Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23431 |
|---|---|
| ensemblid | ENSG00000081014.11 |
| hgncid | 573 |
| symbol | AP4E1 |
| name | adaptor related protein complex 4 subunit epsilon 1 |
| refseq_nuc | NM_007347.5 |
| refseq_prot | NP_031373.2 |
| ensembl_nuc | ENST00000261842.10 |
| ensembl_prot | ENSP00000261842.5 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 50908683 |
| end | 51005895 |
| strand | + |
| ver | v1.2 |
| region | chr15:50908683-51005895 |
| region5000 | chr15:50903683-51010895 |
| regionname0 | AP4E1_chr15_50908683_51005895 |
| regionname5000 | AP4E1_chr15_50903683_51010895 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1137 | 192 | 59 | 41 | 62 | 6 | 22 | 49 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002 | 0/0 | 1137 | 183 | 19 | 32 | 108 | 8 | 16 | 83 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0003 | 0/0 | 1137 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0004 | 0/0 | 1137 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0005 | 0/0 | 1137 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0006 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0007 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0008 | 0/0 | 1137 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0009 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0010 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0011 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| 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 | 1/1 | 3414 | 191 | 59 | 41 | 61 | 6 | 22 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| c0002 | 0/0 | 3414 | 95 | 2 | 14 | 67 | 4 | 8 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| c0003 | 0/0 | 3414 | 86 | 15 | 18 | 41 | 4 | 8 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| c0004 | 0/0 | 3414 | 6 | 6 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| c0005 | 0/0 | 3414 | 3 | 0 | 0 | 3 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| c0006 | 0/0 | 3414 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| c0007 | 0/0 | 3414 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| c0008 | 0/0 | 3414 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| c0009 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| c0010 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| c0011 | 0/0 | 3414 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| c0012 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| c0013 | 0/0 | 3414 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| c0014 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| 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 | 3330 | 114 | 16 | 24 | 62 | 1 | 10 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0002 | 0/0 | 3330 | 89 | 2 | 12 | 65 | 4 | 6 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0003 | 0/1 | 3330 | 81 | 7 | 15 | 40 | 6 | 12 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0004 | 0/0 | 3330 | 39 | 14 | 12 | 3 | 3 | 7 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0005 | 0/0 | 3330 | 19 | 17 | 2 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0006 | 0/0 | 3330 | 7 | 6 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0007 | 0/0 | 3330 | 4 | 4 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0008 | 0/0 | 3330 | 4 | 4 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0009 | 0/0 | 3330 | 4 | 4 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0010 | 0/0 | 3330 | 3 | 1 | 2 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0011 | 0/0 | 3330 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0012 | 0/0 | 3330 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0013 | 0/0 | 3330 | 2 | 0 | 2 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0014 | 0/0 | 3330 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0015 | 0/0 | 3330 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0016 | 0/0 | 3330 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0017 | 0/0 | 3330 | 2 | 0 | 1 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0018 | 0/0 | 3330 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0019 | 0/0 | 3330 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0020 | 0/0 | 3348 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0021 | 0/0 | 3330 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0022 | 0/0 | 3330 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0023 | 0/0 | 3330 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0024 | 0/0 | 3330 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0025 | 0/0 | 3330 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0026 | 0/0 | 3330 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0027 | 0/0 | 3330 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0028 | 0/0 | 3330 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| t0029 | 0/0 | 3318 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| 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 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0312 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0375 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0382 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0386 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| 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 | 1/1 | 3414 | 191 | 59 | 41 | 61 | 6 | 22 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0001c0010 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0002 | 0/0 | 3414 | 95 | 2 | 14 | 67 | 4 | 8 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0003 | 0/0 | 3414 | 86 | 15 | 18 | 41 | 4 | 8 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0006 | 0/0 | 3414 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0003c0004 | 0/0 | 3414 | 6 | 6 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0004c0005 | 0/0 | 3414 | 3 | 0 | 0 | 3 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0005c0007 | 0/0 | 3414 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0006c0012 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0007c0011 | 0/0 | 3414 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0008c0013 | 0/0 | 3414 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0009c0014 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0010c0008 | 0/0 | 3414 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0011c0009 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6743 | 106 | 16 | 23 | 55 | 1 | 10 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0001c0001t0003 | 0/1 | 6743 | 14 | 2 | 3 | 1 | 2 | 5 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0001c0001t0004 | 0/0 | 6743 | 39 | 14 | 12 | 3 | 3 | 7 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0001c0001t0005 | 0/0 | 6743 | 17 | 16 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0001c0001t0008 | 0/0 | 6743 | 4 | 4 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0001c0001t0009 | 0/0 | 6743 | 4 | 4 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0001c0001t0019 | 0/0 | 6743 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0001c0001t0025 | 0/0 | 6743 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0001c0001t0026 | 0/0 | 6743 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0001c0001t0027 | 0/0 | 6743 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0001c0001t0028 | 0/0 | 6743 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0001c0001t0029 | 0/0 | 6731 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0001c0010t0002 | 0/0 | 6743 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0002t0002 | 0/0 | 6743 | 86 | 1 | 12 | 63 | 4 | 6 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0002t0012 | 0/0 | 6743 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0002t0016 | 0/0 | 6743 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0002t0017 | 0/0 | 6743 | 2 | 0 | 1 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0002t0021 | 0/0 | 6743 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0002t0023 | 0/0 | 6743 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0002t0024 | 0/0 | 6743 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0003t0001 | 0/0 | 6743 | 3 | 0 | 1 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0003t0002 | 0/0 | 6743 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0003t0003 | 0/0 | 6743 | 66 | 5 | 12 | 38 | 4 | 7 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0003t0006 | 0/0 | 6743 | 7 | 6 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0003t0010 | 0/0 | 6743 | 3 | 1 | 2 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0003t0013 | 0/0 | 6743 | 2 | 0 | 2 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0003t0014 | 0/0 | 6743 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0003t0020 | 0/0 | 6761 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0003t0022 | 0/0 | 6743 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0002c0006t0015 | 0/0 | 6743 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0003c0004t0007 | 0/0 | 6743 | 4 | 4 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0003c0004t0018 | 0/0 | 6743 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0004c0005t0001 | 0/0 | 6743 | 3 | 0 | 0 | 3 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0005c0007t0011 | 0/0 | 6743 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0006c0012t0001 | 0/0 | 6743 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0007c0011t0005 | 0/0 | 6743 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0008c0013t0005 | 0/0 | 6743 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0009c0014t0001 | 0/0 | 6743 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0010c0008t0002 | 0/0 | 6743 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| a0011c0009t0003 | 0/0 | 6743 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | copy fasta | chr15 | 50903683 | 51010895 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0312 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0375 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0382 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0386 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0008g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0008g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0008g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0009g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0009g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0009g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0009g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0019g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0019g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0025g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0026g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0027g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0028g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0029g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0010t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0012g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0012g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0016g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0016g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0017g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0017g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0021g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0023g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0024g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0010g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0010g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0013g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0014g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0014g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0020g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0022g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0006t0015g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0006t0015g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0003c0004t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0003c0004t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0003c0004t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0003c0004t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0003c0004t0018g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0003c0004t0018g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0004c0005t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0004c0005t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0004c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0005c0007t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0005c0007t0011g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0006c0012t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0007c0011t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0008c0013t0005g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0009c0014t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0010c0008t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0011c0009t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0382 | EUR | GBR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00099 | hp2 | a0002 | c0003 | t0003 | g0152 | EUR | GBR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0057 | EUR | GBR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0346 | EUR | GBR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0386 | EUR | FIN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0073 | EUR | FIN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00408 | hp2 | a0002 | c0003 | t0003 | g0175 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00438 | hp1 | a0002 | c0003 | t0001 | g0077 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00609 | hp1 | a0002 | c0003 | t0003 | g0133 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00621 | hp2 | a0002 | c0003 | t0003 | g0026 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0376 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00733 | hp1 | a0002 | c0003 | t0003 | g0138 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00735 | hp1 | a0002 | c0003 | t0003 | g0194 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0040 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00741 | hp1 | a0002 | c0002 | t0017 | g0055 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00741 | hp2 | a0002 | c0003 | t0003 | g0163 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0369 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0079 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0370 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0056 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01074 | hp2 | a0002 | c0003 | t0013 | g0001 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0092 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01099 | hp1 | a0002 | c0003 | t0013 | g0001 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0383 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0331 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01109 | hp2 | a0002 | c0003 | t0003 | g0158 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01167 | hp1 | a0002 | c0003 | t0006 | g0186 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01167 | hp2 | a0002 | c0003 | t0010 | g0034 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01168 | hp1 | a0002 | c0003 | t0003 | g0137 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01168 | hp2 | a0002 | c0003 | t0003 | g0025 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01169 | hp1 | a0002 | c0003 | t0010 | g0032 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01169 | hp2 | a0002 | c0003 | t0003 | g0151 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0380 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0125 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01192 | hp1 | a0002 | c0003 | t0003 | g0146 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0122 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01243 | hp1 | a0002 | c0003 | t0003 | g0193 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01255 | hp1 | a0008 | c0013 | t0005 | g0329 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0088 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0365 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01261 | hp1 | a0002 | c0003 | t0003 | g0159 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01346 | hp2 | a0001 | c0001 | t0025 | g0371 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01358 | hp2 | a0002 | c0003 | t0001 | g0071 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0313 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0384 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01496 | hp1 | a0001 | c0001 | t0029 | g0304 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0378 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0375 | EUR | IBS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01515 | hp2 | a0002 | c0003 | t0003 | g0142 | EUR | IBS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0310 | EUR | IBS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0012 | EUR | IBS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01517 | hp1 | a0002 | c0003 | t0003 | g0130 | EUR | IBS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0064 | EUR | IBS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0218 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0336 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01891 | hp1 | a0005 | c0007 | t0011 | g0185 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01891 | hp2 | a0002 | c0003 | t0022 | g0007 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01943 | hp1 | a0002 | c0002 | t0023 | g0042 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01943 | hp2 | a0002 | c0003 | t0003 | g0029 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0372 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0373 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0043 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0374 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02004 | hp1 | a0002 | c0003 | t0003 | g0030 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02027 | hp2 | a0002 | c0003 | t0003 | g0178 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0330 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02056 | hp1 | a0002 | c0003 | t0003 | g0150 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02071 | hp1 | a0002 | c0003 | t0003 | g0166 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02074 | hp1 | a0002 | c0003 | t0003 | g0135 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0322 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02145 | hp2 | a0003 | c0004 | t0018 | g0020 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0115 | EAS | CDX | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CDX | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02257 | hp1 | a0002 | c0006 | t0015 | g0347 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0308 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0341 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0207 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02280 | hp1 | a0002 | c0003 | t0003 | g0170 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0317 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0385 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0219 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0379 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02615 | hp1 | a0002 | c0003 | t0006 | g0187 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02615 | hp2 | a0003 | c0004 | t0007 | g0024 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0319 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0356 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0333 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0363 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02647 | hp2 | a0007 | c0011 | t0005 | g0339 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0050 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0357 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0309 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0340 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02809 | hp2 | a0010 | c0008 | t0002 | g0005 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02818 | hp1 | a0002 | c0003 | t0014 | g0017 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0318 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02895 | hp2 | a0002 | c0003 | t0003 | g0140 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0358 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02897 | hp2 | a0002 | c0003 | t0003 | g0128 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02922 | hp1 | a0002 | c0003 | t0014 | g0018 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02922 | hp2 | a0003 | c0004 | t0007 | g0021 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0301 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0349 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02976 | hp2 | a0001 | c0001 | t0028 | g0216 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03041 | hp1 | a0005 | c0007 | t0011 | g0184 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03041 | hp2 | a0002 | c0002 | t0021 | g0006 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0334 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03098 | hp2 | a0002 | c0003 | t0003 | g0132 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0320 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0303 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0352 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03195 | hp1 | a0003 | c0004 | t0018 | g0019 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0361 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0306 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03209 | hp2 | a0002 | c0006 | t0015 | g0348 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0381 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0302 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03239 | hp1 | a0002 | c0003 | t0003 | g0155 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0081 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0350 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0338 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0362 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0307 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03491 | hp1 | a0002 | c0003 | t0003 | g0127 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0011 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0316 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03492 | hp2 | a0002 | c0003 | t0003 | g0134 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0328 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03516 | hp2 | a0002 | c0003 | t0006 | g0192 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0337 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0321 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0221 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0305 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0387 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0342 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0377 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03704 | hp2 | a0002 | c0003 | t0003 | g0183 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03710 | hp1 | a0002 | c0003 | t0020 | g0008 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03710 | hp2 | a0002 | c0002 | t0017 | g0054 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0367 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03834 | hp2 | a0002 | c0003 | t0003 | g0139 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03927 | hp1 | a0002 | c0003 | t0003 | g0144 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0327 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0090 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04115 | hp1 | a0002 | c0003 | t0003 | g0167 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0048 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0368 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04199 | hp1 | a0002 | c0002 | t0024 | g0047 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0366 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0388 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | YRI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0351 | AFR | YRI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | CHB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18612 | hp2 | a0002 | c0003 | t0003 | g0148 | EAS | CHB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | CHB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18747 | hp2 | a0002 | c0003 | t0003 | g0181 | EAS | CHB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0360 | AFR | YRI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18906 | hp2 | a0003 | c0004 | t0007 | g0022 | AFR | YRI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18939 | hp1 | a0002 | c0003 | t0003 | g0153 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0359 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18943 | hp2 | a0002 | c0003 | t0003 | g0180 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18944 | hp2 | a0004 | c0005 | t0001 | g0238 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18946 | hp1 | a0002 | c0003 | t0003 | g0171 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18947 | hp2 | a0002 | c0003 | t0003 | g0147 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18948 | hp1 | a0002 | c0003 | t0003 | g0027 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18948 | hp2 | a0002 | c0003 | t0003 | g0164 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18949 | hp2 | a0002 | c0002 | t0012 | g0111 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18956 | hp2 | a0002 | c0003 | t0003 | g0160 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18959 | hp1 | a0002 | c0003 | t0003 | g0162 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18960 | hp1 | a0002 | c0003 | t0003 | g0172 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18962 | hp1 | a0004 | c0005 | t0001 | g0239 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18964 | hp2 | a0002 | c0003 | t0003 | g0143 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18965 | hp1 | a0002 | c0003 | t0003 | g0154 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18967 | hp2 | a0002 | c0003 | t0003 | g0174 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0354 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18974 | hp2 | a0006 | c0012 | t0001 | g0289 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18975 | hp1 | a0002 | c0003 | t0003 | g0182 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18975 | hp2 | a0004 | c0005 | t0001 | g0235 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18978 | hp2 | a0002 | c0003 | t0003 | g0136 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18979 | hp1 | a0002 | c0003 | t0003 | g0031 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18981 | hp2 | a0002 | c0003 | t0003 | g0177 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18982 | hp1 | a0002 | c0003 | t0003 | g0157 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18984 | hp2 | a0002 | c0003 | t0003 | g0149 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18986 | hp1 | a0002 | c0003 | t0003 | g0126 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18986 | hp2 | a0001 | c0001 | t0019 | g0215 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18990 | hp2 | a0002 | c0003 | t0003 | g0131 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18992 | hp1 | a0002 | c0003 | t0003 | g0028 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18993 | hp1 | a0009 | c0014 | t0001 | g0231 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18993 | hp2 | a0002 | c0003 | t0003 | g0165 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0353 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19000 | hp2 | a0002 | c0003 | t0003 | g0179 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19004 | hp1 | a0002 | c0003 | t0003 | g0156 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19012 | hp2 | a0002 | c0002 | t0016 | g0068 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | LWK | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0364 | AFR | LWK | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0335 | AFR | LWK | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19057 | hp1 | a0002 | c0003 | t0003 | g0173 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19058 | hp1 | a0011 | c0009 | t0003 | g0161 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19060 | hp2 | a0001 | c0001 | t0019 | g0230 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19067 | hp1 | a0002 | c0003 | t0003 | g0141 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19072 | hp2 | a0002 | c0002 | t0016 | g0116 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19074 | hp2 | a0002 | c0003 | t0003 | g0129 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19079 | hp1 | a0002 | c0003 | t0003 | g0176 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19088 | hp1 | a0002 | c0003 | t0003 | g0145 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19088 | hp2 | a0002 | c0002 | t0012 | g0112 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19090 | hp2 | a0002 | c0003 | t0002 | g0123 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0220 | AFR | YRI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19240 | hp2 | a0001 | c0001 | t0026 | g0294 | AFR | YRI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA20129 | hp1 | a0002 | c0003 | t0006 | g0190 | AFR | ASW | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA20129 | hp2 | a0003 | c0004 | t0007 | g0023 | AFR | ASW | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0311 | EUR | TSI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA20752 | hp2 | a0002 | c0003 | t0003 | g0168 | EUR | TSI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0076 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0315 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02109 | hp1 | a0002 | c0003 | t0006 | g0189 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02109 | hp2 | a0001 | c0001 | t0027 | g0224 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02486 | hp1 | a0002 | c0003 | t0006 | g0188 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02486 | hp2 | a0002 | c0003 | t0003 | g0169 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG06807 | hp1 | a0002 | c0003 | t0010 | g0033 | AFR | USA | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG06807 | hp2 | a0002 | c0003 | t0006 | g0191 | AFR | USA | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18955 | hp2 | a0001 | c0010 | t0002 | g0355 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0332 | AFR | USA | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0083 | AFR | LWK | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | LWK | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0312 | REF | REF | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0038 | REF | REF | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:50925164
|
T | C | 5 | a0002a0003a0005others(2): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
missense_variant | MODERATE | c.487T>C | p.Cys163Arg | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/21 | 583/6743 | 487/3414 | 163/1137 | chr15 | 50925164 | ||
| chr15:50930893
|
A | G | 1 | a0011 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.791A>G | p.Asn264Ser | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/21 | 887/6743 | 791/3414 | 264/1137 | chr15 | 50930893 | ||
| chr15:50941684
|
A | G | 1 | a0010 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1085A>G | p.Tyr362Cys | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/21 | 1181/6743 | 1085/3414 | 362/1137 | chr15 | 50941684 | ||
| chr15:50948126
|
A | G | 1 | a0005 | 2 | HG01891.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.1283A>G | p.Asn428Ser | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/21 | 1379/6743 | 1283/3414 | 428/1137 | chr15 | 50948126 | ||
| chr15:50958529
|
C | T | 1 | a0010 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1586C>T | p.Thr529Met | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/21 | 1682/6743 | 1586/3414 | 529/1137 | chr15 | 50958529 | ||
| chr15:50958637
|
C | T | 1 | a0009 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.1694C>T | p.Ala565Val | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/21 | 1790/6743 | 1694/3414 | 565/1137 | chr15 | 50958637 | ||
| chr15:50968362
|
C | G | 1 | a0008 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.1951C>G | p.Leu651Val | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/21 | 2047/6743 | 1951/3414 | 651/1137 | chr15 | 50968362 | ||
| chr15:50997359
|
A | G | 1 | a0006 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.2380A>G | p.Arg794Gly | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/21 | 2476/6743 | 2380/3414 | 794/1137 | chr15 | 50997359 | ||
| chr15:50997408
|
C | T | 1 | a0003 | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
missense_variant | MODERATE | c.2429C>T | p.Thr810Ile | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/21 | 2525/6743 | 2429/3414 | 810/1137 | chr15 | 50997408 | ||
| chr15:50997597
|
C | G | 1 | a0007 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.2618C>G | p.Ser873Cys | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/21 | 2714/6743 | 2618/3414 | 873/1137 | chr15 | 50997597 | ||
| chr15:50997734
|
A | G | 1 | a0005 | 2 | HG01891.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.2755A>G | p.Met919Val | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/21 | 2851/6743 | 2755/3414 | 919/1137 | chr15 | 50997734 | ||
| chr15:51001147
|
C | A | 1 | a0004 | 3 | NA18944.hp2 NA18962.hp1 NA18975.hp2 |
missense_variant | MODERATE | c.3217C>A | p.Gln1073Lys | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/21 | 3313/6743 | 3217/3414 | 1073/1137 | chr15 | 51001147 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:50912098
|
G | A | 1 | a0002c0006 | 2 | HG02257.hp1 HG03209.hp2 |
synonymous_variant | LOW | c.171G>A | p.Gln57Gln | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/21 | 267/6743 | 171/3414 | 57/1137 | chr15 | 50912098 | ||
| chr15:51002635
|
G | A | 3 | a0001c0010a0002c0002a0010c0008 | 97 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(94): Show |
synonymous_variant | LOW | c.3387G>A | p.Gln1129Gln | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 3483/6743 | 3387/3414 | 1129/1137 | chr15 | 51002635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:50908702
|
C | T | 1 | a0001c0001t0019 | 2 | NA18986.hp2 NA19060.hp2 |
5_prime_UTR_variant | MODIFIER | c.-77C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/21 | 77 | chr15 | 50908702 | |||||
| chr15:50908713
|
GGCCGGGC others(5): Show |
G | 1 | a0001c0001t0029 | 1 | HG01496.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58_-47delATGAAGCC others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/21 | 47 | INFO_REALIGN_3_PRIME | chr15 | 50908713 | ||||
| chr15:50908741
|
G | GATCGCGG others(11): Show |
1 | a0002c0003t0020 | 1 | HG03710.hp1 | 5_prime_UTR_variant | MODIFIER | c.-19_-2dupATCGCGGGC others(9): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/21 | 1 | INFO_REALIGN_3_PRIME | chr15 | 50908741 | ||||
| chr15:51002798
|
G | A | 23 | a0001c0001t0003a0001c0010t0002a0002c0002t0002others(20): Show | 205 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*136G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 136 | chr15 | 51002798 | |||||
| chr15:51002821
|
C | T | 1 | a0001c0001t0028 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*159C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 159 | chr15 | 51002821 | |||||
| chr15:51003057
|
A | G | 1 | a0003c0004t0018 | 2 | HG02145.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*395A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 395 | chr15 | 51003057 | |||||
| chr15:51003215
|
G | C | 1 | a0002c0002t0021 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*553G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 553 | chr15 | 51003215 | |||||
| chr15:51003284
|
G | A | 1 | a0005c0007t0011 | 2 | HG01891.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*622G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 622 | chr15 | 51003284 | |||||
| chr15:51003382
|
T | A | 1 | a0002c0002t0012 | 2 | NA18949.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*720T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 720 | chr15 | 51003382 | |||||
| chr15:51003451
|
C | A | 1 | a0002c0003t0013 | 2 | HG01074.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*789C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 789 | chr15 | 51003451 | |||||
| chr15:51003535
|
C | T | 1 | a0001c0001t0009 | 4 | HG02622.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*873C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 873 | chr15 | 51003535 | |||||
| chr15:51003583
|
C | T | 1 | a0001c0001t0027 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*921C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 921 | chr15 | 51003583 | |||||
| chr15:51003736
|
A | C | 2 | a0003c0004t0007a0003c0004t0018 | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1074A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1074 | chr15 | 51003736 | |||||
| chr15:51003737
|
G | A | 10 | a0001c0001t0003a0002c0003t0003a0002c0003t0010others(7): Show | 96 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*1075G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1075 | chr15 | 51003737 | |||||
| chr15:51003818
|
G | A | 2 | a0001c0001t0004a0001c0001t0025 | 40 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1156G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1156 | chr15 | 51003818 | |||||
| chr15:51003990
|
C | T | 1 | a0002c0003t0014 | 2 | HG02818.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1328C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1328 | chr15 | 51003990 | |||||
| chr15:51004036
|
T | C | 1 | a0001c0001t0026 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1374T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1374 | chr15 | 51004036 | |||||
| chr15:51004045
|
A | G | 1 | a0001c0001t0019 | 2 | NA18986.hp2 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1383A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1383 | chr15 | 51004045 | |||||
| chr15:51004210
|
T | C | 28 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(25): Show | 229 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*1548T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1548 | chr15 | 51004210 | |||||
| chr15:51004221
|
G | T | 2 | a0002c0003t0010a0002c0003t0014 | 5 | HG01167.hp2 HG01169.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1559G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1559 | chr15 | 51004221 | |||||
| chr15:51004364
|
A | G | 1 | a0002c0002t0017 | 2 | HG00741.hp1 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1702A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1702 | chr15 | 51004364 | |||||
| chr15:51004572
|
T | C | 1 | a0002c0006t0015 | 2 | HG02257.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1910T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1910 | chr15 | 51004572 | |||||
| chr15:51004765
|
A | T | 5 | a0001c0001t0005a0001c0001t0009a0001c0001t0029others(2): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2103A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 2103 | chr15 | 51004765 | |||||
| chr15:51004842
|
C | T | 1 | a0002c0002t0024 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2180C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 2180 | chr15 | 51004842 | |||||
| chr15:51004856
|
T | A | 1 | a0002c0003t0006 | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2194T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 2194 | chr15 | 51004856 | |||||
| chr15:51005097
|
G | A | 1 | a0002c0003t0022 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2435G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 2435 | chr15 | 51005097 | |||||
| chr15:51005166
|
G | A | 1 | a0001c0001t0008 | 4 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2504G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 2504 | chr15 | 51005166 | |||||
| chr15:51005389
|
G | A | 1 | a0001c0001t0025 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2727G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 2727 | chr15 | 51005389 | |||||
| chr15:51005693
|
T | G | 1 | a0002c0002t0016 | 2 | NA19012.hp2 NA19072.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3031T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 3031 | chr15 | 51005693 | |||||
| chr15:51005694
|
G | A | 1 | a0002c0002t0023 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3032G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 3032 | chr15 | 51005694 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:50908961
|
A | G | 40 | a0001c0001t0004g0349a0001c0001t0004g0350a0001c0001t0004g0351others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.150+33A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50908961 | ||||||
| chr15:50909084
|
A | G | 24 | a0001c0001t0004g0365a0001c0001t0004g0366a0001c0001t0004g0367others(21): Show | 24 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.150+156A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909084 | ||||||
| chr15:50909160
|
G | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.150+232G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909160 | ||||||
| chr15:50909167
|
C | T | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.150+239C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909167 | ||||||
| chr15:50909187
|
C | T | 1 | a0001c0001t0004g0388 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.150+259C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909187 | ||||||
| chr15:50909204
|
A | T | 1 | a0001c0001t0004g0364 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.150+276A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909204 | ||||||
| chr15:50909323
|
C | T | 2 | a0002c0003t0003g0193a0002c0003t0003g0194 | 2 | HG00735.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.150+395C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909323 | ||||||
| chr15:50909440
|
C | T | 9 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(6): Show | 9 | HG01167.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.150+512C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909440 | ||||||
| chr15:50909498
|
G | T | 4 | a0001c0001t0001g0343a0001c0001t0001g0344a0001c0001t0001g0345others(1): Show | 4 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+570G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909498 | ||||||
| chr15:50909583
|
A | C | 61 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(58): Show | 62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.150+655A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909583 | ||||||
| chr15:50909585
|
T | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.150+657T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909585 | ||||||
| chr15:50909710
|
C | T | 1 | a0002c0003t0003g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.150+782C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909710 | ||||||
| chr15:50909804
|
C | T | 1 | a0001c0001t0003g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.150+876C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909804 | ||||||
| chr15:50909843
|
G | A | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 198 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.150+915G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909843 | ||||||
| chr15:50909869
|
T | A | 2 | a0002c0002t0021g0006a0010c0008t0002g0005 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.150+941T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909869 | ||||||
| chr15:50909888
|
T | C | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.150+960T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909888 | ||||||
| chr15:50910032
|
G | T | 1 | a0002c0003t0003g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.150+1104G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910032 | ||||||
| chr15:50910140
|
C | G | 13 | a0001c0001t0005g0330a0001c0001t0005g0331a0001c0001t0005g0332others(10): Show | 13 | HG01109.hp1 HG01255.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.150+1212C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910140 | ||||||
| chr15:50910338
|
A | G | 2 | a0002c0002t0021g0006a0010c0008t0002g0005 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.150+1410A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910338 | ||||||
| chr15:50910346
|
A | G | 1 | a0002c0003t0003g0181 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.150+1418A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910346 | ||||||
| chr15:50910686
|
C | T | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 198 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.151-1392C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910686 | ||||||
| chr15:50910700
|
G | A | 1 | a0002c0003t0022g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.151-1378G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910700 | ||||||
| chr15:50910704
|
G | A | 1 | a0002c0003t0020g0008 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.151-1374G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910704 | ||||||
| chr15:50910974
|
A | G | 40 | a0001c0001t0004g0349a0001c0001t0004g0350a0001c0001t0004g0351others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.151-1104A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910974 | ||||||
| chr15:50911213
|
G | C | 1 | a0001c0001t0001g0195 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.151-865G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50911213 | ||||||
| chr15:50911264
|
G | A | 6 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(3): Show | 6 | HG01993.hp1 HG02074.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-814G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50911264 | ||||||
| chr15:50911431
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.151-647T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50911431 | ||||||
| chr15:50911479
|
A | AT | 11 | a0002c0002t0002g0120a0002c0002t0002g0121a0002c0002t0002g0122others(8): Show | 11 | HG01175.hp2 HG01192.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-577dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr15 | 50911479 | |||||
| chr15:50911479
|
AT | A | 50 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325others(47): Show | 50 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.151-577delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr15 | 50911479 | |||||
| chr15:50911479
|
ATT | A | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 187 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.151-578_151-577del others(2): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr15 | 50911479 | |||||
| chr15:50911479
|
ATTT | A | 6 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(3): Show | 6 | HG00408.hp1 HG01257.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-579_151-577del others(3): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr15 | 50911479 | |||||
| chr15:50911629
|
C | T | 1 | a0001c0001t0005g0322 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.151-449C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50911629 | ||||||
| chr15:50911666
|
C | CG | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 198 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.151-408dupG | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr15 | 50911666 | |||||
| chr15:50911773
|
C | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.151-305C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50911773 | ||||||
| chr15:50911936
|
C | T | 81 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(78): Show | 82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.151-142C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50911936 | ||||||
| chr15:50912167
|
G | A | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 198 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.222+18G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912167 | ||||||
| chr15:50912197
|
C | CT | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.222+48_222+49insT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912197 | ||||||
| chr15:50912223
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.222+74A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912223 | ||||||
| chr15:50912303
|
C | T | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.222+154C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912303 | ||||||
| chr15:50912358
|
G | A | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.222+209G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912358 | ||||||
| chr15:50912364
|
GTGA | G | 4 | a0001c0001t0005g0321a0001c0001t0009g0318a0001c0001t0009g0319others(1): Show | 4 | HG02622.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+223_222+225del others(3): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr15 | 50912364 | |||||
| chr15:50912472
|
A | T | 1 | a0005c0007t0011g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.222+323A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912472 | ||||||
| chr15:50912519
|
A | G | 9 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(6): Show | 9 | HG01167.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+370A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912519 | ||||||
| chr15:50912552
|
C | T | 287 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(284): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.222+403C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912552 | ||||||
| chr15:50912657
|
A | AT | 9 | a0002c0002t0002g0119a0002c0002t0002g0125a0002c0003t0003g0173others(6): Show | 9 | HG00408.hp2 HG00735.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+526dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr15 | 50912657 | |||||
| chr15:50912657
|
ATTTT | A | 9 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0295others(6): Show | 9 | HG01243.hp2 HG02148.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+523_222+526del others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr15 | 50912657 | |||||
| chr15:50912657
|
ATTTTT | A | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0195others(140): Show | 145 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.222+522_222+526del others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr15 | 50912657 | |||||
| chr15:50912657
|
ATTTTTT | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+521_222+526del others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr15 | 50912657 | |||||
| chr15:50912788
|
G | A | 2 | a0002c0003t0014g0017a0002c0003t0014g0018 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.222+639G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912788 | ||||||
| chr15:50912806
|
G | T | 1 | a0001c0001t0004g0387 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.222+657G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912806 | ||||||
| chr15:50912811
|
C | T | 2 | a0002c0003t0003g0171a0002c0003t0003g0172 | 2 | NA18946.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.222+662C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912811 | ||||||
| chr15:50912823
|
T | C | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+674T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912823 | ||||||
| chr15:50912988
|
A | G | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.222+839A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912988 | ||||||
| chr15:50913091
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.222+942A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50913091 | ||||||
| chr15:50913126
|
G | A | 2 | a0002c0002t0002g0035a0002c0002t0002g0036 | 2 | HG02135.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.222+977G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50913126 | ||||||
| chr15:50913913
|
A | G | 13 | a0002c0002t0002g0107a0002c0002t0002g0108a0002c0002t0002g0109others(10): Show | 13 | HG02071.hp2 HG02155.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.223-1535A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50913913 | ||||||
| chr15:50914107
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.223-1341A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914107 | ||||||
| chr15:50914170
|
T | G | 1 | a0010c0008t0002g0005 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.223-1278T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914170 | ||||||
| chr15:50914212
|
T | C | 60 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(57): Show | 61 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.223-1236T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914212 | ||||||
| chr15:50914303
|
T | C | 1 | a0001c0001t0004g0350 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.223-1145T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914303 | ||||||
| chr15:50914381
|
T | C | 1 | a0002c0002t0002g0037 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.223-1067T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914381 | ||||||
| chr15:50914448
|
T | G | 1 | a0002c0003t0003g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.223-1000T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914448 | ||||||
| chr15:50914512
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0004g0366 | 2 | HG04199.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.223-936G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914512 | ||||||
| chr15:50914637
|
C | T | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.223-811C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914637 | ||||||
| chr15:50914638
|
G | A | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.223-810G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914638 | ||||||
| chr15:50914650
|
CA | C | 7 | a0001c0001t0001g0214a0001c0001t0004g0367a0001c0001t0019g0215others(4): Show | 7 | HG01167.hp1 HG01256.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-777delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr15 | 50914650 | |||||
| chr15:50914650
|
CAA | C | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(274): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.223-778_223-777del others(2): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr15 | 50914650 | |||||
| chr15:50914885
|
C | T | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.223-563C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914885 | ||||||
| chr15:50914946
|
T | A | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-502T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914946 | ||||||
| chr15:50915008
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.223-440A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50915008 | ||||||
| chr15:50915070
|
A | C | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0195others(103): Show | 108 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.223-378A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50915070 | ||||||
| chr15:50915367
|
C | T | 1 | a0002c0003t0003g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.223-81C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50915367 | ||||||
| chr15:50915416
|
T | C | 1 | a0002c0003t0022g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.223-32T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50915416 | ||||||
| chr15:50915621
|
G | C | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.346+50G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50915621 | ||||||
| chr15:50915752
|
T | G | 1 | a0002c0003t0003g0174 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.346+181T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50915752 | ||||||
| chr15:50915786
|
G | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.346+215G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50915786 | ||||||
| chr15:50915800
|
G | A | 4 | a0001c0001t0005g0321a0001c0001t0009g0318a0001c0001t0009g0319others(1): Show | 4 | HG02622.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+229G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50915800 | ||||||
| chr15:50915807
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.346+236C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50915807 | ||||||
| chr15:50915892
|
C | G | 1 | a0002c0002t0002g0105 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.346+321C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50915892 | ||||||
| chr15:50916055
|
T | G | 1 | a0001c0001t0005g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.346+484T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916055 | ||||||
| chr15:50916195
|
G | T | 3 | a0002c0003t0010g0032a0002c0003t0010g0033a0002c0003t0010g0034 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.346+624G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916195 | ||||||
| chr15:50916237
|
C | T | 1 | a0002c0003t0003g0168 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.346+666C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916237 | ||||||
| chr15:50916276
|
G | C | 1 | a0001c0001t0004g0368 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.346+705G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916276 | ||||||
| chr15:50916371
|
G | T | 1 | a0001c0001t0005g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.346+800G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916371 | ||||||
| chr15:50916387
|
A | T | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.346+816A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916387 | ||||||
| chr15:50916537
|
G | T | 13 | a0002c0002t0002g0093a0002c0002t0002g0094a0002c0002t0002g0095others(10): Show | 13 | HG00438.hp2 NA18747.hp1 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.346+966G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916537 | ||||||
| chr15:50916551
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+980C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916551 | ||||||
| chr15:50916611
|
G | A | 14 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(11): Show | 14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+1040G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916611 | ||||||
| chr15:50916648
|
C | G | 13 | a0001c0001t0005g0330a0001c0001t0005g0331a0001c0001t0005g0332others(10): Show | 13 | HG01109.hp1 HG01255.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.346+1077C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916648 | ||||||
| chr15:50916751
|
A | G | 230 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(227): Show | 231 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.346+1180A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916751 | ||||||
| chr15:50916861
|
C | G | 1 | a0002c0003t0003g0181 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.346+1290C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916861 | ||||||
| chr15:50916861
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+1290C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916861 | ||||||
| chr15:50916896
|
C | G | 14 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(11): Show | 14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+1325C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916896 | ||||||
| chr15:50916985
|
A | G | 1 | a0006c0012t0001g0289 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.346+1414A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916985 | ||||||
| chr15:50917071
|
T | C | 14 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(11): Show | 14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+1500T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917071 | ||||||
| chr15:50917073
|
A | G | 1 | a0001c0001t0003g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.346+1502A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917073 | ||||||
| chr15:50917173
|
C | A | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+1602C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917173 | ||||||
| chr15:50917238
|
G | A | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.346+1667G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917238 | ||||||
| chr15:50917282
|
T | A | 1 | a0002c0003t0003g0126 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.346+1711T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917282 | ||||||
| chr15:50917374
|
G | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.346+1803G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917374 | ||||||
| chr15:50917388
|
G | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.346+1817G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917388 | ||||||
| chr15:50917442
|
T | C | 23 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0305others(20): Show | 23 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.346+1871T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917442 | ||||||
| chr15:50917477
|
A | G | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(287): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.346+1906A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917477 | ||||||
| chr15:50917496
|
C | A | 4 | a0001c0001t0005g0321a0001c0001t0009g0318a0001c0001t0009g0319others(1): Show | 4 | HG02622.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+1925C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917496 | ||||||
| chr15:50917536
|
CAG | C | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+1967_346+1968d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50917536 | |||||
| chr15:50917658
|
A | G | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 174 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.346+2087A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917658 | ||||||
| chr15:50917678
|
A | G | 1 | a0002c0002t0002g0091 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.346+2107A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917678 | ||||||
| chr15:50917718
|
C | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0323others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+2147C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917718 | ||||||
| chr15:50917777
|
G | A | 75 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(72): Show | 76 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.346+2206G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917777 | ||||||
| chr15:50917795
|
CAG | C | 6 | a0001c0001t0001g0217a0001c0001t0008g0218a0001c0001t0008g0219others(3): Show | 6 | HG01884.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+2226_346+2227d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50917795 | |||||
| chr15:50917851
|
G | A | 1 | a0001c0001t0001g0343 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.346+2280G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917851 | ||||||
| chr15:50917957
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.346+2386A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917957 | ||||||
| chr15:50917989
|
A | G | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 174 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.346+2418A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917989 | ||||||
| chr15:50918358
|
C | T | 3 | a0002c0003t0010g0032a0002c0003t0010g0033a0002c0003t0010g0034 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.346+2787C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918358 | ||||||
| chr15:50918366
|
T | G | 13 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(10): Show | 13 | HG01123.hp2 HG01433.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.346+2795T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918366 | ||||||
| chr15:50918388
|
C | G | 2 | a0002c0002t0002g0015a0002c0002t0002g0090 | 2 | HG03490.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.346+2817C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918388 | ||||||
| chr15:50918443
|
AGTAG | A | 4 | a0001c0001t0008g0218a0001c0001t0008g0219a0001c0001t0008g0220others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+2873_346+2876d others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918443 | ||||||
| chr15:50918444
|
G | A | 283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(280): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.346+2873G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918444 | ||||||
| chr15:50918452
|
T | A | 4 | a0001c0001t0008g0218a0001c0001t0008g0219a0001c0001t0008g0220others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+2881T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918452 | ||||||
| chr15:50918674
|
T | G | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.346+3103T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918674 | ||||||
| chr15:50918830
|
A | G | 1 | a0002c0003t0003g0031 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.346+3259A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918830 | ||||||
| chr15:50918913
|
T | G | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.346+3342T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918913 | ||||||
| chr15:50918934
|
T | A | 287 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(284): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.346+3363T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918934 | ||||||
| chr15:50918936
|
T | A | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 160 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.346+3365T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918936 | ||||||
| chr15:50918995
|
G | A | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.346+3424G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918995 | ||||||
| chr15:50919150
|
A | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.346+3579A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919150 | ||||||
| chr15:50919186
|
C | A | 1 | a0001c0001t0001g0222 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.346+3615C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919186 | ||||||
| chr15:50919301
|
G | C | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.346+3730G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919301 | ||||||
| chr15:50919535
|
A | AAAAT | 6 | a0002c0002t0002g0045a0002c0002t0002g0046a0002c0003t0003g0127others(3): Show | 6 | HG00609.hp1 HG03098.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+4003_346+4006d others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50919535 | |||||
| chr15:50919535
|
AAAAT | A | 92 | a0001c0001t0001g0217a0001c0001t0001g0226a0001c0001t0003g0307others(89): Show | 92 | HG00438.hp2 HG00639.hp2 HG01109.hp1 others(89): Show |
intron_variant | MODIFIER | c.346+4003_346+4006d others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50919535 | |||||
| chr15:50919535
|
AAAATAAA others(1): Show |
A | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0195others(103): Show | 108 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.346+3999_346+4006d others(10): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50919535 | |||||
| chr15:50919535
|
AAAATAAA others(5): Show |
A | 14 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(11): Show | 15 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.346+3995_346+4006d others(14): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50919535 | |||||
| chr15:50919535
|
AAAATAAA others(9): Show |
A | 7 | a0001c0001t0004g0380a0001c0001t0004g0381a0001c0001t0004g0382others(4): Show | 7 | HG00099.hp1 HG00323.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+3991_346+4006d others(18): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50919535 | |||||
| chr15:50919570
|
ATAAATAA others(1): Show |
A | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0027g0224 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.346+4007_346+4014d others(10): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50919570 | |||||
| chr15:50919685
|
C | G | 1 | a0002c0002t0002g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.346+4114C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919685 | ||||||
| chr15:50919719
|
C | T | 8 | a0001c0001t0001g0286a0002c0003t0006g0186a0002c0003t0006g0187others(5): Show | 8 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.346+4148C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919719 | ||||||
| chr15:50919812
|
A | G | 1 | a0002c0002t0002g0082 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.347-4119A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919812 | ||||||
| chr15:50919926
|
G | A | 230 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(227): Show | 231 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.347-4005G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919926 | ||||||
| chr15:50919980
|
G | T | 14 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(11): Show | 14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.347-3951G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919980 | ||||||
| chr15:50919999
|
C | T | 1 | a0002c0002t0002g0081 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.347-3932C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919999 | ||||||
| chr15:50920019
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-3912G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920019 | ||||||
| chr15:50920047
|
A | G | 5 | a0002c0003t0010g0032a0002c0003t0010g0033a0002c0003t0010g0034others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-3884A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920047 | ||||||
| chr15:50920050
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0283a0001c0001t0001g0284others(2): Show | 6 | NA18940.hp2 NA18941.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-3881C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920050 | ||||||
| chr15:50920075
|
T | TA | 7 | a0001c0001t0001g0203a0001c0001t0001g0227a0001c0001t0001g0228others(4): Show | 7 | HG01981.hp1 HG02738.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.347-3836dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50920075 | |||||
| chr15:50920075
|
T | TC | 4 | a0001c0001t0005g0330a0001c0001t0005g0331a0002c0003t0003g0135others(1): Show | 4 | HG01109.hp1 HG01255.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-3856_347-3855i others(3): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920075 | ||||||
| chr15:50920075
|
TA | T | 100 | a0001c0001t0001g0199a0002c0002t0002g0009a0002c0002t0002g0010others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.347-3836delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50920075 | |||||
| chr15:50920076
|
A | C | 127 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(124): Show | 128 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.347-3855A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920076 | ||||||
| chr15:50920077
|
A | C | 98 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(95): Show | 98 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.347-3854A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920077 | ||||||
| chr15:50920078
|
A | C | 1 | a0002c0002t0002g0092 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.347-3853A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920078 | ||||||
| chr15:50920109
|
C | CCTT | 79 | a0001c0001t0003g0328a0002c0002t0002g0080a0002c0002t0002g0082others(76): Show | 80 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.347-3821_347-3819d others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50920109 | |||||
| chr15:50920110
|
C | CT | 11 | a0001c0001t0001g0229a0001c0001t0001g0276a0001c0001t0001g0277others(8): Show | 11 | HG00140.hp2 HG01978.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.347-3800dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50920110 | |||||
| chr15:50920110
|
CT | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(43): Show | 47 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.347-3800delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50920110 | |||||
| chr15:50920111
|
T | TTC | 120 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(117): Show | 120 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.347-3819_347-3818i others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50920111 | |||||
| chr15:50920112
|
T | TC | 26 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(23): Show | 26 | HG01109.hp1 HG01167.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.347-3819_347-3818i others(3): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920112 | ||||||
| chr15:50920145
|
G | A | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.347-3786G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920145 | ||||||
| chr15:50920277
|
C | G | 1 | a0001c0001t0004g0366 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.347-3654C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920277 | ||||||
| chr15:50920338
|
C | T | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-3593C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920338 | ||||||
| chr15:50920415
|
C | CT | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0195others(105): Show | 110 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.347-3503dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50920415 | |||||
| chr15:50920964
|
G | A | 2 | a0002c0003t0014g0017a0002c0003t0014g0018 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.347-2967G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920964 | ||||||
| chr15:50921028
|
C | T | 2 | a0001c0001t0019g0215a0001c0001t0019g0230 | 2 | NA18986.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.347-2903C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921028 | ||||||
| chr15:50921080
|
G | A | 75 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(72): Show | 76 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.347-2851G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921080 | ||||||
| chr15:50921116
|
A | AT | 287 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(284): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.347-2807dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50921116 | |||||
| chr15:50921162
|
A | G | 4 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-2769A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921162 | ||||||
| chr15:50921183
|
T | A | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.347-2748T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921183 | ||||||
| chr15:50921321
|
T | G | 1 | a0002c0002t0002g0016 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.347-2610T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921321 | ||||||
| chr15:50921332
|
T | C | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-2599T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921332 | ||||||
| chr15:50921410
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-2521G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921410 | ||||||
| chr15:50921427
|
A | C | 287 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(284): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.347-2504A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921427 | ||||||
| chr15:50921598
|
G | C | 1 | a0002c0002t0002g0109 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.347-2333G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921598 | ||||||
| chr15:50921680
|
T | C | 38 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(35): Show | 38 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.347-2251T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921680 | ||||||
| chr15:50921705
|
A | G | 1 | a0002c0003t0003g0031 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.347-2226A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921705 | ||||||
| chr15:50921791
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-2140G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921791 | ||||||
| chr15:50922163
|
C | CA | 95 | a0001c0001t0001g0227a0001c0001t0001g0276a0001c0001t0001g0283others(92): Show | 96 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.347-1747dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50922163 | |||||
| chr15:50922163
|
C | CAA | 86 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(83): Show | 86 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.347-1748_347-1747d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50922163 | |||||
| chr15:50922163
|
C | CAAA | 15 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0002g0039others(12): Show | 15 | HG00423.hp1 HG02071.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.347-1749_347-1747d others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50922163 | |||||
| chr15:50922186
|
T | C | 100 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.347-1745T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922186 | ||||||
| chr15:50922191
|
C | T | 3 | a0002c0002t0002g0117a0002c0002t0002g0118a0002c0002t0016g0116 | 3 | NA18950.hp1 NA18971.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.347-1740C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922191 | ||||||
| chr15:50922338
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.347-1593C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922338 | ||||||
| chr15:50922361
|
G | A | 1 | a0002c0002t0002g0049 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.347-1570G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922361 | ||||||
| chr15:50922437
|
C | T | 1 | a0001c0001t0003g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.347-1494C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922437 | ||||||
| chr15:50922524
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.347-1407A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922524 | ||||||
| chr15:50922526
|
G | A | 282 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(279): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.347-1405G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922526 | ||||||
| chr15:50922729
|
T | C | 61 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(58): Show | 62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.347-1202T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922729 | ||||||
| chr15:50922782
|
C | CT | 96 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.347-1136dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50922782 | |||||
| chr15:50922793
|
T | C | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-1138T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922793 | ||||||
| chr15:50922880
|
C | A | 40 | a0001c0001t0004g0349a0001c0001t0004g0350a0001c0001t0004g0351others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.347-1051C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922880 | ||||||
| chr15:50922881
|
C | A | 1 | a0001c0001t0001g0232 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.347-1050C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922881 | ||||||
| chr15:50922978
|
C | T | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-953C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922978 | ||||||
| chr15:50923007
|
A | G | 192 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(189): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.347-924A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923007 | ||||||
| chr15:50923050
|
A | T | 230 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(227): Show | 231 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.347-881A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923050 | ||||||
| chr15:50923094
|
G | A | 2 | a0002c0002t0017g0054a0002c0002t0017g0055 | 2 | HG00741.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.347-837G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923094 | ||||||
| chr15:50923139
|
A | T | 1 | a0001c0001t0001g0271 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.347-792A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923139 | ||||||
| chr15:50923352
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-579G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923352 | ||||||
| chr15:50923461
|
C | T | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-470C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923461 | ||||||
| chr15:50923467
|
C | G | 281 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(278): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.347-464C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923467 | ||||||
| chr15:50923494
|
A | G | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-437A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923494 | ||||||
| chr15:50923537
|
GT | G | 9 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(6): Show | 9 | HG01167.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.347-386delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50923537 | |||||
| chr15:50923829
|
G | C | 1 | a0002c0002t0002g0040 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.347-102G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923829 | ||||||
| chr15:50924239
|
T | G | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.420+235T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50924239 | ||||||
| chr15:50924289
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.420+285G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50924289 | ||||||
| chr15:50924489
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.420+485A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50924489 | ||||||
| chr15:50924552
|
TAGAG | T | 3 | a0001c0001t0004g0349a0001c0001t0004g0351a0001c0001t0004g0352 | 3 | HG02976.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.421-538_421-535del others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | 50924552 | |||||
| chr15:50924623
|
C | T | 100 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.421-475C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50924623 | ||||||
| chr15:50924677
|
A | G | 1 | a0001c0001t0005g0331 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421-421A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50924677 | ||||||
| chr15:50924759
|
T | A | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.421-339T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50924759 | ||||||
| chr15:50924899
|
CTTTA | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.421-195_421-192del others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | 50924899 | |||||
| chr15:50924929
|
A | C | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.421-169A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50924929 | ||||||
| chr15:50925045
|
T | A | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.421-53T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50925045 | ||||||
| chr15:50925078
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0233 | 2 | NA18942.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.421-20T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50925078 | ||||||
| chr15:50925230
|
T | G | 3 | a0002c0003t0006g0188a0002c0003t0006g0189a0002c0003t0006g0192 | 3 | HG02109.hp1 HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.542+11T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50925230 | ||||||
| chr15:50925267
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.542+48C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50925267 | ||||||
| chr15:50925278
|
G | A | 230 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(227): Show | 231 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.542+59G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50925278 | ||||||
| chr15:50925477
|
A | G | 61 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(58): Show | 62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.542+258A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50925477 | ||||||
| chr15:50925632
|
C | CT | 70 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0292others(67): Show | 71 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.542+428dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50925632 | |||||
| chr15:50925632
|
C | CTT | 100 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.542+427_542+428dup others(2): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50925632 | |||||
| chr15:50925796
|
AT | A | 185 | a0001c0001t0001g0223a0001c0001t0001g0228a0002c0002t0002g0009others(182): Show | 186 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.542+594delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50925796 | |||||
| chr15:50925877
|
G | A | 1 | a0002c0003t0003g0164 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.542+658G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50925877 | ||||||
| chr15:50925926
|
G | C | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.542+707G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50925926 | ||||||
| chr15:50925933
|
T | A | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.542+714T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50925933 | ||||||
| chr15:50926065
|
T | G | 38 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(35): Show | 38 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.542+846T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926065 | ||||||
| chr15:50926206
|
C | T | 23 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0305others(20): Show | 23 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.542+987C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926206 | ||||||
| chr15:50926207
|
G | A | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+988G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926207 | ||||||
| chr15:50926347
|
C | T | 10 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0305others(7): Show | 10 | HG01496.hp1 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.542+1128C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926347 | ||||||
| chr15:50926428
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.542+1209G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926428 | ||||||
| chr15:50926603
|
T | A | 8 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(5): Show | 8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.542+1384T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926603 | ||||||
| chr15:50926648
|
G | T | 2 | a0002c0002t0002g0079a0002c0002t0002g0083 | 2 | HG01070.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.542+1429G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926648 | ||||||
| chr15:50926940
|
A | T | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+1721A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926940 | ||||||
| chr15:50926993
|
T | A | 1 | a0001c0001t0001g0325 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.542+1774T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926993 | ||||||
| chr15:50927045
|
A | G | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+1826A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50927045 | ||||||
| chr15:50927087
|
T | C | 63 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(60): Show | 64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.542+1868T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50927087 | ||||||
| chr15:50927096
|
A | C | 230 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(227): Show | 231 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.542+1877A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50927096 | ||||||
| chr15:50927285
|
TATGGCCA others(6): Show |
T | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.543-1723_543-1711d others(15): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50927285 | ||||||
| chr15:50927516
|
G | GT | 105 | a0001c0001t0001g0200a0001c0001t0001g0282a0001c0001t0009g0318others(102): Show | 105 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.543-1477dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50927516 | |||||
| chr15:50927516
|
G | GTT | 121 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(118): Show | 122 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.543-1478_543-1477d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50927516 | |||||
| chr15:50927671
|
C | CT | 14 | a0001c0001t0001g0217a0001c0001t0008g0218a0001c0001t0008g0219others(11): Show | 14 | HG01167.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.543-1327dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50927671 | |||||
| chr15:50927765
|
G | A | 57 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0129others(54): Show | 58 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.543-1244G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50927765 | ||||||
| chr15:50927890
|
T | C | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.543-1119T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50927890 | ||||||
| chr15:50927937
|
A | ATTTGCAG others(7): Show |
1 | a0002c0003t0003g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.543-1071_543-1070i others(16): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50927937 | |||||
| chr15:50928114
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.543-895C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928114 | ||||||
| chr15:50928186
|
C | A | 1 | a0001c0001t0001g0234 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.543-823C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928186 | ||||||
| chr15:50928193
|
A | G | 192 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(189): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.543-816A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928193 | ||||||
| chr15:50928230
|
A | T | 25 | a0001c0001t0001g0270a0001c0001t0005g0301a0001c0001t0005g0302others(22): Show | 25 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.543-779A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928230 | ||||||
| chr15:50928390
|
C | T | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.543-619C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928390 | ||||||
| chr15:50928402
|
C | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.543-607C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928402 | ||||||
| chr15:50928566
|
G | T | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.543-443G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928566 | ||||||
| chr15:50928571
|
A | T | 1 | a0001c0001t0004g0379 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.543-438A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928571 | ||||||
| chr15:50928714
|
GT | G | 119 | a0001c0001t0001g0228a0001c0001t0004g0349a0001c0001t0004g0380others(116): Show | 119 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.543-282delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50928714 | |||||
| chr15:50928714
|
GTT | G | 81 | a0001c0001t0001g0217a0001c0001t0008g0218a0001c0001t0008g0219others(78): Show | 82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.543-283_543-282del others(2): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50928714 | |||||
| chr15:50928792
|
G | A | 81 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(78): Show | 82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.543-217G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928792 | ||||||
| chr15:50928813
|
C | T | 1 | a0001c0001t0019g0230 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.543-196C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928813 | ||||||
| chr15:50929392
|
A | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0324 | 2 | HG01261.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.702+224A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50929392 | ||||||
| chr15:50929404
|
A | G | 11 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(8): Show | 11 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.702+236A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50929404 | ||||||
| chr15:50929526
|
G | A | 8 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(5): Show | 8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.702+358G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50929526 | ||||||
| chr15:50929711
|
T | C | 2 | a0002c0002t0002g0035a0002c0002t0002g0036 | 2 | HG02135.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.702+543T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50929711 | ||||||
| chr15:50929742
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.702+574A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50929742 | ||||||
| chr15:50929861
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.702+693G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50929861 | ||||||
| chr15:50929940
|
G | T | 1 | a0001c0001t0005g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.702+772G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50929940 | ||||||
| chr15:50930035
|
A | G | 8 | a0002c0002t0002g0093a0002c0002t0002g0098a0002c0002t0002g0099others(5): Show | 8 | HG00438.hp2 NA18747.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.703-770A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50930035 | ||||||
| chr15:50930264
|
A | ACCATGTT others(356): Show |
4 | a0001c0001t0001g0004a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 5 | NA18941.hp1 NA18960.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.703-519_703-518ins others(363): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930264
|
A | ACCATGTT others(357): Show |
1 | a0001c0001t0001g0285 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.703-519_703-518ins others(364): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930264
|
A | ACCATGTT others(344): Show |
6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-519_703-518ins others(351): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930264
|
A | ACCATGTT others(350): Show |
1 | a0005c0007t0011g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.703-519_703-518ins others(357): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930264
|
A | ACCATGTT others(351): Show |
1 | a0005c0007t0011g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.703-519_703-518ins others(358): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930264
|
A | ACCATGTT others(352): Show |
1 | a0002c0006t0015g0347 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.703-519_703-518ins others(359): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930264
|
A | ACCATGTT others(353): Show |
1 | a0002c0006t0015g0348 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.703-519_703-518ins others(360): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930264
|
A | ACCATGTT others(354): Show |
2 | a0002c0003t0003g0142a0002c0003t0003g0175 | 2 | HG00408.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.703-519_703-518ins others(361): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930264
|
A | ACCATGTT others(355): Show |
209 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.703-519_703-518ins others(362): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930264
|
A | ACCATGTT others(356): Show |
130 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0196others(127): Show | 131 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.703-519_703-518ins others(363): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930264
|
A | ACCATGTT others(356): Show |
1 | a0001c0001t0001g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.703-519_703-518ins others(363): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930264
|
A | ACCATGTT others(357): Show |
24 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(21): Show | 24 | HG00609.hp2 HG01261.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.703-519_703-518ins others(364): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930264
|
A | ACCATGTT others(357): Show |
1 | a0002c0003t0006g0186 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.703-519_703-518ins others(364): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930264
|
A | ACCATGTT others(358): Show |
2 | a0001c0001t0001g0228a0001c0001t0001g0266 | 2 | HG03942.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.703-519_703-518ins others(365): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930264
|
A | ACCATGTT others(359): Show |
3 | a0001c0001t0001g0229a0001c0001t0001g0281a0001c0001t0001g0299 | 3 | HG01981.hp1 HG02293.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.703-519_703-518ins others(366): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | |||||
| chr15:50930309
|
C | T | 2 | a0002c0003t0003g0029a0002c0003t0003g0030 | 2 | HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.703-496C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50930309 | ||||||
| chr15:50930347
|
G | A | 1 | a0002c0003t0003g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.703-458G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50930347 | ||||||
| chr15:50930674
|
G | C | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.703-131G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50930674 | ||||||
| chr15:50930770
|
G | A | 1 | a0002c0003t0003g0171 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.703-35G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50930770 | ||||||
| chr15:50931046
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.869+75T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931046 | ||||||
| chr15:50931179
|
C | A | 1 | a0002c0003t0006g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.869+208C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931179 | ||||||
| chr15:50931180
|
A | T | 1 | a0002c0003t0006g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.869+209A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931180 | ||||||
| chr15:50931252
|
C | G | 61 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(58): Show | 62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.869+281C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931252 | ||||||
| chr15:50931324
|
C | CT | 387 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(384): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.869+355dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr15 | 50931324 | |||||
| chr15:50931363
|
T | G | 1 | a0001c0001t0004g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.869+392T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931363 | ||||||
| chr15:50931425
|
G | A | 13 | a0001c0001t0005g0330a0001c0001t0005g0331a0001c0001t0005g0332others(10): Show | 13 | HG01109.hp1 HG01255.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.869+454G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931425 | ||||||
| chr15:50931436
|
C | T | 1 | a0005c0007t0011g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.869+465C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931436 | ||||||
| chr15:50931524
|
C | T | 1 | a0002c0003t0010g0032 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.869+553C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931524 | ||||||
| chr15:50931560
|
T | C | 6 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(3): Show | 6 | HG01993.hp1 HG02074.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.869+589T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931560 | ||||||
| chr15:50931732
|
G | A | 280 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(277): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.869+761G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931732 | ||||||
| chr15:50932072
|
C | T | 2 | a0002c0003t0014g0017a0002c0003t0014g0018 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.869+1101C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932072 | ||||||
| chr15:50932140
|
C | T | 1 | a0002c0003t0001g0071 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.869+1169C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932140 | ||||||
| chr15:50932235
|
T | C | 1 | a0002c0003t0003g0158 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.869+1264T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932235 | ||||||
| chr15:50932268
|
C | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.869+1297C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932268 | ||||||
| chr15:50932269
|
G | A | 1 | a0001c0001t0004g0358 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.869+1298G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932269 | ||||||
| chr15:50932290
|
T | C | 3 | a0001c0001t0003g0310a0001c0001t0003g0311a0001c0001t0003g0312 | 3 | HG01516.hp1 NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.869+1319T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932290 | ||||||
| chr15:50932366
|
A | T | 1 | a0001c0001t0001g0257 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.869+1395A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932366 | ||||||
| chr15:50932417
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0323others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.869+1446G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932417 | ||||||
| chr15:50932445
|
A | G | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.869+1474A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932445 | ||||||
| chr15:50932472
|
G | A | 5 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0305others(2): Show | 5 | HG01496.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.869+1501G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932472 | ||||||
| chr15:50932484
|
A | G | 1 | a0001c0001t0005g0321 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.869+1513A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932484 | ||||||
| chr15:50932699
|
G | T | 192 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(189): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.869+1728G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932699 | ||||||
| chr15:50932824
|
A | G | 100 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.870-1800A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932824 | ||||||
| chr15:50932929
|
C | T | 61 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(58): Show | 62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.870-1695C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932929 | ||||||
| chr15:50932950
|
C | A | 4 | a0002c0003t0003g0143a0002c0003t0003g0173a0002c0003t0003g0178others(1): Show | 4 | HG02027.hp2 NA18964.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-1674C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932950 | ||||||
| chr15:50933219
|
A | G | 14 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(11): Show | 14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.870-1405A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933219 | ||||||
| chr15:50933486
|
T | C | 100 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.870-1138T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933486 | ||||||
| chr15:50933560
|
A | G | 14 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(11): Show | 14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.870-1064A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933560 | ||||||
| chr15:50933571
|
T | A | 38 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(35): Show | 38 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.870-1053T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933571 | ||||||
| chr15:50933572
|
T | G | 1 | a0001c0001t0001g0271 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.870-1052T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933572 | ||||||
| chr15:50933573
|
T | A | 2 | a0002c0002t0021g0006a0010c0008t0002g0005 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.870-1051T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933573 | ||||||
| chr15:50933578
|
T | G | 34 | a0001c0001t0001g0226a0001c0001t0001g0236a0001c0001t0001g0237others(31): Show | 34 | HG00423.hp2 HG00621.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.870-1046T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933578 | ||||||
| chr15:50933628
|
A | G | 199 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(196): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.870-996A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933628 | ||||||
| chr15:50933652
|
G | A | 3 | a0004c0005t0001g0235a0004c0005t0001g0238a0004c0005t0001g0239 | 3 | NA18944.hp2 NA18962.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.870-972G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933652 | ||||||
| chr15:50933902
|
A | G | 214 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0254others(211): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.870-722A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933902 | ||||||
| chr15:50934038
|
T | C | 38 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(35): Show | 38 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.870-586T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50934038 | ||||||
| chr15:50934070
|
TAC | T | 5 | a0001c0001t0001g0253a0001c0001t0001g0265a0001c0001t0001g0267others(2): Show | 5 | HG01261.hp2 NA19001.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.870-553_870-552del others(2): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50934070 | ||||||
| chr15:50934285
|
A | G | 4 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-339A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50934285 | ||||||
| chr15:50934390
|
G | A | 1 | a0002c0003t0003g0031 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.870-234G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50934390 | ||||||
| chr15:50934415
|
G | T | 1 | a0001c0001t0001g0267 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.870-209G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50934415 | ||||||
| chr15:50935024
|
C | T | 1 | a0001c0001t0004g0388 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.943+327C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50935024 | ||||||
| chr15:50935055
|
A | G | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.943+358A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50935055 | ||||||
| chr15:50935276
|
A | G | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.943+579A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50935276 | ||||||
| chr15:50935363
|
A | AGAGACAA others(2075): Show |
1 | a0002c0003t0006g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.943+682_943+683ins others(2082): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr15 | 50935363 | |||||
| chr15:50935363
|
A | AGAGACAA others(2075): Show |
5 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(2): Show | 5 | HG01167.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+682_943+683ins others(2082): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr15 | 50935363 | |||||
| chr15:50935363
|
A | AGAGACAA others(2076): Show |
1 | a0002c0003t0006g0189 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.943+682_943+683ins others(2083): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr15 | 50935363 | |||||
| chr15:50935940
|
T | C | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.943+1243T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50935940 | ||||||
| chr15:50936255
|
A | C | 109 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(106): Show | 109 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.943+1558A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936255 | ||||||
| chr15:50936303
|
G | A | 6 | a0001c0001t0001g0217a0001c0001t0008g0218a0001c0001t0008g0219others(3): Show | 6 | HG01884.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.943+1606G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936303 | ||||||
| chr15:50936311
|
T | A | 1 | a0001c0001t0001g0271 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.943+1614T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936311 | ||||||
| chr15:50936337
|
T | G | 1 | a0001c0001t0001g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.943+1640T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936337 | ||||||
| chr15:50936504
|
A | G | 3 | a0001c0001t0001g0256a0001c0001t0001g0263a0001c0001t0001g0264 | 3 | HG00609.hp2 NA18961.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.943+1807A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936504 | ||||||
| chr15:50936511
|
C | G | 1 | a0001c0001t0004g0357 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.943+1814C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936511 | ||||||
| chr15:50936636
|
C | G | 1 | a0001c0001t0004g0365 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.943+1939C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936636 | ||||||
| chr15:50936739
|
A | C | 1 | a0001c0001t0001g0252 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.943+2042A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936739 | ||||||
| chr15:50936896
|
T | C | 1 | a0002c0002t0002g0098 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.943+2199T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936896 | ||||||
| chr15:50936939
|
CA | C | 25 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(22): Show | 25 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.943+2254delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr15 | 50936939 | |||||
| chr15:50936956
|
T | A | 1 | a0002c0002t0012g0112 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.943+2259T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936956 | ||||||
| chr15:50936980
|
C | G | 281 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(278): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.943+2283C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936980 | ||||||
| chr15:50937284
|
T | C | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.943+2587T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50937284 | ||||||
| chr15:50937611
|
G | A | 60 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(57): Show | 61 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.943+2914G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50937611 | ||||||
| chr15:50937826
|
G | C | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.943+3129G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50937826 | ||||||
| chr15:50937919
|
G | A | 3 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0277 | 3 | HG01952.hp1 HG01978.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.943+3222G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50937919 | ||||||
| chr15:50938106
|
A | G | 1 | a0002c0002t0021g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.944-3336A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938106 | ||||||
| chr15:50938358
|
T | G | 231 | a0001c0001t0001g0259a0001c0001t0003g0307a0001c0001t0003g0308others(228): Show | 232 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.944-3084T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938358 | ||||||
| chr15:50938577
|
T | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2865T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938577 | ||||||
| chr15:50938579
|
T | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2863T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938579 | ||||||
| chr15:50938582
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2860A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938582 | ||||||
| chr15:50938584
|
T | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2858T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938584 | ||||||
| chr15:50938585
|
T | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2857T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938585 | ||||||
| chr15:50938586
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2856T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938586 | ||||||
| chr15:50938589
|
C | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2853C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938589 | ||||||
| chr15:50938591
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2851A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938591 | ||||||
| chr15:50938592
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2850T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938592 | ||||||
| chr15:50938596
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2846G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938596 | ||||||
| chr15:50938598
|
AGTAGGGA others(15): Show |
A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2843_944-2822d others(24): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938598 | ||||||
| chr15:50938626
|
T | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2816T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938626 | ||||||
| chr15:50938632
|
T | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2810T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938632 | ||||||
| chr15:50938637
|
A | C | 101 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(98): Show | 101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.944-2805A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938637 | ||||||
| chr15:50938640
|
G | T | 1 | a0001c0001t0004g0362 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.944-2802G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938640 | ||||||
| chr15:50938643
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.944-2799C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938643 | ||||||
| chr15:50938644
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2798G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938644 | ||||||
| chr15:50938653
|
G | GATCACCT others(8): Show |
1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2789_944-2788i others(17): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938653 | ||||||
| chr15:50938655
|
T | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2787T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938655 | ||||||
| chr15:50938659
|
A | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2783A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938659 | ||||||
| chr15:50938664
|
A | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2778A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938664 | ||||||
| chr15:50938672
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2770T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938672 | ||||||
| chr15:50938674
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2768G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938674 | ||||||
| chr15:50938677
|
A | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2765A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938677 | ||||||
| chr15:50938681
|
A | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2761A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938681 | ||||||
| chr15:50938682
|
G | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2760G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938682 | ||||||
| chr15:50938683
|
A | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2759A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938683 | ||||||
| chr15:50938687
|
T | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2755T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938687 | ||||||
| chr15:50938688
|
C | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2754C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938688 | ||||||
| chr15:50938689
|
C | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2753C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938689 | ||||||
| chr15:50938691
|
C | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2751C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938691 | ||||||
| chr15:50938693
|
C | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2749C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938693 | ||||||
| chr15:50938694
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2748C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938694 | ||||||
| chr15:50938695
|
T | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2747T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938695 | ||||||
| chr15:50938696
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2746G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938696 | ||||||
| chr15:50938699
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2743C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938699 | ||||||
| chr15:50938704
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2738A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938704 | ||||||
| chr15:50938705
|
T | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2737T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938705 | ||||||
| chr15:50938706
|
A | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2736A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938706 | ||||||
| chr15:50938707
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2735A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938707 | ||||||
| chr15:50938710
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2732A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938710 | ||||||
| chr15:50938711
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2731G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938711 | ||||||
| chr15:50938712
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.944-2730G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938712 | ||||||
| chr15:50938713
|
C | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2729C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938713 | ||||||
| chr15:50938714
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2728C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938714 | ||||||
| chr15:50938717
|
T | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2725T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938717 | ||||||
| chr15:50938719
|
C | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2723C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938719 | ||||||
| chr15:50938721
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2721T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938721 | ||||||
| chr15:50938722
|
C | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2720C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938722 | ||||||
| chr15:50938723
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2719A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938723 | ||||||
| chr15:50938728
|
G | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2714G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938728 | ||||||
| chr15:50938729
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2713T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938729 | ||||||
| chr15:50938734
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2708G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938734 | ||||||
| chr15:50938768
|
T | C | 14 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(11): Show | 14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.944-2674T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938768 | ||||||
| chr15:50939195
|
G | A | 1 | a0001c0001t0003g0327 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.944-2247G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939195 | ||||||
| chr15:50939337
|
A | G | 192 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(189): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.944-2105A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939337 | ||||||
| chr15:50939339
|
G | A | 1 | a0002c0003t0003g0166 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.944-2103G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939339 | ||||||
| chr15:50939351
|
T | C | 190 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(187): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.944-2091T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939351 | ||||||
| chr15:50939416
|
A | C | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.944-2026A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939416 | ||||||
| chr15:50939420
|
C | T | 5 | a0002c0002t0002g0107a0002c0002t0002g0108a0002c0002t0002g0109others(2): Show | 5 | HG02155.hp1 NA18941.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.944-2022C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939420 | ||||||
| chr15:50939659
|
T | C | 2 | a0002c0002t0002g0079a0002c0003t0003g0144 | 2 | HG01070.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.944-1783T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939659 | ||||||
| chr15:50939792
|
A | G | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.944-1650A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939792 | ||||||
| chr15:50939854
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.944-1588G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939854 | ||||||
| chr15:50939939
|
G | A | 2 | a0002c0003t0014g0017a0002c0003t0014g0018 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.944-1503G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939939 | ||||||
| chr15:50940005
|
G | T | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.944-1437G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50940005 | ||||||
| chr15:50940129
|
T | C | 230 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(227): Show | 231 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.944-1313T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50940129 | ||||||
| chr15:50940359
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.944-1083T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50940359 | ||||||
| chr15:50940947
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.944-495A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50940947 | ||||||
| chr15:50940980
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.944-462C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50940980 | ||||||
| chr15:50941116
|
T | C | 1 | a0002c0002t0002g0016 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.944-326T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50941116 | ||||||
| chr15:50941234
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0323others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-208A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50941234 | ||||||
| chr15:50941615
|
T | C | 100 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1066+51T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 9/20 | chr15 | 50941615 | ||||||
| chr15:50941625
|
T | C | 1 | a0002c0003t0003g0174 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1067-41T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 9/20 | chr15 | 50941625 | ||||||
| chr15:50941650
|
G | A | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1067-16G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 9/20 | chr15 | 50941650 | ||||||
| chr15:50941893
|
T | C | 2 | a0002c0002t0002g0014a0002c0002t0002g0091 | 2 | NA19060.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1176+118T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50941893 | ||||||
| chr15:50941981
|
A | G | 190 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(187): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1176+206A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50941981 | ||||||
| chr15:50942012
|
G | T | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1176+237G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50942012 | ||||||
| chr15:50942398
|
A | G | 38 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(35): Show | 38 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.1176+623A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50942398 | ||||||
| chr15:50942475
|
T | A | 1 | a0002c0003t0003g0025 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1176+700T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50942475 | ||||||
| chr15:50942750
|
A | G | 1 | a0001c0001t0001g0252 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1176+975A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50942750 | ||||||
| chr15:50943003
|
T | C | 1 | a0001c0001t0003g0313 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1176+1228T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50943003 | ||||||
| chr15:50943012
|
G | A | 1 | a0001c0001t0005g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1176+1237G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50943012 | ||||||
| chr15:50943272
|
A | G | 100 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1176+1497A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50943272 | ||||||
| chr15:50943638
|
C | T | 3 | a0001c0001t0001g0344a0001c0001t0001g0345a0001c0001t0001g0346 | 3 | HG00140.hp2 HG01099.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1176+1863C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50943638 | ||||||
| chr15:50943835
|
T | C | 3 | a0002c0002t0002g0072a0002c0002t0002g0080a0002c0002t0002g0121 | 3 | NA18980.hp2 NA18981.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1176+2060T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50943835 | ||||||
| chr15:50944107
|
C | T | 216 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(213): Show | 217 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.1176+2332C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944107 | ||||||
| chr15:50944155
|
G | A | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1176+2380G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944155 | ||||||
| chr15:50944212
|
A | G | 1 | a0001c0001t0005g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1176+2437A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944212 | ||||||
| chr15:50944223
|
C | T | 1 | a0002c0003t0003g0165 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1176+2448C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944223 | ||||||
| chr15:50944318
|
A | G | 1 | a0001c0001t0004g0365 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1176+2543A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944318 | ||||||
| chr15:50944511
|
A | G | 5 | a0001c0001t0001g0217a0001c0001t0008g0218a0001c0001t0008g0219others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1176+2736A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944511 | ||||||
| chr15:50944562
|
G | C | 1 | a0002c0003t0003g0145 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1176+2787G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944562 | ||||||
| chr15:50944586
|
TA | T | 192 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(189): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1176+2823delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr15 | 50944586 | |||||
| chr15:50944640
|
C | T | 109 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(106): Show | 109 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1176+2865C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944640 | ||||||
| chr15:50944641
|
C | T | 100 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1176+2866C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944641 | ||||||
| chr15:50944724
|
C | T | 1 | a0001c0001t0003g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1176+2949C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944724 | ||||||
| chr15:50944846
|
G | T | 1 | a0001c0001t0004g0356 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1176+3071G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944846 | ||||||
| chr15:50944974
|
T | C | 2 | a0002c0002t0021g0006a0010c0008t0002g0005 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1177-3046T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944974 | ||||||
| chr15:50945007
|
G | A | 1 | a0002c0002t0002g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1177-3013G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945007 | ||||||
| chr15:50945013
|
A | T | 1 | a0002c0002t0024g0047 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1177-3007A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945013 | ||||||
| chr15:50945045
|
G | T | 2 | a0002c0003t0003g0138a0002c0003t0003g0139 | 2 | HG00733.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1177-2975G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945045 | ||||||
| chr15:50945152
|
T | C | 61 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(58): Show | 62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1177-2868T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945152 | ||||||
| chr15:50945285
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1177-2735A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945285 | ||||||
| chr15:50945522
|
C | T | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1177-2498C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945522 | ||||||
| chr15:50945660
|
C | G | 192 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(189): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1177-2360C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945660 | ||||||
| chr15:50945713
|
T | C | 40 | a0001c0001t0004g0349a0001c0001t0004g0350a0001c0001t0004g0351others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1177-2307T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945713 | ||||||
| chr15:50945833
|
C | T | 2 | a0002c0003t0003g0136a0002c0003t0003g0157 | 2 | NA18978.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1177-2187C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945833 | ||||||
| chr15:50945863
|
A | G | 100 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1177-2157A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945863 | ||||||
| chr15:50945898
|
G | A | 100 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1177-2122G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945898 | ||||||
| chr15:50945978
|
T | C | 230 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(227): Show | 231 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1177-2042T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945978 | ||||||
| chr15:50946028
|
A | G | 1 | a0002c0002t0021g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1177-1992A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946028 | ||||||
| chr15:50946154
|
A | C | 3 | a0002c0003t0006g0188a0002c0003t0006g0189a0002c0003t0006g0192 | 3 | HG02109.hp1 HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1177-1866A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946154 | ||||||
| chr15:50946285
|
A | G | 2 | a0002c0002t0002g0013a0002c0002t0002g0070 | 2 | NA18942.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1177-1735A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946285 | ||||||
| chr15:50946497
|
T | C | 3 | a0001c0001t0003g0313a0002c0006t0015g0347a0002c0006t0015g0348 | 3 | HG01433.hp1 HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1177-1523T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946497 | ||||||
| chr15:50946559
|
C | T | 3 | a0001c0001t0004g0377a0001c0001t0004g0379a0001c0001t0004g0387 | 3 | HG02602.hp2 HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1177-1461C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946559 | ||||||
| chr15:50946560
|
G | A | 2 | a0002c0002t0021g0006a0010c0008t0002g0005 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1177-1460G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946560 | ||||||
| chr15:50946563
|
GA | G | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1177-1447delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr15 | 50946563 | |||||
| chr15:50946607
|
T | A | 1 | a0001c0001t0001g0195 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1177-1413T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946607 | ||||||
| chr15:50946712
|
A | G | 2 | a0002c0003t0014g0017a0002c0003t0014g0018 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1177-1308A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946712 | ||||||
| chr15:50946758
|
A | T | 100 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1177-1262A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946758 | ||||||
| chr15:50946787
|
G | A | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1177-1233G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946787 | ||||||
| chr15:50946882
|
C | T | 3 | a0001c0001t0001g0256a0001c0001t0001g0263a0001c0001t0001g0264 | 3 | HG00609.hp2 NA18961.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1177-1138C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946882 | ||||||
| chr15:50946894
|
T | G | 192 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(189): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1177-1126T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946894 | ||||||
| chr15:50946896
|
C | T | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1177-1124C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946896 | ||||||
| chr15:50946968
|
C | T | 192 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(189): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1177-1052C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946968 | ||||||
| chr15:50947107
|
G | A | 4 | a0002c0002t0002g0107a0002c0002t0002g0108a0002c0002t0002g0109others(1): Show | 4 | NA18941.hp2 NA18962.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177-913G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50947107 | ||||||
| chr15:50947151
|
C | T | 1 | a0002c0002t0002g0075 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1177-869C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50947151 | ||||||
| chr15:50947193
|
A | G | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1177-827A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50947193 | ||||||
| chr15:50947323
|
G | A | 100 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1177-697G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50947323 | ||||||
| chr15:50947415
|
CA | C | 113 | a0001c0001t0001g0275a0001c0001t0001g0326a0001c0001t0003g0307others(110): Show | 113 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1177-586delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr15 | 50947415 | |||||
| chr15:50947415
|
CAA | C | 78 | a0002c0002t0002g0043a0002c0002t0002g0069a0002c0002t0002g0108others(75): Show | 79 | HG00099.hp2 HG00408.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1177-587_1177-586d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr15 | 50947415 | |||||
| chr15:50947494
|
T | G | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1177-526T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50947494 | ||||||
| chr15:50947550
|
C | G | 1 | a0002c0002t0021g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1177-470C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50947550 | ||||||
| chr15:50947838
|
C | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1177-182C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50947838 | ||||||
| chr15:50948011
|
T | C | 1 | a0002c0003t0020g0008 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1177-9T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50948011 | ||||||
| chr15:50948016
|
A | G | 1 | a0002c0002t0002g0053 | 1 | NA19002.hp1 | splice_region_variant&intron_variant | LOW | c.1177-4A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50948016 | ||||||
| chr15:50948201
|
ATGCAGTG others(4): Show |
A | 100 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1316+44_1316+54del others(11): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr15 | 50948201 | |||||
| chr15:50948249
|
G | A | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1316+90G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948249 | ||||||
| chr15:50948339
|
C | CTTT | 10 | a0001c0001t0003g0307a0001c0001t0003g0309a0001c0001t0003g0310others(7): Show | 10 | HG01516.hp1 HG02293.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1316+196_1316+198d others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr15 | 50948339 | |||||
| chr15:50948339
|
CT | C | 163 | a0001c0001t0001g0257a0002c0002t0002g0009a0002c0002t0002g0010others(160): Show | 164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1316+198delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr15 | 50948339 | |||||
| chr15:50948339
|
CTT | C | 17 | a0002c0002t0002g0015a0002c0003t0003g0137a0002c0003t0003g0170others(14): Show | 17 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1316+197_1316+198d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr15 | 50948339 | |||||
| chr15:50948339
|
CTTT | C | 8 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(5): Show | 8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1316+196_1316+198d others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr15 | 50948339 | |||||
| chr15:50948503
|
G | A | 190 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(187): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1316+344G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948503 | ||||||
| chr15:50948597
|
A | C | 1 | a0002c0002t0021g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1316+438A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948597 | ||||||
| chr15:50948675
|
A | G | 1 | a0002c0003t0003g0163 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1316+516A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948675 | ||||||
| chr15:50948723
|
A | G | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1316+564A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948723 | ||||||
| chr15:50948823
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1316+664T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948823 | ||||||
| chr15:50948840
|
C | T | 1 | a0002c0003t0003g0156 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1316+681C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948840 | ||||||
| chr15:50948894
|
A | C | 231 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(228): Show | 232 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.1316+735A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948894 | ||||||
| chr15:50948972
|
CA | C | 12 | a0001c0001t0001g0233a0001c0001t0001g0237a0001c0001t0005g0335others(9): Show | 12 | HG01257.hp2 HG02145.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1316+829delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr15 | 50948972 | |||||
| chr15:50948986
|
A | G | 8 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(5): Show | 8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1316+827A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948986 | ||||||
| chr15:50949067
|
T | C | 1 | a0002c0002t0002g0113 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1317-759T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949067 | ||||||
| chr15:50949087
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1317-739C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949087 | ||||||
| chr15:50949412
|
C | CA | 34 | a0001c0001t0001g0260a0001c0001t0001g0295a0001c0001t0001g0298others(31): Show | 34 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.1317-398dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr15 | 50949412 | |||||
| chr15:50949429
|
G | A | 1 | a0002c0003t0003g0028 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1317-397G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949429 | ||||||
| chr15:50949431
|
A | G | 1 | a0002c0003t0003g0028 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1317-395A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949431 | ||||||
| chr15:50949447
|
C | A | 1 | a0001c0001t0001g0286 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1317-379C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949447 | ||||||
| chr15:50949512
|
A | G | 5 | a0001c0001t0001g0217a0001c0001t0008g0218a0001c0001t0008g0219others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1317-314A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949512 | ||||||
| chr15:50949531
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1317-295G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949531 | ||||||
| chr15:50949575
|
T | C | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1317-251T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949575 | ||||||
| chr15:50949582
|
G | C | 1 | a0002c0003t0003g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1317-244G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949582 | ||||||
| chr15:50949714
|
G | A | 5 | a0002c0003t0010g0032a0002c0003t0010g0033a0002c0003t0010g0034others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1317-112G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949714 | ||||||
| chr15:50949949
|
T | C | 3 | a0002c0002t0002g0072a0002c0002t0002g0080a0002c0002t0002g0121 | 3 | NA18980.hp2 NA18981.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1429+11T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 12/20 | chr15 | 50949949 | ||||||
| chr15:50950423
|
C | T | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1548+254C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50950423 | ||||||
| chr15:50950428
|
G | A | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548+259G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50950428 | ||||||
| chr15:50950463
|
A | G | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1548+294A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50950463 | ||||||
| chr15:50950585
|
T | G | 99 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(96): Show | 99 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1548+416T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50950585 | ||||||
| chr15:50950652
|
A | T | 1 | a0002c0003t0022g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1548+483A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50950652 | ||||||
| chr15:50951064
|
C | CA | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548+897dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50951064 | |||||
| chr15:50951374
|
G | A | 2 | a0002c0003t0003g0129a0002c0003t0003g0147 | 2 | NA18947.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1548+1205G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50951374 | ||||||
| chr15:50951726
|
C | CT | 30 | a0001c0001t0001g0255a0001c0001t0001g0300a0001c0001t0005g0330others(27): Show | 30 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1548+1575dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50951726 | |||||
| chr15:50951726
|
C | CTT | 70 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(67): Show | 71 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1548+1574_1548+157 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50951726 | |||||
| chr15:50951726
|
C | T | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1548+1557C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50951726 | ||||||
| chr15:50951767
|
A | C | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1548+1598A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50951767 | ||||||
| chr15:50951786
|
G | A | 75 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(72): Show | 76 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1548+1617G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50951786 | ||||||
| chr15:50951792
|
A | T | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1548+1623A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50951792 | ||||||
| chr15:50951816
|
T | G | 1 | a0001c0001t0001g0213 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1548+1647T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50951816 | ||||||
| chr15:50952077
|
T | G | 1 | a0001c0001t0004g0388 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1548+1908T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952077 | ||||||
| chr15:50952098
|
A | G | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1548+1929A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952098 | ||||||
| chr15:50952180
|
A | G | 1 | a0001c0001t0001g0343 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1548+2011A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952180 | ||||||
| chr15:50952220
|
G | C | 191 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(188): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1548+2051G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952220 | ||||||
| chr15:50952238
|
C | T | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1548+2069C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952238 | ||||||
| chr15:50952239
|
G | A | 2 | a0002c0002t0002g0059a0002c0002t0002g0060 | 2 | HG02040.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.1548+2070G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952239 | ||||||
| chr15:50952292
|
C | T | 1 | a0002c0003t0006g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1548+2123C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952292 | ||||||
| chr15:50952466
|
C | T | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1548+2297C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952466 | ||||||
| chr15:50952509
|
CA | C | 8 | a0001c0001t0001g0250a0001c0001t0001g0256a0001c0001t0004g0369others(5): Show | 8 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1548+2357delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50952509 | |||||
| chr15:50952624
|
T | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0261 | 2 | NA18947.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1548+2455T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952624 | ||||||
| chr15:50952625
|
C | G | 1 | a0001c0001t0004g0386 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1548+2456C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952625 | ||||||
| chr15:50952765
|
C | CT | 231 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(228): Show | 232 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.1548+2597dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50952765 | |||||
| chr15:50952804
|
G | A | 2 | a0002c0003t0006g0187a0002c0003t0006g0190 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1548+2635G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952804 | ||||||
| chr15:50953262
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1548+3093G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50953262 | ||||||
| chr15:50953483
|
T | C | 63 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(60): Show | 64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1548+3314T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50953483 | ||||||
| chr15:50953654
|
C | T | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1548+3485C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50953654 | ||||||
| chr15:50953678
|
C | T | 1 | a0001c0001t0003g0328 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1548+3509C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50953678 | ||||||
| chr15:50954217
|
AT | A | 110 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(107): Show | 110 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1548+4053delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50954217 | |||||
| chr15:50954578
|
G | C | 2 | a0002c0002t0002g0048a0002c0002t0002g0050 | 2 | HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1549-3914G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50954578 | ||||||
| chr15:50954767
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1549-3725C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50954767 | ||||||
| chr15:50954840
|
T | C | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1549-3652T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50954840 | ||||||
| chr15:50954857
|
A | G | 101 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(98): Show | 101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1549-3635A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50954857 | ||||||
| chr15:50954914
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1549-3578A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50954914 | ||||||
| chr15:50954914
|
A | T | 1 | a0001c0001t0005g0305 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1549-3578A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50954914 | ||||||
| chr15:50954939
|
C | T | 3 | a0002c0002t0012g0111a0002c0006t0015g0347a0002c0006t0015g0348 | 3 | HG02257.hp1 HG03209.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1549-3553C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50954939 | ||||||
| chr15:50955630
|
A | G | 1 | a0001c0001t0004g0362 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1549-2862A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50955630 | ||||||
| chr15:50955731
|
C | G | 1 | a0001c0001t0028g0216 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1549-2761C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50955731 | ||||||
| chr15:50955945
|
C | T | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1549-2547C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50955945 | ||||||
| chr15:50955997
|
G | C | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1549-2495G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50955997 | ||||||
| chr15:50956024
|
G | T | 1 | a0002c0002t0002g0057 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1549-2468G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956024 | ||||||
| chr15:50956025
|
C | T | 1 | a0002c0002t0002g0057 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1549-2467C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956025 | ||||||
| chr15:50956061
|
G | A | 7 | a0002c0003t0003g0143a0002c0003t0003g0145a0002c0003t0003g0148others(4): Show | 7 | HG02027.hp2 NA18612.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.1549-2431G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956061 | ||||||
| chr15:50956106
|
T | C | 130 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(127): Show | 130 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1549-2386T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956106 | ||||||
| chr15:50956120
|
G | T | 13 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(10): Show | 13 | HG01123.hp2 HG01433.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.1549-2372G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956120 | ||||||
| chr15:50956473
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1549-2019T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956473 | ||||||
| chr15:50956500
|
A | T | 1 | a0002c0002t0002g0103 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1549-1992A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956500 | ||||||
| chr15:50956640
|
C | G | 38 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(35): Show | 38 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.1549-1852C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956640 | ||||||
| chr15:50956877
|
G | A | 63 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(60): Show | 64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1549-1615G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956877 | ||||||
| chr15:50956931
|
T | C | 63 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(60): Show | 64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1549-1561T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956931 | ||||||
| chr15:50956964
|
C | T | 281 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(278): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1549-1528C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956964 | ||||||
| chr15:50956967
|
T | G | 39 | a0001c0001t0004g0349a0001c0001t0004g0350a0001c0001t0004g0351others(36): Show | 39 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1549-1525T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956967 | ||||||
| chr15:50956986
|
C | CAAAACTC others(320): Show |
1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1549-1491_1549-149 others(331): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50956986 | |||||
| chr15:50956997
|
A | G | 1 | a0002c0003t0003g0178 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1549-1495A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956997 | ||||||
| chr15:50956998
|
T | A | 1 | a0002c0003t0003g0178 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1549-1494T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956998 | ||||||
| chr15:50957049
|
A | G | 38 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(35): Show | 38 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.1549-1443A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957049 | ||||||
| chr15:50957065
|
T | G | 3 | a0001c0001t0001g0257a0005c0007t0011g0184a0005c0007t0011g0185 | 3 | HG01891.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1549-1427T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957065 | ||||||
| chr15:50957092
|
C | T | 1 | a0006c0012t0001g0289 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1549-1400C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957092 | ||||||
| chr15:50957238
|
C | T | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1549-1254C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957238 | ||||||
| chr15:50957332
|
C | A | 63 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(60): Show | 64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1549-1160C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957332 | ||||||
| chr15:50957362
|
C | T | 2 | a0002c0002t0002g0058a0002c0002t0002g0065 | 2 | NA18969.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1549-1130C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957362 | ||||||
| chr15:50957504
|
G | A | 1 | a0004c0005t0001g0238 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1549-988G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957504 | ||||||
| chr15:50957654
|
G | T | 63 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(60): Show | 64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1549-838G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957654 | ||||||
| chr15:50957671
|
C | CT | 33 | a0001c0001t0001g0217a0001c0001t0001g0248a0001c0001t0001g0249others(30): Show | 33 | HG00621.hp2 HG01123.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.1549-798dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50957671 | |||||
| chr15:50957671
|
C | CTT | 13 | a0001c0001t0003g0307a0001c0001t0005g0336a0002c0003t0003g0028others(10): Show | 13 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1549-799_1549-798d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50957671 | |||||
| chr15:50957671
|
C | CTTT | 32 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0003g0311others(29): Show | 32 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.1549-800_1549-798d others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50957671 | |||||
| chr15:50957671
|
CT | C | 6 | a0001c0001t0004g0358a0002c0002t0002g0011a0002c0002t0002g0105others(3): Show | 6 | HG02280.hp1 HG02897.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1549-798delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50957671 | |||||
| chr15:50957671
|
CTTTTTTT others(4): Show |
C | 2 | a0002c0003t0014g0017a0002c0003t0014g0018 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1549-808_1549-798d others(13): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50957671 | |||||
| chr15:50957677
|
T | C | 2 | a0002c0002t0002g0009a0002c0002t0002g0010 | 2 | NA18959.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1549-815T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957677 | ||||||
| chr15:50957700
|
G | A | 38 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(35): Show | 38 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.1549-792G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957700 | ||||||
| chr15:50957822
|
G | A | 2 | a0002c0002t0002g0067a0002c0003t0003g0031 | 2 | NA18979.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1549-670G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957822 | ||||||
| chr15:50957827
|
C | A | 1 | a0001c0001t0008g0218 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1549-665C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957827 | ||||||
| chr15:50957940
|
G | A | 1 | a0002c0003t0022g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1549-552G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957940 | ||||||
| chr15:50958015
|
G | C | 1 | a0002c0003t0003g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1549-477G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50958015 | ||||||
| chr15:50958048
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1549-444C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50958048 | ||||||
| chr15:50958139
|
G | A | 1 | a0002c0002t0002g0061 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1549-353G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50958139 | ||||||
| chr15:50958200
|
A | G | 2 | a0002c0003t0003g0128a0002c0003t0003g0140 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1549-292A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50958200 | ||||||
| chr15:50958251
|
A | G | 20 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(17): Show | 20 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1549-241A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50958251 | ||||||
| chr15:50958400
|
C | T | 1 | a0002c0002t0002g0050 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1549-92C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50958400 | ||||||
| chr15:50958413
|
G | A | 1 | a0002c0002t0002g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1549-79G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50958413 | ||||||
| chr15:50958924
|
C | G | 1 | a0001c0001t0001g0267 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1851+130C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50958924 | ||||||
| chr15:50958925
|
T | G | 63 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(60): Show | 64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1851+131T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50958925 | ||||||
| chr15:50958935
|
A | G | 4 | a0001c0001t0008g0218a0001c0001t0008g0219a0001c0001t0008g0220others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1851+141A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50958935 | ||||||
| chr15:50958972
|
G | A | 98 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(95): Show | 98 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1851+178G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50958972 | ||||||
| chr15:50959115
|
A | G | 217 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(214): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1851+321A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959115 | ||||||
| chr15:50959152
|
A | G | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1851+358A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959152 | ||||||
| chr15:50959242
|
A | G | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1851+448A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959242 | ||||||
| chr15:50959296
|
G | C | 6 | a0001c0001t0001g0217a0001c0001t0008g0218a0001c0001t0008g0219others(3): Show | 6 | HG01884.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1851+502G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959296 | ||||||
| chr15:50959426
|
T | G | 1 | a0001c0001t0001g0227 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1851+632T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959426 | ||||||
| chr15:50959676
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1851+882T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959676 | ||||||
| chr15:50959878
|
A | G | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1851+1084A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959878 | ||||||
| chr15:50959899
|
A | T | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1851+1105A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959899 | ||||||
| chr15:50960004
|
GA | G | 100 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1851+1218delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50960004 | |||||
| chr15:50960040
|
A | G | 2 | a0002c0003t0006g0187a0002c0003t0006g0190 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1851+1246A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50960040 | ||||||
| chr15:50960157
|
A | G | 14 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(11): Show | 14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.1851+1363A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50960157 | ||||||
| chr15:50960344
|
A | G | 1 | a0001c0001t0003g0317 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1851+1550A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50960344 | ||||||
| chr15:50960408
|
A | G | 1 | a0002c0002t0002g0053 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1851+1614A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50960408 | ||||||
| chr15:50960455
|
T | C | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1851+1661T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50960455 | ||||||
| chr15:50960467
|
G | T | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1851+1673G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50960467 | ||||||
| chr15:50960488
|
TA | T | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1851+1696delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50960488 | |||||
| chr15:50960819
|
C | CA | 10 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0254others(7): Show | 10 | HG01981.hp1 HG02293.hp2 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.1851+2035dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50960819 | |||||
| chr15:50961109
|
A | G | 8 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(5): Show | 8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1851+2315A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50961109 | ||||||
| chr15:50961222
|
A | G | 11 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(8): Show | 11 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1851+2428A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50961222 | ||||||
| chr15:50961314
|
C | CTACAAGC others(81): Show |
5 | a0001c0001t0001g0222a0001c0001t0001g0269a0004c0005t0001g0235others(2): Show | 5 | HG04115.hp2 NA18944.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.1851+2525_1851+261 others(92): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50961314 | |||||
| chr15:50961729
|
A | T | 1 | a0001c0001t0001g0284 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1851+2935A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50961729 | ||||||
| chr15:50961876
|
C | A | 11 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(8): Show | 11 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1851+3082C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50961876 | ||||||
| chr15:50962017
|
A | AAATAC | 99 | a0001c0001t0003g0313a0001c0010t0002g0355a0002c0002t0002g0009others(96): Show | 99 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1851+3244_1851+324 others(9): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962017 | |||||
| chr15:50962017
|
A | AAATACAA others(3): Show |
20 | a0002c0002t0002g0015a0002c0002t0002g0061a0002c0002t0002g0088others(17): Show | 20 | HG00621.hp2 HG01167.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.1851+3239_1851+324 others(14): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962017 | |||||
| chr15:50962017
|
A | AAATACAA others(8): Show |
11 | a0002c0003t0003g0029a0002c0003t0003g0030a0002c0003t0006g0188others(8): Show | 11 | HG01943.hp2 HG02004.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1851+3234_1851+324 others(19): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962017 | |||||
| chr15:50962152
|
A | G | 2 | a0001c0001t0005g0330a0001c0001t0005g0334 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1851+3358A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962152 | ||||||
| chr15:50962209
|
A | G | 1 | a0001c0001t0019g0230 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1851+3415A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962209 | ||||||
| chr15:50962305
|
A | G | 130 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(127): Show | 130 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1851+3511A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962305 | ||||||
| chr15:50962446
|
C | A | 7 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0062others(4): Show | 7 | HG00544.hp2 HG00621.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.1851+3652C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962446 | ||||||
| chr15:50962472
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1851+3678C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962472 | ||||||
| chr15:50962572
|
C | T | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1851+3778C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962572 | ||||||
| chr15:50962722
|
C | T | 1 | a0001c0001t0003g0328 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1851+3928C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962722 | ||||||
| chr15:50962822
|
G | A | 101 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(98): Show | 101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1851+4028G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962822 | ||||||
| chr15:50962829
|
G | A | 8 | a0001c0001t0003g0307a0001c0001t0003g0309a0001c0001t0003g0310others(5): Show | 8 | HG01516.hp1 HG02293.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1851+4035G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962829 | ||||||
| chr15:50962834
|
A | G | 2 | a0002c0003t0003g0141a0002c0003t0003g0181 | 2 | NA18747.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1851+4040A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962834 | ||||||
| chr15:50962889
|
C | CA | 57 | a0001c0001t0001g0195a0001c0001t0001g0199a0001c0001t0001g0205others(54): Show | 57 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1851+4122dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAA | 10 | a0001c0001t0001g0256a0001c0001t0003g0328a0001c0001t0004g0352others(7): Show | 10 | HG01891.hp1 HG02027.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.1851+4121_1851+412 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAA | 28 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0004g0365others(25): Show | 28 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1851+4120_1851+412 others(7): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAA | 11 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0004g0367others(8): Show | 12 | HG01891.hp2 HG02257.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.1851+4119_1851+412 others(8): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0004g0350a0001c0001t0004g0351a0001c0001t0004g0356others(1): Show | 4 | HG02630.hp1 HG03453.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1851+4113_1851+412 others(14): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0004g0363 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1851+4112_1851+412 others(15): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0004g0353a0001c0001t0005g0331a0001c0001t0005g0340 | 3 | HG01109.hp1 HG02809.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1851+4109_1851+412 others(18): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(8): Show |
5 | a0001c0001t0004g0354a0001c0001t0005g0303a0001c0001t0005g0321others(2): Show | 5 | HG01496.hp1 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1851+4108_1851+412 others(19): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0005g0322a0001c0001t0005g0332a0001c0001t0005g0334 | 3 | HG02145.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1851+4107_1851+412 others(20): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0005g0302a0001c0001t0005g0330 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1851+4106_1851+412 others(21): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0004g0362a0001c0001t0005g0335a0001c0001t0005g0336 | 3 | HG01884.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1851+4105_1851+412 others(22): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0005g0301a0001c0001t0005g0341 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1851+4104_1851+412 others(23): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(14): Show |
3 | a0001c0001t0004g0358a0001c0001t0009g0319a0001c0001t0009g0320 | 3 | HG02622.hp2 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1851+4102_1851+412 others(25): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0004g0359 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1851+4101_1851+412 others(26): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0005g0305 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1851+4100_1851+412 others(27): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(18): Show |
2 | a0001c0001t0004g0357a0001c0001t0005g0338 | 2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1851+4098_1851+412 others(29): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0009g0337 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1851+4096_1851+412 others(31): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0009g0318 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1851+4122_1851+412 others(36): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0005g0306 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1851+4122_1851+412 others(37): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
C | CAAAAAAA others(29): Show |
1 | a0001c0001t0004g0364 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1851+4122_1851+412 others(40): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
CA | C | 35 | a0001c0001t0001g0286a0001c0001t0003g0307a0001c0001t0003g0309others(32): Show | 35 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1851+4122delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
CAA | C | 46 | a0002c0002t0002g0016a0002c0003t0003g0126a0002c0003t0003g0127others(43): Show | 47 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1851+4121_1851+412 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
CAAAA | C | 10 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(7): Show | 10 | HG00621.hp2 HG02004.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1851+4119_1851+412 others(8): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
CAAAAAAA others(2): Show |
C | 6 | a0002c0003t0006g0187a0002c0003t0006g0188a0002c0003t0006g0189others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1851+4114_1851+412 others(13): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
CAAAAAAA others(3): Show |
C | 1 | a0002c0003t0006g0186 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1851+4113_1851+412 others(14): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962889
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0253 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1851+4112_1851+412 others(15): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | |||||
| chr15:50962917
|
T | A | 1 | a0001c0001t0004g0353 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1851+4123T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962917 | ||||||
| chr15:50963020
|
C | T | 4 | a0002c0003t0003g0133a0002c0003t0003g0144a0002c0003t0003g0146others(1): Show | 4 | HG00609.hp1 HG01192.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1851+4226C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963020 | ||||||
| chr15:50963181
|
CAG | C | 23 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0305others(20): Show | 23 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1851+4392_1851+439 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50963181 | |||||
| chr15:50963195
|
A | T | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1851+4401A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963195 | ||||||
| chr15:50963284
|
T | A | 1 | a0002c0002t0002g0050 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1851+4490T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963284 | ||||||
| chr15:50963289
|
G | T | 3 | a0001c0001t0005g0330a0001c0001t0005g0332a0001c0001t0005g0334 | 3 | HG02055.hp2 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1851+4495G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963289 | ||||||
| chr15:50963555
|
C | G | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1852-4708C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963555 | ||||||
| chr15:50963667
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1852-4596A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963667 | ||||||
| chr15:50963677
|
G | A | 14 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(11): Show | 14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.1852-4586G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963677 | ||||||
| chr15:50963815
|
T | C | 63 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(60): Show | 64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1852-4448T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963815 | ||||||
| chr15:50963845
|
C | T | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1852-4418C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963845 | ||||||
| chr15:50963904
|
A | T | 1 | a0001c0001t0001g0290 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1852-4359A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963904 | ||||||
| chr15:50963907
|
A | G | 1 | a0002c0002t0016g0068 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1852-4356A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963907 | ||||||
| chr15:50963919
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1852-4344G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963919 | ||||||
| chr15:50963947
|
A | G | 5 | a0001c0001t0001g0217a0001c0001t0008g0218a0001c0001t0008g0219others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-4316A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963947 | ||||||
| chr15:50963974
|
G | A | 10 | a0001c0001t0004g0349a0001c0001t0004g0350a0001c0001t0004g0351others(7): Show | 10 | HG01891.hp1 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1852-4289G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963974 | ||||||
| chr15:50964086
|
A | G | 2 | a0002c0002t0002g0035a0002c0002t0002g0036 | 2 | HG02135.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1852-4177A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964086 | ||||||
| chr15:50964144
|
G | C | 3 | a0001c0001t0005g0330a0001c0001t0005g0332a0001c0001t0005g0334 | 3 | HG02055.hp2 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1852-4119G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964144 | ||||||
| chr15:50964190
|
A | C | 1 | a0002c0002t0002g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1852-4073A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964190 | ||||||
| chr15:50964315
|
G | A | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1852-3948G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964315 | ||||||
| chr15:50964505
|
T | C | 1 | a0002c0002t0016g0116 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1852-3758T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964505 | ||||||
| chr15:50964612
|
G | C | 13 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(10): Show | 13 | HG01123.hp2 HG01433.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.1852-3651G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964612 | ||||||
| chr15:50964623
|
G | A | 3 | a0002c0003t0010g0032a0002c0003t0010g0033a0002c0003t0010g0034 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1852-3640G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964623 | ||||||
| chr15:50964687
|
A | G | 2 | a0001c0001t0004g0366a0001c0001t0004g0375 | 2 | HG01515.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1852-3576A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964687 | ||||||
| chr15:50964953
|
T | A | 5 | a0001c0001t0001g0217a0001c0001t0008g0218a0001c0001t0008g0219others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-3310T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964953 | ||||||
| chr15:50964954
|
A | C | 5 | a0001c0001t0001g0217a0001c0001t0008g0218a0001c0001t0008g0219others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-3309A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964954 | ||||||
| chr15:50964955
|
C | CA | 5 | a0001c0001t0001g0217a0001c0001t0008g0218a0001c0001t0008g0219others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-3308_1852-330 others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964955 | ||||||
| chr15:50964955
|
C | CACACACA others(14): Show |
2 | a0002c0002t0017g0054a0002c0003t0006g0186 | 2 | HG01167.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1852-3308_1852-330 others(25): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964955 | ||||||
| chr15:50964955
|
C | CCA | 43 | a0001c0001t0001g0002a0001c0001t0001g0197a0001c0001t0001g0198others(40): Show | 44 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.1852-3272_1852-327 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCACA | 64 | a0001c0001t0001g0196a0001c0001t0001g0258a0001c0001t0001g0269others(61): Show | 65 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1852-3274_1852-327 others(8): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCACACA | 15 | a0001c0001t0001g0199a0001c0001t0004g0354a0001c0001t0004g0359others(12): Show | 15 | HG01496.hp1 HG02055.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.1852-3276_1852-327 others(10): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCACACAC others(1): Show |
21 | a0001c0001t0003g0342a0001c0001t0004g0350a0001c0001t0004g0351others(18): Show | 21 | HG00140.hp1 HG01109.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1852-3278_1852-327 others(12): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCACACAC others(3): Show |
12 | a0001c0001t0004g0349a0001c0001t0004g0352a0001c0001t0004g0357others(9): Show | 12 | HG00099.hp1 HG00323.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.1852-3280_1852-327 others(14): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCACACAC others(5): Show |
26 | a0001c0001t0004g0358a0001c0001t0004g0366a0001c0001t0004g0367others(23): Show | 26 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1852-3282_1852-327 others(16): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCACACAC others(7): Show |
35 | a0001c0001t0004g0365a0001c0001t0004g0372a0001c0001t0004g0378others(32): Show | 35 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1852-3284_1852-327 others(18): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCACACAC others(9): Show |
36 | a0001c0001t0004g0368a0001c0001t0004g0377a0001c0001t0004g0379others(33): Show | 36 | HG00438.hp1 HG00438.hp2 HG01943.hp1 others(33): Show |
intron_variant | MODIFIER | c.1852-3286_1852-327 others(20): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCACACAC others(11): Show |
16 | a0001c0001t0001g0286a0002c0002t0002g0013a0002c0002t0002g0040others(13): Show | 16 | HG00423.hp1 HG00544.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1852-3288_1852-327 others(22): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCACACAC others(13): Show |
10 | a0001c0001t0004g0376a0002c0002t0002g0036a0002c0002t0002g0044others(7): Show | 10 | HG00639.hp2 HG00741.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.1852-3290_1852-327 others(24): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCACACAC others(15): Show |
3 | a0002c0002t0002g0050a0002c0002t0002g0056a0002c0003t0022g0007 | 3 | HG01074.hp1 HG01891.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1852-3292_1852-327 others(26): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCACACAC others(17): Show |
4 | a0002c0003t0006g0188a0002c0003t0006g0189a0003c0004t0018g0019others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1852-3294_1852-327 others(28): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCCACACA others(26): Show |
1 | a0002c0003t0003g0026 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1852-3307_1852-330 others(37): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCCCACAC others(13): Show |
1 | a0002c0003t0003g0025 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1852-3307_1852-330 others(24): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCCCACAC others(19): Show |
3 | a0002c0003t0003g0031a0002c0003t0010g0032a0002c0003t0010g0034 | 3 | HG01167.hp2 HG01169.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1852-3307_1852-330 others(30): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCCCACAC others(23): Show |
3 | a0002c0003t0003g0028a0002c0003t0003g0029a0002c0003t0003g0030 | 3 | HG01943.hp2 HG02004.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1852-3307_1852-330 others(34): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCCCACAC others(25): Show |
3 | a0002c0003t0003g0027a0002c0003t0010g0033a0002c0003t0020g0008 | 3 | HG03710.hp1 HG06807.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1852-3307_1852-330 others(36): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCCCCCCC others(21): Show |
1 | a0002c0003t0014g0018 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1852-3307_1852-330 others(32): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
C | CCCCCCCC others(22): Show |
1 | a0002c0003t0014g0017 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1852-3307_1852-330 others(33): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
CCACACA | C | 4 | a0001c0001t0001g0277a0001c0001t0001g0344a0001c0001t0001g0345others(1): Show | 4 | HG00140.hp2 HG01099.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1852-3276_1852-327 others(10): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50964955
|
CCACACAC others(7): Show |
C | 2 | a0001c0001t0009g0318a0001c0001t0009g0337 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1852-3284_1852-327 others(18): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | |||||
| chr15:50965007
|
C | T | 13 | a0001c0001t0005g0321a0001c0001t0005g0330a0001c0001t0005g0331others(10): Show | 13 | HG01109.hp1 HG01255.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1852-3256C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965007 | ||||||
| chr15:50965020
|
G | A | 217 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(214): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1852-3243G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965020 | ||||||
| chr15:50965115
|
T | C | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1852-3148T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965115 | ||||||
| chr15:50965121
|
G | A | 9 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(6): Show | 9 | HG01167.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1852-3142G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965121 | ||||||
| chr15:50965134
|
C | T | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1852-3129C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965134 | ||||||
| chr15:50965221
|
T | TGGC | 3 | a0002c0003t0010g0032a0002c0003t0010g0033a0002c0003t0010g0034 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1852-3041_1852-303 others(7): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50965221 | |||||
| chr15:50965222
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1852-3041G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965222 | ||||||
| chr15:50965424
|
A | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1852-2839A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965424 | ||||||
| chr15:50965494
|
C | T | 1 | a0001c0001t0019g0230 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1852-2769C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965494 | ||||||
| chr15:50965593
|
A | G | 63 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(60): Show | 64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1852-2670A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965593 | ||||||
| chr15:50965770
|
T | A | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1852-2493T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965770 | ||||||
| chr15:50965889
|
T | C | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1852-2374T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965889 | ||||||
| chr15:50965948
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(85): Show | 89 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1852-2315C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965948 | ||||||
| chr15:50965996
|
T | C | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1852-2267T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965996 | ||||||
| chr15:50966066
|
C | T | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1852-2197C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966066 | ||||||
| chr15:50966118
|
A | G | 64 | a0002c0002t0002g0088a0002c0003t0003g0126a0002c0003t0003g0127others(61): Show | 65 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1852-2145A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966118 | ||||||
| chr15:50966196
|
G | C | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1852-2067G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966196 | ||||||
| chr15:50966375
|
G | A | 2 | a0001c0001t0001g0296a0001c0001t0026g0294 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1852-1888G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966375 | ||||||
| chr15:50966415
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1852-1848T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966415 | ||||||
| chr15:50966457
|
G | A | 2 | a0004c0005t0001g0238a0004c0005t0001g0239 | 2 | NA18944.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1852-1806G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966457 | ||||||
| chr15:50966464
|
C | G | 81 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(78): Show | 82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1852-1799C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966464 | ||||||
| chr15:50966466
|
A | C | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1852-1797A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966466 | ||||||
| chr15:50966473
|
C | T | 101 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(98): Show | 101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1852-1790C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966473 | ||||||
| chr15:50966531
|
C | CT | 7 | a0001c0001t0001g0292a0001c0001t0001g0343a0001c0001t0004g0353others(4): Show | 7 | HG00733.hp2 HG02738.hp1 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.1852-1710dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50966531 | |||||
| chr15:50966531
|
CT | C | 211 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0237others(208): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.1852-1710delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50966531 | |||||
| chr15:50966531
|
CTT | C | 8 | a0002c0002t0002g0065a0002c0002t0002g0070a0002c0002t0002g0099others(5): Show | 8 | HG02922.hp2 NA18747.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1852-1711_1852-171 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50966531 | |||||
| chr15:50966685
|
C | T | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1852-1578C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966685 | ||||||
| chr15:50967149
|
A | G | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1852-1114A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50967149 | ||||||
| chr15:50967397
|
C | T | 1 | a0002c0003t0022g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1852-866C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50967397 | ||||||
| chr15:50967437
|
C | T | 1 | a0002c0003t0003g0149 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1852-826C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50967437 | ||||||
| chr15:50967555
|
A | G | 2 | a0004c0005t0001g0238a0004c0005t0001g0239 | 2 | NA18944.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1852-708A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50967555 | ||||||
| chr15:50967580
|
A | G | 1 | a0011c0009t0003g0161 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1852-683A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50967580 | ||||||
| chr15:50968196
|
A | T | 1 | a0002c0003t0003g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1852-67A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50968196 | ||||||
| chr15:50968678
|
T | A | 231 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(228): Show | 232 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.1966+301T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50968678 | ||||||
| chr15:50968827
|
A | G | 1 | a0001c0001t0004g0358 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1966+450A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50968827 | ||||||
| chr15:50968832
|
G | T | 1 | a0001c0001t0027g0224 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1966+455G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50968832 | ||||||
| chr15:50968851
|
T | TC | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1966+475dupC | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50968851 | |||||
| chr15:50968898
|
G | A | 25 | a0001c0001t0001g0270a0001c0001t0005g0301a0001c0001t0005g0302others(22): Show | 25 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.1966+521G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50968898 | ||||||
| chr15:50969001
|
T | C | 1 | a0001c0010t0002g0355 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1966+624T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969001 | ||||||
| chr15:50969032
|
T | A | 61 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(58): Show | 62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1966+655T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969032 | ||||||
| chr15:50969111
|
G | A | 1 | a0002c0003t0003g0180 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1966+734G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969111 | ||||||
| chr15:50969232
|
T | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1966+855T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969232 | ||||||
| chr15:50969246
|
G | T | 1 | a0001c0001t0001g0242 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1966+869G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969246 | ||||||
| chr15:50969314
|
G | T | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1966+937G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969314 | ||||||
| chr15:50969512
|
A | AATTTT | 230 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(227): Show | 231 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1966+1136_1966+114 others(9): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50969512 | |||||
| chr15:50969530
|
A | G | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1966+1153A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969530 | ||||||
| chr15:50969660
|
C | CT | 45 | a0001c0001t0001g0196a0001c0001t0001g0296a0001c0001t0004g0350others(42): Show | 45 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1966+1300dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50969660 | |||||
| chr15:50969759
|
T | C | 1 | a0001c0001t0001g0325 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1966+1382T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969759 | ||||||
| chr15:50969773
|
C | G | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1966+1396C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969773 | ||||||
| chr15:50969801
|
A | G | 1 | a0001c0001t0001g0325 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1966+1424A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969801 | ||||||
| chr15:50969804
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1966+1427G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969804 | ||||||
| chr15:50969807
|
G | A | 1 | a0001c0001t0004g0381 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1966+1430G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969807 | ||||||
| chr15:50969807
|
G | C | 1 | a0001c0001t0001g0325 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1966+1430G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969807 | ||||||
| chr15:50969808
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1966+1431G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969808 | ||||||
| chr15:50969850
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1966+1473A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969850 | ||||||
| chr15:50969861
|
A | G | 198 | a0001c0001t0001g0292a0001c0001t0004g0380a0001c0001t0004g0381others(195): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1966+1484A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969861 | ||||||
| chr15:50969910
|
T | C | 2 | a0002c0003t0003g0137a0002c0003t0003g0151 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1966+1533T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969910 | ||||||
| chr15:50969936
|
G | A | 1 | a0001c0001t0003g0314 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1966+1559G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969936 | ||||||
| chr15:50969954
|
C | T | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1966+1577C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969954 | ||||||
| chr15:50970111
|
G | C | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1966+1734G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970111 | ||||||
| chr15:50970171
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1966+1794T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970171 | ||||||
| chr15:50970215
|
T | C | 1 | a0002c0003t0003g0166 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1966+1838T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970215 | ||||||
| chr15:50970503
|
C | G | 61 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(58): Show | 62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1966+2126C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970503 | ||||||
| chr15:50970550
|
G | A | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1966+2173G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970550 | ||||||
| chr15:50970566
|
A | G | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0298others(2): Show | 5 | HG01243.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1966+2189A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970566 | ||||||
| chr15:50970576
|
T | C | 81 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(78): Show | 82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1966+2199T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970576 | ||||||
| chr15:50970593
|
G | T | 39 | a0001c0001t0004g0349a0001c0001t0004g0350a0001c0001t0004g0351others(36): Show | 39 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1966+2216G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970593 | ||||||
| chr15:50970927
|
CA | C | 61 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(58): Show | 62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1966+2551delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970927 | ||||||
| chr15:50970998
|
G | T | 1 | a0002c0003t0002g0123 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1966+2621G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970998 | ||||||
| chr15:50971108
|
A | G | 1 | a0002c0003t0003g0165 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1966+2731A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971108 | ||||||
| chr15:50971299
|
G | C | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1966+2922G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971299 | ||||||
| chr15:50971634
|
T | A | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1966+3257T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971634 | ||||||
| chr15:50971712
|
C | T | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1966+3335C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971712 | ||||||
| chr15:50971724
|
G | A | 1 | a0001c0001t0005g0336 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1966+3347G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971724 | ||||||
| chr15:50971929
|
C | A | 191 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(188): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1966+3552C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971929 | ||||||
| chr15:50971950
|
T | C | 5 | a0001c0001t0001g0217a0001c0001t0008g0218a0001c0001t0008g0219others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1966+3573T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971950 | ||||||
| chr15:50971967
|
G | A | 110 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(107): Show | 110 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1966+3590G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971967 | ||||||
| chr15:50972056
|
C | G | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1966+3679C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972056 | ||||||
| chr15:50972086
|
T | C | 1 | a0001c0001t0004g0349 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1966+3709T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972086 | ||||||
| chr15:50972198
|
GTTTC | G | 191 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(188): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1966+3841_1966+384 others(8): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50972198 | |||||
| chr15:50972222
|
T | C | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1966+3845T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972222 | ||||||
| chr15:50972267
|
G | A | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1966+3890G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972267 | ||||||
| chr15:50972342
|
G | T | 1 | a0001c0001t0004g0372 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1966+3965G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972342 | ||||||
| chr15:50972368
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1966+3991C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972368 | ||||||
| chr15:50972401
|
G | A | 81 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(78): Show | 82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1966+4024G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972401 | ||||||
| chr15:50972463
|
C | T | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1966+4086C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972463 | ||||||
| chr15:50972816
|
A | G | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1966+4439A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972816 | ||||||
| chr15:50972848
|
A | T | 1 | a0002c0003t0003g0139 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1966+4471A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972848 | ||||||
| chr15:50972942
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1966+4565A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972942 | ||||||
| chr15:50972949
|
G | A | 1 | a0001c0001t0004g0363 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1966+4572G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972949 | ||||||
| chr15:50973042
|
G | A | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1966+4665G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50973042 | ||||||
| chr15:50973347
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0323others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1966+4970C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50973347 | ||||||
| chr15:50973662
|
C | T | 1 | a0002c0003t0003g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1966+5285C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50973662 | ||||||
| chr15:50973696
|
T | G | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1966+5319T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50973696 | ||||||
| chr15:50973789
|
A | G | 57 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0129others(54): Show | 58 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1966+5412A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50973789 | ||||||
| chr15:50973842
|
G | A | 101 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(98): Show | 101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1966+5465G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50973842 | ||||||
| chr15:50973914
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1966+5537T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50973914 | ||||||
| chr15:50974008
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0283a0001c0001t0001g0284others(2): Show | 6 | NA18940.hp2 NA18941.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1966+5631T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50974008 | ||||||
| chr15:50974020
|
C | T | 3 | a0002c0003t0006g0188a0002c0003t0006g0189a0002c0003t0006g0192 | 3 | HG02109.hp1 HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1966+5643C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50974020 | ||||||
| chr15:50974266
|
A | AT | 47 | a0001c0001t0001g0195a0001c0001t0001g0227a0001c0001t0001g0232others(44): Show | 47 | HG01106.hp2 HG01192.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.1966+5907dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50974266 | |||||
| chr15:50974266
|
AT | A | 11 | a0001c0001t0001g0263a0002c0003t0006g0186a0002c0003t0006g0187others(8): Show | 11 | HG01167.hp1 HG01167.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1966+5907delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50974266 | |||||
| chr15:50974720
|
G | T | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1966+6343G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50974720 | ||||||
| chr15:50974776
|
T | G | 1 | a0002c0002t0002g0095 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1966+6399T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50974776 | ||||||
| chr15:50974850
|
T | C | 1 | a0001c0001t0004g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1966+6473T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50974850 | ||||||
| chr15:50974940
|
T | C | 13 | a0001c0001t0001g0004a0001c0001t0001g0203a0001c0001t0001g0210others(10): Show | 14 | HG02148.hp2 HG02155.hp2 NA18940.hp2 others(11): Show |
intron_variant | MODIFIER | c.1966+6563T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50974940 | ||||||
| chr15:50975080
|
C | T | 13 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(10): Show | 13 | HG01123.hp2 HG01433.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.1966+6703C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975080 | ||||||
| chr15:50975153
|
C | T | 1 | a0002c0003t0003g0029 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1966+6776C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975153 | ||||||
| chr15:50975164
|
A | G | 217 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(214): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1966+6787A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975164 | ||||||
| chr15:50975180
|
T | C | 1 | a0002c0002t0002g0122 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1966+6803T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975180 | ||||||
| chr15:50975200
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1966+6823G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975200 | ||||||
| chr15:50975227
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1966+6850G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975227 | ||||||
| chr15:50975253
|
A | C | 3 | a0001c0001t0004g0349a0001c0001t0004g0351a0001c0001t0004g0352 | 3 | HG02976.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1966+6876A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975253 | ||||||
| chr15:50975383
|
C | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1966+7006C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975383 | ||||||
| chr15:50975552
|
CTG | C | 75 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(72): Show | 76 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1966+7177_1966+717 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50975552 | |||||
| chr15:50975946
|
A | G | 4 | a0002c0002t0002g0040a0002c0002t0002g0043a0002c0002t0002g0044others(1): Show | 4 | HG00735.hp2 HG01943.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1966+7569A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975946 | ||||||
| chr15:50975956
|
C | CAG | 9 | a0001c0001t0001g0196a0001c0001t0001g0200a0001c0001t0001g0237others(6): Show | 9 | HG00639.hp2 HG01255.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1966+7603_1966+760 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50975956 | |||||
| chr15:50975956
|
CAG | C | 177 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(174): Show | 178 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.1966+7603_1966+760 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50975956 | |||||
| chr15:50975956
|
CAGAGAGA others(9): Show |
C | 1 | a0002c0002t0002g0043 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1966+7589_1966+760 others(20): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50975956 | |||||
| chr15:50975970
|
G | C | 3 | a0002c0003t0006g0188a0002c0003t0006g0189a0002c0003t0006g0192 | 3 | HG02109.hp1 HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1966+7593G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975970 | ||||||
| chr15:50976097
|
C | CA | 81 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(78): Show | 82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1966+7728dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50976097 | |||||
| chr15:50976234
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1967-7788A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50976234 | ||||||
| chr15:50976255
|
G | A | 20 | a0002c0003t0003g0127a0002c0003t0003g0130a0002c0003t0003g0133others(17): Show | 21 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1967-7767G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50976255 | ||||||
| chr15:50976538
|
G | A | 1 | a0002c0002t0002g0011 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1967-7484G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50976538 | ||||||
| chr15:50976791
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1967-7231A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50976791 | ||||||
| chr15:50976792
|
A | G | 4 | a0001c0001t0001g0296a0001c0001t0004g0358a0001c0001t0004g0362others(1): Show | 4 | HG02280.hp2 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1967-7230A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50976792 | ||||||
| chr15:50977084
|
T | C | 2 | a0001c0001t0004g0366a0001c0001t0004g0375 | 2 | HG01515.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1967-6938T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977084 | ||||||
| chr15:50977107
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1967-6915G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977107 | ||||||
| chr15:50977185
|
A | G | 14 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(11): Show | 14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.1967-6837A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977185 | ||||||
| chr15:50977193
|
G | A | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1967-6829G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977193 | ||||||
| chr15:50977201
|
A | C | 1 | a0002c0002t0002g0037 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1967-6821A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977201 | ||||||
| chr15:50977278
|
T | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1967-6744T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977278 | ||||||
| chr15:50977432
|
A | G | 283 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1967-6590A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977432 | ||||||
| chr15:50977478
|
C | A | 1 | a0001c0001t0005g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1967-6544C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977478 | ||||||
| chr15:50977497
|
A | C | 1 | a0002c0003t0003g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1967-6525A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977497 | ||||||
| chr15:50977563
|
T | G | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1967-6459T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977563 | ||||||
| chr15:50977706
|
G | GT | 12 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0200others(9): Show | 12 | HG00639.hp1 HG01081.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1967-6296dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977706 | |||||
| chr15:50977706
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0003g0307 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1967-6305_1967-629 others(14): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977706 | |||||
| chr15:50977706
|
G | GTTTTTTT others(4): Show |
20 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0003g0311others(17): Show | 20 | HG01123.hp2 HG01433.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.1967-6306_1967-629 others(15): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977706 | |||||
| chr15:50977706
|
G | GTTTTTTT others(5): Show |
12 | a0001c0001t0003g0309a0001c0001t0003g0312a0001c0001t0003g0327others(9): Show | 12 | HG01109.hp1 HG01255.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1967-6307_1967-629 others(16): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977706 | |||||
| chr15:50977706
|
G | GTTTTTTT others(7): Show |
3 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0305 | 3 | HG03139.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1967-6309_1967-629 others(18): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977706 | |||||
| chr15:50977706
|
G | GTTTTTTT others(8): Show |
2 | a0001c0001t0005g0322a0001c0001t0029g0304 | 2 | HG01496.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1967-6310_1967-629 others(19): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977706 | |||||
| chr15:50977708
|
T | TTTTTTTT others(1): Show |
64 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(61): Show | 65 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1967-6307_1967-630 others(12): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977708 | |||||
| chr15:50977709
|
T | TTTTTTTG | 10 | a0002c0002t0002g0052a0002c0002t0002g0053a0002c0002t0002g0110others(7): Show | 10 | HG01167.hp1 HG02071.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1967-6307_1967-630 others(11): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977709 | |||||
| chr15:50977709
|
T | TTTTTTTT others(1): Show |
6 | a0002c0003t0010g0032a0002c0003t0010g0033a0002c0003t0010g0034others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1967-6306_1967-630 others(12): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977709 | |||||
| chr15:50977710
|
T | TTTTTTG | 99 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(96): Show | 99 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1967-6307_1967-630 others(10): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977710 | |||||
| chr15:50977710
|
T | TTTTTTTG | 8 | a0002c0002t0002g0087a0002c0003t0003g0025a0002c0003t0003g0026others(5): Show | 8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1967-6306_1967-630 others(11): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977710 | |||||
| chr15:50978030
|
C | T | 1 | a0002c0002t0002g0063 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1967-5992C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978030 | ||||||
| chr15:50978168
|
T | C | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1967-5854T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978168 | ||||||
| chr15:50978209
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1967-5813G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978209 | ||||||
| chr15:50978495
|
T | C | 4 | a0001c0001t0005g0330a0001c0001t0005g0332a0001c0001t0005g0334others(1): Show | 4 | HG01255.hp1 HG02055.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1967-5527T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978495 | ||||||
| chr15:50978685
|
C | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1967-5337C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978685 | ||||||
| chr15:50978686
|
C | G | 3 | a0002c0003t0010g0032a0002c0003t0010g0033a0002c0003t0010g0034 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1967-5336C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978686 | ||||||
| chr15:50978866
|
A | T | 4 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.1967-5156A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978866 | ||||||
| chr15:50978980
|
G | A | 61 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(58): Show | 62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1967-5042G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978980 | ||||||
| chr15:50979032
|
G | C | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1967-4990G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979032 | ||||||
| chr15:50979059
|
G | A | 1 | a0002c0002t0002g0073 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1967-4963G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979059 | ||||||
| chr15:50979138
|
GTA | G | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1967-4882_1967-488 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50979138 | |||||
| chr15:50979226
|
A | G | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1967-4796A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979226 | ||||||
| chr15:50979381
|
C | T | 267 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(264): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1967-4641C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979381 | ||||||
| chr15:50979384
|
G | A | 217 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(214): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1967-4638G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979384 | ||||||
| chr15:50979611
|
A | C | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1967-4411A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979611 | ||||||
| chr15:50979611
|
A | G | 191 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(188): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1967-4411A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979611 | ||||||
| chr15:50979857
|
T | C | 1 | a0002c0002t0002g0081 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1967-4165T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979857 | ||||||
| chr15:50980043
|
G | C | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1967-3979G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980043 | ||||||
| chr15:50980448
|
G | A | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1967-3574G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980448 | ||||||
| chr15:50980476
|
G | T | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1967-3546G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980476 | ||||||
| chr15:50980509
|
T | A | 191 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(188): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1967-3513T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980509 | ||||||
| chr15:50980634
|
C | G | 1 | a0003c0004t0007g0023 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1967-3388C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980634 | ||||||
| chr15:50980685
|
T | C | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1967-3337T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980685 | ||||||
| chr15:50980792
|
C | T | 1 | a0001c0001t0005g0333 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1967-3230C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980792 | ||||||
| chr15:50980897
|
A | G | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1967-3125A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980897 | ||||||
| chr15:50980979
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1967-3043G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980979 | ||||||
| chr15:50981201
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1967-2821A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50981201 | ||||||
| chr15:50981209
|
G | A | 2 | a0002c0002t0021g0006a0010c0008t0002g0005 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1967-2813G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50981209 | ||||||
| chr15:50981486
|
G | T | 38 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(35): Show | 38 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.1967-2536G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50981486 | ||||||
| chr15:50981522
|
A | T | 15 | a0001c0001t0001g0214a0001c0001t0001g0234a0001c0001t0001g0236others(12): Show | 15 | HG00423.hp2 HG01261.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1967-2500A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50981522 | ||||||
| chr15:50981915
|
G | A | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1967-2107G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50981915 | ||||||
| chr15:50981931
|
C | T | 5 | a0001c0001t0001g0217a0001c0001t0008g0218a0001c0001t0008g0219others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967-2091C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50981931 | ||||||
| chr15:50982009
|
C | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1967-2013C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982009 | ||||||
| chr15:50982086
|
C | CA | 41 | a0001c0001t0001g0199a0001c0001t0001g0204a0001c0001t0001g0229others(38): Show | 41 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1967-1913dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50982086 | |||||
| chr15:50982086
|
C | CAA | 118 | a0001c0001t0005g0321a0001c0001t0005g0322a0001c0001t0005g0330others(115): Show | 118 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1967-1914_1967-191 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50982086 | |||||
| chr15:50982086
|
C | CAAA | 59 | a0002c0002t0002g0046a0002c0002t0002g0074a0002c0002t0002g0082others(56): Show | 60 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1967-1915_1967-191 others(7): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50982086 | |||||
| chr15:50982086
|
C | CAAAA | 10 | a0002c0003t0003g0147a0002c0003t0003g0158a0002c0003t0003g0160others(7): Show | 10 | HG00735.hp1 HG01109.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1967-1916_1967-191 others(8): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50982086 | |||||
| chr15:50982140
|
A | G | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1967-1882A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982140 | ||||||
| chr15:50982238
|
T | G | 1 | a0002c0003t0003g0177 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1967-1784T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982238 | ||||||
| chr15:50982251
|
A | C | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1967-1771A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982251 | ||||||
| chr15:50982308
|
C | T | 191 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(188): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1967-1714C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982308 | ||||||
| chr15:50982309
|
G | A | 1 | a0001c0001t0028g0216 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1967-1713G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982309 | ||||||
| chr15:50982350
|
G | A | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1967-1672G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982350 | ||||||
| chr15:50982693
|
CATT | C | 75 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(72): Show | 76 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1967-1322_1967-132 others(7): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50982693 | |||||
| chr15:50982853
|
A | T | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1967-1169A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982853 | ||||||
| chr15:50983100
|
G | A | 1 | a0005c0007t0011g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1967-922G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983100 | ||||||
| chr15:50983188
|
C | T | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1967-834C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983188 | ||||||
| chr15:50983280
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1967-742G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983280 | ||||||
| chr15:50983372
|
C | G | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1967-650C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983372 | ||||||
| chr15:50983469
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1967-553G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983469 | ||||||
| chr15:50983510
|
A | G | 2 | a0002c0003t0003g0171a0002c0003t0003g0172 | 2 | NA18946.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1967-512A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983510 | ||||||
| chr15:50983526
|
T | C | 1 | a0001c0001t0004g0380 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1967-496T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983526 | ||||||
| chr15:50983568
|
G | C | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1967-454G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983568 | ||||||
| chr15:50983604
|
A | G | 1 | a0001c0001t0001g0326 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1967-418A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983604 | ||||||
| chr15:50983632
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1967-390C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983632 | ||||||
| chr15:50983705
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1967-317C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983705 | ||||||
| chr15:50983895
|
A | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0262 | 2 | NA18967.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1967-127A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983895 | ||||||
| chr15:50983911
|
T | A | 4 | a0001c0001t0004g0377a0001c0001t0004g0379a0001c0001t0004g0387others(1): Show | 4 | HG02602.hp2 HG03669.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1967-111T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983911 | ||||||
| chr15:50983919
|
G | C | 1 | a0001c0001t0001g0245 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1967-103G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983919 | ||||||
| chr15:50983931
|
A | G | 265 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1967-91A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983931 | ||||||
| chr15:50984317
|
T | A | 1 | a0002c0002t0002g0073 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2090+172T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984317 | ||||||
| chr15:50984328
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2090+183T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984328 | ||||||
| chr15:50984521
|
A | T | 217 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(214): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.2090+376A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984521 | ||||||
| chr15:50984577
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2090+432G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984577 | ||||||
| chr15:50984614
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2090+469G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984614 | ||||||
| chr15:50984769
|
C | T | 1 | a0002c0002t0002g0067 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2090+624C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984769 | ||||||
| chr15:50984785
|
T | A | 1 | a0002c0003t0022g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2090+640T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984785 | ||||||
| chr15:50984834
|
T | G | 2 | a0001c0001t0004g0349a0001c0001t0004g0352 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2090+689T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984834 | ||||||
| chr15:50984878
|
A | G | 193 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.2090+733A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984878 | ||||||
| chr15:50984881
|
A | C | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2090+736A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984881 | ||||||
| chr15:50984983
|
T | A | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090+838T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984983 | ||||||
| chr15:50985017
|
G | C | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2090+872G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985017 | ||||||
| chr15:50985084
|
G | T | 1 | a0002c0003t0003g0178 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2090+939G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985084 | ||||||
| chr15:50985126
|
A | G | 1 | a0001c0001t0003g0313 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2090+981A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985126 | ||||||
| chr15:50985159
|
G | GT | 27 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(24): Show | 27 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.2090+1022dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50985159 | |||||
| chr15:50985349
|
A | T | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2090+1204A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985349 | ||||||
| chr15:50985392
|
C | T | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2090+1247C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985392 | ||||||
| chr15:50985527
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2090+1382G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985527 | ||||||
| chr15:50985592
|
G | C | 1 | a0001c0001t0001g0206 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2090+1447G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985592 | ||||||
| chr15:50985593
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2090+1448T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985593 | ||||||
| chr15:50985615
|
G | A | 60 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(57): Show | 61 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2090+1470G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985615 | ||||||
| chr15:50985664
|
G | A | 2 | a0002c0003t0014g0017a0002c0003t0014g0018 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2090+1519G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985664 | ||||||
| chr15:50985702
|
T | C | 1 | a0002c0003t0003g0144 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2090+1557T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985702 | ||||||
| chr15:50985741
|
G | A | 2 | a0002c0003t0014g0017a0002c0003t0014g0018 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2090+1596G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985741 | ||||||
| chr15:50985742
|
A | C | 2 | a0002c0003t0014g0017a0002c0003t0014g0018 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2090+1597A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985742 | ||||||
| chr15:50985791
|
C | T | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2090+1646C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985791 | ||||||
| chr15:50986008
|
G | C | 3 | a0002c0002t0002g0069a0002c0002t0002g0082a0002c0002t0002g0120 | 3 | HG00621.hp1 NA18965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2090+1863G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986008 | ||||||
| chr15:50986018
|
G | A | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2090+1873G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986018 | ||||||
| chr15:50986075
|
T | A | 1 | a0001c0001t0001g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2090+1930T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986075 | ||||||
| chr15:50986191
|
CT | C | 60 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(57): Show | 61 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2090+2048delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50986191 | |||||
| chr15:50986216
|
G | A | 217 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(214): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.2090+2071G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986216 | ||||||
| chr15:50986237
|
A | G | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2090+2092A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986237 | ||||||
| chr15:50986338
|
C | T | 2 | a0002c0002t0002g0113a0002c0002t0002g0119 | 2 | NA18954.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2090+2193C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986338 | ||||||
| chr15:50986449
|
A | G | 3 | a0001c0001t0001g0205a0001c0001t0001g0247a0001c0001t0001g0297 | 3 | HG00408.hp1 NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2090+2304A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986449 | ||||||
| chr15:50986452
|
A | G | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2090+2307A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986452 | ||||||
| chr15:50986484
|
C | G | 1 | a0001c0001t0004g0350 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2090+2339C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986484 | ||||||
| chr15:50986521
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2090+2376C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986521 | ||||||
| chr15:50986607
|
C | T | 1 | a0001c0001t0004g0363 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2090+2462C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986607 | ||||||
| chr15:50986608
|
G | A | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2090+2463G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986608 | ||||||
| chr15:50986621
|
T | C | 2 | a0003c0004t0007g0021a0003c0004t0007g0022 | 2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2090+2476T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986621 | ||||||
| chr15:50986636
|
C | G | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2090+2491C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986636 | ||||||
| chr15:50986855
|
A | G | 1 | a0002c0003t0014g0018 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2090+2710A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986855 | ||||||
| chr15:50986941
|
A | C | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090+2796A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986941 | ||||||
| chr15:50987052
|
C | G | 4 | a0001c0001t0001g0206a0001c0001t0001g0244a0001c0001t0001g0246others(1): Show | 4 | HG00544.hp1 HG01069.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.2090+2907C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50987052 | ||||||
| chr15:50987145
|
G | A | 1 | a0002c0003t0002g0123 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2090+3000G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50987145 | ||||||
| chr15:50987190
|
C | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | NA19012.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2090+3045C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50987190 | ||||||
| chr15:50987217
|
C | A | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.2090+3072C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50987217 | ||||||
| chr15:50987402
|
C | A | 1 | a0001c0001t0001g0271 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2090+3257C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50987402 | ||||||
| chr15:50987409
|
A | G | 1 | a0001c0001t0001g0271 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2090+3264A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50987409 | ||||||
| chr15:50987558
|
G | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0300 | 2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2090+3413G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50987558 | ||||||
| chr15:50988066
|
G | A | 14 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(11): Show | 14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.2090+3921G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988066 | ||||||
| chr15:50988137
|
T | A | 81 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(78): Show | 82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.2090+3992T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988137 | ||||||
| chr15:50988224
|
G | T | 1 | a0002c0002t0002g0063 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2090+4079G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988224 | ||||||
| chr15:50988385
|
A | G | 231 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(228): Show | 232 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.2090+4240A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988385 | ||||||
| chr15:50988403
|
CT | C | 191 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(188): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.2090+4260delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50988403 | |||||
| chr15:50988407
|
TGG | T | 191 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(188): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.2090+4264_2090+426 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50988407 | |||||
| chr15:50988427
|
G | T | 1 | a0001c0001t0003g0313 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2090+4282G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988427 | ||||||
| chr15:50988507
|
G | A | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2090+4362G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988507 | ||||||
| chr15:50988532
|
C | T | 81 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(78): Show | 82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.2090+4387C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988532 | ||||||
| chr15:50988733
|
C | CT | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090+4589dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50988733 | |||||
| chr15:50988735
|
A | G | 1 | a0002c0002t0002g0104 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2090+4590A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988735 | ||||||
| chr15:50988782
|
T | C | 44 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0209others(41): Show | 45 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.2091-4588T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988782 | ||||||
| chr15:50989004
|
G | A | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2091-4366G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989004 | ||||||
| chr15:50989034
|
G | A | 8 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(5): Show | 8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.2091-4336G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989034 | ||||||
| chr15:50989409
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2091-3961G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989409 | ||||||
| chr15:50989426
|
G | T | 61 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(58): Show | 62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2091-3944G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989426 | ||||||
| chr15:50989487
|
CT | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0208a0001c0001t0001g0323others(3): Show | 7 | HG02145.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2091-3871delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50989487 | |||||
| chr15:50989635
|
G | C | 1 | a0002c0002t0002g0059 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2091-3735G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989635 | ||||||
| chr15:50989743
|
G | A | 1 | a0008c0013t0005g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2091-3627G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989743 | ||||||
| chr15:50989746
|
G | T | 2 | a0002c0003t0003g0137a0002c0003t0003g0151 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2091-3624G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989746 | ||||||
| chr15:50989826
|
T | A | 1 | a0001c0001t0001g0229 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2091-3544T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989826 | ||||||
| chr15:50989830
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2091-3540A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989830 | ||||||
| chr15:50989896
|
G | T | 4 | a0001c0001t0009g0318a0001c0001t0009g0319a0001c0001t0009g0320others(1): Show | 4 | HG02622.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2091-3474G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989896 | ||||||
| chr15:50989926
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2091-3444G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989926 | ||||||
| chr15:50990016
|
G | A | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2091-3354G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990016 | ||||||
| chr15:50990114
|
T | C | 1 | a0002c0003t0006g0186 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2091-3256T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990114 | ||||||
| chr15:50990174
|
G | A | 191 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(188): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.2091-3196G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990174 | ||||||
| chr15:50990316
|
A | G | 1 | a0002c0002t0002g0056 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2091-3054A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990316 | ||||||
| chr15:50990344
|
T | TTTA | 21 | a0001c0001t0001g0204a0001c0001t0001g0222a0001c0001t0001g0233others(18): Show | 21 | HG00609.hp2 HG01167.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.2091-2996_2091-299 others(7): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990344 | |||||
| chr15:50990344
|
T | TTTATTA | 31 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(28): Show | 31 | HG00408.hp2 HG00621.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.2091-2999_2091-299 others(10): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990344 | |||||
| chr15:50990344
|
T | TTTATTAT others(2): Show |
70 | a0001c0001t0001g0279a0001c0001t0005g0301a0001c0001t0005g0306others(67): Show | 71 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.2091-3002_2091-299 others(13): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990344 | |||||
| chr15:50990344
|
T | TTTATTAT others(5): Show |
36 | a0001c0001t0005g0302a0001c0001t0005g0305a0001c0001t0009g0318others(33): Show | 36 | HG00438.hp2 HG01175.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.2091-3005_2091-299 others(16): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990344 | |||||
| chr15:50990344
|
T | TTTATTAT others(8): Show |
76 | a0001c0001t0005g0303a0001c0001t0005g0322a0001c0001t0009g0319others(73): Show | 76 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.2091-3008_2091-299 others(19): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990344 | |||||
| chr15:50990344
|
T | TTTATTAT others(11): Show |
4 | a0002c0002t0002g0049a0002c0002t0002g0087a0002c0003t0002g0123others(1): Show | 4 | HG02080.hp1 HG02615.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.2091-3011_2091-299 others(22): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990344 | |||||
| chr15:50990344
|
TTTA | T | 5 | a0002c0003t0003g0031a0002c0003t0022g0007a0002c0006t0015g0347others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2091-2996_2091-299 others(7): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990344 | |||||
| chr15:50990360
|
T | TTATTATT others(5): Show |
1 | a0010c0008t0002g0005 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2091-2999_2091-299 others(16): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990360 | |||||
| chr15:50990628
|
C | T | 1 | a0001c0001t0003g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2091-2742C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990628 | ||||||
| chr15:50990635
|
CTCAGCGT others(20): Show |
C | 3 | a0002c0002t0002g0013a0002c0002t0002g0052a0002c0002t0002g0070 | 3 | NA18942.hp2 NA18946.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.2091-2733_2091-270 others(31): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990635 | |||||
| chr15:50990641
|
G | A | 1 | a0001c0001t0001g0343 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2091-2729G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990641 | ||||||
| chr15:50990678
|
G | A | 9 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0232others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.2091-2692G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990678 | ||||||
| chr15:50990737
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2091-2633G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990737 | ||||||
| chr15:50991319
|
T | C | 2 | a0002c0006t0015g0347a0002c0006t0015g0348 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2091-2051T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50991319 | ||||||
| chr15:50991369
|
A | C | 38 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(35): Show | 38 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.2091-2001A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50991369 | ||||||
| chr15:50991891
|
A | AT | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2091-1473dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50991891 | |||||
| chr15:50991923
|
G | A | 101 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(98): Show | 101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2091-1447G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50991923 | ||||||
| chr15:50991962
|
CT | C | 93 | a0001c0001t0001g0237a0001c0001t0004g0354a0001c0001t0004g0358others(90): Show | 94 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.2091-1390delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50991962 | |||||
| chr15:50991962
|
CTT | C | 6 | a0002c0003t0003g0148a0002c0003t0003g0183a0002c0003t0022g0007others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2091-1391_2091-139 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50991962 | |||||
| chr15:50992009
|
C | T | 24 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(21): Show | 24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.2091-1361C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50992009 | ||||||
| chr15:50992098
|
G | A | 1 | a0002c0003t0003g0168 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2091-1272G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50992098 | ||||||
| chr15:50992108
|
T | A | 1 | a0002c0002t0002g0082 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2091-1262T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50992108 | ||||||
| chr15:50992213
|
A | G | 1 | a0002c0002t0016g0116 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2091-1157A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50992213 | ||||||
| chr15:50992483
|
G | A | 81 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(78): Show | 82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.2091-887G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50992483 | ||||||
| chr15:50992503
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2091-867T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50992503 | ||||||
| chr15:50992930
|
T | A | 191 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(188): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.2091-440T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50992930 | ||||||
| chr15:50993838
|
G | C | 1 | a0001c0001t0001g0253 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2346+213G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50993838 | ||||||
| chr15:50993896
|
A | G | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2346+271A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50993896 | ||||||
| chr15:50993929
|
C | T | 101 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(98): Show | 101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2346+304C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50993929 | ||||||
| chr15:50993967
|
C | A | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2346+342C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50993967 | ||||||
| chr15:50994339
|
A | G | 1 | a0002c0002t0002g0091 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2346+714A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50994339 | ||||||
| chr15:50994379
|
C | T | 75 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(72): Show | 76 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.2346+754C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50994379 | ||||||
| chr15:50994858
|
G | A | 14 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(11): Show | 14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.2346+1233G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50994858 | ||||||
| chr15:50994886
|
G | A | 217 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(214): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.2346+1261G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50994886 | ||||||
| chr15:50995358
|
C | T | 6 | a0001c0001t0001g0217a0001c0001t0008g0218a0001c0001t0008g0219others(3): Show | 6 | HG01884.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2346+1733C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50995358 | ||||||
| chr15:50995362
|
G | T | 2 | a0001c0001t0004g0367a0001c0001t0004g0368 | 2 | HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2346+1737G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50995362 | ||||||
| chr15:50995399
|
C | CT | 109 | a0001c0001t0001g0195a0001c0001t0005g0333a0001c0010t0002g0355others(106): Show | 109 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.2346+1790dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50995399 | |||||
| chr15:50995399
|
C | CTT | 7 | a0002c0002t0024g0047a0002c0003t0003g0026a0002c0003t0003g0027others(4): Show | 7 | HG00621.hp2 HG01943.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.2346+1789_2346+179 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50995399 | |||||
| chr15:50995483
|
C | T | 1 | a0002c0003t0003g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2347-1843C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50995483 | ||||||
| chr15:50995651
|
G | T | 3 | a0002c0003t0001g0071a0002c0003t0001g0077a0002c0003t0001g0078 | 3 | HG00438.hp1 HG01358.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.2347-1675G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50995651 | ||||||
| chr15:50995672
|
C | T | 8 | a0002c0002t0002g0106a0002c0003t0006g0186a0002c0003t0006g0187others(5): Show | 8 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2347-1654C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50995672 | ||||||
| chr15:50995719
|
A | G | 8 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(5): Show | 8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.2347-1607A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50995719 | ||||||
| chr15:50995883
|
A | G | 1 | a0002c0002t0002g0052 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2347-1443A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50995883 | ||||||
| chr15:50995980
|
C | CT | 32 | a0001c0001t0001g0002a0001c0001t0001g0196a0001c0001t0001g0225others(29): Show | 33 | HG00544.hp1 HG01243.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.2347-1320dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50995980 | |||||
| chr15:50995980
|
CT | C | 84 | a0001c0001t0001g0262a0001c0001t0003g0310a0001c0001t0004g0350others(81): Show | 85 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.2347-1320delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50995980 | |||||
| chr15:50995980
|
CTT | C | 19 | a0001c0001t0005g0341a0002c0002t0002g0069a0002c0003t0003g0025others(16): Show | 19 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.2347-1321_2347-132 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50995980 | |||||
| chr15:50995980
|
CTTTTTTT others(11): Show |
C | 1 | a0002c0003t0003g0136 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2347-1337_2347-132 others(22): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50995980 | |||||
| chr15:50996069
|
A | G | 6 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2347-1257A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996069 | ||||||
| chr15:50996092
|
A | G | 1 | a0002c0003t0003g0166 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2347-1234A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996092 | ||||||
| chr15:50996113
|
C | G | 1 | a0002c0002t0002g0092 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2347-1213C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996113 | ||||||
| chr15:50996113
|
C | T | 1 | a0002c0003t0003g0180 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2347-1213C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996113 | ||||||
| chr15:50996155
|
A | AT | 60 | a0001c0001t0001g0227a0001c0001t0001g0271a0001c0001t0001g0281others(57): Show | 61 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2347-1150dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50996155 | |||||
| chr15:50996155
|
AT | A | 125 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0310others(122): Show | 125 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.2347-1150delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50996155 | |||||
| chr15:50996155
|
ATT | A | 37 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(34): Show | 37 | HG00558.hp2 HG01109.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.2347-1151_2347-115 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50996155 | |||||
| chr15:50996350
|
G | A | 1 | a0002c0002t0002g0065 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2347-976G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996350 | ||||||
| chr15:50996352
|
T | C | 2 | a0003c0004t0007g0021a0003c0004t0007g0022 | 2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2347-974T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996352 | ||||||
| chr15:50996370
|
G | A | 1 | a0002c0002t0002g0057 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2347-956G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996370 | ||||||
| chr15:50996454
|
G | A | 188 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(185): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.2347-872G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996454 | ||||||
| chr15:50996571
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2347-755A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996571 | ||||||
| chr15:50996577
|
T | C | 3 | a0002c0002t0002g0110a0002c0002t0002g0113a0002c0002t0002g0119 | 3 | HG02071.hp2 NA18954.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2347-749T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996577 | ||||||
| chr15:50996594
|
C | G | 3 | a0001c0001t0001g0344a0001c0001t0001g0345a0001c0001t0001g0346 | 3 | HG00140.hp2 HG01099.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.2347-732C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996594 | ||||||
| chr15:50996595
|
C | T | 40 | a0001c0001t0004g0207a0001c0001t0004g0349a0001c0001t0004g0350others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.2347-731C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996595 | ||||||
| chr15:50996959
|
A | G | 1 | a0001c0001t0004g0357 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2347-367A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996959 | ||||||
| chr15:50997145
|
T | C | 3 | a0003c0004t0007g0021a0003c0004t0007g0022a0003c0004t0007g0023 | 3 | HG02922.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2347-181T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50997145 | ||||||
| chr15:50997198
|
T | C | 101 | a0001c0010t0002g0355a0002c0002t0002g0009a0002c0002t0002g0010others(98): Show | 101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2347-128T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50997198 | ||||||
| chr15:50997201
|
T | G | 1 | a0002c0002t0002g0119 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2347-125T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50997201 | ||||||
| chr15:50997959
|
T | A | 2 | a0002c0003t0003g0138a0002c0003t0003g0139 | 2 | HG00733.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2904+76T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50997959 | ||||||
| chr15:50998193
|
TTGG | T | 202 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(199): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.2904+314_2904+316d others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr15 | 50998193 | |||||
| chr15:50998371
|
C | T | 1 | a0001c0001t0004g0373 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2904+488C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50998371 | ||||||
| chr15:50998503
|
A | G | 1 | a0001c0001t0005g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2905-569A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50998503 | ||||||
| chr15:50998599
|
T | C | 228 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(225): Show | 229 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.2905-473T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50998599 | ||||||
| chr15:50998638
|
AG | A | 8 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(5): Show | 8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.2905-433delG | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50998638 | ||||||
| chr15:50998780
|
A | G | 2 | a0005c0007t0011g0184a0005c0007t0011g0185 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2905-292A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50998780 | ||||||
| chr15:50998859
|
A | C | 62 | a0002c0003t0003g0126a0002c0003t0003g0127a0002c0003t0003g0128others(59): Show | 63 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2905-213A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50998859 | ||||||
| chr15:50998997
|
T | C | 1 | a0001c0001t0001g0344 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2905-75T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50998997 | ||||||
| chr15:50999064
|
A | G | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.2905-8A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50999064 | ||||||
| chr15:50999379
|
G | A | 202 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(199): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.3095+117G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | chr15 | 50999379 | ||||||
| chr15:50999401
|
A | T | 1 | a0002c0002t0002g0050 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3095+139A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | chr15 | 50999401 | ||||||
| chr15:50999423
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3095+161A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | chr15 | 50999423 | ||||||
| chr15:50999703
|
CTTTTT | C | 10 | a0001c0001t0001g0222a0001c0001t0001g0237a0001c0001t0001g0266others(7): Show | 10 | HG01257.hp2 HG03834.hp1 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.3095+445_3095+449d others(7): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr15 | 50999703 | |||||
| chr15:50999904
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3095+642T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | chr15 | 50999904 | ||||||
| chr15:51000141
|
C | CT | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.3096-865dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr15 | 51000141 | |||||
| chr15:51000141
|
C | CTT | 27 | a0001c0001t0001g0195a0001c0001t0001g0229a0001c0001t0001g0277others(24): Show | 27 | HG01081.hp1 HG01123.hp2 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.3096-866_3096-865d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr15 | 51000141 | |||||
| chr15:51000306
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3096-720A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | chr15 | 51000306 | ||||||
| chr15:51000658
|
C | T | 1 | a0002c0002t0002g0096 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3096-368C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | chr15 | 51000658 | ||||||
| chr15:51000967
|
G | GT | 228 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(225): Show | 229 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.3096-57dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr15 | 51000967 | |||||
| chr15:51001371
|
T | G | 1 | a0001c0001t0004g0380 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3253+188T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51001371 | ||||||
| chr15:51001447
|
A | G | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3253+264A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51001447 | ||||||
| chr15:51001531
|
C | T | 1 | a0002c0003t0003g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3253+348C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51001531 | ||||||
| chr15:51001752
|
T | C | 4 | a0002c0003t0003g0130a0002c0003t0003g0142a0002c0003t0003g0155others(1): Show | 4 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.3253+569T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51001752 | ||||||
| chr15:51001966
|
C | T | 5 | a0003c0004t0007g0021a0003c0004t0007g0023a0003c0004t0007g0024others(2): Show | 5 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3254-536C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51001966 | ||||||
| chr15:51002004
|
G | A | 7 | a0002c0003t0006g0186a0002c0003t0006g0187a0002c0003t0006g0188others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3254-498G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51002004 | ||||||
| chr15:51002004
|
G | T | 1 | a0002c0003t0003g0146 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3254-498G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51002004 | ||||||
| chr15:51002250
|
C | T | 1 | a0002c0003t0003g0146 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3254-252C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51002250 | ||||||
| chr15:51002274
|
C | T | 1 | a0002c0003t0003g0146 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3254-228C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51002274 | ||||||
| chr15:51002300
|
A | G | 89 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(86): Show | 90 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.3254-202A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51002300 | ||||||
| chr15:51002367
|
A | G | 2 | a0002c0003t0006g0187a0002c0003t0006g0190 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3254-135A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51002367 |