Search by Gene
| geneid | 55435 |
|---|---|
| ensemblid | ENSG00000138660.12 |
| hgncid | 28808 |
| symbol | AP1AR |
| name | adaptor related protein complex 1 associated regulatory protein |
| refseq_nuc | NM_018569.6 |
| refseq_prot | NP_061039.3 |
| ensembl_nuc | ENST00000274000.10 |
| ensembl_prot | ENSP00000274000.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 112231787 |
| end | 112273110 |
| strand | + |
| ver | v1.2 |
| region | chr4:112231787-112273110 |
| region5000 | chr4:112226787-112278110 |
| regionname0 | AP1AR_chr4_112231787_112273110 |
| regionname5000 | AP1AR_chr4_112226787_112278110 |
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 | 302 | 395 | 87 | 72 | 189 | 12 | 33 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0002 | 0/0 | 302 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0003 | 0/0 | 302 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0004 | 0/0 | 302 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | 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 | 909 | 388 | 83 | 70 | 188 | 12 | 33 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| c0002 | 0/0 | 909 | 5 | 4 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| c0003 | 0/0 | 909 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| c0004 | 0/0 | 909 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| c0005 | 0/0 | 909 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| c0006 | 0/0 | 909 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| c0007 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | 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 | 0/0 | 5009 | 123 | 40 | 14 | 60 | 2 | 7 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0002 | 1/0 | 5007 | 88 | 8 | 25 | 40 | 3 | 11 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0003 | 0/0 | 5007 | 47 | 0 | 2 | 44 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0004 | 0/0 | 5009 | 36 | 5 | 6 | 20 | 3 | 2 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0005 | 0/0 | 5013 | 25 | 8 | 7 | 5 | 1 | 4 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0006 | 0/1 | 5015 | 20 | 6 | 5 | 4 | 0 | 4 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0007 | 0/0 | 5007 | 8 | 7 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0008 | 0/0 | 5007 | 4 | 1 | 0 | 3 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0009 | 0/0 | 5009 | 3 | 3 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0010 | 0/0 | 5007 | 3 | 0 | 3 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0011 | 0/0 | 5007 | 3 | 2 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0012 | 0/0 | 5007 | 3 | 0 | 2 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0013 | 0/0 | 5019 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0014 | 0/0 | 5017 | 2 | 0 | 1 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0015 | 0/0 | 5009 | 2 | 1 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0016 | 0/0 | 5009 | 2 | 1 | 0 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0017 | 0/0 | 5007 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0018 | 0/0 | 5007 | 2 | 0 | 1 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0019 | 0/0 | 5007 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0020 | 0/0 | 5007 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0021 | 0/0 | 5015 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0022 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0023 | 0/0 | 5007 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0024 | 0/0 | 5013 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0025 | 0/0 | 5021 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0026 | 0/0 | 5015 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0027 | 0/0 | 5013 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0028 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0029 | 0/0 | 5009 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0030 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0031 | 0/0 | 5009 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0032 | 0/0 | 5009 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0033 | 0/0 | 5009 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0034 | 0/0 | 5009 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0035 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0036 | 0/0 | 5007 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0037 | 0/0 | 5007 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0038 | 0/0 | 5007 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0039 | 0/0 | 5007 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| t0040 | 0/0 | 5009 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | 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 | 34 | 0 | 1 | 33 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0002 | 0/0 | 29 | 1 | 11 | 11 | 1 | 5 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0003 | 0/0 | 19 | 2 | 6 | 8 | 1 | 2 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0004 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0005 | 0/0 | 15 | 1 | 0 | 13 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0006 | 0/0 | 13 | 0 | 1 | 11 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0007 | 0/0 | 11 | 5 | 2 | 3 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0008 | 0/0 | 9 | 0 | 5 | 0 | 3 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0009 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0010 | 0/1 | 6 | 0 | 3 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0012 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0013 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0017 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0036 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| 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 | 388 | 83 | 70 | 188 | 12 | 33 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0003c0007 | a0003 | c0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0004c0004 | a0004 | c0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | 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 | 0/0 | 117 | 36 | 13 | 59 | 2 | 7 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 1/0 | 87 | 8 | 25 | 40 | 3 | 10 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 47 | 0 | 2 | 44 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 35 | 5 | 5 | 20 | 3 | 2 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 24 | 8 | 7 | 4 | 1 | 4 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/1 | 20 | 6 | 5 | 4 | 0 | 4 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0020 | a0001 | c0001 | t0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0021 | a0001 | c0001 | t0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0022 | a0001 | c0001 | t0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0023 | a0001 | c0001 | t0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0024 | a0001 | c0001 | t0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0025 | a0001 | c0001 | t0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0026 | a0001 | c0001 | t0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0027 | a0001 | c0001 | t0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0028 | a0001 | c0001 | t0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0029 | a0001 | c0001 | t0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0031 | a0001 | c0001 | t0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0032 | a0001 | c0001 | t0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0033 | a0001 | c0001 | t0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0034 | a0001 | c0001 | t0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0035 | a0001 | c0001 | t0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0036 | a0001 | c0001 | t0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0037 | a0001 | c0001 | t0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0038 | a0001 | c0001 | t0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0039 | a0001 | c0001 | t0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0001t0040 | a0001 | c0001 | t0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0002t0030 | a0001 | c0002 | t0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0005t0004 | a0001 | c0005 | t0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0001c0006t0005 | a0001 | c0006 | t0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0002c0003t0001 | a0002 | c0003 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0003c0007t0001 | a0003 | c0007 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR | copy fasta |
| a0004c0004t0002 | a0004 | c0004 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 17 | 0 | 0 | 17 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 12 | 1 | 0 | 11 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 11 | 5 | 2 | 3 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0002 | a0001 | c0001 | t0002 | g0002 | 0/0 | 22 | 0 | 7 | 11 | 0 | 4 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0009 | a0001 | c0001 | t0002 | g0009 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0011 | a0001 | c0001 | t0002 | g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0015 | a0001 | c0001 | t0002 | g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0016 | a0001 | c0001 | t0002 | g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0023 | a0001 | c0001 | t0002 | g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0029 | a0001 | c0001 | t0002 | g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0036 | a0001 | c0001 | t0002 | g0036 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0037 | a0001 | c0001 | t0002 | g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0038 | a0001 | c0001 | t0002 | g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0040 | a0001 | c0001 | t0002 | g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0041 | a0001 | c0001 | t0002 | g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0042 | a0001 | c0001 | t0002 | g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0071 | a0001 | c0001 | t0002 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0106 | a0001 | c0001 | t0002 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0107 | a0001 | c0001 | t0002 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0108 | a0001 | c0001 | t0002 | g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0109 | a0001 | c0001 | t0002 | g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0110 | a0001 | c0001 | t0002 | g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0111 | a0001 | c0001 | t0002 | g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0112 | a0001 | c0001 | t0002 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0113 | a0001 | c0001 | t0002 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0114 | a0001 | c0001 | t0002 | g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0115 | a0001 | c0001 | t0002 | g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0116 | a0001 | c0001 | t0002 | g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0118 | a0001 | c0001 | t0002 | g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0119 | a0001 | c0001 | t0002 | g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0120 | a0001 | c0001 | t0002 | g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0121 | a0001 | c0001 | t0002 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0122 | a0001 | c0001 | t0002 | g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0123 | a0001 | c0001 | t0002 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0124 | a0001 | c0001 | t0002 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0125 | a0001 | c0001 | t0002 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0126 | a0001 | c0001 | t0002 | g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0128 | a0001 | c0001 | t0002 | g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0129 | a0001 | c0001 | t0002 | g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0131 | a0001 | c0001 | t0002 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0132 | a0001 | c0001 | t0002 | g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0133 | a0001 | c0001 | t0002 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0157 | a0001 | c0001 | t0002 | g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0002g0178 | a0001 | c0001 | t0002 | g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0003g0001 | a0001 | c0001 | t0003 | g0001 | 0/0 | 33 | 0 | 1 | 32 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0003g0018 | a0001 | c0001 | t0003 | g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0003g0027 | a0001 | c0001 | t0003 | g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0003g0050 | a0001 | c0001 | t0003 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0003g0051 | a0001 | c0001 | t0003 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0003g0052 | a0001 | c0001 | t0003 | g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0003g0053 | a0001 | c0001 | t0003 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0003g0054 | a0001 | c0001 | t0003 | g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0003g0055 | a0001 | c0001 | t0003 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0003g0056 | a0001 | c0001 | t0003 | g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0003g0057 | a0001 | c0001 | t0003 | g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0003g0058 | a0001 | c0001 | t0003 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0004g0006 | a0001 | c0001 | t0004 | g0006 | 0/0 | 13 | 0 | 1 | 11 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0004g0008 | a0001 | c0001 | t0004 | g0008 | 0/0 | 8 | 0 | 4 | 0 | 3 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0004g0022 | a0001 | c0001 | t0004 | g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0004g0035 | a0001 | c0001 | t0004 | g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0004g0097 | a0001 | c0001 | t0004 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0004g0098 | a0001 | c0001 | t0004 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0004g0099 | a0001 | c0001 | t0004 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0004g0100 | a0001 | c0001 | t0004 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0004g0101 | a0001 | c0001 | t0004 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0004g0102 | a0001 | c0001 | t0004 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0004g0103 | a0001 | c0001 | t0004 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0004g0105 | a0001 | c0001 | t0004 | g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0004g0158 | a0001 | c0001 | t0004 | g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0005g0003 | a0001 | c0001 | t0005 | g0003 | 0/0 | 12 | 2 | 5 | 3 | 1 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0005g0043 | a0001 | c0001 | t0005 | g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0005g0045 | a0001 | c0001 | t0005 | g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0005g0082 | a0001 | c0001 | t0005 | g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0005g0104 | a0001 | c0001 | t0005 | g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0005g0142 | a0001 | c0001 | t0005 | g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0005g0143 | a0001 | c0001 | t0005 | g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0005g0145 | a0001 | c0001 | t0005 | g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0005g0150 | a0001 | c0001 | t0005 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0005g0153 | a0001 | c0001 | t0005 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0005g0159 | a0001 | c0001 | t0005 | g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0006g0003 | a0001 | c0001 | t0006 | g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0006g0005 | a0001 | c0001 | t0006 | g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0006g0010 | a0001 | c0001 | t0006 | g0010 | 0/1 | 6 | 0 | 3 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0006g0031 | a0001 | c0001 | t0006 | g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0006g0044 | a0001 | c0001 | t0006 | g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0006g0069 | a0001 | c0001 | t0006 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0006g0070 | a0001 | c0001 | t0006 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0006g0134 | a0001 | c0001 | t0006 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0006g0139 | a0001 | c0001 | t0006 | g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0006g0141 | a0001 | c0001 | t0006 | g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0006g0156 | a0001 | c0001 | t0006 | g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0006g0164 | a0001 | c0001 | t0006 | g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0006g0170 | a0001 | c0001 | t0006 | g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0007g0012 | a0001 | c0001 | t0007 | g0012 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0007g0166 | a0001 | c0001 | t0007 | g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0007g0167 | a0001 | c0001 | t0007 | g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0007g0168 | a0001 | c0001 | t0007 | g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0008g0003 | a0001 | c0001 | t0008 | g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0008g0005 | a0001 | c0001 | t0008 | g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0008g0087 | a0001 | c0001 | t0008 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0008g0094 | a0001 | c0001 | t0008 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0009g0048 | a0001 | c0001 | t0009 | g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0009g0171 | a0001 | c0001 | t0009 | g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0010g0017 | a0001 | c0001 | t0010 | g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0011g0136 | a0001 | c0001 | t0011 | g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0011g0152 | a0001 | c0001 | t0011 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0011g0169 | a0001 | c0001 | t0011 | g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0012g0002 | a0001 | c0001 | t0012 | g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0013g0003 | a0001 | c0001 | t0013 | g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0013g0144 | a0001 | c0001 | t0013 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0014g0135 | a0001 | c0001 | t0014 | g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0014g0140 | a0001 | c0001 | t0014 | g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0015g0021 | a0001 | c0001 | t0015 | g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0016g0146 | a0001 | c0001 | t0016 | g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0016g0147 | a0001 | c0001 | t0016 | g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0017g0046 | a0001 | c0001 | t0017 | g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0018g0002 | a0001 | c0001 | t0018 | g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0018g0049 | a0001 | c0001 | t0018 | g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0019g0039 | a0001 | c0001 | t0019 | g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0020g0002 | a0001 | c0001 | t0020 | g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0021g0004 | a0001 | c0001 | t0021 | g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0022g0060 | a0001 | c0001 | t0022 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0023g0160 | a0001 | c0001 | t0023 | g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0024g0003 | a0001 | c0001 | t0024 | g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0025g0151 | a0001 | c0001 | t0025 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0026g0003 | a0001 | c0001 | t0026 | g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0027g0003 | a0001 | c0001 | t0027 | g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0028g0161 | a0001 | c0001 | t0028 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0029g0009 | a0001 | c0001 | t0029 | g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0031g0020 | a0001 | c0001 | t0031 | g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0032g0089 | a0001 | c0001 | t0032 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0033g0014 | a0001 | c0001 | t0033 | g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0034g0028 | a0001 | c0001 | t0034 | g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0035g0002 | a0001 | c0001 | t0035 | g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0036g0002 | a0001 | c0001 | t0036 | g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0037g0001 | a0001 | c0001 | t0037 | g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0038g0059 | a0001 | c0001 | t0038 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0039g0117 | a0001 | c0001 | t0039 | g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0001t0040g0005 | a0001 | c0001 | t0040 | g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0002t0001g0024 | a0001 | c0002 | t0001 | g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0002t0001g0138 | a0001 | c0002 | t0001 | g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0002t0030g0137 | a0001 | c0002 | t0030 | g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0005t0004g0008 | a0001 | c0005 | t0004 | g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0001c0006t0005g0003 | a0001 | c0006 | t0005 | g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0002c0003t0001g0019 | a0002 | c0003 | t0001 | g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0003c0007t0001g0068 | a0003 | c0007 | t0001 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1AR_chr4_112226787_112278110 | AP1AR |
| a0004c0004t0002g0130 | a0004 | c0004 | t0002 | g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1AR_chr4_112226787_112278110 | AP1AR |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0016 | g0147 | EUR | GBR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0003 | EUR | GBR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0111 | EUR | GBR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | FIN | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00323 | hp2 | a0001 | c0001 | t0018 | g0049 | EUR | FIN | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00544 | hp2 | a0001 | c0001 | t0032 | g0089 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00609 | hp1 | a0001 | c0001 | t0024 | g0003 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00642 | hp1 | a0001 | c0001 | t0036 | g0002 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00733 | hp2 | a0001 | c0001 | t0034 | g0028 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0044 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00738 | hp1 | a0001 | c0001 | t0015 | g0021 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01069 | hp1 | a0001 | c0001 | t0010 | g0017 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01071 | hp1 | a0001 | c0001 | t0010 | g0017 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01074 | hp2 | a0001 | c0001 | t0027 | g0003 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01099 | hp1 | a0001 | c0001 | t0010 | g0017 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0012 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01175 | hp2 | a0001 | c0001 | t0012 | g0002 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01192 | hp1 | a0001 | c0001 | t0012 | g0002 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01358 | hp1 | a0001 | c0005 | t0004 | g0008 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01361 | hp2 | a0001 | c0001 | t0018 | g0002 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01433 | hp1 | a0001 | c0001 | t0014 | g0140 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | IBS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | IBS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01517 | hp2 | a0001 | c0001 | t0012 | g0002 | EUR | IBS | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01975 | hp1 | a0001 | c0001 | t0029 | g0009 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0104 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02040 | hp2 | a0001 | c0001 | t0013 | g0144 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02135 | hp1 | a0001 | c0001 | t0013 | g0003 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02148 | hp1 | a0001 | c0001 | t0006 | g0044 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02155 | hp1 | a0001 | c0001 | t0025 | g0151 | EAS | CDX | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | CDX | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CDX | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CDX | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02257 | hp1 | a0001 | c0001 | t0017 | g0046 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02258 | hp1 | a0003 | c0007 | t0001 | g0068 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02258 | hp2 | a0001 | c0001 | t0016 | g0146 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PEL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0168 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02602 | hp2 | a0004 | c0004 | t0002 | g0130 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02630 | hp1 | a0001 | c0001 | t0022 | g0060 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0141 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0003 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0167 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0164 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | ESN | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02965 | hp1 | a0001 | c0001 | t0028 | g0161 | AFR | ESN | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | ESN | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | ESN | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | ESN | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0143 | AFR | ESN | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | MSL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0136 | AFR | MSL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | MSL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | MSL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0166 | AFR | MSL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | MSL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03540 | hp2 | a0001 | c0001 | t0017 | g0046 | AFR | GWD | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03579 | hp1 | a0001 | c0002 | t0030 | g0137 | AFR | MSL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0087 | AFR | MSL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03654 | hp2 | a0001 | c0001 | t0026 | g0003 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03688 | hp1 | a0001 | c0001 | t0020 | g0002 | SAS | STU | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0156 | SAS | STU | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0005 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03704 | hp2 | a0001 | c0001 | t0006 | g0170 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0145 | SAS | PJL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0139 | SAS | BEB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03834 | hp2 | a0001 | c0001 | t0023 | g0160 | SAS | BEB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03927 | hp1 | a0001 | c0001 | t0014 | g0135 | SAS | BEB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03927 | hp2 | a0001 | c0001 | t0039 | g0117 | SAS | BEB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | STU | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0171 | AFR | YRI | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18612 | hp1 | a0002 | c0003 | t0001 | g0019 | EAS | CHB | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | CHB | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | CHB | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | YRI | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18944 | hp2 | a0001 | c0001 | t0038 | g0059 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18956 | hp2 | a0001 | c0001 | t0031 | g0020 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18972 | hp2 | a0001 | c0001 | t0037 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18978 | hp1 | a0001 | c0001 | t0008 | g0094 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18978 | hp2 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18988 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18992 | hp2 | a0001 | c0001 | t0019 | g0039 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18998 | hp1 | a0001 | c0006 | t0005 | g0003 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19002 | hp2 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19005 | hp1 | a0001 | c0001 | t0011 | g0152 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19030 | hp2 | a0001 | c0001 | t0011 | g0169 | AFR | LWK | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19054 | hp1 | a0001 | c0001 | t0021 | g0004 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19054 | hp2 | a0001 | c0001 | t0006 | g0134 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19055 | hp1 | a0001 | c0001 | t0040 | g0005 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19058 | hp2 | a0001 | c0001 | t0019 | g0039 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19064 | hp2 | a0001 | c0001 | t0033 | g0014 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | YRI | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0150 | AFR | YRI | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0159 | AFR | ASW | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | ASW | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0126 | EUR | TSI | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0120 | EUR | TSI | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0043 | SAS | GIH | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0082 | SAS | GIH | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0097 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0138 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ACB | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | MSL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | MSL | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | USA | AP1AR_chr4_112226787_112278110 | AP1AR |
| HG06807 | hp2 | a0001 | c0001 | t0015 | g0021 | AFR | USA | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA20300 | hp1 | a0001 | c0001 | t0035 | g0002 | AFR | USA | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | USA | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | AP1AR_chr4_112226787_112278110 | AP1AR |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | LWK | AP1AR_chr4_112226787_112278110 | AP1AR |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0006 | g0010 | REF | REF | AP1AR_chr4_112226787_112278110 | AP1AR |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0036 | REF | REF | AP1AR_chr4_112226787_112278110 | AP1AR |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:112232100
|
C | A | 1 | a0002 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.9C>A | p.Asn3Lys | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/10 | 314/5915 | 9/909 | 3/302 | chr4 | 112232100 | ||
| chr4:112232119
|
T | C | 1 | a0004 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.28T>C | p.Phe10Leu | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/10 | 333/5915 | 28/909 | 10/302 | chr4 | 112232119 | ||
| chr4:112268390
|
C | T | 1 | a0003 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.890C>T | p.Thr297Ile | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 1195/5915 | 890/909 | 297/302 | chr4 | 112268390 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:112232142
|
G | A | 1 | a0001c0005 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.51G>A | p.Ala17Ala | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/10 | 356/5915 | 51/909 | 17/302 | chr4 | 112232142 | ||
| chr4:112265755
|
C | T | 1 | a0001c0002 | 5 | HG01975.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
synonymous_variant | LOW | c.462C>T | p.Phe154Phe | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 8/10 | 767/5915 | 462/909 | 154/302 | chr4 | 112265755 | ||
| chr4:112268244
|
T | C | 1 | a0001c0006 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.744T>C | p.Pro248Pro | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 1049/5915 | 744/909 | 248/302 | chr4 | 112268244 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:112231805
|
G | A | 1 | a0001c0001t0020 | 1 | HG03688.hp1 | 5_prime_UTR_variant | MODIFIER | c.-287G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/10 | 287 | chr4 | 112231805 | |||||
| chr4:112231972
|
G | A | 1 | a0001c0001t0021 | 1 | NA19054.hp1 | 5_prime_UTR_variant | MODIFIER | c.-120G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/10 | 120 | chr4 | 112231972 | |||||
| chr4:112231987
|
C | T | 1 | a0001c0001t0040 | 1 | NA19055.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/10 | 105 | chr4 | 112231987 | |||||
| chr4:112232080
|
G | A | 1 | a0001c0001t0022 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/10 | 12 | chr4 | 112232080 | |||||
| chr4:112268668
|
G | C | 1 | a0001c0001t0007 | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*259G>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 259 | chr4 | 112268668 | |||||
| chr4:112268824
|
G | A | 1 | a0001c0001t0023 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*415G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 415 | chr4 | 112268824 | |||||
| chr4:112268931
|
G | A | 1 | a0001c0001t0009 | 3 | HG02970.hp1 HG03540.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*522G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 522 | chr4 | 112268931 | |||||
| chr4:112268948
|
A | G | 1 | a0001c0001t0019 | 2 | NA18992.hp2 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*539A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 539 | chr4 | 112268948 | |||||
| chr4:112269091
|
A | AAG | 2 | a0001c0001t0004a0001c0005t0004 | 36 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*684_*685dupGA | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 686 | INFO_REALIGN_3_PRIME | chr4 | 112269091 | ||||
| chr4:112269093
|
G | GAT | 16 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(13): Show | 141 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*701_*702dupAT | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 703 | INFO_REALIGN_3_PRIME | chr4 | 112269093 | ||||
| chr4:112269093
|
G | GATATAT | 4 | a0001c0001t0005a0001c0001t0024a0001c0001t0027others(1): Show | 27 | HG00099.hp2 HG00609.hp1 HG00735.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*697_*702dupATATAT | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 703 | INFO_REALIGN_3_PRIME | chr4 | 112269093 | ||||
| chr4:112269093
|
G | GATATATA others(1): Show |
3 | a0001c0001t0006a0001c0001t0021a0001c0001t0026 | 22 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*695_*702dupATATAT others(2): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 703 | INFO_REALIGN_3_PRIME | chr4 | 112269093 | ||||
| chr4:112269093
|
G | GATATATA others(3): Show |
1 | a0001c0001t0014 | 2 | HG01433.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*693_*702dupATATAT others(4): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 703 | INFO_REALIGN_3_PRIME | chr4 | 112269093 | ||||
| chr4:112269093
|
G | GATATATA others(5): Show |
1 | a0001c0001t0013 | 2 | HG02040.hp2 HG02135.hp1 |
3_prime_UTR_variant | MODIFIER | c.*691_*702dupATATAT others(6): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 703 | INFO_REALIGN_3_PRIME | chr4 | 112269093 | ||||
| chr4:112269093
|
G | GATATATA others(7): Show |
1 | a0001c0001t0025 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*689_*702dupATATAT others(8): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 703 | INFO_REALIGN_3_PRIME | chr4 | 112269093 | ||||
| chr4:112269112
|
T | A | 1 | a0001c0001t0024 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*703T>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 703 | chr4 | 112269112 | |||||
| chr4:112269215
|
A | G | 1 | a0001c0001t0018 | 2 | HG00323.hp2 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*806A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 806 | chr4 | 112269215 | |||||
| chr4:112269254
|
A | C | 1 | a0001c0001t0039 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*845A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 845 | chr4 | 112269254 | |||||
| chr4:112269403
|
C | G | 3 | a0001c0001t0003a0001c0001t0037a0001c0001t0038 | 49 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*994C>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 994 | chr4 | 112269403 | |||||
| chr4:112269561
|
C | T | 1 | a0001c0001t0022 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1152C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 1152 | chr4 | 112269561 | |||||
| chr4:112269969
|
T | C | 1 | a0001c0001t0015 | 2 | HG00738.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1560T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 1560 | chr4 | 112269969 | |||||
| chr4:112270669
|
G | A | 1 | a0001c0001t0007 | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2260G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 2260 | chr4 | 112270669 | |||||
| chr4:112270691
|
G | A | 1 | a0001c0001t0022 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2282G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 2282 | chr4 | 112270691 | |||||
| chr4:112270938
|
A | C | 1 | a0001c0001t0038 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2529A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 2529 | chr4 | 112270938 | |||||
| chr4:112271013
|
T | C | 1 | a0001c0001t0035 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2604T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 2604 | chr4 | 112271013 | |||||
| chr4:112271047
|
G | T | 1 | a0001c0001t0034 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2638G>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 2638 | chr4 | 112271047 | |||||
| chr4:112271125
|
T | C | 1 | a0001c0001t0007 | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2716T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 2716 | chr4 | 112271125 | |||||
| chr4:112271286
|
C | G | 1 | a0001c0001t0016 | 2 | HG00099.hp1 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2877C>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 2877 | chr4 | 112271286 | |||||
| chr4:112271394
|
G | A | 1 | a0001c0001t0037 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2985G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 2985 | chr4 | 112271394 | |||||
| chr4:112271403
|
C | A | 1 | a0001c0001t0022 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2994C>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 2994 | chr4 | 112271403 | |||||
| chr4:112271479
|
G | C | 2 | a0001c0001t0011a0001c0001t0028 | 4 | HG02965.hp1 HG03225.hp1 NA19005.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3070G>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 3070 | chr4 | 112271479 | |||||
| chr4:112271625
|
A | C | 1 | a0001c0001t0036 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3216A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 3216 | chr4 | 112271625 | |||||
| chr4:112271695
|
GAA | G | 1 | a0001c0001t0010 | 3 | HG01069.hp1 HG01071.hp1 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3288_*3289delAA | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 3288 | INFO_REALIGN_3_PRIME | chr4 | 112271695 | ||||
| chr4:112271910
|
A | G | 3 | a0001c0001t0003a0001c0001t0037a0001c0001t0038 | 49 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3501A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 3501 | chr4 | 112271910 | |||||
| chr4:112271924
|
G | T | 1 | a0001c0001t0017 | 2 | HG02257.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3515G>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 3515 | chr4 | 112271924 | |||||
| chr4:112272096
|
G | A | 1 | a0001c0001t0012 | 3 | HG01175.hp2 HG01192.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3687G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 3687 | chr4 | 112272096 | |||||
| chr4:112272171
|
A | G | 29 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(26): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
3_prime_UTR_variant | MODIFIER | c.*3762A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 3762 | chr4 | 112272171 | |||||
| chr4:112272269
|
G | A | 1 | a0001c0002t0030 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3860G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 3860 | chr4 | 112272269 | |||||
| chr4:112272289
|
A | G | 35 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(32): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
3_prime_UTR_variant | MODIFIER | c.*3880A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 3880 | chr4 | 112272289 | |||||
| chr4:112272384
|
A | T | 31 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(28): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*3975A>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 3975 | chr4 | 112272384 | |||||
| chr4:112272390
|
C | T | 27 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(24): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*3981C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 3981 | chr4 | 112272390 | |||||
| chr4:112272502
|
A | G | 1 | a0001c0001t0033 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4093A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 4093 | chr4 | 112272502 | |||||
| chr4:112272571
|
G | A | 1 | a0001c0001t0026 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4162G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 4162 | chr4 | 112272571 | |||||
| chr4:112272594
|
A | G | 3 | a0001c0001t0003a0001c0001t0037a0001c0001t0038 | 49 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*4185A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 4185 | chr4 | 112272594 | |||||
| chr4:112272603
|
G | C | 1 | a0001c0001t0017 | 2 | HG02257.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4194G>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 4194 | chr4 | 112272603 | |||||
| chr4:112272692
|
C | G | 1 | a0001c0001t0019 | 2 | NA18992.hp2 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4283C>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 4283 | chr4 | 112272692 | |||||
| chr4:112272773
|
C | T | 1 | a0001c0001t0027 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4364C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 4364 | chr4 | 112272773 | |||||
| chr4:112272774
|
G | A | 3 | a0001c0001t0003a0001c0001t0037a0001c0001t0038 | 49 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*4365G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 4365 | chr4 | 112272774 | |||||
| chr4:112272836
|
C | T | 4 | a0001c0001t0003a0001c0001t0032a0001c0001t0037others(1): Show | 50 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*4427C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 4427 | chr4 | 112272836 | |||||
| chr4:112272915
|
A | C | 1 | a0001c0001t0007 | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4506A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 4506 | chr4 | 112272915 | |||||
| chr4:112272964
|
G | A | 1 | a0001c0001t0031 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4555G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 4555 | chr4 | 112272964 | |||||
| chr4:112272969
|
G | T | 1 | a0001c0001t0017 | 2 | HG02257.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4560G>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 4560 | chr4 | 112272969 | |||||
| chr4:112273008
|
G | A | 33 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(30): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*4599G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 10/10 | 4599 | chr4 | 112273008 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:112232207
|
T | A | 1 | a0001c0001t0018g0049 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.83+33T>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112232207 | ||||||
| chr4:112232251
|
C | A | 14 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0003g0027others(11): Show | 49 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.83+77C>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112232251 | ||||||
| chr4:112232308
|
G | A | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.83+134G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112232308 | ||||||
| chr4:112232451
|
A | G | 12 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0173others(9): Show | 18 | HG00621.hp2 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.83+277A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112232451 | ||||||
| chr4:112232561
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.83+387C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112232561 | ||||||
| chr4:112232621
|
G | T | 1 | a0001c0001t0001g0182 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.83+447G>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112232621 | ||||||
| chr4:112232725
|
A | G | 2 | a0001c0001t0009g0048a0001c0001t0009g0171 | 3 | HG02970.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.83+551A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112232725 | ||||||
| chr4:112232954
|
T | C | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(70): Show | 130 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.83+780T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112232954 | ||||||
| chr4:112233108
|
T | G | 1 | a0001c0001t0001g0061 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.83+934T>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112233108 | ||||||
| chr4:112233126
|
A | C | 1 | a0001c0001t0006g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.83+952A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112233126 | ||||||
| chr4:112233170
|
A | G | 1 | a0001c0001t0011g0169 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.83+996A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112233170 | ||||||
| chr4:112233424
|
T | C | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.83+1250T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112233424 | ||||||
| chr4:112233567
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.83+1393C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112233567 | ||||||
| chr4:112233865
|
C | CT | 11 | a0001c0001t0001g0047a0001c0001t0001g0162a0001c0001t0001g0163others(8): Show | 16 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.83+1700dupT | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 112233865 | |||||
| chr4:112233891
|
C | G | 1 | a0001c0001t0005g0159 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.83+1717C>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112233891 | ||||||
| chr4:112234003
|
C | T | 1 | a0001c0001t0004g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.83+1829C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112234003 | ||||||
| chr4:112234316
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.83+2142A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112234316 | ||||||
| chr4:112234500
|
T | A | 1 | a0001c0001t0001g0062 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.83+2326T>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112234500 | ||||||
| chr4:112234524
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.83+2350C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112234524 | ||||||
| chr4:112234608
|
G | C | 15 | a0001c0001t0004g0006a0001c0001t0004g0008a0001c0001t0004g0022others(12): Show | 37 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.83+2434G>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112234608 | ||||||
| chr4:112234621
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.83+2447A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112234621 | ||||||
| chr4:112234636
|
A | G | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(156): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.83+2462A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112234636 | ||||||
| chr4:112234658
|
G | GT | 47 | a0001c0001t0001g0127a0001c0001t0002g0002a0001c0001t0002g0009others(44): Show | 88 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.83+2499dupT | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 112234658 | |||||
| chr4:112234660
|
T | TG | 25 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0154others(22): Show | 58 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.83+2486_83+2487ins others(1): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112234660 | ||||||
| chr4:112234661
|
T | G | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.83+2487T>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112234661 | ||||||
| chr4:112234754
|
C | T | 1 | a0001c0001t0006g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.83+2580C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112234754 | ||||||
| chr4:112234872
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.83+2698C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112234872 | ||||||
| chr4:112234915
|
G | C | 158 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(155): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.83+2741G>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112234915 | ||||||
| chr4:112235091
|
A | G | 1 | a0001c0001t0002g0023 | 3 | HG01255.hp1 HG01358.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.83+2917A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112235091 | ||||||
| chr4:112235126
|
T | C | 1 | a0001c0001t0004g0098 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.83+2952T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112235126 | ||||||
| chr4:112235528
|
C | T | 1 | a0001c0001t0002g0133 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.83+3354C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112235528 | ||||||
| chr4:112235558
|
A | G | 4 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.83+3384A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112235558 | ||||||
| chr4:112235667
|
T | C | 1 | a0001c0001t0006g0134 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.83+3493T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112235667 | ||||||
| chr4:112236155
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.83+3981A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112236155 | ||||||
| chr4:112236261
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.83+4087T>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112236261 | ||||||
| chr4:112236400
|
C | CTT | 150 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(147): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.83+4238_83+4239dup others(2): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 112236400 | |||||
| chr4:112236400
|
C | CTTT | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG00544.hp2 HG00741.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+4237_83+4239dup others(3): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 112236400 | |||||
| chr4:112236413
|
T | C | 1 | a0001c0001t0002g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.83+4239T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112236413 | ||||||
| chr4:112236414
|
C | T | 150 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(147): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.83+4240C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112236414 | ||||||
| chr4:112236445
|
G | A | 1 | a0001c0001t0001g0026 | 3 | HG00621.hp2 NA18960.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.83+4271G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112236445 | ||||||
| chr4:112236490
|
G | A | 4 | a0001c0001t0004g0097a0001c0001t0004g0099a0001c0001t0004g0100others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+4316G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112236490 | ||||||
| chr4:112236653
|
G | A | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.83+4479G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112236653 | ||||||
| chr4:112236813
|
G | A | 1 | a0001c0001t0003g0050 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.83+4639G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112236813 | ||||||
| chr4:112237192
|
C | T | 14 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0003g0027others(11): Show | 49 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.83+5018C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112237192 | ||||||
| chr4:112237229
|
C | T | 1 | a0001c0001t0008g0087 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.83+5055C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112237229 | ||||||
| chr4:112237291
|
A | G | 14 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0003g0027others(11): Show | 49 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.83+5117A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112237291 | ||||||
| chr4:112237345
|
A | G | 136 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(133): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.83+5171A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112237345 | ||||||
| chr4:112237383
|
G | A | 4 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.83+5209G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112237383 | ||||||
| chr4:112237481
|
G | A | 3 | a0001c0002t0001g0024a0001c0002t0001g0138a0001c0002t0030g0137 | 5 | HG01975.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+5307G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112237481 | ||||||
| chr4:112237502
|
G | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.83+5328G>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112237502 | ||||||
| chr4:112237600
|
G | A | 1 | a0001c0001t0017g0046 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.83+5426G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112237600 | ||||||
| chr4:112237711
|
A | G | 2 | a0001c0001t0005g0045a0001c0001t0005g0159 | 3 | HG02559.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.83+5537A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112237711 | ||||||
| chr4:112237840
|
C | T | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0086others(2): Show | 7 | HG00741.hp1 HG01081.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.83+5666C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112237840 | ||||||
| chr4:112237842
|
C | T | 1 | a0001c0001t0004g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.83+5668C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112237842 | ||||||
| chr4:112237851
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.83+5677C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112237851 | ||||||
| chr4:112237977
|
GGT | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(5): Show | 27 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.83+5804_83+5805del others(2): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112237977 | ||||||
| chr4:112237978
|
G | A | 1 | a0001c0001t0011g0169 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.83+5804G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112237978 | ||||||
| chr4:112238159
|
C | T | 1 | a0001c0001t0025g0151 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.83+5985C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112238159 | ||||||
| chr4:112238237
|
A | C | 1 | a0001c0001t0001g0032 | 2 | HG00140.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.83+6063A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112238237 | ||||||
| chr4:112238397
|
AT | A | 14 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0003g0027others(11): Show | 49 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.83+6231delT | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 112238397 | |||||
| chr4:112238411
|
G | A | 2 | a0001c0001t0005g0045a0001c0001t0005g0159 | 3 | HG02559.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.83+6237G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112238411 | ||||||
| chr4:112238762
|
C | T | 3 | a0001c0001t0011g0136a0001c0001t0011g0152a0001c0001t0011g0169 | 3 | HG03225.hp1 NA19005.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.83+6588C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112238762 | ||||||
| chr4:112238821
|
G | A | 15 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0003g0027others(12): Show | 50 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.83+6647G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112238821 | ||||||
| chr4:112238888
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.83+6714C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112238888 | ||||||
| chr4:112239006
|
C | A | 1 | a0001c0001t0006g0139 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.83+6832C>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112239006 | ||||||
| chr4:112239118
|
A | G | 14 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0003g0027others(11): Show | 49 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.83+6944A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112239118 | ||||||
| chr4:112239231
|
C | G | 1 | a0001c0001t0002g0132 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.83+7057C>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112239231 | ||||||
| chr4:112239289
|
C | A | 1 | a0001c0001t0011g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.83+7115C>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112239289 | ||||||
| chr4:112239492
|
C | G | 14 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0003g0027others(11): Show | 49 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.83+7318C>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112239492 | ||||||
| chr4:112239713
|
G | A | 1 | a0001c0001t0002g0107 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.83+7539G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112239713 | ||||||
| chr4:112239810
|
C | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0182 | 2 | NA19005.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.83+7636C>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112239810 | ||||||
| chr4:112239938
|
A | G | 2 | a0001c0001t0004g0035a0001c0001t0005g0150 | 3 | NA18994.hp2 NA19084.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.83+7764A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112239938 | ||||||
| chr4:112240103
|
G | A | 1 | a0001c0001t0028g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.83+7929G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112240103 | ||||||
| chr4:112240190
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.83+8016T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112240190 | ||||||
| chr4:112240222
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.83+8048G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112240222 | ||||||
| chr4:112240400
|
C | T | 1 | a0001c0001t0002g0131 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.83+8226C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112240400 | ||||||
| chr4:112240488
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.83+8314G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112240488 | ||||||
| chr4:112240747
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.83+8573T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112240747 | ||||||
| chr4:112240751
|
A | G | 4 | a0001c0001t0011g0136a0001c0001t0011g0152a0001c0001t0011g0169others(1): Show | 4 | HG02965.hp1 HG03225.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+8577A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112240751 | ||||||
| chr4:112241023
|
C | T | 1 | a0001c0001t0002g0042 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.83+8849C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112241023 | ||||||
| chr4:112241079
|
T | C | 1 | a0003c0007t0001g0068 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.83+8905T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112241079 | ||||||
| chr4:112241091
|
A | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0165a0001c0001t0006g0164 | 4 | HG02896.hp2 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+8917A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112241091 | ||||||
| chr4:112241115
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.83+8941A>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112241115 | ||||||
| chr4:112241182
|
C | T | 1 | a0004c0004t0002g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.83+9008C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112241182 | ||||||
| chr4:112241226
|
A | G | 2 | a0001c0001t0002g0128a0001c0001t0002g0129 | 2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.83+9052A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112241226 | ||||||
| chr4:112241242
|
C | A | 2 | a0001c0001t0001g0028a0001c0001t0034g0028 | 2 | HG00733.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.83+9068C>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112241242 | ||||||
| chr4:112241249
|
TAGTC | T | 3 | a0001c0002t0001g0024a0001c0002t0001g0138a0001c0002t0030g0137 | 5 | HG01975.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+9078_83+9081del others(4): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 112241249 | |||||
| chr4:112241462
|
A | G | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.83+9288A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112241462 | ||||||
| chr4:112241463
|
G | A | 1 | a0001c0001t0002g0037 | 2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.83+9289G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112241463 | ||||||
| chr4:112241481
|
T | G | 1 | a0001c0001t0002g0108 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.83+9307T>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112241481 | ||||||
| chr4:112241670
|
C | T | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.83+9496C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112241670 | ||||||
| chr4:112241939
|
T | C | 1 | a0001c0001t0004g0101 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.83+9765T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112241939 | ||||||
| chr4:112241953
|
A | G | 1 | a0001c0001t0008g0094 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.83+9779A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112241953 | ||||||
| chr4:112241977
|
G | A | 14 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0026others(11): Show | 21 | HG00438.hp1 HG00621.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.83+9803G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112241977 | ||||||
| chr4:112242279
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.83+10105G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112242279 | ||||||
| chr4:112242304
|
C | G | 1 | a0001c0001t0011g0152 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.83+10130C>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112242304 | ||||||
| chr4:112242321
|
G | A | 2 | a0001c0001t0006g0069a0001c0001t0006g0070 | 2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.83+10147G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112242321 | ||||||
| chr4:112242407
|
C | G | 133 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(130): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.83+10233C>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112242407 | ||||||
| chr4:112242452
|
G | GA | 151 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(148): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.83+10287dupA | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 112242452 | |||||
| chr4:112242457
|
A | AG | 4 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.83+10283_83+10284i others(3): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112242457 | ||||||
| chr4:112242611
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.83+10437A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112242611 | ||||||
| chr4:112242729
|
A | T | 5 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0006g0031others(2): Show | 6 | HG02486.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.84-10479A>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112242729 | ||||||
| chr4:112243002
|
C | T | 1 | a0001c0001t0002g0126 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.84-10206C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112243002 | ||||||
| chr4:112243168
|
C | T | 1 | a0004c0004t0002g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.84-10040C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112243168 | ||||||
| chr4:112243214
|
T | C | 1 | a0001c0001t0028g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.84-9994T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112243214 | ||||||
| chr4:112243231
|
C | T | 14 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0003g0027others(11): Show | 49 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.84-9977C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112243231 | ||||||
| chr4:112243389
|
C | T | 1 | a0001c0001t0002g0041 | 2 | HG02155.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.84-9819C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112243389 | ||||||
| chr4:112243476
|
T | G | 1 | a0001c0001t0002g0131 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.84-9732T>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112243476 | ||||||
| chr4:112244042
|
A | G | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(59): Show | 113 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.84-9166A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112244042 | ||||||
| chr4:112244087
|
T | C | 21 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0154others(18): Show | 47 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.84-9121T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112244087 | ||||||
| chr4:112244221
|
T | G | 22 | a0001c0001t0002g0011a0001c0001t0005g0003a0001c0001t0005g0043others(19): Show | 38 | HG00099.hp2 HG00609.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.84-8987T>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112244221 | ||||||
| chr4:112244245
|
G | C | 1 | a0001c0001t0028g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.84-8963G>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112244245 | ||||||
| chr4:112244436
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.84-8772A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112244436 | ||||||
| chr4:112244510
|
C | G | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.84-8698C>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112244510 | ||||||
| chr4:112244514
|
A | T | 2 | a0001c0001t0004g0099a0001c0001t0004g0158 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.84-8694A>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112244514 | ||||||
| chr4:112244540
|
G | T | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.84-8668G>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112244540 | ||||||
| chr4:112244661
|
G | A | 2 | a0001c0001t0016g0146a0001c0001t0016g0147 | 2 | HG00099.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.84-8547G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112244661 | ||||||
| chr4:112244898
|
C | T | 1 | a0001c0001t0028g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.84-8310C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112244898 | ||||||
| chr4:112244911
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.84-8297T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112244911 | ||||||
| chr4:112245114
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.84-8094A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112245114 | ||||||
| chr4:112245192
|
A | G | 1 | a0001c0001t0038g0059 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.84-8016A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112245192 | ||||||
| chr4:112245317
|
T | A | 1 | a0001c0001t0003g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.84-7891T>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112245317 | ||||||
| chr4:112245326
|
A | G | 1 | a0001c0002t0001g0138 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.84-7882A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112245326 | ||||||
| chr4:112245489
|
G | A | 1 | a0001c0001t0007g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.84-7719G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112245489 | ||||||
| chr4:112245903
|
T | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0088a0001c0001t0015g0021 | 4 | HG00738.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-7305T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112245903 | ||||||
| chr4:112245974
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.84-7234A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112245974 | ||||||
| chr4:112246107
|
T | C | 1 | a0001c0001t0004g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.84-7101T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112246107 | ||||||
| chr4:112246248
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.84-6960G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112246248 | ||||||
| chr4:112246265
|
G | A | 1 | a0001c0001t0014g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.84-6943G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112246265 | ||||||
| chr4:112246379
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.84-6829G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112246379 | ||||||
| chr4:112246420
|
C | T | 1 | a0001c0001t0002g0124 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.84-6788C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112246420 | ||||||
| chr4:112246559
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0010g0017 | 4 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-6649G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112246559 | ||||||
| chr4:112246701
|
A | C | 1 | a0001c0001t0001g0032 | 2 | HG00140.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.84-6507A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112246701 | ||||||
| chr4:112246732
|
T | A | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(151): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.84-6476T>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112246732 | ||||||
| chr4:112246813
|
A | T | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.84-6395A>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112246813 | ||||||
| chr4:112246902
|
T | C | 1 | a0001c0001t0006g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.84-6306T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112246902 | ||||||
| chr4:112246918
|
CT | C | 6 | a0001c0001t0005g0045a0001c0001t0005g0159a0001c0001t0006g0010others(3): Show | 13 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.84-6284delT | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 112246918 | |||||
| chr4:112246931
|
A | G | 2 | a0001c0001t0001g0086a0001c0001t0008g0087 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.84-6277A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112246931 | ||||||
| chr4:112247130
|
T | C | 1 | a0001c0001t0002g0111 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.84-6078T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112247130 | ||||||
| chr4:112247190
|
A | G | 4 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.84-6018A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112247190 | ||||||
| chr4:112247286
|
G | A | 1 | a0001c0001t0002g0015 | 4 | NA18947.hp1 NA18957.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-5922G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112247286 | ||||||
| chr4:112247533
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.84-5675A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112247533 | ||||||
| chr4:112247734
|
T | C | 2 | a0001c0001t0009g0048a0001c0001t0009g0171 | 3 | HG02970.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.84-5474T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112247734 | ||||||
| chr4:112247936
|
A | C | 18 | a0001c0001t0005g0003a0001c0001t0005g0104a0001c0001t0005g0143others(15): Show | 29 | HG00099.hp2 HG00609.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.84-5272A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112247936 | ||||||
| chr4:112248396
|
A | T | 2 | a0001c0001t0004g0099a0001c0001t0004g0158 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.84-4812A>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112248396 | ||||||
| chr4:112248531
|
G | A | 1 | a0001c0001t0017g0046 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.84-4677G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112248531 | ||||||
| chr4:112248937
|
C | T | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.84-4271C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112248937 | ||||||
| chr4:112249109
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.84-4099A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112249109 | ||||||
| chr4:112249185
|
T | G | 1 | a0001c0001t0016g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.84-4023T>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112249185 | ||||||
| chr4:112249220
|
G | A | 1 | a0001c0001t0003g0052 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.84-3988G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112249220 | ||||||
| chr4:112249221
|
C | T | 4 | a0001c0001t0002g0009a0001c0001t0002g0016a0001c0001t0002g0123others(1): Show | 13 | HG00733.hp1 HG01070.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.84-3987C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112249221 | ||||||
| chr4:112249222
|
G | A | 3 | a0001c0001t0002g0015a0001c0001t0002g0029a0001c0001t0002g0071 | 7 | HG00558.hp2 HG02080.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-3986G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112249222 | ||||||
| chr4:112249359
|
T | TA | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(128): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.84-3837dupA | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 112249359 | |||||
| chr4:112249359
|
T | TAA | 6 | a0001c0001t0001g0047a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 7 | HG02647.hp2 HG02897.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-3838_84-3837dup others(2): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 112249359 | |||||
| chr4:112249370
|
A | AAG | 3 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167 | 7 | HG01175.hp1 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.84-3837_84-3836ins others(2): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 112249370 | |||||
| chr4:112249370
|
A | C | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.84-3838A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112249370 | ||||||
| chr4:112249372
|
T | A | 2 | a0001c0001t0001g0165a0001c0001t0006g0164 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.84-3836T>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112249372 | ||||||
| chr4:112249481
|
A | G | 4 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.84-3727A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112249481 | ||||||
| chr4:112249605
|
C | T | 1 | a0001c0001t0004g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.84-3603C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112249605 | ||||||
| chr4:112249718
|
C | A | 4 | a0001c0001t0006g0010a0001c0001t0006g0044a0001c0001t0006g0156others(1): Show | 10 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.84-3490C>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112249718 | ||||||
| chr4:112249773
|
G | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0138 | 4 | HG01975.hp2 HG02486.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-3435G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112249773 | ||||||
| chr4:112249800
|
C | T | 1 | a0001c0001t0003g0018 | 3 | NA18984.hp1 NA19079.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.84-3408C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112249800 | ||||||
| chr4:112249842
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.84-3366G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112249842 | ||||||
| chr4:112249951
|
A | T | 1 | a0001c0001t0017g0046 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.84-3257A>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112249951 | ||||||
| chr4:112250127
|
C | T | 2 | a0001c0001t0002g0122a0001c0001t0002g0133 | 2 | NA18990.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.84-3081C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112250127 | ||||||
| chr4:112250128
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.84-3080G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112250128 | ||||||
| chr4:112250347
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.84-2861C>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112250347 | ||||||
| chr4:112250412
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.84-2796T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112250412 | ||||||
| chr4:112250429
|
A | G | 1 | a0001c0001t0005g0082 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.84-2779A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112250429 | ||||||
| chr4:112250632
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.84-2576A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112250632 | ||||||
| chr4:112250801
|
CCAAATAT others(15): Show |
C | 4 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.84-2384_84-2363del others(22): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 112250801 | |||||
| chr4:112250862
|
A | G | 1 | a0001c0001t0002g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84-2346A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112250862 | ||||||
| chr4:112251124
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.84-2084C>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112251124 | ||||||
| chr4:112251360
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(5): Show | 27 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.84-1848T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112251360 | ||||||
| chr4:112251394
|
G | A | 1 | a0001c0001t0004g0105 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.84-1814G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112251394 | ||||||
| chr4:112251405
|
A | G | 14 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0003g0027others(11): Show | 49 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.84-1803A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112251405 | ||||||
| chr4:112251420
|
A | C | 2 | a0001c0001t0002g0040a0001c0001t0002g0121 | 3 | NA18960.hp1 NA18988.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.84-1788A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112251420 | ||||||
| chr4:112251940
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0033g0014 | 4 | NA18973.hp1 NA19000.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-1268A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112251940 | ||||||
| chr4:112252026
|
T | A | 1 | a0001c0001t0001g0073 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.84-1182T>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112252026 | ||||||
| chr4:112252077
|
C | A | 1 | a0001c0001t0001g0074 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.84-1131C>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112252077 | ||||||
| chr4:112252196
|
G | A | 1 | a0001c0001t0017g0046 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.84-1012G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112252196 | ||||||
| chr4:112252326
|
A | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0084others(4): Show | 9 | HG02486.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.84-882A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112252326 | ||||||
| chr4:112252914
|
T | C | 1 | a0001c0001t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.84-294T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112252914 | ||||||
| chr4:112253049
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.84-159T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112253049 | ||||||
| chr4:112253159
|
A | G | 1 | a0001c0001t0003g0027 | 2 | NA19057.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.84-49A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 1/9 | chr4 | 112253159 | ||||||
| chr4:112253323
|
A | G | 1 | a0001c0001t0005g0145 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.132+67A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112253323 | ||||||
| chr4:112253400
|
A | G | 1 | a0001c0001t0002g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.132+144A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112253400 | ||||||
| chr4:112253411
|
A | C | 1 | a0001c0001t0028g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.132+155A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112253411 | ||||||
| chr4:112253544
|
C | T | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(66): Show | 122 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.132+288C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112253544 | ||||||
| chr4:112253594
|
G | C | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.132+338G>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112253594 | ||||||
| chr4:112253606
|
A | G | 2 | a0001c0001t0002g0016a0001c0001t0002g0123 | 5 | NA18964.hp1 NA19004.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+350A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112253606 | ||||||
| chr4:112253682
|
C | T | 1 | a0001c0001t0003g0058 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.132+426C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112253682 | ||||||
| chr4:112253686
|
A | G | 1 | a0001c0001t0017g0046 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.132+430A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112253686 | ||||||
| chr4:112253796
|
C | T | 19 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0154others(16): Show | 45 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.132+540C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112253796 | ||||||
| chr4:112253826
|
C | T | 1 | a0001c0001t0002g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.132+570C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112253826 | ||||||
| chr4:112253944
|
A | T | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.132+688A>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112253944 | ||||||
| chr4:112253956
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.132+700C>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112253956 | ||||||
| chr4:112253962
|
T | TAAAAAAA others(342): Show |
1 | a0001c0001t0005g0142 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.132+722_132+723ins others(349): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 112253962 | |||||
| chr4:112254031
|
A | C | 1 | a0001c0001t0003g0057 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.133-716A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112254031 | ||||||
| chr4:112254037
|
T | C | 1 | a0001c0002t0030g0137 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.133-710T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112254037 | ||||||
| chr4:112254281
|
T | G | 1 | a0001c0001t0017g0046 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.133-466T>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112254281 | ||||||
| chr4:112254420
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.133-327C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112254420 | ||||||
| chr4:112254578
|
G | A | 1 | a0001c0001t0003g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.133-169G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112254578 | ||||||
| chr4:112254578
|
G | T | 1 | a0001c0001t0008g0094 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.133-169G>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112254578 | ||||||
| chr4:112254586
|
A | G | 19 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0154others(16): Show | 45 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.133-161A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 2/9 | chr4 | 112254586 | ||||||
| chr4:112254848
|
G | A | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0086others(2): Show | 7 | HG00741.hp1 HG01081.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+75G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112254848 | ||||||
| chr4:112254984
|
G | T | 1 | a0001c0001t0007g0167 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.159+211G>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112254984 | ||||||
| chr4:112254991
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.159+218C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112254991 | ||||||
| chr4:112255022
|
G | A | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(137): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.159+249G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255022 | ||||||
| chr4:112255023
|
G | T | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(137): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.159+250G>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255023 | ||||||
| chr4:112255024
|
G | C | 3 | a0001c0001t0011g0136a0001c0001t0011g0152a0001c0001t0011g0169 | 3 | HG03225.hp1 NA19005.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.159+251G>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255024 | ||||||
| chr4:112255047
|
G | A | 1 | a0001c0001t0002g0123 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.159+274G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255047 | ||||||
| chr4:112255078
|
G | A | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.159+305G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255078 | ||||||
| chr4:112255105
|
G | A | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.159+332G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255105 | ||||||
| chr4:112255108
|
C | T | 4 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.159+335C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255108 | ||||||
| chr4:112255114
|
T | C | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(137): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.159+341T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255114 | ||||||
| chr4:112255121
|
G | A | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(137): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.159+348G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255121 | ||||||
| chr4:112255195
|
G | A | 4 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.159+422G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255195 | ||||||
| chr4:112255205
|
A | G | 4 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.159+432A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255205 | ||||||
| chr4:112255233
|
T | A | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.159+460T>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255233 | ||||||
| chr4:112255286
|
T | TA | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.159+514dupA | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 112255286 | |||||
| chr4:112255437
|
C | T | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(137): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.159+664C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255437 | ||||||
| chr4:112255489
|
T | C | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(152): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.159+716T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255489 | ||||||
| chr4:112255619
|
A | G | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.159+846A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255619 | ||||||
| chr4:112255957
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.159+1184C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112255957 | ||||||
| chr4:112256015
|
A | G | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.159+1242A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112256015 | ||||||
| chr4:112256035
|
T | TAAAAATG others(286): Show |
1 | a0001c0001t0009g0171 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.159+1278_159+1279i others(295): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 112256035 | |||||
| chr4:112256035
|
T | TAAAAATG others(287): Show |
1 | a0001c0001t0009g0048 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.159+1278_159+1279i others(296): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 112256035 | |||||
| chr4:112256037
|
A | G | 6 | a0001c0001t0005g0045a0001c0001t0005g0159a0001c0001t0006g0010others(3): Show | 13 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+1264A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112256037 | ||||||
| chr4:112256107
|
T | C | 2 | a0001c0001t0009g0048a0001c0001t0009g0171 | 3 | HG02970.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.159+1334T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112256107 | ||||||
| chr4:112256201
|
A | C | 1 | a0001c0001t0017g0046 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.159+1428A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112256201 | ||||||
| chr4:112256257
|
C | T | 4 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.159+1484C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112256257 | ||||||
| chr4:112256291
|
A | G | 1 | a0001c0001t0028g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.160-1481A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112256291 | ||||||
| chr4:112256448
|
G | A | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.160-1324G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112256448 | ||||||
| chr4:112256551
|
C | T | 1 | a0001c0001t0003g0057 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.160-1221C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112256551 | ||||||
| chr4:112256681
|
A | G | 4 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-1091A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112256681 | ||||||
| chr4:112256759
|
A | T | 1 | a0001c0001t0003g0057 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.160-1013A>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112256759 | ||||||
| chr4:112256830
|
C | G | 1 | a0001c0001t0005g0043 | 2 | HG00735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.160-942C>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112256830 | ||||||
| chr4:112256920
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.160-852T>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112256920 | ||||||
| chr4:112257037
|
G | C | 4 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-735G>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112257037 | ||||||
| chr4:112257124
|
C | A | 1 | a0001c0001t0011g0152 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.160-648C>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112257124 | ||||||
| chr4:112257520
|
A | G | 1 | a0001c0001t0014g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.160-252A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112257520 | ||||||
| chr4:112257648
|
G | T | 1 | a0001c0001t0014g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.160-124G>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112257648 | ||||||
| chr4:112257712
|
T | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.160-60T>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | chr4 | 112257712 | ||||||
| chr4:112257738
|
ATTTGT | A | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(151): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.160-30_160-26delGT others(3): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 112257738 | |||||
| chr4:112257810
|
T | TA | 5 | a0001c0001t0001g0047a0001c0001t0001g0076a0001c0001t0001g0165others(2): Show | 6 | HG00423.hp1 HG00544.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+25dupA | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 112257810 | |||||
| chr4:112257921
|
C | T | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(151): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.185+124C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112257921 | ||||||
| chr4:112257924
|
A | T | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(151): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.185+127A>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112257924 | ||||||
| chr4:112257953
|
A | T | 1 | a0001c0001t0011g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.185+156A>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112257953 | ||||||
| chr4:112258047
|
T | C | 1 | a0001c0001t0028g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.185+250T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112258047 | ||||||
| chr4:112258110
|
TCTTTC | T | 1 | a0001c0001t0004g0022 | 3 | NA18612.hp2 NA18953.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.185+317_185+321del others(5): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 112258110 | |||||
| chr4:112258136
|
T | C | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(151): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.185+339T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112258136 | ||||||
| chr4:112258212
|
T | C | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.185+415T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112258212 | ||||||
| chr4:112258244
|
CTT | C | 3 | a0001c0002t0001g0024a0001c0002t0001g0138a0001c0002t0030g0137 | 5 | HG01975.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.185+449_185+450del others(2): Show |
AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 112258244 | |||||
| chr4:112258427
|
A | C | 19 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0154others(16): Show | 45 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.185+630A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112258427 | ||||||
| chr4:112258701
|
T | C | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.185+904T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112258701 | ||||||
| chr4:112258727
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.185+930A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112258727 | ||||||
| chr4:112258789
|
A | C | 1 | a0001c0001t0001g0127 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.185+992A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112258789 | ||||||
| chr4:112258861
|
C | T | 2 | a0001c0001t0004g0008a0001c0005t0004g0008 | 9 | HG00323.hp1 HG01106.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+1064C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112258861 | ||||||
| chr4:112259011
|
T | C | 1 | a0001c0001t0017g0046 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.185+1214T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112259011 | ||||||
| chr4:112259292
|
G | T | 1 | a0001c0001t0001g0177 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.186-1474G>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112259292 | ||||||
| chr4:112259580
|
G | A | 1 | a0001c0001t0003g0055 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.186-1186G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112259580 | ||||||
| chr4:112259623
|
C | T | 15 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0003g0027others(12): Show | 50 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.186-1143C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112259623 | ||||||
| chr4:112259865
|
T | A | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.186-901T>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112259865 | ||||||
| chr4:112259958
|
TA | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0092 | 5 | HG00741.hp1 HG01081.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-800delA | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 112259958 | |||||
| chr4:112260055
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0072 | 3 | HG02572.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.186-711A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112260055 | ||||||
| chr4:112260187
|
T | C | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(151): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.186-579T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112260187 | ||||||
| chr4:112260205
|
G | C | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.186-561G>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112260205 | ||||||
| chr4:112260286
|
G | C | 2 | a0001c0001t0002g0122a0001c0001t0002g0133 | 2 | NA18990.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.186-480G>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112260286 | ||||||
| chr4:112260411
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.186-355T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 4/9 | chr4 | 112260411 | ||||||
| chr4:112261050
|
T | C | 1 | a0001c0001t0002g0038 | 2 | HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.282+188T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | chr4 | 112261050 | ||||||
| chr4:112261098
|
T | C | 1 | a0001c0001t0004g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.282+236T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | chr4 | 112261098 | ||||||
| chr4:112261341
|
A | G | 1 | a0001c0001t0002g0126 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.282+479A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | chr4 | 112261341 | ||||||
| chr4:112261343
|
T | G | 1 | a0001c0001t0002g0126 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.282+481T>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | chr4 | 112261343 | ||||||
| chr4:112261427
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.282+565G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | chr4 | 112261427 | ||||||
| chr4:112261463
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.282+601A>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | chr4 | 112261463 | ||||||
| chr4:112261479
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.282+617T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | chr4 | 112261479 | ||||||
| chr4:112261666
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.282+804T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | chr4 | 112261666 | ||||||
| chr4:112261909
|
T | C | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(154): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.282+1047T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | chr4 | 112261909 | ||||||
| chr4:112261968
|
C | CA | 14 | a0001c0001t0001g0007a0001c0001t0001g0073a0001c0001t0001g0075others(11): Show | 24 | HG01109.hp1 HG01255.hp2 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.283-1008dupA | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 112261968 | |||||
| chr4:112262100
|
G | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0123 | 5 | NA18964.hp1 NA19004.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-888G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | chr4 | 112262100 | ||||||
| chr4:112262387
|
T | G | 1 | a0001c0001t0002g0115 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.283-601T>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | chr4 | 112262387 | ||||||
| chr4:112262447
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.283-541T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | chr4 | 112262447 | ||||||
| chr4:112262540
|
A | C | 1 | a0001c0002t0001g0138 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.283-448A>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | chr4 | 112262540 | ||||||
| chr4:112262596
|
C | T | 19 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0154others(16): Show | 45 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.283-392C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 5/9 | chr4 | 112262596 | ||||||
| chr4:112263298
|
C | T | 1 | a0001c0001t0028g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.381+212C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | chr4 | 112263298 | ||||||
| chr4:112263330
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.381+244C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | chr4 | 112263330 | ||||||
| chr4:112263464
|
G | GT | 14 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0084others(11): Show | 15 | HG00735.hp1 HG02040.hp2 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.381+391dupT | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 112263464 | |||||
| chr4:112263464
|
GT | G | 11 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0007g0012others(8): Show | 16 | HG01175.hp1 HG02257.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.381+391delT | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 112263464 | |||||
| chr4:112263557
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.381+471T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | chr4 | 112263557 | ||||||
| chr4:112263771
|
G | T | 1 | a0001c0001t0002g0111 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.381+685G>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | chr4 | 112263771 | ||||||
| chr4:112263897
|
T | C | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(154): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.381+811T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | chr4 | 112263897 | ||||||
| chr4:112264048
|
T | C | 4 | a0001c0001t0011g0136a0001c0001t0011g0152a0001c0001t0011g0169others(1): Show | 4 | HG02965.hp1 HG03225.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-961T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | chr4 | 112264048 | ||||||
| chr4:112264116
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.382-893A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | chr4 | 112264116 | ||||||
| chr4:112264186
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.382-823A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | chr4 | 112264186 | ||||||
| chr4:112264189
|
A | G | 14 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0003g0027others(11): Show | 49 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.382-820A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | chr4 | 112264189 | ||||||
| chr4:112264393
|
T | A | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(151): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.382-616T>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | chr4 | 112264393 | ||||||
| chr4:112264477
|
G | A | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.382-532G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | chr4 | 112264477 | ||||||
| chr4:112264517
|
T | C | 2 | a0001c0001t0004g0008a0001c0005t0004g0008 | 9 | HG00323.hp1 HG01106.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.382-492T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | chr4 | 112264517 | ||||||
| chr4:112264733
|
A | T | 4 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-276A>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | chr4 | 112264733 | ||||||
| chr4:112264918
|
GA | G | 3 | a0001c0002t0001g0024a0001c0002t0001g0138a0001c0002t0030g0137 | 5 | HG01975.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-84delA | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 112264918 | |||||
| chr4:112265325
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.440+258C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 7/9 | chr4 | 112265325 | ||||||
| chr4:112265371
|
C | G | 1 | a0001c0001t0002g0116 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.440+304C>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 7/9 | chr4 | 112265371 | ||||||
| chr4:112265384
|
A | G | 1 | a0001c0001t0022g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.440+317A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 7/9 | chr4 | 112265384 | ||||||
| chr4:112265693
|
T | C | 2 | a0001c0001t0016g0146a0001c0001t0016g0147 | 2 | HG00099.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.441-41T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 7/9 | chr4 | 112265693 | ||||||
| chr4:112265875
|
C | T | 1 | a0001c0001t0006g0044 | 2 | HG00735.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.514+68C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 8/9 | chr4 | 112265875 | ||||||
| chr4:112265958
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.514+151C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 8/9 | chr4 | 112265958 | ||||||
| chr4:112266017
|
G | T | 1 | a0001c0001t0001g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.514+210G>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 8/9 | chr4 | 112266017 | ||||||
| chr4:112266125
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.514+318A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 8/9 | chr4 | 112266125 | ||||||
| chr4:112266190
|
A | G | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.514+383A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 8/9 | chr4 | 112266190 | ||||||
| chr4:112266230
|
A | G | 1 | a0001c0001t0019g0039 | 2 | NA18992.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.515-358A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 8/9 | chr4 | 112266230 | ||||||
| chr4:112266254
|
T | A | 4 | a0001c0001t0007g0012a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.515-334T>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 8/9 | chr4 | 112266254 | ||||||
| chr4:112266273
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.515-315T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 8/9 | chr4 | 112266273 | ||||||
| chr4:112266532
|
C | T | 1 | a0001c0001t0028g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.515-56C>T | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 8/9 | chr4 | 112266532 | ||||||
| chr4:112266539
|
G | A | 1 | a0001c0001t0003g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.515-49G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 8/9 | chr4 | 112266539 | ||||||
| chr4:112266575
|
G | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0092 | 3 | HG00741.hp1 HG01081.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.515-13G>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 8/9 | chr4 | 112266575 | ||||||
| chr4:112267101
|
A | G | 1 | a0001c0001t0019g0039 | 2 | NA18992.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.643+385A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 9/9 | chr4 | 112267101 | ||||||
| chr4:112267103
|
T | C | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.643+387T>C | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 9/9 | chr4 | 112267103 | ||||||
| chr4:112267594
|
C | A | 1 | a0001c0001t0001g0067 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.644-550C>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 9/9 | chr4 | 112267594 | ||||||
| chr4:112267651
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.644-493G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 9/9 | chr4 | 112267651 | ||||||
| chr4:112267843
|
A | G | 1 | a0001c0001t0003g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.644-301A>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 9/9 | chr4 | 112267843 | ||||||
| chr4:112267902
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.644-242G>A | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 9/9 | chr4 | 112267902 | ||||||
| chr4:112268015
|
T | G | 1 | a0001c0001t0001g0079 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.644-129T>G | AP1AR | ENSG00000138660.12 | transcript | ENST00000274000.10 | protein_coding | 9/9 | chr4 | 112268015 |