+52G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53948369 | ||||||
| chr2:53948380
|
C | G | 1 | a0002c0002t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.500+41G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53948380 | ||||||
| chr2:53948383
|
A | G | 1 | a0002c0003t0002g0072 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.500+38T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53948383 | ||||||
| chr2:53948626
|
T | C | 64 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.384-89A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/46 | chr2 | 53948626 | ||||||
| chr2:53948652
|
T | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.384-115A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/46 | chr2 | 53948652 | ||||||
| chr2:53948765
|
T | C | 1 | a0002c0003t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.384-228A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/46 | chr2 | 53948765 | ||||||
| chr2:53948768
|
G | C | 69 | a0001c0001t0001g0053a0001c0022t0016g0111a0002c0003t0001g0080others(66): Show | 69 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.384-231C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/46 | chr2 | 53948768 | ||||||
| chr2:53948849
|
CAGG | C | 4 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(1): Show | 4 | HG00099.hp1 HG01081.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+291_383+293del others(3): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/46 | chr2 | 53948849 | ||||||
| chr2:53949078
|
C | A | 7 | a0001c0006t0005g0002a0001c0006t0005g0004a0003c0004t0003g0219others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.383+65G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/46 | chr2 | 53949078 | ||||||
| chr2:53949114
|
T | C | 1 | a0016c0014t0002g0067 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.383+29A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/46 | chr2 | 53949114 | ||||||
| chr2:53949321
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.243-38A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949321 | ||||||
| chr2:53949337
|
T | C | 1 | a0001c0006t0005g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.243-54A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949337 | ||||||
| chr2:53949356
|
C | T | 1 | a0001c0005t0001g0317 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.243-73G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949356 | ||||||
| chr2:53949448
|
C | CT | 58 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.243-166dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949448 | ||||||
| chr2:53949448
|
CT | C | 73 | a0001c0001t0001g0053a0001c0005t0001g0313a0001c0005t0001g0320others(70): Show | 73 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.243-166delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949448 | ||||||
| chr2:53949490
|
G | C | 1 | a0001c0001t0001g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.243-207C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949490 | ||||||
| chr2:53949541
|
A | G | 1 | a0009c0027t0003g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.243-258T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949541 | ||||||
| chr2:53949596
|
C | A | 3 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0001g0179 | 3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.243-313G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949596 | ||||||
| chr2:53949740
|
T | C | 1 | a0001c0009t0001g0360 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.243-457A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949740 | ||||||
| chr2:53949824
|
T | C | 1 | a0002c0003t0002g0128 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.243-541A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949824 | ||||||
| chr2:53949979
|
T | C | 1 | a0010c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.243-696A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949979 | ||||||
| chr2:53949993
|
G | T | 72 | a0001c0001t0001g0053a0001c0022t0016g0111a0002c0003t0001g0080others(69): Show | 72 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.243-710C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949993 | ||||||
| chr2:53949994
|
G | A | 1 | a0002c0003t0002g0128 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.243-711C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949994 | ||||||
| chr2:53950055
|
A | G | 132 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0006t0003g0025others(129): Show | 132 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.243-772T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950055 | ||||||
| chr2:53950094
|
G | C | 3 | a0001c0006t0003g0161a0001c0006t0003g0178a0001c0006t0003g0266 | 3 | HG00738.hp2 HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.243-811C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950094 | ||||||
| chr2:53950121
|
A | G | 4 | a0005c0011t0001g0362a0005c0011t0001g0364a0005c0011t0002g0363others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.243-838T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950121 | ||||||
| chr2:53950263
|
G | A | 62 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.243-980C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950263 | ||||||
| chr2:53950275
|
T | G | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.243-992A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950275 | ||||||
| chr2:53950285
|
C | CA | 82 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0053others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.243-1003dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950285 | ||||||
| chr2:53950286
|
A | C | 1 | a0003c0004t0001g0200 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.243-1003T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950286 | ||||||
| chr2:53950311
|
A | G | 1 | a0001c0005t0001g0320 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.243-1028T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950311 | ||||||
| chr2:53950398
|
T | C | 50 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(47): Show | 50 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.243-1115A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950398 | ||||||
| chr2:53950520
|
G | T | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.243-1237C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950520 | ||||||
| chr2:53950550
|
G | A | 1 | a0001c0005t0001g0351 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.243-1267C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950550 | ||||||
| chr2:53950552
|
G | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.243-1269C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950552 | ||||||
| chr2:53950570
|
AGTGGCTC others(3481): Show |
A | 1 | a0003c0004t0001g0194 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.243-4775_243-1288d others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950570 | ||||||
| chr2:53950618
|
G | C | 7 | a0002c0002t0002g0044a0002c0002t0002g0065a0002c0002t0002g0098others(4): Show | 7 | HG02056.hp1 NA18971.hp1 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.243-1335C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950618 | ||||||
| chr2:53950628
|
G | C | 1 | a0002c0010t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.243-1345C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950628 | ||||||
| chr2:53950653
|
C | T | 2 | a0003c0004t0001g0033a0003c0004t0001g0256 | 2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.243-1370G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950653 | ||||||
| chr2:53950668
|
C | A | 1 | a0002c0015t0002g0359 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.243-1385G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950668 | ||||||
| chr2:53950794
|
G | A | 1 | a0002c0002t0002g0357 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.243-1511C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950794 | ||||||
| chr2:53950841
|
C | CA | 17 | a0001c0001t0001g0036a0001c0001t0001g0189a0001c0001t0001g0190others(14): Show | 17 | HG00323.hp2 HG00733.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.243-1559dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950841 | ||||||
| chr2:53950929
|
T | C | 3 | a0001c0006t0005g0002a0001c0006t0005g0004a0003c0004t0003g0219 | 3 | HG01109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.243-1646A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950929 | ||||||
| chr2:53950981
|
T | C | 1 | a0011c0023t0003g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.243-1698A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950981 | ||||||
| chr2:53950995
|
T | G | 69 | a0001c0001t0001g0053a0001c0022t0016g0111a0002c0003t0001g0080others(66): Show | 69 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.243-1712A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950995 | ||||||
| chr2:53951086
|
CTT | C | 5 | a0002c0002t0002g0043a0002c0002t0002g0054a0002c0002t0002g0089others(2): Show | 5 | HG00280.hp2 HG00323.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.243-1805_243-1804d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951086 | ||||||
| chr2:53951149
|
C | G | 7 | a0003c0004t0001g0040a0003c0004t0001g0257a0003c0004t0001g0274others(4): Show | 7 | NA18959.hp2 NA18969.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.243-1866G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951149 | ||||||
| chr2:53951309
|
C | T | 4 | a0005c0011t0001g0362a0005c0011t0001g0364a0005c0011t0002g0363others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.243-2026G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951309 | ||||||
| chr2:53951484
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.243-2201C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951484 | ||||||
| chr2:53951620
|
T | A | 1 | a0001c0005t0001g0347 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.243-2337A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951620 | ||||||
| chr2:53951763
|
C | G | 1 | a0002c0010t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.243-2480G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951763 | ||||||
| chr2:53951772
|
T | C | 250 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0005t0001g0311others(247): Show | 250 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.243-2489A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951772 | ||||||
| chr2:53951881
|
C | T | 118 | a0001c0005t0001g0311a0001c0005t0001g0313a0001c0005t0001g0314others(115): Show | 118 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.243-2598G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951881 | ||||||
| chr2:53951899
|
G | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.243-2616C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951899 | ||||||
| chr2:53951913
|
C | T | 62 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0043others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.243-2630G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951913 | ||||||
| chr2:53952085
|
CA | C | 49 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(46): Show | 49 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.243-2803delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952085 | ||||||
| chr2:53952150
|
T | C | 1 | a0003c0004t0001g0255 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.243-2867A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952150 | ||||||
| chr2:53952161
|
C | T | 1 | a0002c0002t0004g0121 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.243-2878G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952161 | ||||||
| chr2:53952232
|
T | G | 1 | a0002c0003t0002g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.243-2949A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952232 | ||||||
| chr2:53952269
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.243-2986A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952269 | ||||||
| chr2:53952413
|
G | A | 49 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(46): Show | 49 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.243-3130C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952413 | ||||||
| chr2:53952491
|
C | T | 3 | a0001c0001t0001g0173a0001c0006t0003g0174a0001c0006t0003g0218 | 3 | HG02258.hp2 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.243-3208G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952491 | ||||||
| chr2:53952721
|
G | C | 1 | a0008c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.243-3438C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952721 | ||||||
| chr2:53952744
|
T | G | 1 | a0003c0004t0003g0219 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.243-3461A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952744 | ||||||
| chr2:53953224
|
T | C | 1 | a0010c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.243-3941A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953224 | ||||||
| chr2:53953378
|
G | T | 1 | a0001c0007t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.243-4095C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953378 | ||||||
| chr2:53953381
|
G | C | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.243-4098C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953381 | ||||||
| chr2:53953487
|
TA | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0035others(235): Show | 239 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.243-4205delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953487 | ||||||
| chr2:53953487
|
TAA | T | 134 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0001t0001g0180others(131): Show | 134 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.243-4206_243-4205d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953487 | ||||||
| chr2:53953504
|
A | G | 3 | a0002c0003t0002g0016a0002c0003t0002g0057a0002c0003t0002g0072 | 3 | NA18991.hp1 NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.243-4221T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953504 | ||||||
| chr2:53953509
|
A | G | 1 | a0001c0005t0001g0354 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.243-4226T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953509 | ||||||
| chr2:53953570
|
A | G | 42 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(39): Show | 42 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.243-4287T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953570 | ||||||
| chr2:53953597
|
T | C | 1 | a0002c0002t0002g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.243-4314A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953597 | ||||||
| chr2:53953601
|
C | CT | 71 | a0001c0001t0001g0053a0001c0007t0001g0015a0001c0007t0001g0017others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.243-4319dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953601 | ||||||
| chr2:53953601
|
CT | C | 9 | a0001c0005t0001g0337a0001c0006t0005g0002a0001c0006t0005g0004others(6): Show | 9 | HG02145.hp1 HG02559.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.243-4319delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953601 | ||||||
| chr2:53953713
|
C | A | 1 | a0001c0005t0001g0338 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.243-4430G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953713 | ||||||
| chr2:53953844
|
C | T | 1 | a0003c0004t0001g0207 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.243-4561G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953844 | ||||||
| chr2:53953845
|
G | A | 5 | a0001c0006t0003g0167a0001c0006t0003g0168a0001c0006t0003g0170others(2): Show | 5 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.243-4562C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953845 | ||||||
| chr2:53953881
|
C | T | 1 | a0002c0002t0002g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.243-4598G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953881 | ||||||
| chr2:53953955
|
A | C | 4 | a0003c0004t0001g0262a0003c0004t0001g0263a0003c0004t0001g0264others(1): Show | 4 | NA18983.hp2 NA19004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.243-4672T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953955 | ||||||
| chr2:53953998
|
G | A | 3 | a0002c0002t0002g0097a0002c0002t0004g0096a0002c0002t0004g0121 | 3 | HG00621.hp2 HG02523.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.243-4715C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953998 | ||||||
| chr2:53954096
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.243-4813C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954096 | ||||||
| chr2:53954122
|
G | T | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.243-4839C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954122 | ||||||
| chr2:53954126
|
G | A | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0270others(1): Show | 4 | HG01175.hp2 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.243-4843C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954126 | ||||||
| chr2:53954185
|
G | A | 2 | a0003c0004t0001g0033a0003c0004t0001g0256 | 2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.243-4902C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954185 | ||||||
| chr2:53954221
|
G | A | 4 | a0003c0004t0001g0262a0003c0004t0001g0263a0003c0004t0001g0264others(1): Show | 4 | NA18983.hp2 NA19004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.243-4938C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954221 | ||||||
| chr2:53954247
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.243-4964C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954247 | ||||||
| chr2:53954326
|
T | C | 126 | a0001c0005t0001g0311a0001c0005t0001g0313a0001c0005t0001g0314others(123): Show | 126 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.243-5043A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954326 | ||||||
| chr2:53954366
|
G | A | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.243-5083C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954366 | ||||||
| chr2:53954392
|
C | T | 69 | a0001c0001t0001g0053a0001c0022t0016g0111a0002c0003t0001g0080others(66): Show | 69 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.243-5109G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954392 | ||||||
| chr2:53954480
|
T | C | 1 | a0001c0005t0001g0314 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.243-5197A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954480 | ||||||
| chr2:53954733
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.243-5450A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954733 | ||||||
| chr2:53954809
|
C | G | 1 | a0001c0005t0001g0341 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.243-5526G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954809 | ||||||
| chr2:53954900
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.243-5617G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954900 | ||||||
| chr2:53954928
|
C | G | 1 | a0008c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.243-5645G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954928 | ||||||
| chr2:53954972
|
G | A | 5 | a0001c0001t0001g0181a0001c0001t0001g0191a0001c0001t0001g0240others(2): Show | 5 | HG01255.hp2 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.243-5689C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954972 | ||||||
| chr2:53955041
|
C | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0239 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.243-5758G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955041 | ||||||
| chr2:53955142
|
G | C | 1 | a0001c0005t0001g0347 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.243-5859C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955142 | ||||||
| chr2:53955242
|
A | G | 1 | a0002c0029t0002g0307 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.243-5959T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955242 | ||||||
| chr2:53955342
|
C | T | 4 | a0002c0003t0002g0070a0002c0003t0002g0071a0002c0003t0002g0081others(1): Show | 4 | NA18970.hp1 NA18984.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.243-6059G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955342 | ||||||
| chr2:53955361
|
A | C | 1 | a0001c0005t0001g0342 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.243-6078T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955361 | ||||||
| chr2:53955410
|
C | T | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.243-6127G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955410 | ||||||
| chr2:53955411
|
G | A | 2 | a0002c0003t0002g0019a0008c0030t0002g0310 | 2 | HG02717.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.243-6128C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955411 | ||||||
| chr2:53955479
|
C | T | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.243-6196G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955479 | ||||||
| chr2:53955578
|
C | G | 65 | a0001c0001t0001g0053a0001c0007t0001g0015a0001c0007t0001g0017others(62): Show | 65 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.243-6295G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955578 | ||||||
| chr2:53955610
|
A | C | 1 | a0002c0002t0002g0094 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.243-6327T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955610 | ||||||
| chr2:53955761
|
G | C | 254 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0005t0001g0311others(251): Show | 254 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.243-6478C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955761 | ||||||
| chr2:53955836
|
T | A | 2 | a0001c0007t0001g0015a0001c0007t0001g0017 | 2 | HG01081.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.243-6553A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955836 | ||||||
| chr2:53955890
|
C | G | 3 | a0001c0006t0005g0002a0001c0006t0005g0004a0002c0003t0010g0006 | 3 | HG02145.hp1 HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.243-6607G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955890 | ||||||
| chr2:53955922
|
A | C | 1 | a0001c0006t0003g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.243-6639T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955922 | ||||||
| chr2:53955927
|
A | C | 1 | a0002c0010t0002g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.243-6644T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955927 | ||||||
| chr2:53955929
|
C | A | 1 | a0001c0001t0001g0282 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.243-6646G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955929 | ||||||
| chr2:53955987
|
A | T | 1 | a0002c0002t0002g0358 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.243-6704T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955987 | ||||||
| chr2:53955990
|
T | G | 1 | a0003c0004t0001g0039 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.243-6707A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955990 | ||||||
| chr2:53956083
|
G | A | 1 | a0002c0003t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.243-6800C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956083 | ||||||
| chr2:53956094
|
G | C | 1 | a0014c0016t0001g0339 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.243-6811C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956094 | ||||||
| chr2:53956358
|
G | A | 5 | a0002c0002t0002g0047a0002c0002t0002g0068a0002c0002t0002g0092others(2): Show | 5 | HG02040.hp2 NA18965.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.243-7075C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956358 | ||||||
| chr2:53956390
|
C | A | 1 | a0002c0002t0002g0094 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.243-7107G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956390 | ||||||
| chr2:53956445
|
G | A | 5 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(2): Show | 5 | HG01167.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.243-7162C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956445 | ||||||
| chr2:53956617
|
A | T | 1 | a0001c0005t0001g0341 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.243-7334T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956617 | ||||||
| chr2:53956671
|
T | G | 11 | a0003c0004t0001g0183a0003c0004t0001g0195a0003c0004t0001g0258others(8): Show | 11 | HG00558.hp2 HG00735.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.243-7388A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956671 | ||||||
| chr2:53956860
|
T | C | 1 | a0002c0002t0002g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.243-7577A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956860 | ||||||
| chr2:53957116
|
T | A | 1 | a0001c0001t0001g0275 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.243-7833A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957116 | ||||||
| chr2:53957162
|
G | A | 1 | a0005c0011t0001g0364 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.243-7879C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957162 | ||||||
| chr2:53957392
|
A | C | 1 | a0001c0005t0001g0348 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.243-8109T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957392 | ||||||
| chr2:53957408
|
T | C | 73 | a0001c0001t0001g0053a0001c0007t0001g0015a0001c0007t0001g0017others(70): Show | 73 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.243-8125A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957408 | ||||||
| chr2:53957415
|
G | A | 1 | a0002c0002t0002g0355 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.243-8132C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957415 | ||||||
| chr2:53957436
|
T | C | 1 | a0002c0010t0002g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.243-8153A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957436 | ||||||
| chr2:53957665
|
A | G | 3 | a0001c0001t0001g0181a0001c0001t0001g0240a0001c0001t0001g0241 | 3 | HG01255.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.243-8382T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957665 | ||||||
| chr2:53957845
|
A | G | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.243-8562T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957845 | ||||||
| chr2:53957849
|
T | C | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.243-8566A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957849 | ||||||
| chr2:53957891
|
C | A | 2 | a0001c0006t0003g0172a0001c0006t0003g0175 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.243-8608G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957891 | ||||||
| chr2:53957893
|
T | A | 2 | a0001c0006t0003g0172a0001c0006t0003g0175 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.243-8610A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957893 | ||||||
| chr2:53958004
|
A | G | 253 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0005t0001g0311others(250): Show | 253 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.243-8721T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958004 | ||||||
| chr2:53958099
|
T | A | 2 | a0002c0003t0002g0134a0002c0003t0002g0135 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.243-8816A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958099 | ||||||
| chr2:53958155
|
C | T | 1 | a0003c0004t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.243-8872G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958155 | ||||||
| chr2:53958183
|
C | CA | 35 | a0001c0001t0001g0038a0001c0001t0001g0053a0001c0001t0001g0181others(32): Show | 35 | HG00438.hp1 HG00597.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.243-8901dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958183 | ||||||
| chr2:53958183
|
CA | C | 12 | a0001c0001t0001g0215a0001c0001t0001g0223a0001c0001t0007g0224others(9): Show | 12 | HG01069.hp2 HG01070.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.243-8901delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958183 | ||||||
| chr2:53958183
|
CAAAAAAA | C | 8 | a0002c0003t0002g0024a0002c0003t0002g0136a0002c0003t0002g0144others(5): Show | 8 | HG00733.hp2 HG01123.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.243-8907_243-8901d others(9): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958183 | ||||||
| chr2:53958328
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.243-9045C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958328 | ||||||
| chr2:53958356
|
AAAAAAAA others(1): Show |
A | 66 | a0001c0001t0001g0053a0001c0022t0016g0111a0002c0003t0001g0080others(63): Show | 66 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.243-9081_243-9074d others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958356 | ||||||
| chr2:53958467
|
A | C | 2 | a0002c0003t0002g0134a0002c0003t0002g0135 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.243-9184T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958467 | ||||||
| chr2:53958510
|
C | T | 48 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(45): Show | 48 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.243-9227G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958510 | ||||||
| chr2:53958604
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.243-9321T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958604 | ||||||
| chr2:53958607
|
T | C | 5 | a0001c0006t0005g0002a0001c0006t0005g0004a0002c0003t0010g0006others(2): Show | 5 | HG01109.hp1 HG02145.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.243-9324A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958607 | ||||||
| chr2:53958726
|
G | C | 1 | a0003c0004t0001g0257 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.243-9443C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958726 | ||||||
| chr2:53958818
|
T | TA | 12 | a0001c0005t0001g0329a0003c0004t0001g0183a0003c0004t0001g0195others(9): Show | 12 | HG00558.hp2 HG00735.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.243-9536dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958818 | ||||||
| chr2:53958818
|
TA | T | 9 | a0001c0005t0001g0319a0001c0006t0005g0002a0001c0006t0005g0004others(6): Show | 9 | HG01109.hp1 HG01256.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.243-9536delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958818 | ||||||
| chr2:53958834
|
G | A | 1 | a0002c0003t0002g0019 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.243-9551C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958834 | ||||||
| chr2:53958899
|
C | T | 2 | a0003c0004t0001g0192a0003c0004t0001g0245 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.243-9616G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958899 | ||||||
| chr2:53958916
|
A | G | 254 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0005t0001g0311others(251): Show | 254 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.243-9633T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958916 | ||||||
| chr2:53959053
|
C | T | 1 | a0002c0003t0002g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.243-9770G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959053 | ||||||
| chr2:53959107
|
A | G | 3 | a0001c0005t0001g0316a0001c0005t0001g0318a0001c0005t0001g0353 | 3 | HG01515.hp2 HG01517.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.243-9824T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959107 | ||||||
| chr2:53959122
|
G | C | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.243-9839C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959122 | ||||||
| chr2:53959128
|
G | C | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.243-9845C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959128 | ||||||
| chr2:53959268
|
G | C | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.243-9985C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959268 | ||||||
| chr2:53959343
|
T | A | 67 | a0001c0001t0001g0053a0001c0022t0016g0111a0002c0003t0001g0080others(64): Show | 67 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.243-10060A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959343 | ||||||
| chr2:53959399
|
C | T | 67 | a0001c0001t0001g0053a0001c0022t0016g0111a0002c0003t0001g0080others(64): Show | 67 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.243-10116G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959399 | ||||||
| chr2:53959470
|
C | T | 1 | a0003c0004t0001g0183 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.243-10187G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959470 | ||||||
| chr2:53959532
|
A | G | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.243-10249T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959532 | ||||||
| chr2:53959745
|
A | C | 1 | a0008c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.243-10462T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959745 | ||||||
| chr2:53959863
|
G | C | 4 | a0001c0001t0001g0181a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG01255.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.243-10580C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959863 | ||||||
| chr2:53959869
|
C | A | 1 | a0002c0002t0002g0095 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.243-10586G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959869 | ||||||
| chr2:53959876
|
C | T | 1 | a0003c0004t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.243-10593G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959876 | ||||||
| chr2:53959891
|
G | A | 2 | a0001c0005t0001g0352a0002c0003t0004g0340 | 2 | NA19055.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.243-10608C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959891 | ||||||
| chr2:53959922
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.242+10621G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959922 | ||||||
| chr2:53960169
|
G | T | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.242+10374C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960169 | ||||||
| chr2:53960206
|
C | T | 1 | a0002c0002t0002g0115 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.242+10337G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960206 | ||||||
| chr2:53960215
|
C | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.242+10328G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960215 | ||||||
| chr2:53960216
|
A | T | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.242+10327T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960216 | ||||||
| chr2:53960221
|
G | A | 5 | a0001c0009t0001g0360a0001c0009t0001g0366a0001c0009t0001g0367others(2): Show | 5 | HG02717.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+10322C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960221 | ||||||
| chr2:53960269
|
G | T | 1 | a0008c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.242+10274C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960269 | ||||||
| chr2:53960381
|
A | G | 1 | a0002c0002t0002g0115 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.242+10162T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960381 | ||||||
| chr2:53960398
|
C | CA | 8 | a0001c0001t0001g0242a0001c0005t0001g0344a0001c0006t0003g0172others(5): Show | 8 | HG00735.hp2 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.242+10144dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960398 | ||||||
| chr2:53960480
|
A | G | 50 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(47): Show | 50 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.242+10063T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960480 | ||||||
| chr2:53960507
|
C | T | 4 | a0001c0001t0001g0180a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG02630.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+10036G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960507 | ||||||
| chr2:53960523
|
T | C | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.242+10020A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960523 | ||||||
| chr2:53960585
|
C | G | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.242+9958G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960585 | ||||||
| chr2:53960709
|
C | T | 378 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0035others(375): Show | 379 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.242+9834G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960709 | ||||||
| chr2:53960731
|
T | G | 58 | a0002c0029t0002g0307a0003c0004t0001g0032a0003c0004t0001g0033others(55): Show | 58 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.242+9812A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960731 | ||||||
| chr2:53960750
|
G | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.242+9793C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960750 | ||||||
| chr2:53960826
|
G | A | 1 | a0003c0004t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.242+9717C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960826 | ||||||
| chr2:53960889
|
C | T | 7 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(4): Show | 7 | HG00738.hp1 HG01123.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.242+9654G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960889 | ||||||
| chr2:53960906
|
G | C | 2 | a0002c0002t0002g0097a0002c0002t0004g0096 | 2 | HG02523.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.242+9637C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960906 | ||||||
| chr2:53961159
|
A | G | 5 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(2): Show | 5 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+9384T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961159 | ||||||
| chr2:53961257
|
T | A | 2 | a0001c0007t0001g0015a0001c0007t0001g0017 | 2 | HG01081.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.242+9286A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961257 | ||||||
| chr2:53961434
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.242+9109G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961434 | ||||||
| chr2:53961514
|
T | C | 1 | a0007c0012t0002g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.242+9029A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961514 | ||||||
| chr2:53961583
|
T | C | 1 | a0001c0001t0001g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.242+8960A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961583 | ||||||
| chr2:53961672
|
T | C | 5 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(2): Show | 5 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+8871A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961672 | ||||||
| chr2:53961673
|
C | A | 5 | a0001c0007t0006g0012a0001c0007t0006g0014a0001c0007t0006g0196others(2): Show | 5 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+8870G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961673 | ||||||
| chr2:53961932
|
C | T | 61 | a0001c0001t0001g0053a0001c0022t0016g0111a0002c0003t0001g0080others(58): Show | 61 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.242+8611G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961932 | ||||||
| chr2:53962059
|
C | T | 1 | a0003c0004t0001g0298 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.242+8484G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962059 | ||||||
| chr2:53962121
|
G | T | 2 | a0001c0006t0005g0002a0001c0006t0005g0004 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.242+8422C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962121 | ||||||
| chr2:53962140
|
T | C | 13 | a0001c0001t0001g0273a0001c0001t0012g0041a0002c0002t0002g0044others(10): Show | 13 | HG00323.hp2 HG00544.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.242+8403A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962140 | ||||||
| chr2:53962147
|
C | G | 2 | a0002c0003t0002g0144a0012c0024t0001g0312 | 2 | HG03579.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.242+8396G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962147 | ||||||
| chr2:53962150
|
C | T | 2 | a0002c0003t0002g0144a0012c0024t0001g0312 | 2 | HG03579.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.242+8393G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962150 | ||||||
| chr2:53962157
|
G | T | 1 | a0002c0003t0002g0069 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.242+8386C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962157 | ||||||
| chr2:53962240
|
T | C | 4 | a0001c0005t0001g0341a0002c0002t0002g0101a0002c0002t0002g0126others(1): Show | 4 | HG02572.hp2 NA19002.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+8303A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962240 | ||||||
| chr2:53962375
|
G | T | 2 | a0001c0001t0001g0267a0001c0006t0003g0266 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.242+8168C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962375 | ||||||
| chr2:53962589
|
C | A | 1 | a0001c0005t0001g0182 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.242+7954G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962589 | ||||||
| chr2:53962650
|
T | C | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.242+7893A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962650 | ||||||
| chr2:53962700
|
T | C | 1 | a0001c0005t0001g0372 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.242+7843A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962700 | ||||||
| chr2:53962826
|
T | A | 1 | a0002c0003t0002g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.242+7717A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962826 | ||||||
| chr2:53962876
|
T | C | 1 | a0002c0003t0002g0148 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.242+7667A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962876 | ||||||
| chr2:53962941
|
T | C | 1 | a0002c0003t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.242+7602A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962941 | ||||||
| chr2:53962966
|
C | T | 1 | a0001c0007t0006g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.242+7577G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962966 | ||||||
| chr2:53962967
|
G | C | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.242+7576C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962967 | ||||||
| chr2:53963009
|
C | CA | 7 | a0001c0001t0001g0206a0001c0001t0001g0267a0001c0005t0001g0342others(4): Show | 7 | HG00597.hp2 HG01884.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.242+7533dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963009 | ||||||
| chr2:53963009
|
CA | C | 12 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.242+7533delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963009 | ||||||
| chr2:53963025
|
A | G | 3 | a0001c0006t0005g0002a0001c0006t0005g0004a0002c0003t0010g0006 | 3 | HG02145.hp1 HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.242+7518T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963025 | ||||||
| chr2:53963102
|
G | A | 1 | a0002c0003t0002g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.242+7441C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963102 | ||||||
| chr2:53963190
|
G | A | 1 | a0010c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.242+7353C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963190 | ||||||
| chr2:53963237
|
G | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0004a0002c0003t0010g0006 | 3 | HG02145.hp1 HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.242+7306C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963237 | ||||||
| chr2:53963284
|
G | A | 1 | a0001c0006t0003g0172 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.242+7259C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963284 | ||||||
| chr2:53963396
|
A | C | 3 | a0001c0005t0001g0316a0001c0005t0001g0318a0001c0005t0001g0353 | 3 | HG01515.hp2 HG01517.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.242+7147T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963396 | ||||||
| chr2:53963449
|
T | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0004a0002c0003t0010g0006 | 3 | HG02145.hp1 HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.242+7094A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963449 | ||||||
| chr2:53963485
|
A | G | 1 | a0001c0006t0003g0172 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.242+7058T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963485 | ||||||
| chr2:53963613
|
A | T | 5 | a0003c0004t0001g0032a0003c0004t0001g0034a0003c0004t0001g0207others(2): Show | 5 | NA18945.hp1 NA18955.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+6930T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963613 | ||||||
| chr2:53963663
|
A | G | 1 | a0002c0032t0004g0374 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.242+6880T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963663 | ||||||
| chr2:53963832
|
C | T | 1 | a0001c0006t0003g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.242+6711G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963832 | ||||||
| chr2:53963839
|
T | A | 1 | a0009c0027t0003g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.242+6704A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963839 | ||||||
| chr2:53964110
|
T | C | 1 | a0001c0006t0015g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.242+6433A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53964110 | ||||||
| chr2:53964325
|
G | A | 3 | a0002c0010t0002g0018a0002c0010t0002g0051a0002c0010t0002g0056 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.242+6218C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53964325 | ||||||
| chr2:53964337
|
T | G | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.242+6206A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53964337 | ||||||
| chr2:53964370
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.242+6173A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53964370 | ||||||
| chr2:53964657
|
C | T | 9 | a0001c0005t0001g0317a0001c0005t0001g0325a0001c0005t0001g0326others(6): Show | 9 | HG00597.hp1 HG02129.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.242+5886G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53964657 | ||||||
| chr2:53964858
|
G | C | 1 | a0011c0023t0003g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.242+5685C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53964858 | ||||||
| chr2:53964862
|
A | G | 1 | a0009c0027t0003g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.242+5681T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53964862 | ||||||
| chr2:53965020
|
G | A | 246 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0001t0001g0293others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.242+5523C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965020 | ||||||
| chr2:53965068
|
A | C | 5 | a0001c0006t0005g0002a0001c0006t0005g0003a0001c0006t0005g0004others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+5475T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965068 | ||||||
| chr2:53965095
|
A | G | 3 | a0001c0006t0003g0163a0001c0006t0003g0165a0001c0006t0003g0166 | 3 | NA18951.hp2 NA18973.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.242+5448T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965095 | ||||||
| chr2:53965102
|
G | GAC | 3 | a0001c0007t0006g0012a0001c0007t0006g0014a0010c0026t0001g0013 | 3 | HG02559.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.242+5439_242+5440d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965102 | ||||||
| chr2:53965175
|
T | G | 1 | a0002c0029t0002g0307 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.242+5368A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965175 | ||||||
| chr2:53965246
|
A | AT | 19 | a0001c0001t0001g0173a0001c0001t0001g0184a0001c0001t0001g0205others(16): Show | 19 | HG00597.hp1 HG00597.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.242+5296dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965246 | ||||||
| chr2:53965246
|
AT | A | 131 | a0001c0001t0001g0053a0001c0006t0003g0371a0001c0006t0005g0002others(128): Show | 131 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.242+5296delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965246 | ||||||
| chr2:53965328
|
A | G | 1 | a0002c0029t0002g0307 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.242+5215T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965328 | ||||||
| chr2:53965525
|
G | A | 4 | a0002c0002t0002g0356a0002c0002t0002g0357a0002c0002t0002g0358others(1): Show | 4 | HG01255.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+5018C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965525 | ||||||
| chr2:53965554
|
TGAG | T | 126 | a0001c0001t0001g0053a0001c0022t0016g0111a0002c0002t0002g0022others(123): Show | 126 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.242+4986_242+4988d others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965554 | ||||||
| chr2:53965622
|
C | T | 1 | a0003c0004t0001g0271 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.242+4921G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965622 | ||||||
| chr2:53965659
|
T | C | 2 | a0003c0004t0001g0032a0003c0004t0001g0268 | 2 | NA18945.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.242+4884A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965659 | ||||||
| chr2:53965663
|
T | A | 1 | a0009c0027t0003g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.242+4880A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965663 | ||||||
| chr2:53965670
|
G | GT | 225 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0001t0001g0293others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.242+4872dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965670 | ||||||
| chr2:53965670
|
G | GTT | 9 | a0001c0006t0003g0167a0001c0006t0003g0168a0001c0006t0003g0170others(6): Show | 9 | HG00438.hp1 HG02630.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.242+4871_242+4872d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965670 | ||||||
| chr2:53965690
|
G | A | 1 | a0003c0004t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.242+4853C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965690 | ||||||
| chr2:53965779
|
T | C | 382 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0035others(379): Show | 383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.242+4764A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965779 | ||||||
| chr2:53965792
|
C | T | 4 | a0001c0006t0005g0002a0001c0006t0005g0003a0001c0006t0005g0004others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+4751G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965792 | ||||||
| chr2:53965810
|
C | A | 1 | a0001c0007t0001g0015 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.242+4733G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965810 | ||||||
| chr2:53965962
|
A | G | 246 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0001t0001g0293others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.242+4581T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965962 | ||||||
| chr2:53966056
|
T | C | 249 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0001t0001g0198others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.242+4487A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966056 | ||||||
| chr2:53966088
|
C | A | 1 | a0002c0003t0002g0128 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.242+4455G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966088 | ||||||
| chr2:53966237
|
T | C | 4 | a0001c0006t0005g0002a0001c0006t0005g0003a0001c0006t0005g0004others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+4306A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966237 | ||||||
| chr2:53966430
|
G | A | 5 | a0002c0002t0002g0045a0002c0002t0002g0102a0002c0002t0002g0103others(2): Show | 5 | NA18941.hp1 NA18961.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.242+4113C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966430 | ||||||
| chr2:53966443
|
T | C | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.242+4100A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966443 | ||||||
| chr2:53966528
|
G | A | 5 | a0001c0006t0003g0167a0001c0006t0003g0168a0001c0006t0003g0170others(2): Show | 5 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+4015C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966528 | ||||||
| chr2:53966554
|
C | T | 3 | a0003c0004t0001g0200a0003c0004t0001g0201a0003c0004t0001g0202 | 3 | NA18948.hp2 NA18952.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.242+3989G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966554 | ||||||
| chr2:53966659
|
T | A | 1 | a0001c0005t0001g0343 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.242+3884A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966659 | ||||||
| chr2:53966659
|
T | C | 1 | a0002c0002t0002g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.242+3884A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966659 | ||||||
| chr2:53966703
|
G | T | 1 | a0001c0005t0001g0344 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.242+3840C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966703 | ||||||
| chr2:53966716
|
T | C | 7 | a0001c0006t0003g0371a0001c0009t0001g0360a0001c0009t0001g0366others(4): Show | 7 | HG01074.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.242+3827A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966716 | ||||||
| chr2:53966751
|
G | A | 129 | a0001c0001t0001g0053a0001c0005t0001g0324a0001c0007t0001g0015others(126): Show | 129 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.242+3792C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966751 | ||||||
| chr2:53966830
|
G | C | 1 | a0001c0007t0001g0015 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.242+3713C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966830 | ||||||
| chr2:53966920
|
G | A | 1 | a0001c0006t0003g0159 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.242+3623C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966920 | ||||||
| chr2:53966934
|
G | A | 240 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0005t0001g0311others(237): Show | 240 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.242+3609C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966934 | ||||||
| chr2:53966950
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.242+3593C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966950 | ||||||
| chr2:53967044
|
G | A | 1 | a0003c0004t0001g0271 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.242+3499C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967044 | ||||||
| chr2:53967199
|
C | T | 1 | a0002c0003t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.242+3344G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967199 | ||||||
| chr2:53967241
|
C | T | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.242+3302G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967241 | ||||||
| chr2:53967280
|
T | C | 2 | a0001c0001t0001g0272a0001c0001t0001g0273 | 2 | HG00323.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.242+3263A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967280 | ||||||
| chr2:53967294
|
C | T | 124 | a0001c0001t0001g0053a0001c0022t0016g0111a0002c0002t0002g0022others(121): Show | 124 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.242+3249G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967294 | ||||||
| chr2:53967314
|
C | T | 1 | a0002c0003t0002g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.242+3229G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967314 | ||||||
| chr2:53967449
|
C | T | 4 | a0001c0006t0005g0002a0001c0006t0005g0003a0001c0006t0005g0004others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+3094G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967449 | ||||||
| chr2:53967583
|
G | A | 3 | a0001c0006t0003g0031a0001c0006t0003g0176a0001c0006t0003g0177 | 3 | HG02615.hp1 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.242+2960C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967583 | ||||||
| chr2:53967611
|
A | G | 241 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0005t0001g0311others(238): Show | 241 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.242+2932T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967611 | ||||||
| chr2:53967649
|
C | CA | 35 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(32): Show | 35 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.242+2893dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
C | CAA | 12 | a0001c0001t0012g0041a0002c0002t0002g0357a0002c0003t0002g0297others(9): Show | 12 | HG02132.hp1 HG02572.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.242+2892_242+2893d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
C | CAAAA | 7 | a0001c0001t0001g0053a0001c0009t0001g0365a0002c0002t0002g0054others(4): Show | 7 | HG01255.hp1 HG02155.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.242+2890_242+2893d others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
C | CAAAAA | 17 | a0001c0006t0003g0025a0001c0006t0003g0026a0001c0006t0003g0027others(14): Show | 17 | HG00099.hp2 HG01099.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.242+2889_242+2893d others(7): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
C | CAAAAAA | 62 | a0001c0005t0001g0315a0001c0006t0003g0029a0001c0006t0003g0030others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.242+2888_242+2893d others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
C | CAAAAAAA | 54 | a0001c0005t0001g0316a0001c0005t0001g0317a0001c0005t0001g0318others(51): Show | 54 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.242+2887_242+2893d others(9): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
C | CAAAAAAA others(1): Show |
40 | a0001c0005t0001g0326a0001c0005t0001g0327a0001c0005t0001g0328others(37): Show | 40 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.242+2886_242+2893d others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
C | CAAAAAAA others(2): Show |
23 | a0001c0001t0001g0173a0001c0005t0001g0311a0001c0005t0001g0344others(20): Show | 23 | HG00423.hp1 HG00609.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.242+2885_242+2893d others(11): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
C | CAAAAAAA others(3): Show |
5 | a0001c0005t0001g0353a0001c0006t0003g0177a0002c0002t0002g0151others(2): Show | 5 | HG01123.hp2 HG01256.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+2884_242+2893d others(12): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
C | CAAAAAAA others(4): Show |
2 | a0001c0006t0003g0031a0001c0006t0003g0178 | 2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.242+2883_242+2893d others(13): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
C | CAAAAAAA others(5): Show |
1 | a0001c0005t0001g0354 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.242+2882_242+2893d others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
C | CAAAAAAA others(30): Show |
1 | a0001c0005t0001g0325 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.242+2893_242+2894i others(39): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
CA | C | 12 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0190others(9): Show | 12 | HG01361.hp1 HG01516.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.242+2893delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG00738.hp1 HG01123.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.242+2886_242+2893d others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0009t0001g0360 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.242+2882_242+2893d others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
CAAAAAAA others(6): Show |
C | 5 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(2): Show | 5 | HG01167.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+2881_242+2893d others(15): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
CAAAAAAA others(8): Show |
C | 1 | a0010c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.242+2879_242+2893d others(17): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
CAAAAAAA others(10): Show |
C | 1 | a0003c0004t0001g0183 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.242+2877_242+2893d others(19): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967649
|
CAAAAAAA others(12): Show |
C | 1 | a0001c0005t0001g0182 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.242+2875_242+2893d others(21): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | ||||||
| chr2:53967679
|
A | G | 2 | a0001c0006t0005g0002a0001c0006t0005g0003 | 2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.242+2864T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967679 | ||||||
| chr2:53967797
|
C | G | 241 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0005t0001g0311others(238): Show | 241 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.242+2746G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967797 | ||||||
| chr2:53967848
|
T | C | 1 | a0002c0002t0002g0355 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.242+2695A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967848 | ||||||
| chr2:53967908
|
A | G | 4 | a0002c0002t0002g0356a0002c0002t0002g0357a0002c0002t0002g0358others(1): Show | 4 | HG01255.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+2635T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967908 | ||||||
| chr2:53967934
|
T | C | 1 | a0001c0005t0001g0373 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.242+2609A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967934 | ||||||
| chr2:53968139
|
G | C | 1 | a0002c0003t0002g0152 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.242+2404C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53968139 | ||||||
| chr2:53968147
|
C | T | 55 | a0001c0005t0001g0311a0001c0005t0001g0313a0001c0005t0001g0314others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.242+2396G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53968147 | ||||||
| chr2:53968274
|
C | CA | 122 | a0001c0001t0001g0053a0001c0001t0001g0305a0001c0022t0016g0111others(119): Show | 122 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.242+2268dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53968274 | ||||||
| chr2:53968334
|
T | C | 1 | a0001c0007t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.242+2209A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53968334 | ||||||
| chr2:53968424
|
G | T | 1 | a0012c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.242+2119C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53968424 | ||||||
| chr2:53968616
|
T | C | 5 | a0001c0006t0005g0002a0001c0006t0005g0003a0001c0006t0005g0004others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+1927A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53968616 | ||||||
| chr2:53968877
|
T | C | 241 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0005t0001g0311others(238): Show | 241 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.242+1666A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53968877 | ||||||
| chr2:53969013
|
T | C | 1 | a0002c0002t0002g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.242+1530A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969013 | ||||||
| chr2:53969101
|
G | A | 128 | a0001c0001t0001g0053a0001c0007t0001g0015a0001c0007t0001g0017others(125): Show | 128 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.242+1442C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969101 | ||||||
| chr2:53969149
|
T | C | 1 | a0004c0008t0001g0383 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.242+1394A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969149 | ||||||
| chr2:53969247
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.242+1296T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969247 | ||||||
| chr2:53969410
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.242+1133C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969410 | ||||||
| chr2:53969412
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.242+1131C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969412 | ||||||
| chr2:53969435
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.242+1108T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969435 | ||||||
| chr2:53969635
|
T | G | 73 | a0001c0005t0001g0311a0001c0005t0001g0313a0001c0005t0001g0314others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.242+908A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969635 | ||||||
| chr2:53969660
|
CT | C | 236 | a0001c0001t0001g0053a0001c0001t0001g0173a0001c0005t0001g0311others(233): Show | 236 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.242+882delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969660 | ||||||
| chr2:53969672
|
A | C | 32 | a0001c0001t0001g0173a0001c0006t0003g0025a0001c0006t0003g0026others(29): Show | 32 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.242+871T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969672 | ||||||
| chr2:53969673
|
C | A | 2 | a0001c0005t0001g0372a0001c0005t0001g0373 | 2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.242+870G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969673 | ||||||
| chr2:53969687
|
G | GT | 137 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(134): Show | 137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.242+855dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969687 | ||||||
| chr2:53969687
|
G | GTT | 11 | a0001c0007t0001g0015a0001c0007t0001g0017a0001c0007t0006g0012others(8): Show | 11 | HG01081.hp2 HG01192.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.242+854_242+855dup others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969687 | ||||||
| chr2:53969687
|
G | T | 1 | a0002c0002t0002g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.242+856C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969687 | ||||||
| chr2:53969687
|
GT | G | 74 | a0001c0005t0001g0313a0001c0005t0001g0314a0001c0005t0001g0315others(71): Show | 74 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.242+855delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969687 | ||||||
| chr2:53969749
|
A | T | 3 | a0001c0007t0006g0012a0001c0007t0006g0014a0010c0026t0001g0013 | 3 | HG02559.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.242+794T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969749 | ||||||
| chr2:53969808
|
C | T | 1 | a0002c0003t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.242+735G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969808 | ||||||
| chr2:53969916
|
C | CTTAAGAT others(2): Show |
4 | a0001c0006t0005g0002a0001c0006t0005g0003a0001c0006t0005g0004others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+626_242+627ins others(9): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969916 | ||||||
| chr2:53969917
|
A | T | 4 | a0001c0006t0005g0002a0001c0006t0005g0003a0001c0006t0005g0004others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+626T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969917 | ||||||
| chr2:53969989
|
C | A | 72 | a0001c0005t0001g0311a0001c0005t0001g0313a0001c0005t0001g0314others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.242+554G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969989 | ||||||
| chr2:53970390
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.242+153G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53970390 |