Search by Gene
| geneid | 160 |
|---|---|
| ensemblid | ENSG00000196961.13 |
| hgncid | 561 |
| symbol | AP2A1 |
| name | adaptor related protein complex 2 subunit alpha 1 |
| refseq_nuc | NM_130787.3 |
| refseq_prot | NP_570603.2 |
| ensembl_nuc | ENST00000354293.10 |
| ensembl_prot | ENSP00000346246.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 49767001 |
| end | 49807114 |
| strand | + |
| ver | v1.2 |
| region | chr19:49767001-49807114 |
| region5000 | chr19:49762001-49812114 |
| regionname0 | AP2A1_chr19_49767001_49807114 |
| regionname5000 | AP2A1_chr19_49762001_49812114 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 955 | 341 | 82 | 64 | 133 | 14 | 46 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0002 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2868 | 324 | 80 | 61 | 125 | 12 | 44 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| c0002 | 0/0 | 2868 | 4 | 0 | 0 | 3 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| c0003 | 0/0 | 2868 | 3 | 0 | 2 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| c0004 | 0/0 | 2868 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| c0005 | 0/0 | 2868 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| c0006 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| c0007 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| c0008 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| c0009 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| c0010 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| c0011 | 0/0 | 2868 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| c0012 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 490 | 277 | 64 | 55 | 108 | 12 | 36 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| t0002 | 0/0 | 494 | 45 | 8 | 7 | 18 | 2 | 10 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| t0003 | 0/0 | 490 | 13 | 3 | 2 | 8 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| t0004 | 0/0 | 490 | 5 | 5 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| t0005 | 0/0 | 490 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0002 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 324 | 80 | 61 | 125 | 12 | 44 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0007 | a0001 | c0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0009 | a0001 | c0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0010 | a0001 | c0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0011 | a0001 | c0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0012 | a0001 | c0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0002c0008 | a0002 | c0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 262 | 62 | 52 | 100 | 11 | 35 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 42 | 8 | 7 | 17 | 1 | 9 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 13 | 3 | 2 | 8 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0004t0001 | a0001 | c0004 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0005t0001 | a0001 | c0005 | t0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0006t0002 | a0001 | c0006 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0007t0002 | a0001 | c0007 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0009t0001 | a0001 | c0009 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0010t0001 | a0001 | c0010 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0011t0001 | a0001 | c0011 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0001c0012t0002 | a0001 | c0012 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| a0002c0008t0001 | a0002 | c0008 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0187 | a0001 | c0001 | t0001 | g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0193 | a0001 | c0001 | t0001 | g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0203 | a0001 | c0001 | t0001 | g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0212 | a0001 | c0001 | t0001 | g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0213 | a0001 | c0001 | t0001 | g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0215 | a0001 | c0001 | t0001 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0216 | a0001 | c0001 | t0001 | g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0220 | a0001 | c0001 | t0001 | g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0221 | a0001 | c0001 | t0001 | g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0222 | a0001 | c0001 | t0001 | g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0223 | a0001 | c0001 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0226 | a0001 | c0001 | t0001 | g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0227 | a0001 | c0001 | t0001 | g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0229 | a0001 | c0001 | t0001 | g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0231 | a0001 | c0001 | t0001 | g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0233 | a0001 | c0001 | t0001 | g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0234 | a0001 | c0001 | t0001 | g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0235 | a0001 | c0001 | t0001 | g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0236 | a0001 | c0001 | t0001 | g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0237 | a0001 | c0001 | t0001 | g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0238 | a0001 | c0001 | t0001 | g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0239 | a0001 | c0001 | t0001 | g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0240 | a0001 | c0001 | t0001 | g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0241 | a0001 | c0001 | t0001 | g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0242 | a0001 | c0001 | t0001 | g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0244 | a0001 | c0001 | t0001 | g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0245 | a0001 | c0001 | t0001 | g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0246 | a0001 | c0001 | t0001 | g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0248 | a0001 | c0001 | t0001 | g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0249 | a0001 | c0001 | t0001 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0250 | a0001 | c0001 | t0001 | g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0251 | a0001 | c0001 | t0001 | g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0252 | a0001 | c0001 | t0001 | g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0253 | a0001 | c0001 | t0001 | g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0254 | a0001 | c0001 | t0001 | g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0255 | a0001 | c0001 | t0001 | g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0256 | a0001 | c0001 | t0001 | g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0257 | a0001 | c0001 | t0001 | g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0258 | a0001 | c0001 | t0001 | g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0259 | a0001 | c0001 | t0001 | g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0260 | a0001 | c0001 | t0001 | g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0261 | a0001 | c0001 | t0001 | g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0262 | a0001 | c0001 | t0001 | g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0263 | a0001 | c0001 | t0001 | g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0264 | a0001 | c0001 | t0001 | g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0265 | a0001 | c0001 | t0001 | g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0266 | a0001 | c0001 | t0001 | g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0268 | a0001 | c0001 | t0001 | g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0269 | a0001 | c0001 | t0001 | g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0270 | a0001 | c0001 | t0001 | g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0272 | a0001 | c0001 | t0001 | g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0274 | a0001 | c0001 | t0001 | g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0275 | a0001 | c0001 | t0001 | g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0276 | a0001 | c0001 | t0001 | g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0277 | a0001 | c0001 | t0001 | g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0278 | a0001 | c0001 | t0001 | g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0279 | a0001 | c0001 | t0001 | g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0280 | a0001 | c0001 | t0001 | g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0281 | a0001 | c0001 | t0001 | g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0282 | a0001 | c0001 | t0001 | g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0283 | a0001 | c0001 | t0001 | g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0284 | a0001 | c0001 | t0001 | g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0285 | a0001 | c0001 | t0001 | g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0286 | a0001 | c0001 | t0001 | g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0287 | a0001 | c0001 | t0001 | g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0290 | a0001 | c0001 | t0001 | g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0291 | a0001 | c0001 | t0001 | g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0292 | a0001 | c0001 | t0001 | g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0293 | a0001 | c0001 | t0001 | g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0294 | a0001 | c0001 | t0001 | g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0297 | a0001 | c0001 | t0001 | g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0298 | a0001 | c0001 | t0001 | g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0299 | a0001 | c0001 | t0001 | g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0300 | a0001 | c0001 | t0001 | g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0301 | a0001 | c0001 | t0001 | g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0302 | a0001 | c0001 | t0001 | g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0303 | a0001 | c0001 | t0001 | g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0304 | a0001 | c0001 | t0001 | g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0305 | a0001 | c0001 | t0001 | g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0306 | a0001 | c0001 | t0001 | g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0307 | a0001 | c0001 | t0001 | g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0308 | a0001 | c0001 | t0001 | g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0309 | a0001 | c0001 | t0001 | g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0311 | a0001 | c0001 | t0001 | g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0312 | a0001 | c0001 | t0001 | g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0001g0313 | a0001 | c0001 | t0001 | g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0006 | a0001 | c0001 | t0002 | g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0019 | a0001 | c0001 | t0002 | g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0020 | a0001 | c0001 | t0002 | g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0021 | a0001 | c0001 | t0002 | g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0022 | a0001 | c0001 | t0002 | g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0023 | a0001 | c0001 | t0002 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0024 | a0001 | c0001 | t0002 | g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0025 | a0001 | c0001 | t0002 | g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0026 | a0001 | c0001 | t0002 | g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0027 | a0001 | c0001 | t0002 | g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0028 | a0001 | c0001 | t0002 | g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0029 | a0001 | c0001 | t0002 | g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0030 | a0001 | c0001 | t0002 | g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0031 | a0001 | c0001 | t0002 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0032 | a0001 | c0001 | t0002 | g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0033 | a0001 | c0001 | t0002 | g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0034 | a0001 | c0001 | t0002 | g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0036 | a0001 | c0001 | t0002 | g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0037 | a0001 | c0001 | t0002 | g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0038 | a0001 | c0001 | t0002 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0040 | a0001 | c0001 | t0002 | g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0041 | a0001 | c0001 | t0002 | g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0042 | a0001 | c0001 | t0002 | g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0043 | a0001 | c0001 | t0002 | g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0044 | a0001 | c0001 | t0002 | g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0045 | a0001 | c0001 | t0002 | g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0046 | a0001 | c0001 | t0002 | g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0047 | a0001 | c0001 | t0002 | g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0048 | a0001 | c0001 | t0002 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0050 | a0001 | c0001 | t0002 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0051 | a0001 | c0001 | t0002 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0052 | a0001 | c0001 | t0002 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0053 | a0001 | c0001 | t0002 | g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0054 | a0001 | c0001 | t0002 | g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0055 | a0001 | c0001 | t0002 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0056 | a0001 | c0001 | t0002 | g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0057 | a0001 | c0001 | t0002 | g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0058 | a0001 | c0001 | t0002 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0059 | a0001 | c0001 | t0002 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0060 | a0001 | c0001 | t0002 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0002g0208 | a0001 | c0001 | t0002 | g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0003g0010 | a0001 | c0001 | t0003 | g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0003g0075 | a0001 | c0001 | t0003 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0003g0082 | a0001 | c0001 | t0003 | g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0003g0086 | a0001 | c0001 | t0003 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0003g0092 | a0001 | c0001 | t0003 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0003g0101 | a0001 | c0001 | t0003 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0003g0111 | a0001 | c0001 | t0003 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0003g0121 | a0001 | c0001 | t0003 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0003g0168 | a0001 | c0001 | t0003 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0003g0271 | a0001 | c0001 | t0003 | g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0003g0288 | a0001 | c0001 | t0003 | g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0003g0289 | a0001 | c0001 | t0003 | g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0003g0296 | a0001 | c0001 | t0003 | g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0004g0198 | a0001 | c0001 | t0004 | g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0004g0199 | a0001 | c0001 | t0004 | g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0004g0200 | a0001 | c0001 | t0004 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0004g0206 | a0001 | c0001 | t0004 | g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0004g0207 | a0001 | c0001 | t0004 | g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0005g0224 | a0001 | c0001 | t0005 | g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0001t0005g0225 | a0001 | c0001 | t0005 | g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0002t0001g0228 | a0001 | c0002 | t0001 | g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0002t0001g0230 | a0001 | c0002 | t0001 | g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0002t0001g0243 | a0001 | c0002 | t0001 | g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0002t0001g0247 | a0001 | c0002 | t0001 | g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0003t0001g0218 | a0001 | c0003 | t0001 | g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0003t0001g0219 | a0001 | c0003 | t0001 | g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0003t0001g0273 | a0001 | c0003 | t0001 | g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0004t0001g0211 | a0001 | c0004 | t0001 | g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0004t0001g0310 | a0001 | c0004 | t0001 | g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0005t0001g0184 | a0001 | c0005 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0005t0001g0190 | a0001 | c0005 | t0001 | g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0006t0002g0039 | a0001 | c0006 | t0002 | g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0007t0002g0035 | a0001 | c0007 | t0002 | g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0009t0001g0267 | a0001 | c0009 | t0001 | g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0010t0001g0122 | a0001 | c0010 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0011t0001g0214 | a0001 | c0011 | t0001 | g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0001c0012t0002g0049 | a0001 | c0012 | t0002 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| a0002c0008t0001g0295 | a0002 | c0008 | t0001 | g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | GBR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | FIN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0043 | EUR | FIN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0273 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0218 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01256 | hp2 | a0001 | c0011 | t0001 | g0214 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0271 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0219 | EUR | IBS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | IBS | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02083 | hp2 | a0001 | c0009 | t0001 | g0267 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | CDX | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0224 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0243 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0288 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0207 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0289 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0225 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03453 | hp2 | a0001 | c0004 | t0001 | g0211 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | YRI | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18959 | hp1 | a0001 | c0012 | t0002 | g0049 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18963 | hp2 | a0001 | c0010 | t0001 | g0122 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0310 | AFR | LWK | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19065 | hp1 | a0002 | c0008 | t0001 | g0295 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19068 | hp2 | a0001 | c0005 | t0001 | g0184 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19087 | hp1 | a0001 | c0005 | t0001 | g0190 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | YRI | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0299 | EUR | TSI | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | TSI | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA20805 | hp2 | a0001 | c0007 | t0002 | g0035 | EUR | TSI | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA20905 | hp1 | a0001 | c0006 | t0002 | g0039 | SAS | GIH | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | GIH | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | USA | AP2A1_chr19_49762001_49812114 | AP2A1 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | USA | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | USA | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | AP2A1_chr19_49762001_49812114 | AP2A1 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | AP2A1_chr19_49762001_49812114 | AP2A1 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0177 | REF | REF | AP2A1_chr19_49762001_49812114 | AP2A1 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0066 | REF | REF | AP2A1_chr19_49762001_49812114 | AP2A1 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49803322
|
G | A | 1 | a0002 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.2290G>A | p.Val764Met | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/23 | 2423/3357 | 2290/2868 | 764/955 | chr19 | 49803322 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49782552
|
C | T | 1 | a0001c0003 | 3 | HG01169.hp2 HG01192.hp1 HG01517.hp1 |
synonymous_variant | LOW | c.301C>T | p.Leu101Leu | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/23 | 434/3357 | 301/2868 | 101/955 | chr19 | 49782552 | ||
| chr19:49782683
|
C | T | 1 | a0001c0012 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.432C>T | p.Gly144Gly | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/23 | 565/3357 | 432/2868 | 144/955 | chr19 | 49782683 | ||
| chr19:49792031
|
G | A | 1 | a0001c0006 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.570G>A | p.Ala190Ala | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/23 | 703/3357 | 570/2868 | 190/955 | chr19 | 49792031 | ||
| chr19:49799456
|
C | T | 1 | a0001c0011 | 1 | HG01256.hp2 | synonymous_variant | LOW | c.1095C>T | p.Ala365Ala | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 9/23 | 1228/3357 | 1095/2868 | 365/955 | chr19 | 49799456 | ||
| chr19:49799640
|
C | T | 1 | a0001c0002 | 4 | HG00438.hp2 HG02071.hp1 HG02683.hp2 others(1): Show |
synonymous_variant | LOW | c.1146C>T | p.Asp382Asp | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 10/23 | 1279/3357 | 1146/2868 | 382/955 | chr19 | 49799640 | ||
| chr19:49799742
|
A | G | 1 | a0001c0005 | 2 | NA19068.hp2 NA19087.hp1 |
synonymous_variant | LOW | c.1248A>G | p.Ala416Ala | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 10/23 | 1381/3357 | 1248/2868 | 416/955 | chr19 | 49799742 | ||
| chr19:49800054
|
G | T | 1 | a0001c0010 | 1 | NA18963.hp2 | synonymous_variant | LOW | c.1359G>T | p.Ala453Ala | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/23 | 1492/3357 | 1359/2868 | 453/955 | chr19 | 49800054 | ||
| chr19:49801582
|
G | A | 1 | a0001c0007 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.1746G>A | p.Glu582Glu | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 13/23 | 1879/3357 | 1746/2868 | 582/955 | chr19 | 49801582 | ||
| chr19:49805661
|
G | A | 1 | a0001c0004 | 2 | HG03453.hp2 NA19030.hp2 |
splice_region_variant&synonymous_variant | LOW | c.2469G>A | p.Arg823Arg | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 20/23 | 2602/3357 | 2469/2868 | 823/955 | chr19 | 49805661 | ||
| chr19:49806729
|
C | T | 1 | a0001c0009 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.2839C>T | p.Leu947Leu | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 23/23 | 2972/3357 | 2839/2868 | 947/955 | chr19 | 49806729 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49767008
|
A | AGCCC | 4 | a0001c0001t0002a0001c0006t0002a0001c0007t0002others(1): Show | 45 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-125_-122dupGCCC | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/23 | 121 | INFO_REALIGN_3_PRIME | chr19 | 49767008 | ||||
| chr19:49767028
|
C | G | 1 | a0001c0001t0005 | 2 | HG02258.hp2 HG03098.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-106C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/23 | chr19 | 49767028 | ||||||
| chr19:49806760
|
C | T | 1 | a0001c0001t0004 | 5 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 23/23 | 2 | chr19 | 49806760 | |||||
| chr19:49807074
|
C | T | 1 | a0001c0001t0003 | 13 | HG00438.hp1 HG01433.hp2 HG01952.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*316C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 23/23 | 316 | chr19 | 49807074 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49767238
|
A | AG | 8 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(5): Show | 8 | HG00621.hp1 HG00741.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+44dupG | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49767238 | |||||
| chr19:49767452
|
T | TG | 24 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0286others(21): Show | 27 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(24): Show |
intron_variant | MODIFIER | c.67+253dupG | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49767452 | |||||
| chr19:49767529
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.67+329T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49767529 | ||||||
| chr19:49767830
|
G | A | 43 | a0001c0001t0002g0006a0001c0001t0002g0019a0001c0001t0002g0020others(40): Show | 44 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.67+630G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49767830 | ||||||
| chr19:49767853
|
C | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.67+653C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49767853 | ||||||
| chr19:49767906
|
A | C | 1 | a0001c0001t0001g0285 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.67+706A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49767906 | ||||||
| chr19:49768062
|
T | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(294): Show | 325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.67+862T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49768062 | ||||||
| chr19:49768099
|
G | A | 43 | a0001c0001t0002g0006a0001c0001t0002g0019a0001c0001t0002g0020others(40): Show | 44 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.67+899G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49768099 | ||||||
| chr19:49768129
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.67+929A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49768129 | ||||||
| chr19:49768245
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(113): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.67+1045T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49768245 | ||||||
| chr19:49768601
|
T | A | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0178others(18): Show | 23 | HG01074.hp2 HG01934.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.67+1401T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49768601 | ||||||
| chr19:49768667
|
G | T | 81 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(78): Show | 85 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.67+1467G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49768667 | ||||||
| chr19:49768801
|
C | T | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060 | 3 | HG02622.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.67+1601C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49768801 | ||||||
| chr19:49769194
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.67+1994G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769194 | ||||||
| chr19:49769243
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+2043C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769243 | ||||||
| chr19:49769258
|
TA | T | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.67+2067delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49769258 | |||||
| chr19:49769264
|
AAAAG | A | 7 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0212others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+2068_67+2071del others(4): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49769264 | |||||
| chr19:49769283
|
G | C | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(3): Show | 6 | HG00609.hp1 HG00621.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+2083G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769283 | ||||||
| chr19:49769435
|
C | T | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.67+2235C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769435 | ||||||
| chr19:49769555
|
G | A | 1 | a0001c0011t0001g0214 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.67+2355G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769555 | ||||||
| chr19:49769595
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.67+2395A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769595 | ||||||
| chr19:49769719
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.67+2519T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769719 | ||||||
| chr19:49769741
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.67+2541C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769741 | ||||||
| chr19:49769869
|
G | A | 42 | a0001c0001t0002g0006a0001c0001t0002g0019a0001c0001t0002g0020others(39): Show | 43 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.67+2669G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769869 | ||||||
| chr19:49769892
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.67+2692C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769892 | ||||||
| chr19:49769951
|
C | G | 1 | a0001c0001t0001g0304 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.67+2751C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769951 | ||||||
| chr19:49769994
|
C | T | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.67+2794C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769994 | ||||||
| chr19:49770029
|
T | C | 1 | a0001c0001t0003g0082 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.67+2829T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49770029 | ||||||
| chr19:49770308
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0285 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67+3108C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49770308 | ||||||
| chr19:49770344
|
A | AGAATCAG others(1597): Show |
1 | a0001c0001t0001g0194 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.67+3163_67+3164ins others(1604): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49770344 | |||||
| chr19:49770518
|
A | G | 1 | a0001c0001t0001g0177 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.67+3318A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49770518 | ||||||
| chr19:49770863
|
A | G | 44 | a0001c0001t0001g0176a0001c0001t0002g0006a0001c0001t0002g0019others(41): Show | 45 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.67+3663A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49770863 | ||||||
| chr19:49771228
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.67+4028G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49771228 | ||||||
| chr19:49771265
|
C | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.67+4065C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49771265 | ||||||
| chr19:49771277
|
G | A | 23 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0287others(20): Show | 26 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(23): Show |
intron_variant | MODIFIER | c.67+4077G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49771277 | ||||||
| chr19:49771303
|
T | TA | 29 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0076others(26): Show | 32 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.67+4126dupA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49771303 | |||||
| chr19:49771303
|
T | TAA | 38 | a0001c0001t0001g0176a0001c0001t0001g0287a0001c0001t0001g0312others(35): Show | 39 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.67+4125_67+4126dup others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49771303 | |||||
| chr19:49771303
|
TA | T | 24 | a0001c0001t0001g0016a0001c0001t0001g0169a0001c0001t0001g0170others(21): Show | 25 | HG00280.hp1 HG01169.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.67+4126delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49771303 | |||||
| chr19:49771303
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0001g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67+4116_67+4126del others(11): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49771303 | |||||
| chr19:49771448
|
TTG | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.67+4251_67+4252del others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49771448 | |||||
| chr19:49771581
|
G | A | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.67+4381G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49771581 | ||||||
| chr19:49771704
|
T | C | 64 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0176others(61): Show | 67 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.67+4504T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49771704 | ||||||
| chr19:49771921
|
G | A | 45 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0305others(42): Show | 46 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.67+4721G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49771921 | ||||||
| chr19:49771925
|
C | A | 1 | a0001c0001t0001g0217 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.67+4725C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49771925 | ||||||
| chr19:49772023
|
A | C | 1 | a0001c0001t0001g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.67+4823A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772023 | ||||||
| chr19:49772069
|
C | A | 1 | a0001c0001t0001g0309 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.67+4869C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772069 | ||||||
| chr19:49772101
|
C | T | 66 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(63): Show | 70 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.67+4901C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772101 | ||||||
| chr19:49772121
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0220a0001c0001t0001g0221others(1): Show | 5 | HG02723.hp1 HG03195.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+4921G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772121 | ||||||
| chr19:49772195
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.67+4995C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772195 | ||||||
| chr19:49772246
|
G | GT | 12 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0071others(9): Show | 12 | HG00741.hp2 HG01257.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.67+5077dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49772246 | |||||
| chr19:49772246
|
GT | G | 74 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(71): Show | 79 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.67+5077delT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49772246 | |||||
| chr19:49772246
|
GTT | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(102): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.67+5076_67+5077del others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49772246 | |||||
| chr19:49772253
|
T | TTTTTGTT others(3): Show |
1 | a0001c0001t0001g0191 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.67+5057_67+5058ins others(10): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49772253 | |||||
| chr19:49772254
|
T | C | 2 | a0001c0001t0003g0288a0001c0001t0003g0289 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.67+5054T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772254 | ||||||
| chr19:49772254
|
T | TTTTGTTT others(2): Show |
11 | a0001c0001t0001g0178a0001c0001t0001g0189a0001c0001t0002g0044others(8): Show | 11 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.67+5057_67+5058ins others(9): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49772254 | |||||
| chr19:49772255
|
T | TTTGTTTT others(1): Show |
51 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0176others(48): Show | 54 | HG00280.hp2 HG00621.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.67+5057_67+5058ins others(8): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49772255 | |||||
| chr19:49772256
|
T | G | 6 | a0001c0001t0001g0085a0001c0001t0001g0272a0001c0001t0003g0271others(3): Show | 6 | HG01192.hp1 HG01256.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+5056T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772256 | ||||||
| chr19:49772260
|
T | G | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 4 | HG00621.hp2 HG02155.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+5060T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772260 | ||||||
| chr19:49772388
|
G | A | 1 | a0001c0001t0003g0086 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.67+5188G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772388 | ||||||
| chr19:49772534
|
C | G | 2 | a0001c0001t0001g0280a0001c0001t0001g0285 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67+5334C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772534 | ||||||
| chr19:49772640
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.67+5440C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772640 | ||||||
| chr19:49772790
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.67+5590G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772790 | ||||||
| chr19:49772875
|
G | A | 90 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(87): Show | 94 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.67+5675G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772875 | ||||||
| chr19:49772881
|
A | G | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0004t0001g0211others(1): Show | 4 | HG02486.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+5681A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772881 | ||||||
| chr19:49772898
|
C | CT | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0178others(17): Show | 22 | HG01074.hp2 HG01934.hp1 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.67+5699dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49772898 | |||||
| chr19:49772924
|
G | T | 67 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0176others(64): Show | 70 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.67+5724G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772924 | ||||||
| chr19:49773157
|
G | C | 67 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0088others(64): Show | 70 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.67+5957G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49773157 | ||||||
| chr19:49773408
|
C | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0240 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.67+6208C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49773408 | ||||||
| chr19:49773411
|
C | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01099.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.67+6211C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49773411 | ||||||
| chr19:49773599
|
A | G | 68 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0088others(65): Show | 71 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.67+6399A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49773599 | ||||||
| chr19:49773611
|
T | C | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.67+6411T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49773611 | ||||||
| chr19:49773785
|
TCTAA | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0197others(19): Show | 25 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(22): Show |
intron_variant | MODIFIER | c.67+6590_67+6593del others(4): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49773785 | |||||
| chr19:49773884
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.67+6684T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49773884 | ||||||
| chr19:49774026
|
AG | A | 309 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(306): Show | 337 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.67+6830delG | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49774026 | |||||
| chr19:49774435
|
G | C | 1 | a0001c0001t0001g0309 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.67+7235G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49774435 | ||||||
| chr19:49774704
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.68-7053C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49774704 | ||||||
| chr19:49774918
|
C | CA | 10 | a0001c0001t0001g0067a0001c0001t0001g0091a0001c0001t0001g0138others(7): Show | 10 | HG00621.hp1 HG01175.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.68-6824dupA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49774918 | |||||
| chr19:49774918
|
CA | C | 166 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(163): Show | 176 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.68-6824delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49774918 | |||||
| chr19:49774918
|
CAA | C | 12 | a0001c0001t0001g0064a0001c0001t0002g0040a0001c0001t0002g0041others(9): Show | 12 | HG00280.hp2 HG00642.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-6825_68-6824del others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49774918 | |||||
| chr19:49774961
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-6796C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49774961 | ||||||
| chr19:49774995
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0220a0001c0001t0001g0221others(5): Show | 9 | HG00733.hp2 HG02258.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-6762G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49774995 | ||||||
| chr19:49775008
|
G | C | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.68-6749G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775008 | ||||||
| chr19:49775029
|
G | A | 56 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(53): Show | 59 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.68-6728G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775029 | ||||||
| chr19:49775180
|
A | G | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG00733.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.68-6577A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775180 | ||||||
| chr19:49775341
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.68-6416A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775341 | ||||||
| chr19:49775402
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0308 | 2 | HG02155.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.68-6355C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775402 | ||||||
| chr19:49775557
|
C | T | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060 | 3 | HG02622.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.68-6200C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775557 | ||||||
| chr19:49775576
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.68-6181A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775576 | ||||||
| chr19:49775669
|
C | T | 1 | a0001c0001t0001g0309 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.68-6088C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775669 | ||||||
| chr19:49775765
|
G | A | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0281 | 3 | HG02055.hp2 HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.68-5992G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775765 | ||||||
| chr19:49775965
|
C | A | 8 | a0001c0001t0001g0272a0001c0001t0001g0280a0001c0001t0001g0285others(5): Show | 8 | HG01169.hp2 HG01192.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-5792C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775965 | ||||||
| chr19:49776080
|
C | T | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060 | 3 | HG02622.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.68-5677C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776080 | ||||||
| chr19:49776082
|
G | A | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.68-5675G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776082 | ||||||
| chr19:49776097
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.68-5660C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776097 | ||||||
| chr19:49776196
|
G | GC | 9 | a0001c0001t0001g0064a0001c0001t0001g0085a0001c0001t0001g0143others(6): Show | 9 | HG00621.hp1 HG01978.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-5556dupC | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49776196 | |||||
| chr19:49776248
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.68-5509G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776248 | ||||||
| chr19:49776268
|
T | A | 1 | a0001c0001t0001g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.68-5489T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776268 | ||||||
| chr19:49776400
|
G | A | 68 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0064others(65): Show | 71 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.68-5357G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776400 | ||||||
| chr19:49776404
|
C | G | 8 | a0001c0001t0001g0272a0001c0001t0001g0280a0001c0001t0001g0285others(5): Show | 8 | HG01169.hp2 HG01192.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-5353C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776404 | ||||||
| chr19:49776501
|
G | T | 1 | a0001c0001t0002g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.68-5256G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776501 | ||||||
| chr19:49776631
|
CCT | C | 73 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(70): Show | 77 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.68-5125_68-5124del others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776631 | ||||||
| chr19:49776676
|
G | T | 6 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0067others(3): Show | 6 | HG01515.hp1 HG01517.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-5081G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776676 | ||||||
| chr19:49776721
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.68-5036A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776721 | ||||||
| chr19:49776809
|
G | C | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.68-4948G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776809 | ||||||
| chr19:49776853
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.68-4904C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776853 | ||||||
| chr19:49777076
|
G | GAAA | 6 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(3): Show | 6 | HG01255.hp1 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-4671_68-4669dup others(3): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49777076 | |||||
| chr19:49777076
|
G | GAAAA | 56 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0088others(53): Show | 59 | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.68-4672_68-4669dup others(4): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49777076 | |||||
| chr19:49777076
|
G | GAAAAA | 7 | a0001c0001t0001g0064a0001c0001t0001g0189a0001c0001t0001g0191others(4): Show | 7 | HG00621.hp2 HG04199.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-4673_68-4669dup others(5): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49777076 | |||||
| chr19:49777119
|
C | T | 16 | a0001c0001t0001g0015a0001c0001t0001g0216a0001c0001t0001g0217others(13): Show | 17 | HG00423.hp1 HG00738.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.68-4638C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777119 | ||||||
| chr19:49777219
|
A | C | 1 | a0001c0001t0001g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.68-4538A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777219 | ||||||
| chr19:49777307
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(112): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.68-4450A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777307 | ||||||
| chr19:49777357
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0285 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.68-4400C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777357 | ||||||
| chr19:49777392
|
T | A | 1 | a0001c0002t0001g0243 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.68-4365T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777392 | ||||||
| chr19:49777507
|
C | T | 5 | a0001c0001t0004g0198a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-4250C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777507 | ||||||
| chr19:49777614
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.68-4143G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777614 | ||||||
| chr19:49777622
|
G | A | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0281 | 3 | HG02055.hp2 HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.68-4135G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777622 | ||||||
| chr19:49777634
|
C | CAA | 59 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0064others(56): Show | 62 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.68-4109_68-4108dup others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49777634 | |||||
| chr19:49777634
|
C | CAAA | 6 | a0001c0001t0001g0181a0001c0001t0002g0020a0001c0001t0002g0021others(3): Show | 6 | HG02055.hp1 HG03669.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-4110_68-4108dup others(3): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49777634 | |||||
| chr19:49777799
|
C | T | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.68-3958C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777799 | ||||||
| chr19:49777809
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.68-3948T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777809 | ||||||
| chr19:49777833
|
TG | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(109): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.68-3921delG | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49777833 | |||||
| chr19:49778112
|
C | G | 68 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0064others(65): Show | 71 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.68-3645C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778112 | ||||||
| chr19:49778120
|
A | C | 1 | a0001c0001t0001g0061 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.68-3637A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778120 | ||||||
| chr19:49778139
|
G | A | 4 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(1): Show | 4 | HG02145.hp2 HG02647.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-3618G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778139 | ||||||
| chr19:49778166
|
A | G | 1 | a0001c0001t0001g0309 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.68-3591A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778166 | ||||||
| chr19:49778280
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(110): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.68-3477T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778280 | ||||||
| chr19:49778303
|
C | G | 1 | a0001c0001t0001g0136 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.68-3454C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778303 | ||||||
| chr19:49778335
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.68-3422C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778335 | ||||||
| chr19:49778341
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.68-3416G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778341 | ||||||
| chr19:49778349
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-3408G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778349 | ||||||
| chr19:49778379
|
T | C | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.68-3378T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778379 | ||||||
| chr19:49778586
|
G | T | 1 | a0001c0001t0001g0191 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.68-3171G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778586 | ||||||
| chr19:49778680
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.68-3077C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778680 | ||||||
| chr19:49778796
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0286others(14): Show | 20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-2961G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778796 | ||||||
| chr19:49778828
|
T | TA | 7 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0298others(4): Show | 7 | HG02683.hp1 HG02698.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-2926dupA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49778828 | |||||
| chr19:49778902
|
CAT | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.68-2845_68-2844del others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49778902 | |||||
| chr19:49779002
|
C | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0286others(14): Show | 20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-2755C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779002 | ||||||
| chr19:49779033
|
C | CA | 98 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(95): Show | 102 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.68-2707dupA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779033 | |||||
| chr19:49779050
|
A | T | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.68-2707A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779050 | ||||||
| chr19:49779062
|
C | T | 69 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0064others(66): Show | 72 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.68-2695C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779062 | ||||||
| chr19:49779063
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.68-2694G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779063 | ||||||
| chr19:49779240
|
G | A | 1 | a0001c0004t0001g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.68-2517G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779240 | ||||||
| chr19:49779305
|
C | G | 2 | a0001c0001t0003g0288a0001c0001t0003g0289 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.68-2452C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779305 | ||||||
| chr19:49779332
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.68-2425G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779332 | ||||||
| chr19:49779336
|
C | CA | 8 | a0001c0001t0001g0067a0001c0001t0001g0216a0001c0001t0001g0217others(5): Show | 8 | HG03453.hp2 HG03486.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-2400dupA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779336 | |||||
| chr19:49779336
|
CA | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.68-2400delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779336 | |||||
| chr19:49779336
|
CAA | C | 9 | a0001c0001t0001g0135a0001c0001t0001g0160a0001c0001t0001g0171others(6): Show | 9 | HG01515.hp2 HG01884.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-2401_68-2400del others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779336 | |||||
| chr19:49779363
|
T | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(1): Show | 4 | HG02145.hp2 HG02647.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-2394T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779363 | ||||||
| chr19:49779460
|
T | C | 68 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0064others(65): Show | 71 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.68-2297T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779460 | ||||||
| chr19:49779487
|
C | CA | 35 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(32): Show | 35 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.68-2246dupA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779487 | |||||
| chr19:49779487
|
C | CAA | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(67): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.68-2247_68-2246dup others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779487 | |||||
| chr19:49779487
|
C | CAAA | 32 | a0001c0001t0001g0008a0001c0001t0001g0079a0001c0001t0001g0084others(29): Show | 33 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.68-2248_68-2246dup others(3): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779487 | |||||
| chr19:49779487
|
C | CAAAAAAA others(1365): Show |
1 | a0001c0001t0001g0180 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.68-2118_68-2117ins others(1372): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779487 | |||||
| chr19:49779487
|
C | CAAAAAAA others(2737): Show |
1 | a0001c0001t0001g0187 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.68-2247_68-2246ins others(2744): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779487 | |||||
| chr19:49779487
|
CA | C | 51 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0064others(48): Show | 54 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.68-2246delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779487 | |||||
| chr19:49779500
|
A | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0286others(14): Show | 20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-2257A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779500 | ||||||
| chr19:49779511
|
A | AAAC | 11 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0125others(8): Show | 11 | HG01109.hp1 HG01109.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-2246_68-2245ins others(3): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779511 | ||||||
| chr19:49779511
|
A | AAC | 6 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-2246_68-2245ins others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779511 | ||||||
| chr19:49779640
|
G | A | 64 | a0001c0001t0001g0011a0001c0001t0001g0064a0001c0001t0001g0088others(61): Show | 66 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.68-2117G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779640 | ||||||
| chr19:49780080
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0220a0001c0001t0001g0221others(5): Show | 9 | HG00733.hp2 HG02258.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-1677A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780080 | ||||||
| chr19:49780122
|
C | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(298): Show | 329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.68-1635C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780122 | ||||||
| chr19:49780188
|
C | T | 1 | a0001c0001t0002g0038 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.68-1569C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780188 | ||||||
| chr19:49780215
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.68-1542G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780215 | ||||||
| chr19:49780378
|
C | A | 1 | a0001c0001t0001g0094 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.68-1379C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780378 | ||||||
| chr19:49780382
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.68-1375G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780382 | ||||||
| chr19:49780467
|
G | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0148 | 2 | NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.68-1290G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780467 | ||||||
| chr19:49780910
|
C | T | 5 | a0001c0001t0001g0239a0001c0001t0001g0259a0001c0001t0001g0268others(2): Show | 5 | HG00738.hp1 HG01074.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-847C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780910 | ||||||
| chr19:49780933
|
TGGA | T | 8 | a0001c0001t0001g0065a0001c0001t0001g0071a0001c0001t0001g0272others(5): Show | 8 | HG01169.hp2 HG01192.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-819_68-817delGA others(1): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49780933 | |||||
| chr19:49780950
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.68-807C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780950 | ||||||
| chr19:49781312
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-445T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49781312 | ||||||
| chr19:49781440
|
G | C | 1 | a0001c0001t0001g0263 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.68-317G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49781440 | ||||||
| chr19:49781675
|
G | C | 3 | a0001c0001t0001g0244a0001c0001t0001g0250a0001c0001t0002g0208 | 3 | NA18961.hp1 NA18969.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.68-82G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49781675 | ||||||
| chr19:49781834
|
G | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.136+9G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 2/22 | chr19 | 49781834 | ||||||
| chr19:49781839
|
C | T | 4 | a0001c0001t0004g0198a0001c0001t0004g0199a0001c0001t0004g0200others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+14C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 2/22 | chr19 | 49781839 | ||||||
| chr19:49782135
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.279+46C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 3/22 | chr19 | 49782135 | ||||||
| chr19:49782136
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.279+47G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 3/22 | chr19 | 49782136 | ||||||
| chr19:49782217
|
G | A | 1 | a0001c0005t0001g0190 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.279+128G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 3/22 | chr19 | 49782217 | ||||||
| chr19:49782252
|
G | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0286others(14): Show | 20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.279+163G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 3/22 | chr19 | 49782252 | ||||||
| chr19:49782388
|
T | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.280-143T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 3/22 | chr19 | 49782388 | ||||||
| chr19:49782479
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.280-52G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 3/22 | chr19 | 49782479 | ||||||
| chr19:49782742
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.473+18C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49782742 | ||||||
| chr19:49782743
|
G | A | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0004t0001g0211others(1): Show | 4 | HG02486.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.473+19G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49782743 | ||||||
| chr19:49782970
|
T | A | 1 | a0001c0001t0001g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.473+246T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49782970 | ||||||
| chr19:49782971
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.473+247T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49782971 | ||||||
| chr19:49783081
|
C | T | 83 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(80): Show | 87 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.473+357C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783081 | ||||||
| chr19:49783125
|
T | C | 78 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(75): Show | 82 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.473+401T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783125 | ||||||
| chr19:49783517
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.473+793C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783517 | ||||||
| chr19:49783593
|
A | T | 2 | a0001c0001t0002g0026a0001c0001t0002g0027 | 2 | HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.473+869A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783593 | ||||||
| chr19:49783679
|
G | C | 24 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0178others(21): Show | 26 | HG01074.hp2 HG01934.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.473+955G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783679 | ||||||
| chr19:49783736
|
C | G | 19 | a0001c0001t0001g0013a0001c0001t0001g0127a0001c0001t0001g0128others(16): Show | 20 | HG00733.hp2 HG01346.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.473+1012C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783736 | ||||||
| chr19:49783840
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.473+1116G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783840 | ||||||
| chr19:49783922
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.473+1198A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783922 | ||||||
| chr19:49783943
|
T | C | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 10 | HG01346.hp2 HG02257.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.473+1219T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783943 | ||||||
| chr19:49783998
|
A | G | 77 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(74): Show | 81 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.473+1274A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783998 | ||||||
| chr19:49784062
|
A | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.473+1338A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784062 | ||||||
| chr19:49784145
|
A | C | 1 | a0001c0001t0002g0037 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.473+1421A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784145 | ||||||
| chr19:49784340
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1616G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784340 | ||||||
| chr19:49784346
|
C | G | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1622C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784346 | ||||||
| chr19:49784347
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1623A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784347 | ||||||
| chr19:49784348
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1624C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784348 | ||||||
| chr19:49784351
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1627G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784351 | ||||||
| chr19:49784352
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1628A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784352 | ||||||
| chr19:49784353
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1629A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784353 | ||||||
| chr19:49784355
|
C | A | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1631C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784355 | ||||||
| chr19:49784356
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1632C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784356 | ||||||
| chr19:49784364
|
A | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1640A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784364 | ||||||
| chr19:49784366
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1642A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784366 | ||||||
| chr19:49784367
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1643G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784367 | ||||||
| chr19:49784368
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.473+1644G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784368 | ||||||
| chr19:49784368
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1644G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784368 | ||||||
| chr19:49784368
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.473+1644G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784368 | ||||||
| chr19:49784370
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1646T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784370 | ||||||
| chr19:49784372
|
C | A | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1648C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784372 | ||||||
| chr19:49784374
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1650G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784374 | ||||||
| chr19:49784378
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1654G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784378 | ||||||
| chr19:49784381
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1657G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784381 | ||||||
| chr19:49784384
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1660A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784384 | ||||||
| chr19:49784386
|
C | G | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1662C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784386 | ||||||
| chr19:49784387
|
A | G | 209 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(206): Show | 219 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.473+1663A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784387 | ||||||
| chr19:49784389
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1665G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784389 | ||||||
| chr19:49784390
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1666C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784390 | ||||||
| chr19:49784391
|
C | G | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1667C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784391 | ||||||
| chr19:49784392
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1668A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784392 | ||||||
| chr19:49784397
|
A | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1673A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784397 | ||||||
| chr19:49784406
|
T | TCCCAAAG others(5): Show |
1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1682_473+1683i others(14): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784406 | ||||||
| chr19:49784409
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1685G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784409 | ||||||
| chr19:49784411
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1687G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784411 | ||||||
| chr19:49784420
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1696A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784420 | ||||||
| chr19:49784421
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1697G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784421 | ||||||
| chr19:49784429
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1705C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784429 | ||||||
| chr19:49784431
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1707C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784431 | ||||||
| chr19:49784431
|
CA | C | 95 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(92): Show | 99 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.473+1719delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49784431 | |||||
| chr19:49784432
|
AAAAAAAA others(26): Show |
A | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1709_473+1741d others(35): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784432 | ||||||
| chr19:49784469
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1745G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784469 | ||||||
| chr19:49784470
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1746G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784470 | ||||||
| chr19:49784471
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1747A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784471 | ||||||
| chr19:49784472
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1748A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784472 | ||||||
| chr19:49784481
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1757A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784481 | ||||||
| chr19:49784483
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1759A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784483 | ||||||
| chr19:49784486
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1762G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784486 | ||||||
| chr19:49784498
|
A | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1774A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784498 | ||||||
| chr19:49784499
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1775G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784499 | ||||||
| chr19:49784501
|
A | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1777A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784501 | ||||||
| chr19:49784502
|
T | A | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1778T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784502 | ||||||
| chr19:49784503
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1779A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784503 | ||||||
| chr19:49784505
|
T | G | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1781T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784505 | ||||||
| chr19:49784510
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1786A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784510 | ||||||
| chr19:49784544
|
T | C | 94 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(91): Show | 98 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.473+1820T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784544 | ||||||
| chr19:49784817
|
A | G | 94 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(91): Show | 98 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.473+2093A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784817 | ||||||
| chr19:49784882
|
A | C | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.473+2158A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784882 | ||||||
| chr19:49784887
|
C | A | 11 | a0001c0001t0001g0155a0001c0001t0001g0197a0001c0001t0001g0212others(8): Show | 11 | HG02486.hp2 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.473+2163C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784887 | ||||||
| chr19:49784902
|
A | G | 6 | a0001c0001t0001g0197a0001c0001t0004g0198a0001c0001t0004g0199others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+2178A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784902 | ||||||
| chr19:49785550
|
A | C | 6 | a0001c0001t0001g0197a0001c0001t0004g0198a0001c0001t0004g0199others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+2826A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49785550 | ||||||
| chr19:49785636
|
G | T | 1 | a0001c0001t0001g0238 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.473+2912G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49785636 | ||||||
| chr19:49786054
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0285 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.473+3330C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786054 | ||||||
| chr19:49786160
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.473+3436T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786160 | ||||||
| chr19:49786171
|
C | CAAGAGGC others(13): Show |
83 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(80): Show | 87 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.473+3459_473+3460i others(22): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49786171 | |||||
| chr19:49786338
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.473+3614G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786338 | ||||||
| chr19:49786393
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.473+3669T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786393 | ||||||
| chr19:49786497
|
G | C | 1 | a0001c0006t0002g0039 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.473+3773G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786497 | ||||||
| chr19:49786599
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.473+3875G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786599 | ||||||
| chr19:49786602
|
G | A | 204 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(201): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.473+3878G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786602 | ||||||
| chr19:49786691
|
A | G | 73 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(70): Show | 77 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.473+3967A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786691 | ||||||
| chr19:49786749
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.473+4025G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786749 | ||||||
| chr19:49787329
|
TTTTTGTT others(18): Show |
T | 4 | a0001c0001t0001g0013a0001c0001t0001g0220a0001c0001t0001g0221others(1): Show | 5 | HG02723.hp1 HG03195.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-4601_474-4577d others(27): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787329 | |||||
| chr19:49787331
|
TTTGTTTG others(9): Show |
T | 3 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0055 | 3 | HG03704.hp1 NA18955.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.474-4601_474-4586d others(18): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787331 | |||||
| chr19:49787332
|
TTGTTTGT others(8): Show |
T | 71 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(68): Show | 75 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.474-4601_474-4587d others(17): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787332 | |||||
| chr19:49787333
|
TGTTTGTT others(7): Show |
T | 4 | a0001c0001t0001g0191a0001c0001t0002g0029a0001c0001t0002g0036others(1): Show | 4 | HG02083.hp2 NA18990.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-4601_474-4588d others(16): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787333 | ||||||
| chr19:49787334
|
G | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.474-4601G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787334 | ||||||
| chr19:49787338
|
G | GT | 26 | a0001c0001t0001g0080a0001c0001t0001g0124a0001c0001t0001g0129others(23): Show | 26 | HG00438.hp2 HG00738.hp1 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.474-4589dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787338 | |||||
| chr19:49787338
|
G | T | 8 | a0001c0001t0001g0196a0001c0001t0001g0201a0001c0001t0001g0202others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.474-4597G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787338 | ||||||
| chr19:49787341
|
T | G | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.474-4594T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787341 | ||||||
| chr19:49787342
|
T | G | 5 | a0001c0001t0001g0196a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-4593T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787342 | ||||||
| chr19:49787346
|
T | G | 1 | a0001c0001t0001g0213 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.474-4589T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787346 | ||||||
| chr19:49787346
|
TG | T | 3 | a0001c0001t0001g0167a0001c0001t0005g0224a0001c0001t0005g0225 | 3 | HG02258.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.474-4588delG | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787346 | ||||||
| chr19:49787347
|
G | GT | 17 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0201others(14): Show | 20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.474-4582dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787347 | |||||
| chr19:49787347
|
G | GTT | 12 | a0001c0001t0001g0272a0001c0001t0001g0280a0001c0001t0001g0285others(9): Show | 12 | HG01169.hp2 HG01256.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.474-4583_474-4582d others(4): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787347 | |||||
| chr19:49787347
|
G | T | 71 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0061others(68): Show | 72 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.474-4588G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787347 | ||||||
| chr19:49787353
|
T | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.474-4582T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787353 | ||||||
| chr19:49787354
|
G | T | 194 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(191): Show | 202 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.474-4581G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787354 | ||||||
| chr19:49787356
|
T | G | 14 | a0001c0001t0001g0015a0001c0001t0001g0062a0001c0001t0001g0063others(11): Show | 15 | HG00099.hp1 HG00423.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.474-4579T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787356 | ||||||
| chr19:49787513
|
A | AT | 9 | a0001c0001t0001g0163a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 9 | HG02109.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-4406dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787513 | |||||
| chr19:49787513
|
AT | A | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(94): Show | 101 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.474-4406delT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787513 | |||||
| chr19:49787592
|
A | G | 204 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(201): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.474-4343A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787592 | ||||||
| chr19:49787644
|
C | T | 6 | a0001c0001t0001g0197a0001c0001t0004g0198a0001c0001t0004g0199others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-4291C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787644 | ||||||
| chr19:49787796
|
C | T | 3 | a0001c0001t0001g0290a0001c0001t0001g0298a0001c0001t0001g0302 | 3 | HG02683.hp1 HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.474-4139C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787796 | ||||||
| chr19:49787876
|
A | G | 4 | a0001c0001t0001g0155a0001c0001t0002g0058a0001c0001t0002g0059others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-4059A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787876 | ||||||
| chr19:49787889
|
C | G | 12 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(9): Show | 12 | HG00099.hp1 HG00741.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.474-4046C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787889 | ||||||
| chr19:49787925
|
C | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0004t0001g0211others(1): Show | 4 | HG02486.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.474-4010C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787925 | ||||||
| chr19:49787983
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.474-3952G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787983 | ||||||
| chr19:49787992
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.474-3943G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787992 | ||||||
| chr19:49788009
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.474-3926T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788009 | ||||||
| chr19:49788238
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.474-3697C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788238 | ||||||
| chr19:49788240
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.474-3695C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788240 | ||||||
| chr19:49788260
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0109 | 3 | HG01257.hp2 HG01258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.474-3675T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788260 | ||||||
| chr19:49788301
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.474-3634C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788301 | ||||||
| chr19:49788416
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.474-3519A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788416 | ||||||
| chr19:49788424
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.474-3511G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788424 | ||||||
| chr19:49788449
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.474-3486G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788449 | ||||||
| chr19:49788521
|
C | T | 10 | a0001c0001t0001g0155a0001c0001t0001g0197a0001c0001t0002g0058others(7): Show | 10 | HG02486.hp2 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.474-3414C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788521 | ||||||
| chr19:49788550
|
T | A | 22 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(19): Show | 22 | HG00099.hp1 HG00741.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.474-3385T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788550 | ||||||
| chr19:49788578
|
A | G | 73 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(70): Show | 77 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.474-3357A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788578 | ||||||
| chr19:49788707
|
C | T | 4 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0005g0224others(1): Show | 4 | HG00733.hp2 HG02258.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.474-3228C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788707 | ||||||
| chr19:49788798
|
G | A | 2 | a0001c0001t0001g0292a0001c0001t0001g0297 | 2 | HG00597.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.474-3137G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788798 | ||||||
| chr19:49789086
|
C | A | 10 | a0001c0001t0001g0155a0001c0001t0001g0197a0001c0001t0002g0058others(7): Show | 10 | HG02486.hp2 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.474-2849C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789086 | ||||||
| chr19:49789400
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474-2535C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789400 | ||||||
| chr19:49789590
|
C | CT | 55 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(52): Show | 63 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.474-2326dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49789590 | |||||
| chr19:49789590
|
CT | C | 129 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(126): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.474-2326delT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49789590 | |||||
| chr19:49789590
|
CTT | C | 6 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0068others(3): Show | 6 | HG01515.hp1 HG01517.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-2327_474-2326d others(4): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49789590 | |||||
| chr19:49789607
|
T | G | 4 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(1): Show | 4 | HG02145.hp2 HG02647.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.474-2328T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789607 | ||||||
| chr19:49789753
|
C | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0123others(4): Show | 9 | HG00609.hp2 HG00673.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-2182C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789753 | ||||||
| chr19:49789826
|
C | A | 1 | a0001c0001t0002g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.474-2109C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789826 | ||||||
| chr19:49789853
|
T | G | 95 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(92): Show | 99 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.474-2082T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789853 | ||||||
| chr19:49789968
|
C | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0044 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.474-1967C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789968 | ||||||
| chr19:49789972
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.474-1963C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789972 | ||||||
| chr19:49790154
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.474-1781C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790154 | ||||||
| chr19:49790171
|
A | T | 12 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(9): Show | 12 | HG00099.hp1 HG00741.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.474-1764A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790171 | ||||||
| chr19:49790178
|
G | A | 83 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(80): Show | 87 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.474-1757G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790178 | ||||||
| chr19:49790361
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.474-1574C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790361 | ||||||
| chr19:49790443
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.474-1492T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790443 | ||||||
| chr19:49790484
|
C | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0220a0001c0001t0001g0221others(1): Show | 5 | HG02723.hp1 HG03195.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-1451C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790484 | ||||||
| chr19:49790495
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.474-1440C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790495 | ||||||
| chr19:49790647
|
A | G | 22 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(19): Show | 22 | HG00099.hp1 HG00741.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.474-1288A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790647 | ||||||
| chr19:49790755
|
C | A | 8 | a0001c0001t0001g0272a0001c0001t0001g0280a0001c0001t0001g0285others(5): Show | 8 | HG01169.hp2 HG01192.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.474-1180C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790755 | ||||||
| chr19:49790837
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.474-1098A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790837 | ||||||
| chr19:49790893
|
G | A | 109 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(106): Show | 114 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.474-1042G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790893 | ||||||
| chr19:49791110
|
A | G | 101 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(98): Show | 105 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.474-825A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791110 | ||||||
| chr19:49791200
|
T | G | 73 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(70): Show | 77 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.474-735T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791200 | ||||||
| chr19:49791258
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.474-677C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791258 | ||||||
| chr19:49791353
|
C | T | 1 | a0001c0002t0001g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.474-582C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791353 | ||||||
| chr19:49791384
|
C | T | 76 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0018others(73): Show | 78 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.474-551C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791384 | ||||||
| chr19:49791453
|
A | G | 1 | a0001c0001t0001g0181 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.474-482A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791453 | ||||||
| chr19:49791502
|
T | C | 99 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(96): Show | 103 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.474-433T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791502 | ||||||
| chr19:49791806
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.474-129G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791806 | ||||||
| chr19:49791808
|
C | G | 1 | a0001c0001t0001g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.474-127C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791808 | ||||||
| chr19:49791891
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0285 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.474-44G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791891 | ||||||
| chr19:49792169
|
C | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0136others(1): Show | 5 | HG01243.hp2 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.603+105C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792169 | ||||||
| chr19:49792198
|
C | T | 6 | a0001c0001t0001g0197a0001c0001t0004g0198a0001c0001t0004g0199others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.603+134C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792198 | ||||||
| chr19:49792210
|
GGGGCTCC others(105): Show |
G | 3 | a0001c0001t0001g0157a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG02055.hp2 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.603+220_603+331del | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr19 | 49792210 | |||||
| chr19:49792232
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0004g0199a0001c0001t0004g0200 | 3 | HG02622.hp1 HG02717.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.603+168C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792232 | ||||||
| chr19:49792233
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.603+169G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792233 | ||||||
| chr19:49792239
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.603+175G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792239 | ||||||
| chr19:49792281
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.603+217G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792281 | ||||||
| chr19:49792303
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.603+239C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792303 | ||||||
| chr19:49792307
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.603+243C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792307 | ||||||
| chr19:49792350
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.603+286C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792350 | ||||||
| chr19:49792448
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.603+384G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792448 | ||||||
| chr19:49792451
|
G | C | 87 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(84): Show | 91 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.603+387G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792451 | ||||||
| chr19:49792540
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.604-451C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792540 | ||||||
| chr19:49792640
|
C | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0109 | 3 | HG01257.hp2 HG01258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.604-351C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792640 | ||||||
| chr19:49792838
|
C | T | 4 | a0001c0002t0001g0228a0001c0002t0001g0230a0001c0002t0001g0243others(1): Show | 4 | HG00438.hp2 HG02071.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.604-153C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792838 | ||||||
| chr19:49792878
|
A | G | 4 | a0001c0001t0001g0176a0001c0001t0002g0006a0001c0001t0002g0036others(1): Show | 5 | NA18960.hp2 NA18961.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-113A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792878 | ||||||
| chr19:49792888
|
T | C | 87 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(84): Show | 91 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.604-103T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792888 | ||||||
| chr19:49792892
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.604-99C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792892 | ||||||
| chr19:49792976
|
C | T | 3 | a0001c0001t0001g0215a0001c0001t0001g0233a0001c0001t0001g0248 | 3 | HG03834.hp1 NA18989.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.604-15C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792976 | ||||||
| chr19:49793134
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.705+42C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793134 | ||||||
| chr19:49793186
|
C | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0004t0001g0211others(1): Show | 4 | HG02486.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+94C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793186 | ||||||
| chr19:49793236
|
C | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0004t0001g0211others(1): Show | 4 | HG02486.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+144C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793236 | ||||||
| chr19:49793291
|
G | C | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0004t0001g0211others(1): Show | 4 | HG02486.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+199G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793291 | ||||||
| chr19:49793393
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.705+301G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793393 | ||||||
| chr19:49793403
|
C | T | 2 | a0001c0001t0003g0082a0001c0001t0003g0168 | 2 | HG01952.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.705+311C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793403 | ||||||
| chr19:49793461
|
T | C | 1 | a0001c0011t0001g0214 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.705+369T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793461 | ||||||
| chr19:49793636
|
A | C | 3 | a0001c0001t0001g0135a0001c0001t0001g0156a0001c0001t0001g0157 | 3 | HG01884.hp2 HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.705+544A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793636 | ||||||
| chr19:49793747
|
A | C | 87 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(84): Show | 91 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.705+655A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793747 | ||||||
| chr19:49793898
|
C | CT | 101 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(98): Show | 105 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.705+833dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr19 | 49793898 | |||||
| chr19:49793898
|
C | CTT | 20 | a0001c0001t0001g0070a0001c0001t0001g0138a0001c0001t0001g0186others(17): Show | 20 | HG00642.hp2 HG00741.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.705+832_705+833dup others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr19 | 49793898 | |||||
| chr19:49793898
|
CT | C | 26 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0110others(23): Show | 29 | HG00280.hp1 HG00597.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.705+833delT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr19 | 49793898 | |||||
| chr19:49794012
|
A | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0105a0001c0001t0001g0160others(1): Show | 4 | HG02559.hp1 HG02602.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+920A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794012 | ||||||
| chr19:49794017
|
T | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0105a0001c0001t0001g0160others(1): Show | 4 | HG02559.hp1 HG02602.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+925T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794017 | ||||||
| chr19:49794026
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0123others(2): Show | 7 | HG00609.hp2 HG00738.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.705+934G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794026 | ||||||
| chr19:49794133
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.705+1041C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794133 | ||||||
| chr19:49794135
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.705+1043C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794135 | ||||||
| chr19:49794143
|
ACCCGCCT others(295): Show |
A | 1 | a0001c0001t0001g0251 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.705+1060_706-1177d others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr19 | 49794143 | |||||
| chr19:49794179
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.705+1087C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794179 | ||||||
| chr19:49794221
|
G | GT | 97 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(94): Show | 101 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.705+1143dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr19 | 49794221 | |||||
| chr19:49794255
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.705+1163G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794255 | ||||||
| chr19:49794263
|
T | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0286others(14): Show | 20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.705+1171T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794263 | ||||||
| chr19:49794297
|
C | A | 73 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(70): Show | 77 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.705+1205C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794297 | ||||||
| chr19:49794357
|
G | A | 73 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(70): Show | 77 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.705+1265G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794357 | ||||||
| chr19:49794407
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.706-1223G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794407 | ||||||
| chr19:49794412
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.706-1218C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794412 | ||||||
| chr19:49794557
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.706-1073G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794557 | ||||||
| chr19:49794684
|
T | C | 1 | a0001c0001t0001g0244 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.706-946T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794684 | ||||||
| chr19:49794736
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.706-894C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794736 | ||||||
| chr19:49794860
|
A | G | 204 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(201): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.706-770A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794860 | ||||||
| chr19:49794916
|
G | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0287others(8): Show | 14 | HG00597.hp1 HG02135.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.706-714G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794916 | ||||||
| chr19:49794965
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.706-665G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794965 | ||||||
| chr19:49794972
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.706-658C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794972 | ||||||
| chr19:49795162
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.706-468T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49795162 | ||||||
| chr19:49795368
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.706-262T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49795368 | ||||||
| chr19:49795399
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.706-231G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49795399 | ||||||
| chr19:49795469
|
C | T | 1 | a0001c0001t0001g0311 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.706-161C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49795469 | ||||||
| chr19:49795476
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0113 | 2 | HG01934.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.706-154G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49795476 | ||||||
| chr19:49795547
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.706-83C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49795547 | ||||||
| chr19:49795808
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.814+70G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49795808 | ||||||
| chr19:49796063
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.814+325C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796063 | ||||||
| chr19:49796151
|
T | G | 169 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(166): Show | 176 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.814+413T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796151 | ||||||
| chr19:49796226
|
G | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0071a0001c0001t0001g0232 | 3 | HG02602.hp1 HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.814+488G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796226 | ||||||
| chr19:49796349
|
C | T | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0104others(16): Show | 21 | HG01934.hp1 HG01978.hp2 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.814+611C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796349 | ||||||
| chr19:49796456
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.814+718G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796456 | ||||||
| chr19:49796497
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.814+759T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796497 | ||||||
| chr19:49796500
|
A | G | 170 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(167): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.814+762A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796500 | ||||||
| chr19:49796608
|
C | T | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0064others(36): Show | 41 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.814+870C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796608 | ||||||
| chr19:49796609
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0179others(15): Show | 21 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.814+871G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796609 | ||||||
| chr19:49796644
|
T | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0105a0001c0001t0001g0160others(1): Show | 4 | HG02559.hp1 HG02602.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.814+906T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796644 | ||||||
| chr19:49796659
|
CCT | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0102a0001c0001t0001g0116others(9): Show | 14 | HG00609.hp2 HG00673.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.814+922_814+923del others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796659 | ||||||
| chr19:49796769
|
A | G | 120 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(117): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.814+1031A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796769 | ||||||
| chr19:49796808
|
A | G | 1 | a0001c0011t0001g0214 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.814+1070A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796808 | ||||||
| chr19:49796910
|
T | C | 1 | a0001c0001t0004g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.814+1172T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796910 | ||||||
| chr19:49797068
|
C | G | 6 | a0001c0001t0001g0196a0001c0001t0001g0201a0001c0001t0001g0203others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.814+1330C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49797068 | ||||||
| chr19:49797220
|
C | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0179others(18): Show | 24 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.814+1482C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49797220 | ||||||
| chr19:49797522
|
C | T | 12 | a0001c0001t0001g0088a0001c0001t0001g0176a0001c0001t0002g0006others(9): Show | 13 | HG01975.hp1 NA18952.hp1 NA18959.hp1 others(10): Show |
intron_variant | MODIFIER | c.815-1280C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49797522 | ||||||
| chr19:49797851
|
CAGA | C | 30 | a0001c0001t0001g0018a0001c0001t0001g0118a0001c0001t0001g0193others(27): Show | 30 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.815-948_815-946del others(3): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr19 | 49797851 | |||||
| chr19:49797877
|
T | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.815-925T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49797877 | ||||||
| chr19:49797895
|
A | T | 67 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0061others(64): Show | 69 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.815-907A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49797895 | ||||||
| chr19:49797913
|
CA | C | 118 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.815-883delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr19 | 49797913 | |||||
| chr19:49797961
|
C | T | 5 | a0001c0001t0004g0198a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.815-841C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49797961 | ||||||
| chr19:49798030
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0179others(15): Show | 21 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.815-772C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798030 | ||||||
| chr19:49798151
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.815-651T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798151 | ||||||
| chr19:49798172
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.815-630C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798172 | ||||||
| chr19:49798178
|
A | C | 1 | a0001c0001t0002g0024 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.815-624A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798178 | ||||||
| chr19:49798287
|
G | C | 1 | a0001c0001t0002g0020 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.815-515G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798287 | ||||||
| chr19:49798288
|
G | A | 118 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.815-514G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798288 | ||||||
| chr19:49798338
|
C | T | 2 | a0001c0004t0001g0211a0001c0004t0001g0310 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.815-464C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798338 | ||||||
| chr19:49798396
|
A | G | 179 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(176): Show | 188 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.815-406A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798396 | ||||||
| chr19:49798542
|
C | T | 2 | a0001c0004t0001g0211a0001c0004t0001g0310 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.815-260C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798542 | ||||||
| chr19:49798563
|
A | G | 42 | a0001c0001t0001g0018a0001c0001t0001g0118a0001c0001t0001g0127others(39): Show | 42 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.815-239A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798563 | ||||||
| chr19:49798587
|
T | G | 118 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.815-215T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798587 | ||||||
| chr19:49798618
|
C | G | 5 | a0001c0001t0004g0198a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.815-184C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798618 | ||||||
| chr19:49799031
|
G | C | 1 | a0001c0001t0001g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.965+79G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 8/22 | chr19 | 49799031 | ||||||
| chr19:49799251
|
T | C | 1 | a0001c0001t0001g0299 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.966-76T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 8/22 | chr19 | 49799251 | ||||||
| chr19:49799579
|
G | C | 1 | a0001c0001t0001g0272 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1135-50G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 9/22 | chr19 | 49799579 | ||||||
| chr19:49799941
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1273-27A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 10/22 | chr19 | 49799941 | ||||||
| chr19:49799943
|
T | A | 1 | a0001c0001t0001g0080 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1273-25T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 10/22 | chr19 | 49799943 | ||||||
| chr19:49800202
|
G | C | 1 | a0001c0001t0001g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1455+52G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800202 | ||||||
| chr19:49800227
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1455+77G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800227 | ||||||
| chr19:49800267
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1455+117G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800267 | ||||||
| chr19:49800356
|
G | C | 45 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0118others(42): Show | 45 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1455+206G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800356 | ||||||
| chr19:49800403
|
G | A | 21 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0179others(18): Show | 24 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455+253G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800403 | ||||||
| chr19:49800410
|
T | C | 2 | a0001c0004t0001g0211a0001c0004t0001g0310 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1455+260T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800410 | ||||||
| chr19:49800449
|
T | TTTTG | 22 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0162others(19): Show | 25 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1455+319_1455+322d others(6): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr19 | 49800449 | |||||
| chr19:49800482
|
G | A | 25 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0088others(22): Show | 27 | HG01934.hp1 HG01975.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.1455+332G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800482 | ||||||
| chr19:49800496
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1455+346T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800496 | ||||||
| chr19:49800532
|
G | A | 6 | a0001c0001t0001g0196a0001c0001t0001g0201a0001c0001t0001g0203others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+382G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800532 | ||||||
| chr19:49801079
|
A | G | 120 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(117): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1553+21A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 12/22 | chr19 | 49801079 | ||||||
| chr19:49801132
|
G | GTCCCAGG others(16): Show |
1 | a0001c0001t0001g0261 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1553+76_1553+77ins others(23): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr19 | 49801132 | |||||
| chr19:49801135
|
T | C | 120 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(117): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1553+77T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 12/22 | chr19 | 49801135 | ||||||
| chr19:49801182
|
T | C | 120 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(117): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1553+124T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 12/22 | chr19 | 49801182 | ||||||
| chr19:49801189
|
A | G | 1 | a0001c0010t0001g0122 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1553+131A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 12/22 | chr19 | 49801189 | ||||||
| chr19:49801190
|
G | C | 1 | a0001c0010t0001g0122 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1553+132G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 12/22 | chr19 | 49801190 | ||||||
| chr19:49801191
|
C | G | 1 | a0001c0010t0001g0122 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1553+133C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 12/22 | chr19 | 49801191 | ||||||
| chr19:49801635
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1785+14C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 13/22 | chr19 | 49801635 | ||||||
| chr19:49801664
|
C | T | 1 | a0001c0010t0001g0122 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1785+43C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 13/22 | chr19 | 49801664 | ||||||
| chr19:49801694
|
C | A | 1 | a0001c0001t0001g0242 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1786-28C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 13/22 | chr19 | 49801694 | ||||||
| chr19:49801909
|
CCCTGCCA others(18): Show |
C | 1 | a0001c0001t0001g0115 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1953+27_1954-41del others(25): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr19 | 49801909 | |||||
| chr19:49801968
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0284 | 2 | HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1954-13G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 14/22 | chr19 | 49801968 | ||||||
| chr19:49802230
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2114+89C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802230 | ||||||
| chr19:49802304
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2114+163C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802304 | ||||||
| chr19:49802346
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2114+205G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802346 | ||||||
| chr19:49802361
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2114+220T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802361 | ||||||
| chr19:49802362
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2114+221C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802362 | ||||||
| chr19:49802423
|
C | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0248others(8): Show | 14 | HG00597.hp1 HG02135.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.2114+282C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802423 | ||||||
| chr19:49802431
|
G | C | 117 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(114): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2114+290G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802431 | ||||||
| chr19:49802463
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2114+322C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802463 | ||||||
| chr19:49802505
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2114+364C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802505 | ||||||
| chr19:49802557
|
A | G | 1 | a0001c0001t0002g0024 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2115-392A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802557 | ||||||
| chr19:49802558
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2115-391G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802558 | ||||||
| chr19:49802637
|
G | C | 7 | a0001c0001t0001g0216a0001c0001t0001g0237a0001c0001t0001g0238others(4): Show | 7 | HG02129.hp2 HG02735.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2115-312G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802637 | ||||||
| chr19:49802683
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2115-266G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802683 | ||||||
| chr19:49802924
|
A | G | 3 | a0001c0001t0002g0023a0001c0001t0002g0032a0001c0001t0002g0044 | 3 | HG02055.hp1 HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2115-25A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802924 | ||||||
| chr19:49802941
|
G | T | 42 | a0001c0001t0001g0018a0001c0001t0001g0118a0001c0001t0001g0127others(39): Show | 42 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(39): Show |
splice_region_variant&intron_variant | LOW | c.2115-8G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802941 | ||||||
| chr19:49802943
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0285 | 2 | HG02717.hp2 NA19240.hp1 |
splice_region_variant&intron_variant | LOW | c.2115-6C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802943 | ||||||
| chr19:49803048
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2171+43G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 16/22 | chr19 | 49803048 | ||||||
| chr19:49803059
|
C | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0240 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2172-48C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 16/22 | chr19 | 49803059 | ||||||
| chr19:49803277
|
C | T | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0104others(18): Show | 23 | HG01891.hp2 HG01934.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.2255-10C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 17/22 | chr19 | 49803277 | ||||||
| chr19:49803479
|
T | C | 2 | a0001c0004t0001g0211a0001c0004t0001g0310 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2344+103T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803479 | ||||||
| chr19:49803493
|
G | A | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2344+117G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803493 | ||||||
| chr19:49803513
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2344+137T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803513 | ||||||
| chr19:49803554
|
A | G | 1 | a0001c0001t0001g0177 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2344+178A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803554 | ||||||
| chr19:49803602
|
C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 6 | HG02723.hp1 HG03041.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2344+226C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803602 | ||||||
| chr19:49803681
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0307 | 2 | HG00741.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2344+305G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803681 | ||||||
| chr19:49803722
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0073 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2344+346C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803722 | ||||||
| chr19:49803756
|
AC | A | 3 | a0001c0001t0001g0149a0001c0001t0001g0195a0001c0001t0001g0236 | 3 | HG00423.hp1 HG02071.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2344+381delC | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803756 | ||||||
| chr19:49803806
|
C | T | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0104others(17): Show | 22 | HG01934.hp1 HG01978.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.2344+430C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803806 | ||||||
| chr19:49803811
|
C | A | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2344+435C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803811 | ||||||
| chr19:49803812
|
T | A | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2344+436T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803812 | ||||||
| chr19:49803813
|
T | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2344+437T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803813 | ||||||
| chr19:49803814
|
CCTCATAG others(3): Show |
C | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2344+439_2344+448d others(12): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803814 | ||||||
| chr19:49803898
|
T | G | 21 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0179others(18): Show | 24 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.2344+522T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803898 | ||||||
| chr19:49804008
|
G | A | 2 | a0001c0004t0001g0211a0001c0004t0001g0310 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2344+632G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804008 | ||||||
| chr19:49804087
|
C | T | 177 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(174): Show | 186 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.2344+711C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804087 | ||||||
| chr19:49804144
|
G | A | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0064others(41): Show | 46 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.2344+768G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804144 | ||||||
| chr19:49804151
|
G | A | 114 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(111): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.2344+775G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804151 | ||||||
| chr19:49804184
|
C | A | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2344+808C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804184 | ||||||
| chr19:49804210
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2344+834T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804210 | ||||||
| chr19:49804233
|
AAAAAG | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0179others(17): Show | 23 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.2344+867_2344+871d others(7): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr19 | 49804233 | |||||
| chr19:49804323
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0253 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2344+947C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804323 | ||||||
| chr19:49804337
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2344+961C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804337 | ||||||
| chr19:49804401
|
C | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0248others(14): Show | 20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.2344+1025C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804401 | ||||||
| chr19:49804457
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0114a0001c0001t0001g0171 | 3 | HG00733.hp1 HG01243.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2345-996C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804457 | ||||||
| chr19:49804500
|
G | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0280a0001c0001t0001g0285 | 3 | HG02280.hp2 HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2345-953G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804500 | ||||||
| chr19:49804540
|
G | GA | 116 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2345-896dupA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr19 | 49804540 | |||||
| chr19:49804540
|
G | GAA | 9 | a0001c0001t0001g0245a0001c0001t0001g0260a0001c0001t0001g0272others(6): Show | 9 | HG01175.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2345-897_2345-896d others(4): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr19 | 49804540 | |||||
| chr19:49804540
|
GA | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0166others(12): Show | 18 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.2345-896delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr19 | 49804540 | |||||
| chr19:49804557
|
AT | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0104others(14): Show | 19 | HG01934.hp1 HG01978.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.2345-894delT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr19 | 49804557 | |||||
| chr19:49804558
|
T | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0204 | 2 | HG01891.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2345-895T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804558 | ||||||
| chr19:49804825
|
C | T | 3 | a0001c0001t0001g0119a0001c0001t0002g0019a0001c0001t0002g0022 | 3 | HG00621.hp2 HG02155.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.2345-628C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804825 | ||||||
| chr19:49804860
|
C | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0248others(14): Show | 20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.2345-593C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804860 | ||||||
| chr19:49804877
|
G | C | 122 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(119): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2345-576G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804877 | ||||||
| chr19:49805285
|
C | G | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0104others(18): Show | 23 | HG01891.hp2 HG01934.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.2345-168C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49805285 | ||||||
| chr19:49805346
|
C | A | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0104others(18): Show | 23 | HG01891.hp2 HG01934.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.2345-107C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49805346 | ||||||
| chr19:49805412
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2345-41C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49805412 | ||||||
| chr19:49805616
|
G | A | 7 | a0001c0001t0001g0090a0001c0001t0001g0098a0001c0001t0001g0141others(4): Show | 7 | HG00280.hp1 HG01099.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.2468+40G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 19/22 | chr19 | 49805616 | ||||||
| chr19:49805636
|
T | C | 124 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(121): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.2469-25T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 19/22 | chr19 | 49805636 | ||||||
| chr19:49805794
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2585+17G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 20/22 | chr19 | 49805794 | ||||||
| chr19:49805833
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0253 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2586-39G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 20/22 | chr19 | 49805833 | ||||||
| chr19:49806018
|
G | C | 5 | a0001c0001t0004g0198a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2655+77G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 21/22 | chr19 | 49806018 | ||||||
| chr19:49806093
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2656-26T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 21/22 | chr19 | 49806093 | ||||||
| chr19:49806103
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2656-16C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 21/22 | chr19 | 49806103 | ||||||
| chr19:49806108
|
C | G | 1 | a0001c0001t0002g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2656-11C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 21/22 | chr19 | 49806108 | ||||||
| chr19:49806358
|
CCCT | C | 163 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(160): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.2790+113_2790+115d others(5): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr19 | 49806358 | |||||
| chr19:49806383
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2790+130C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | chr19 | 49806383 | ||||||
| chr19:49806436
|
T | G | 1 | a0001c0002t0001g0228 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2790+183T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | chr19 | 49806436 | ||||||
| chr19:49806507
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2791-174T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | chr19 | 49806507 | ||||||
| chr19:49806509
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2791-172T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | chr19 | 49806509 | ||||||
| chr19:49806531
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2791-150C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | chr19 | 49806531 | ||||||
| chr19:49806603
|
TC | T | 168 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(165): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.2791-76delC | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr19 | 49806603 | |||||
| chr19:49806626
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0248others(14): Show | 20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.2791-55G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | chr19 | 49806626 |