Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 164 |
|---|---|
| ensemblid | ENSG00000166747.13 |
| hgncid | 555 |
| symbol | AP1G1 |
| name | adaptor related protein complex 1 subunit gamma 1 |
| refseq_nuc | NM_001128.6 |
| refseq_prot | NP_001119.3 |
| ensembl_nuc | ENST00000299980.9 |
| ensembl_prot | ENSP00000299980.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 71729000 |
| end | 71808834 |
| strand | - |
| ver | v1.2 |
| region | chr16:71729000-71808834 |
| region5000 | chr16:71724000-71813834 |
| regionname0 | AP1G1_chr16_71729000_71808834 |
| regionname5000 | AP1G1_chr16_71724000_71813834 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 822 | 234 | 79 | 43 | 80 | 13 | 17 | 56 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0002 | 0/0 | 822 | 82 | 5 | 19 | 36 | 3 | 19 | 31 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0003 | 0/0 | 822 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0004 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0005 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2469 | 217 | 66 | 40 | 80 | 12 | 17 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| c0002 | 0/0 | 2469 | 82 | 5 | 19 | 36 | 3 | 19 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| c0003 | 0/0 | 2469 | 11 | 11 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| c0004 | 0/0 | 2469 | 4 | 0 | 3 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| c0005 | 0/0 | 2469 | 2 | 0 | 0 | 0 | 0 | 2 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| c0006 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| c0007 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| c0008 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| c0009 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4135 | 58 | 5 | 6 | 30 | 2 | 15 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0002 | 0/0 | 4134 | 57 | 11 | 12 | 27 | 2 | 5 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0003 | 0/0 | 4135 | 30 | 3 | 7 | 17 | 0 | 3 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0004 | 1/0 | 4134 | 28 | 13 | 7 | 4 | 3 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0005 | 0/0 | 4136 | 25 | 18 | 2 | 1 | 1 | 3 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0006 | 0/0 | 4135 | 17 | 0 | 12 | 3 | 0 | 2 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0007 | 0/0 | 4136 | 15 | 1 | 8 | 2 | 3 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0008 | 0/0 | 4133 | 13 | 12 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0009 | 0/0 | 4137 | 11 | 0 | 3 | 4 | 2 | 2 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0010 | 0/0 | 4133 | 8 | 7 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0011 | 0/0 | 4134 | 8 | 0 | 0 | 8 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0012 | 0/0 | 4134 | 6 | 0 | 0 | 6 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0013 | 0/0 | 4134 | 6 | 0 | 0 | 6 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0014 | 0/0 | 4133 | 5 | 1 | 1 | 0 | 1 | 2 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0015 | 0/0 | 4134 | 5 | 4 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0016 | 0/0 | 4133 | 2 | 2 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0017 | 0/0 | 4134 | 2 | 0 | 0 | 1 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0018 | 0/0 | 4135 | 2 | 1 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0019 | 0/0 | 4133 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0020 | 0/0 | 4134 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0021 | 0/0 | 4135 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0022 | 0/0 | 4136 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0023 | 0/0 | 4136 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0024 | 0/0 | 4137 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0025 | 0/0 | 4135 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0026 | 0/0 | 4134 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0027 | 0/0 | 4134 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0028 | 0/0 | 4134 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0029 | 0/0 | 4134 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0030 | 0/1 | 4136 | 1 | 0 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0031 | 0/0 | 4135 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0032 | 0/0 | 4135 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0033 | 0/0 | 4135 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0034 | 0/0 | 4136 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0035 | 0/0 | 4135 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0036 | 0/0 | 4135 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0037 | 0/0 | 4137 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0038 | 0/0 | 4137 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0039 | 0/0 | 4135 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| t0040 | 0/0 | 4134 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0024 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2469 | 217 | 66 | 40 | 80 | 12 | 17 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0003 | 0/0 | 2469 | 11 | 11 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0004 | 0/0 | 2469 | 4 | 0 | 3 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0008 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0009 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0002c0002 | 0/0 | 2469 | 82 | 5 | 19 | 36 | 3 | 19 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0003c0005 | 0/0 | 2469 | 2 | 0 | 0 | 0 | 0 | 2 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0004c0007 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0005c0006 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 6602 | 57 | 11 | 12 | 27 | 2 | 5 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0003 | 0/0 | 6603 | 30 | 3 | 7 | 17 | 0 | 3 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0004 | 1/0 | 6602 | 27 | 13 | 7 | 3 | 3 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0005 | 0/0 | 6604 | 24 | 18 | 2 | 0 | 1 | 3 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0007 | 0/0 | 6604 | 11 | 1 | 5 | 2 | 2 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0008 | 0/0 | 6601 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0009 | 0/0 | 6605 | 11 | 0 | 3 | 4 | 2 | 2 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0010 | 0/0 | 6601 | 8 | 7 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0011 | 0/0 | 6602 | 8 | 0 | 0 | 8 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0012 | 0/0 | 6602 | 6 | 0 | 0 | 6 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0013 | 0/0 | 6602 | 6 | 0 | 0 | 6 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0014 | 0/0 | 6601 | 5 | 1 | 1 | 0 | 1 | 2 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0015 | 0/0 | 6602 | 5 | 4 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0016 | 0/0 | 6601 | 2 | 2 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0018 | 0/0 | 6603 | 2 | 1 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0020 | 0/0 | 6602 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0023 | 0/0 | 6604 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0024 | 0/0 | 6605 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0025 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0026 | 0/0 | 6602 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0027 | 0/0 | 6602 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0028 | 0/0 | 6602 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0029 | 0/0 | 6602 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0030 | 0/1 | 6604 | 1 | 0 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0035 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0036 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0037 | 0/0 | 6605 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0038 | 0/0 | 6605 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0001t0040 | 0/0 | 6602 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0003t0008 | 0/0 | 6601 | 11 | 11 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0004t0007 | 0/0 | 6604 | 4 | 0 | 3 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0008t0008 | 0/0 | 6601 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0001c0009t0019 | 0/0 | 6601 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0002c0002t0001 | 0/0 | 6603 | 54 | 5 | 6 | 28 | 2 | 13 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0002c0002t0004 | 0/0 | 6602 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0002c0002t0005 | 0/0 | 6604 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0002c0002t0006 | 0/0 | 6603 | 17 | 0 | 12 | 3 | 0 | 2 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0002c0002t0017 | 0/0 | 6602 | 2 | 0 | 0 | 1 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0002c0002t0021 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0002c0002t0022 | 0/0 | 6604 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0002c0002t0031 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0002c0002t0032 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0002c0002t0033 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0002c0002t0034 | 0/0 | 6604 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0002c0002t0039 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0003c0005t0001 | 0/0 | 6603 | 2 | 0 | 0 | 0 | 0 | 2 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0004c0007t0001 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| a0005c0006t0001 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | copy fasta | chr16 | 71724000 | 71813834 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0024 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0008g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0012g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0012g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0012g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0012g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0012g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0012g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0013g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0013g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0013g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0013g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0013g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0013g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0014g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0014g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0014g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0014g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0014g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0015g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0015g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0015g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0015g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0015g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0016g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0016g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0018g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0018g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0020g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0023g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0024g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0025g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0026g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0027g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0028g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0029g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0030g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0035g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0036g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0037g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0038g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0040g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0004t0007g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0004t0007g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0004t0007g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0004t0007g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0008t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0009t0019g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0017g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0017g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0021g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0022g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0031g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0032g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0033g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0034g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0039g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0003c0005t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0003c0005t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0004c0007t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0005c0006t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0028 | EUR | GBR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0020 | EUR | GBR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0075 | EUR | GBR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00140 | hp2 | a0001 | c0001 | t0014 | g0252 | EUR | GBR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00323 | hp1 | a0002 | c0002 | t0017 | g0129 | EUR | FIN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0131 | EUR | FIN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00408 | hp1 | a0001 | c0001 | t0013 | g0280 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00609 | hp1 | a0001 | c0001 | t0011 | g0247 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00609 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00621 | hp2 | a0001 | c0001 | t0013 | g0289 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00642 | hp2 | a0002 | c0002 | t0006 | g0173 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0052 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0081 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00738 | hp1 | a0002 | c0002 | t0006 | g0171 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0007 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00741 | hp1 | a0002 | c0002 | t0006 | g0099 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01071 | hp1 | a0002 | c0002 | t0006 | g0127 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0155 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0025 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01106 | hp1 | a0001 | c0004 | t0007 | g0068 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0078 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0125 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0077 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01175 | hp1 | a0001 | c0001 | t0014 | g0195 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0062 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01192 | hp2 | a0001 | c0004 | t0007 | g0076 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01255 | hp1 | a0002 | c0002 | t0006 | g0105 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0208 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01256 | hp2 | a0001 | c0001 | t0009 | g0073 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01257 | hp1 | a0002 | c0002 | t0006 | g0179 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01257 | hp2 | a0001 | c0001 | t0007 | g0080 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01258 | hp1 | a0002 | c0002 | t0006 | g0101 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0072 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01358 | hp2 | a0001 | c0001 | t0009 | g0085 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0063 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0216 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01515 | hp1 | a0001 | c0001 | t0015 | g0037 | EUR | IBS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0294 | EUR | IBS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01516 | hp1 | a0001 | c0004 | t0007 | g0091 | EUR | IBS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01516 | hp2 | a0001 | c0001 | t0009 | g0086 | EUR | IBS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01517 | hp1 | a0001 | c0001 | t0009 | g0065 | EUR | IBS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0239 | EUR | IBS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01891 | hp1 | a0001 | c0003 | t0008 | g0183 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0008 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01934 | hp1 | a0001 | c0004 | t0007 | g0074 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0159 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01981 | hp1 | a0002 | c0002 | t0006 | g0104 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01993 | hp1 | a0002 | c0002 | t0034 | g0098 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02040 | hp1 | a0001 | c0001 | t0011 | g0222 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0108 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02056 | hp1 | a0001 | c0001 | t0011 | g0248 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02071 | hp2 | a0002 | c0002 | t0039 | g0318 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02074 | hp1 | a0001 | c0001 | t0027 | g0263 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02074 | hp2 | a0005 | c0006 | t0001 | g0132 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02083 | hp2 | a0001 | c0001 | t0011 | g0246 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02132 | hp2 | a0001 | c0001 | t0011 | g0256 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0093 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02148 | hp1 | a0002 | c0002 | t0006 | g0103 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | CDX | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | CDX | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02257 | hp1 | a0001 | c0001 | t0016 | g0041 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0084 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02258 | hp2 | a0001 | c0003 | t0008 | g0190 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02293 | hp1 | a0002 | c0002 | t0006 | g0106 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02293 | hp2 | a0001 | c0001 | t0018 | g0225 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02300 | hp1 | a0002 | c0002 | t0006 | g0102 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02300 | hp2 | a0001 | c0001 | t0008 | g0029 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0317 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02451 | hp2 | a0001 | c0009 | t0019 | g0010 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02523 | hp1 | a0001 | c0001 | t0040 | g0238 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0004 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0304 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0157 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0050 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0005 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0115 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02647 | hp1 | a0001 | c0001 | t0018 | g0314 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0313 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02683 | hp1 | a0002 | c0002 | t0006 | g0100 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0051 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0150 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0110 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0128 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0277 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02809 | hp2 | a0001 | c0008 | t0008 | g0181 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02818 | hp1 | a0001 | c0001 | t0037 | g0082 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02886 | hp1 | a0001 | c0001 | t0015 | g0038 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0003 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02895 | hp1 | a0001 | c0001 | t0026 | g0311 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0039 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02897 | hp1 | a0001 | c0001 | t0015 | g0035 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0006 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0107 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02965 | hp2 | a0001 | c0003 | t0008 | g0193 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0113 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02970 | hp2 | a0001 | c0003 | t0008 | g0185 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03017 | hp1 | a0002 | c0002 | t0031 | g0160 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03017 | hp2 | a0002 | c0002 | t0032 | g0140 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03130 | hp1 | a0001 | c0003 | t0008 | g0192 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0112 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03209 | hp1 | a0001 | c0001 | t0016 | g0042 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0310 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0056 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03225 | hp2 | a0001 | c0001 | t0020 | g0064 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03239 | hp1 | a0002 | c0002 | t0006 | g0168 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0054 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03490 | hp1 | a0001 | c0001 | t0014 | g0204 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03490 | hp2 | a0001 | c0001 | t0009 | g0079 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03491 | hp1 | a0003 | c0005 | t0001 | g0166 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03492 | hp1 | a0001 | c0001 | t0009 | g0069 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03492 | hp2 | a0003 | c0005 | t0001 | g0165 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0057 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0303 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03540 | hp2 | a0001 | c0003 | t0008 | g0189 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03654 | hp2 | a0002 | c0002 | t0021 | g0097 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0262 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0182 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0174 | SAS | STU | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03688 | hp2 | a0001 | c0001 | t0014 | g0266 | SAS | STU | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03710 | hp1 | a0002 | c0002 | t0022 | g0094 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0154 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0196 | SAS | BEB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0158 | SAS | BEB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0268 | SAS | BEB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0148 | SAS | BEB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0164 | SAS | BEB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0089 | SAS | BEB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG04204 | hp1 | a0001 | c0001 | t0024 | g0088 | SAS | STU | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0135 | SAS | STU | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | STU | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0071 | SAS | STU | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18612 | hp1 | a0001 | c0001 | t0013 | g0287 | EAS | CHB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | CHB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0114 | AFR | YRI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18906 | hp2 | a0001 | c0003 | t0008 | g0188 | AFR | YRI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18941 | hp1 | a0002 | c0002 | t0006 | g0177 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18941 | hp2 | a0002 | c0002 | t0017 | g0047 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18946 | hp1 | a0004 | c0007 | t0001 | g0176 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18950 | hp1 | a0001 | c0001 | t0029 | g0267 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18951 | hp1 | a0001 | c0001 | t0011 | g0199 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18951 | hp2 | a0002 | c0002 | t0033 | g0152 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18952 | hp1 | a0001 | c0001 | t0013 | g0288 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18952 | hp2 | a0001 | c0001 | t0012 | g0202 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18954 | hp1 | a0001 | c0001 | t0012 | g0292 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18957 | hp2 | a0002 | c0002 | t0004 | g0149 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18959 | hp1 | a0001 | c0001 | t0012 | g0200 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18965 | hp1 | a0001 | c0001 | t0035 | g0234 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18966 | hp2 | a0001 | c0001 | t0011 | g0235 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18968 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18968 | hp2 | a0001 | c0001 | t0011 | g0259 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18970 | hp1 | a0001 | c0001 | t0012 | g0203 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0087 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18971 | hp2 | a0001 | c0001 | t0028 | g0251 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18973 | hp1 | a0001 | c0001 | t0009 | g0070 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18973 | hp2 | a0001 | c0001 | t0025 | g0217 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18985 | hp1 | a0001 | c0001 | t0013 | g0282 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18990 | hp1 | a0002 | c0002 | t0006 | g0045 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18993 | hp2 | a0001 | c0001 | t0036 | g0271 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18994 | hp2 | a0001 | c0001 | t0009 | g0067 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18999 | hp2 | a0001 | c0001 | t0013 | g0286 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19011 | hp1 | a0001 | c0001 | t0012 | g0197 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19011 | hp2 | a0002 | c0002 | t0005 | g0142 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0308 | AFR | LWK | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0036 | AFR | LWK | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19043 | hp1 | a0001 | c0003 | t0008 | g0187 | AFR | LWK | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | LWK | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19054 | hp2 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19091 | hp2 | a0002 | c0002 | t0006 | g0046 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19240 | hp1 | a0001 | c0003 | t0008 | g0186 | AFR | YRI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0300 | AFR | YRI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ASW | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20129 | hp2 | a0001 | c0001 | t0023 | g0121 | AFR | ASW | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0130 | EUR | TSI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0053 | EUR | TSI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0027 | EUR | TSI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0066 | EUR | TSI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01123 | hp1 | a0002 | c0002 | t0006 | g0172 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0116 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02109 | hp2 | a0001 | c0003 | t0008 | g0184 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0315 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0119 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02559 | hp2 | a0001 | c0001 | t0038 | g0083 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0117 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG06807 | hp1 | a0001 | c0003 | t0008 | g0191 | AFR | USA | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | USA | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18955 | hp1 | a0001 | c0001 | t0012 | g0207 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | USA | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | USA | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | LWK | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0306 | AFR | LWK | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0030 | g0049 | REF | REF | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0024 | REF | REF | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71739018
|
G | A | 1 | a0005 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.2192C>T | p.Thr731Ile | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/23 | 2267/6602 | 2192/2469 | 731/822 | chr16 | 71739018 | ||
| chr16:71739287
|
G | T | 4 | a0002a0003a0004others(1): Show | 86 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(83): Show |
missense_variant | MODERATE | c.2054C>A | p.Pro685His | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 20/23 | 2129/6602 | 2054/2469 | 685/822 | chr16 | 71739287 | ||
| chr16:71745206
|
G | A | 1 | a0004 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.1937C>T | p.Thr646Ile | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/23 | 2012/6602 | 1937/2469 | 646/822 | chr16 | 71745206 | ||
| chr16:71745593
|
C | A | 1 | a0003 | 2 | HG03491.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.1752G>T | p.Met584Ile | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 18/23 | 1827/6602 | 1752/2469 | 584/822 | chr16 | 71745593 | ||
| chr16:71745604
|
G | A | 1 | a0003 | 2 | HG03491.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.1741C>T | p.Leu581Phe | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 18/23 | 1816/6602 | 1741/2469 | 581/822 | chr16 | 71745604 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71756129
|
T | C | 1 | a0001c0003 | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
synonymous_variant | LOW | c.1119A>G | p.Val373Val | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/23 | 1194/6602 | 1119/2469 | 373/822 | chr16 | 71756129 | ||
| chr16:71769668
|
T | C | 1 | a0001c0008 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.597A>G | p.Thr199Thr | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/23 | 672/6602 | 597/2469 | 199/822 | chr16 | 71769668 | ||
| chr16:71769686
|
T | C | 1 | a0001c0009 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.579A>G | p.Thr193Thr | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/23 | 654/6602 | 579/2469 | 193/822 | chr16 | 71769686 | ||
| chr16:71773329
|
C | A | 1 | a0001c0004 | 4 | HG01106.hp1 HG01192.hp2 HG01516.hp1 others(1): Show |
synonymous_variant | LOW | c.360G>T | p.Gly120Gly | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/23 | 435/6602 | 360/2469 | 120/822 | chr16 | 71773329 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71729016
|
A | G | 1 | a0001c0001t0026 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4042T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 4042 | chr16 | 71729016 | |||||
| chr16:71729159
|
A | AT | 24 | a0001c0001t0005a0001c0001t0007a0001c0001t0009others(21): Show | 141 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*3898dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3898 | chr16 | 71729159 | |||||
| chr16:71729159
|
AT | A | 1 | a0001c0001t0010 | 8 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3898delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3898 | chr16 | 71729159 | |||||
| chr16:71729182
|
A | G | 1 | a0002c0002t0033 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3876T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3876 | chr16 | 71729182 | |||||
| chr16:71729432
|
G | GA | 14 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(11): Show | 77 | HG00423.hp1 HG00609.hp2 HG00733.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3625dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3625 | chr16 | 71729432 | |||||
| chr16:71729432
|
GA | G | 7 | a0001c0001t0008a0001c0001t0014a0001c0001t0016others(4): Show | 23 | HG00140.hp2 HG00323.hp1 HG01175.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3625delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3625 | chr16 | 71729432 | |||||
| chr16:71729451
|
A | C | 1 | a0002c0002t0032 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3607T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3607 | chr16 | 71729451 | |||||
| chr16:71729452
|
C | A | 3 | a0001c0001t0011a0001c0001t0027a0001c0001t0035 | 10 | HG00609.hp1 HG02040.hp1 HG02056.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3606G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3606 | chr16 | 71729452 | |||||
| chr16:71729876
|
C | A | 2 | a0002c0002t0006a0002c0002t0034 | 18 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3182G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3182 | chr16 | 71729876 | |||||
| chr16:71729914
|
A | G | 1 | a0002c0002t0031 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3144T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3144 | chr16 | 71729914 | |||||
| chr16:71730460
|
C | G | 1 | a0001c0009t0019 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2598G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 2598 | chr16 | 71730460 | |||||
| chr16:71730512
|
C | G | 3 | a0001c0001t0016a0001c0001t0020a0001c0009t0019 | 4 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2546G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 2546 | chr16 | 71730512 | |||||
| chr16:71730754
|
G | A | 1 | a0001c0001t0010 | 8 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2304C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 2304 | chr16 | 71730754 | |||||
| chr16:71730922
|
A | G | 1 | a0001c0001t0030 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2136T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 2136 | chr16 | 71730922 | |||||
| chr16:71730923
|
G | C | 1 | a0001c0001t0013 | 6 | HG00408.hp1 HG00621.hp2 NA18612.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2135C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 2135 | chr16 | 71730923 | |||||
| chr16:71730931
|
C | T | 15 | a0001c0001t0002a0001c0001t0003a0001c0001t0011others(12): Show | 121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2127G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 2127 | chr16 | 71730931 | |||||
| chr16:71731329
|
A | C | 1 | a0001c0001t0035 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1729T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1729 | chr16 | 71731329 | |||||
| chr16:71731490
|
A | G | 1 | a0001c0001t0024 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1568T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1568 | chr16 | 71731490 | |||||
| chr16:71731502
|
T | C | 1 | a0001c0001t0028 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1556A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1556 | chr16 | 71731502 | |||||
| chr16:71731510
|
A | G | 1 | a0001c0001t0015 | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1548T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1548 | chr16 | 71731510 | |||||
| chr16:71731513
|
G | T | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0011others(10): Show | 119 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1545C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1545 | chr16 | 71731513 | |||||
| chr16:71731534
|
C | CT | 6 | a0001c0001t0007a0001c0001t0009a0001c0001t0024others(3): Show | 29 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1523dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1523 | chr16 | 71731534 | |||||
| chr16:71731562
|
G | C | 3 | a0001c0001t0011a0001c0001t0035a0001c0001t0036 | 10 | HG00609.hp1 HG02040.hp1 HG02056.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1496C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1496 | chr16 | 71731562 | |||||
| chr16:71731583
|
A | G | 1 | a0001c0001t0023 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1475T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1475 | chr16 | 71731583 | |||||
| chr16:71731634
|
A | G | 1 | a0001c0001t0037 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1424T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1424 | chr16 | 71731634 | |||||
| chr16:71732133
|
T | C | 2 | a0001c0001t0037a0001c0001t0038 | 2 | HG02559.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*925A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 925 | chr16 | 71732133 | |||||
| chr16:71732375
|
C | T | 1 | a0001c0001t0016 | 2 | HG02257.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*683G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 683 | chr16 | 71732375 | |||||
| chr16:71732415
|
G | A | 1 | a0002c0002t0039 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*643C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 643 | chr16 | 71732415 | |||||
| chr16:71732650
|
G | T | 1 | a0001c0001t0012 | 6 | NA18952.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*408C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 408 | chr16 | 71732650 | |||||
| chr16:71732748
|
A | G | 2 | a0002c0002t0021a0002c0002t0022 | 2 | HG03654.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*310T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 310 | chr16 | 71732748 | |||||
| chr16:71732972
|
T | C | 1 | a0001c0001t0040 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*86A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 86 | chr16 | 71732972 | |||||
| chr16:71732980
|
G | T | 2 | a0001c0001t0020a0001c0009t0019 | 2 | HG02451.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*78C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 78 | chr16 | 71732980 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71733162
|
A | G | 3 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0040g0238 | 3 | HG00408.hp2 HG02523.hp1 NA19056.hp2 |
splice_region_variant&intron_variant | LOW | c.2368-3T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733162 | ||||||
| chr16:71733384
|
C | T | 1 | a0002c0002t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2368-225G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733384 | ||||||
| chr16:71733410
|
T | A | 1 | a0001c0001t0004g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2368-251A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733410 | ||||||
| chr16:71733416
|
G | T | 1 | a0001c0001t0004g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2368-257C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733416 | ||||||
| chr16:71733510
|
G | GGCTCACC others(68): Show |
283 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(280): Show | 284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.2368-352_2368-351i others(77): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733510 | ||||||
| chr16:71733510
|
G | GGCTCACC others(68): Show |
3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2368-352_2368-351i others(77): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733510 | ||||||
| chr16:71733557
|
G | A | 1 | a0001c0001t0002g0302 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2368-398C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733557 | ||||||
| chr16:71733747
|
T | C | 1 | a0001c0001t0002g0278 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2368-588A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733747 | ||||||
| chr16:71733758
|
C | T | 122 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2368-599G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733758 | ||||||
| chr16:71733895
|
A | G | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2367+714T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733895 | ||||||
| chr16:71733933
|
G | A | 122 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2367+676C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733933 | ||||||
| chr16:71734135
|
T | A | 1 | a0002c0002t0001g0150 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2367+474A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71734135 | ||||||
| chr16:71734148
|
G | A | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2367+461C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71734148 | ||||||
| chr16:71734151
|
G | A | 1 | a0002c0002t0001g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2367+458C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71734151 | ||||||
| chr16:71734422
|
C | A | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2367+187G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71734422 | ||||||
| chr16:71734571
|
A | C | 1 | a0002c0002t0001g0111 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2367+38T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71734571 | ||||||
| chr16:71734597
|
T | C | 123 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(120): Show | 123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.2367+12A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71734597 | ||||||
| chr16:71734748
|
A | G | 2 | a0001c0001t0009g0001a0001c0001t0009g0070 | 3 | HG00609.hp2 NA18968.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.2269-41T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71734748 | ||||||
| chr16:71734758
|
G | C | 1 | a0001c0001t0004g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2269-51C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71734758 | ||||||
| chr16:71735011
|
G | A | 1 | a0002c0002t0001g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2269-304C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71735011 | ||||||
| chr16:71735019
|
C | G | 1 | a0002c0002t0001g0141 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2269-312G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71735019 | ||||||
| chr16:71735229
|
T | C | 1 | a0001c0001t0005g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2269-522A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71735229 | ||||||
| chr16:71735420
|
T | G | 27 | a0002c0002t0001g0092a0002c0002t0001g0107a0002c0002t0001g0108others(24): Show | 27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.2269-713A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71735420 | ||||||
| chr16:71735632
|
GGCAACAG others(1): Show |
G | 12 | a0001c0001t0002g0228a0001c0001t0002g0278a0001c0001t0002g0279others(9): Show | 12 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.2269-933_2269-926d others(10): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71735632 | ||||||
| chr16:71735659
|
A | C | 123 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(120): Show | 123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.2269-952T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71735659 | ||||||
| chr16:71735866
|
G | A | 7 | a0001c0001t0002g0201a0001c0001t0012g0197a0001c0001t0012g0200others(4): Show | 7 | NA18952.hp2 NA18954.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.2269-1159C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71735866 | ||||||
| chr16:71736011
|
A | C | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2269-1304T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736011 | ||||||
| chr16:71736098
|
C | CAAA | 9 | a0001c0001t0004g0040a0001c0001t0004g0061a0001c0001t0010g0002others(6): Show | 9 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2269-1394_2269-139 others(7): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | ||||||
| chr16:71736098
|
C | CAAAAAAA others(3): Show |
13 | a0001c0001t0002g0194a0001c0001t0002g0233a0001c0001t0002g0240others(10): Show | 13 | HG00735.hp1 HG01169.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.2269-1401_2269-139 others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | ||||||
| chr16:71736098
|
C | CAAAAAAA others(4): Show |
16 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0250others(13): Show | 16 | HG00423.hp1 HG01081.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.2269-1402_2269-139 others(15): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | ||||||
| chr16:71736098
|
C | CAAAAAAA others(5): Show |
33 | a0001c0001t0002g0221a0001c0001t0002g0224a0001c0001t0002g0226others(30): Show | 33 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.2269-1403_2269-139 others(16): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | ||||||
| chr16:71736098
|
C | CAAAAAAA others(6): Show |
19 | a0001c0001t0002g0198a0001c0001t0002g0210a0001c0001t0002g0215others(16): Show | 19 | HG00609.hp1 HG00621.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.2269-1404_2269-139 others(17): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | ||||||
| chr16:71736098
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0002g0230a0001c0001t0002g0297a0001c0001t0003g0277 | 3 | HG00733.hp2 HG02738.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.2269-1405_2269-139 others(18): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | ||||||
| chr16:71736098
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0002g0276a0001c0001t0002g0290a0001c0001t0011g0199others(1): Show | 4 | HG02148.hp2 NA18951.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.2269-1406_2269-139 others(19): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | ||||||
| chr16:71736098
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0014g0303 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2269-1407_2269-139 others(20): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | ||||||
| chr16:71736115
|
A | AT | 4 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0191others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2269-1409_2269-140 others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736115 | ||||||
| chr16:71736115
|
A | T | 2 | a0001c0003t0008g0189a0001c0003t0008g0193 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2269-1408T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736115 | ||||||
| chr16:71736115
|
AAAATAT | A | 13 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(10): Show | 13 | HG00733.hp1 HG01358.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.2269-1414_2269-140 others(10): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736115 | ||||||
| chr16:71736115
|
AAAATATA others(7): Show |
A | 1 | a0002c0002t0001g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2269-1422_2269-140 others(18): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736115 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0002g0264 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(22): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0002g0265 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(21): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0003g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(19): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0002g0316 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(27): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(7): Show |
2 | a0001c0001t0002g0242a0001c0001t0002g0310 | 2 | HG03209.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(18): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0002g0302 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(20): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(6): Show |
2 | a0001c0001t0002g0306a0001c0001t0011g0256 | 2 | HG02132.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(17): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(8): Show |
3 | a0001c0001t0002g0301a0001c0001t0002g0305a0001c0001t0011g0235 | 3 | HG02280.hp1 HG03540.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(19): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0040g0238 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(21): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(5): Show |
4 | a0001c0001t0002g0291a0001c0001t0003g0268a0001c0001t0003g0304others(1): Show | 4 | HG02572.hp2 HG03834.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(16): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0002g0312 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(18): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(9): Show |
2 | a0001c0001t0002g0249a0001c0001t0002g0307 | 2 | HG00621.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(20): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(4): Show |
2 | a0001c0001t0002g0201a0001c0001t0012g0202 | 2 | NA18952.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(15): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(6): Show |
2 | a0001c0001t0002g0239a0001c0001t0002g0294 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(17): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0002g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0026g0311 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(18): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0002g0313 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(15): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | AT | 4 | a0001c0003t0008g0185a0001c0003t0008g0186a0001c0003t0008g0187others(1): Show | 4 | HG02970.hp2 NA18906.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
A | T | 11 | a0001c0001t0004g0020a0001c0001t0004g0022a0001c0001t0004g0023others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.2269-1410T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
AAT | A | 9 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2269-1412_2269-141 others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
AATAT | A | 14 | a0001c0001t0003g0255a0001c0001t0004g0300a0001c0001t0015g0035others(11): Show | 14 | HG00642.hp2 HG02071.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.2269-1414_2269-141 others(8): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
AATATAT | A | 38 | a0001c0001t0005g0058a0001c0001t0005g0112a0001c0001t0005g0114others(35): Show | 39 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2269-1416_2269-141 others(10): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736117
|
AATATATA others(5): Show |
A | 1 | a0001c0001t0004g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2269-1422_2269-141 others(16): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | ||||||
| chr16:71736118
|
ATAT | A | 5 | a0001c0001t0015g0037a0001c0001t0015g0039a0002c0002t0001g0135others(2): Show | 5 | HG01515.hp1 HG02895.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.2269-1414_2269-141 others(7): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736118 | ||||||
| chr16:71736118
|
ATATAT | A | 71 | a0001c0001t0005g0043a0001c0001t0005g0093a0001c0001t0005g0122others(68): Show | 71 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.2269-1416_2269-141 others(9): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736118 | ||||||
| chr16:71736118
|
ATATATAT | A | 5 | a0001c0001t0005g0113a0001c0001t0007g0078a0001c0001t0016g0041others(2): Show | 5 | HG01168.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2269-1418_2269-141 others(11): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736118 | ||||||
| chr16:71736119
|
T | A | 78 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(75): Show | 78 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.2269-1412A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736119 | ||||||
| chr16:71736121
|
T | A | 50 | a0001c0001t0002g0198a0001c0001t0002g0215a0001c0001t0002g0220others(47): Show | 50 | HG00099.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.2269-1414A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736121 | ||||||
| chr16:71736123
|
T | A | 35 | a0001c0001t0002g0279a0001c0001t0003g0257a0001c0001t0003g0273others(32): Show | 35 | HG00099.hp1 HG00642.hp2 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.2269-1416A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736123 | ||||||
| chr16:71736125
|
T | A | 128 | a0001c0001t0003g0257a0001c0001t0004g0028a0001c0001t0004g0300others(125): Show | 129 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.2269-1418A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736125 | ||||||
| chr16:71736127
|
T | A | 111 | a0001c0001t0004g0300a0001c0001t0005g0093a0001c0001t0005g0112others(108): Show | 111 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.2269-1420A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736127 | ||||||
| chr16:71736129
|
T | A | 61 | a0001c0001t0005g0093a0001c0001t0005g0112a0001c0001t0005g0113others(58): Show | 61 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.2269-1422A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736129 | ||||||
| chr16:71736131
|
T | A | 17 | a0001c0001t0004g0018a0001c0001t0005g0093a0001c0001t0005g0112others(14): Show | 17 | HG02109.hp1 HG02145.hp2 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.2269-1424A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736131 | ||||||
| chr16:71736231
|
A | G | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2269-1524T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736231 | ||||||
| chr16:71736350
|
G | A | 1 | a0001c0001t0003g0260 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2269-1643C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736350 | ||||||
| chr16:71736384
|
C | CT | 8 | a0001c0001t0003g0260a0001c0001t0003g0277a0001c0001t0004g0032others(5): Show | 8 | HG01981.hp1 HG01993.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.2269-1678dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736384 | ||||||
| chr16:71736480
|
A | G | 1 | a0001c0001t0014g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2269-1773T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736480 | ||||||
| chr16:71736526
|
G | A | 15 | a0001c0001t0002g0133a0001c0001t0002g0301a0001c0001t0002g0302others(12): Show | 15 | HG01433.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2269-1819C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736526 | ||||||
| chr16:71736541
|
C | A | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2269-1834G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736541 | ||||||
| chr16:71736541
|
C | T | 4 | a0001c0001t0002g0301a0001c0001t0002g0305a0001c0001t0002g0309others(1): Show | 4 | HG02280.hp1 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2269-1834G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736541 | ||||||
| chr16:71736551
|
A | ATTAT | 6 | a0001c0001t0003g0293a0001c0001t0003g0304a0001c0001t0040g0238others(3): Show | 6 | HG02523.hp1 HG02572.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.2269-1848_2269-184 others(8): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736551 | ||||||
| chr16:71736551
|
ATTAT | A | 99 | a0001c0001t0002g0232a0001c0001t0002g0250a0001c0001t0002g0253others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.2269-1848_2269-184 others(8): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736551 | ||||||
| chr16:71736551
|
ATTATTTA others(1): Show |
A | 60 | a0001c0001t0002g0307a0001c0001t0004g0017a0001c0001t0004g0026others(57): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2269-1852_2269-184 others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736551 | ||||||
| chr16:71736551
|
ATTATTTA others(5): Show |
A | 3 | a0001c0001t0002g0297a0001c0001t0003g0206a0002c0002t0001g0154 | 3 | HG00733.hp2 HG03710.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2269-1856_2269-184 others(16): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736551 | ||||||
| chr16:71736551
|
ATTATTTA others(9): Show |
A | 2 | a0001c0001t0004g0061a0001c0001t0004g0315 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2269-1860_2269-184 others(20): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736551 | ||||||
| chr16:71736598
|
A | T | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2269-1891T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736598 | ||||||
| chr16:71736602
|
T | A | 1 | a0001c0001t0002g0291 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2269-1895A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736602 | ||||||
| chr16:71736616
|
C | T | 2 | a0001c0001t0015g0035a0001c0001t0015g0039 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2269-1909G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736616 | ||||||
| chr16:71736678
|
C | T | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2269-1971G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736678 | ||||||
| chr16:71736682
|
C | T | 1 | a0002c0002t0001g0135 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2269-1975G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736682 | ||||||
| chr16:71736730
|
C | T | 85 | a0002c0002t0001g0048a0002c0002t0001g0092a0002c0002t0001g0095others(82): Show | 85 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.2269-2023G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736730 | ||||||
| chr16:71736746
|
C | T | 1 | a0001c0001t0007g0080 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2269-2039G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736746 | ||||||
| chr16:71736752
|
AT | A | 103 | a0001c0001t0002g0210a0001c0001t0002g0276a0001c0001t0003g0212others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.2269-2046delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736752 | ||||||
| chr16:71736752
|
ATT | A | 170 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(167): Show | 171 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.2269-2047_2269-204 others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736752 | ||||||
| chr16:71736875
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2268+2067C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736875 | ||||||
| chr16:71736933
|
G | A | 122 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2268+2009C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736933 | ||||||
| chr16:71737053
|
A | G | 12 | a0001c0001t0005g0093a0001c0001t0005g0112a0001c0001t0005g0113others(9): Show | 12 | HG02109.hp1 HG02145.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2268+1889T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737053 | ||||||
| chr16:71737063
|
T | C | 15 | a0001c0001t0002g0133a0001c0001t0002g0301a0001c0001t0002g0302others(12): Show | 15 | HG01433.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2268+1879A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737063 | ||||||
| chr16:71737204
|
T | C | 1 | a0001c0001t0027g0263 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2268+1738A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737204 | ||||||
| chr16:71737318
|
C | G | 1 | a0001c0001t0015g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2268+1624G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737318 | ||||||
| chr16:71737439
|
G | A | 1 | a0002c0002t0001g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2268+1503C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737439 | ||||||
| chr16:71737560
|
C | T | 2 | a0001c0001t0016g0041a0001c0001t0016g0042 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2268+1382G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737560 | ||||||
| chr16:71737747
|
C | T | 3 | a0001c0001t0004g0061a0001c0001t0004g0300a0001c0001t0018g0314 | 3 | HG02647.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2268+1195G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737747 | ||||||
| chr16:71737886
|
G | C | 1 | a0005c0006t0001g0132 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2268+1056C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737886 | ||||||
| chr16:71737911
|
C | T | 1 | a0001c0001t0005g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2268+1031G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737911 | ||||||
| chr16:71737992
|
C | T | 1 | a0001c0001t0004g0026 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2268+950G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737992 | ||||||
| chr16:71738183
|
T | C | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2268+759A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738183 | ||||||
| chr16:71738211
|
C | T | 2 | a0001c0001t0020g0064a0001c0009t0019g0010 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2268+731G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738211 | ||||||
| chr16:71738212
|
G | T | 151 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(148): Show | 152 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.2268+730C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738212 | ||||||
| chr16:71738217
|
A | AT | 61 | a0001c0001t0009g0067a0002c0002t0001g0048a0002c0002t0001g0089others(58): Show | 61 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.2268+724dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738217 | ||||||
| chr16:71738218
|
T | C | 2 | a0001c0001t0020g0064a0001c0009t0019g0010 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2268+724A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738218 | ||||||
| chr16:71738350
|
C | T | 2 | a0001c0001t0005g0112a0001c0001t0005g0116 | 2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2268+592G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738350 | ||||||
| chr16:71738424
|
A | T | 28 | a0001c0001t0007g0066a0001c0001t0007g0071a0001c0001t0007g0072others(25): Show | 29 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.2268+518T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738424 | ||||||
| chr16:71738474
|
C | T | 1 | a0001c0001t0002g0201 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2268+468G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738474 | ||||||
| chr16:71738475
|
G | A | 3 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0006g0177 | 3 | NA18941.hp1 NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2268+467C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738475 | ||||||
| chr16:71738496
|
T | C | 286 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(283): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.2268+446A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738496 | ||||||
| chr16:71738519
|
T | C | 2 | a0001c0001t0004g0300a0001c0001t0018g0314 | 2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2268+423A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738519 | ||||||
| chr16:71738637
|
A | G | 2 | a0001c0001t0004g0300a0001c0001t0018g0314 | 2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2268+305T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738637 | ||||||
| chr16:71738757
|
C | T | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2268+185G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738757 | ||||||
| chr16:71738821
|
T | C | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2268+121A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738821 | ||||||
| chr16:71738880
|
TG | T | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2268+61delC | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738880 | ||||||
| chr16:71738892
|
G | A | 295 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(292): Show | 296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.2268+50C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738892 | ||||||
| chr16:71739151
|
G | A | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2108-49C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 20/22 | chr16 | 71739151 | ||||||
| chr16:71739363
|
A | T | 1 | a0001c0001t0002g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2000-22T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71739363 | ||||||
| chr16:71739381
|
C | CA | 122 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2000-41dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71739381 | ||||||
| chr16:71739388
|
AAGCTTAC others(11): Show |
A | 3 | a0001c0001t0004g0061a0001c0001t0004g0300a0001c0001t0018g0314 | 3 | HG02647.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2000-65_2000-48del others(18): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71739388 | ||||||
| chr16:71739575
|
C | T | 3 | a0002c0002t0001g0159a0002c0002t0001g0319a0002c0002t0039g0318 | 3 | HG01978.hp1 HG02071.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2000-234G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71739575 | ||||||
| chr16:71739804
|
T | C | 1 | a0001c0001t0002g0250 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2000-463A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71739804 | ||||||
| chr16:71739886
|
T | A | 1 | a0001c0001t0002g0264 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2000-545A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71739886 | ||||||
| chr16:71740196
|
G | A | 1 | a0001c0001t0002g0295 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2000-855C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740196 | ||||||
| chr16:71740487
|
G | A | 122 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2000-1146C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740487 | ||||||
| chr16:71740512
|
T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2000-1171A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740512 | ||||||
| chr16:71740538
|
T | C | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2000-1197A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740538 | ||||||
| chr16:71740605
|
G | A | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2000-1264C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740605 | ||||||
| chr16:71740653
|
G | A | 22 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(19): Show | 22 | HG00738.hp2 HG01515.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2000-1312C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740653 | ||||||
| chr16:71740794
|
G | T | 122 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2000-1453C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740794 | ||||||
| chr16:71740845
|
A | G | 1 | a0002c0002t0001g0143 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2000-1504T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740845 | ||||||
| chr16:71740861
|
A | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2000-1520T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740861 | ||||||
| chr16:71740863
|
T | C | 3 | a0001c0001t0010g0005a0001c0001t0010g0006a0001c0001t0010g0007 | 3 | HG00738.hp2 HG02622.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2000-1522A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740863 | ||||||
| chr16:71740945
|
G | A | 1 | a0001c0001t0035g0234 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2000-1604C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740945 | ||||||
| chr16:71740993
|
T | G | 147 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(144): Show | 147 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.2000-1652A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740993 | ||||||
| chr16:71741086
|
G | T | 27 | a0002c0002t0001g0092a0002c0002t0001g0107a0002c0002t0001g0108others(24): Show | 27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.2000-1745C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741086 | ||||||
| chr16:71741107
|
G | C | 3 | a0002c0002t0001g0096a0002c0002t0001g0136a0002c0002t0001g0137 | 3 | NA18965.hp2 NA19002.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.2000-1766C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741107 | ||||||
| chr16:71741117
|
G | A | 4 | a0001c0001t0016g0041a0001c0001t0016g0042a0001c0001t0020g0064others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2000-1776C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741117 | ||||||
| chr16:71741177
|
C | T | 122 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2000-1836G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741177 | ||||||
| chr16:71741284
|
T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2000-1943A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741284 | ||||||
| chr16:71741403
|
C | T | 1 | a0001c0001t0030g0049 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2000-2062G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741403 | ||||||
| chr16:71741440
|
G | A | 12 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(9): Show | 12 | HG00323.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2000-2099C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741440 | ||||||
| chr16:71741493
|
G | A | 86 | a0001c0001t0005g0043a0002c0002t0001g0048a0002c0002t0001g0092others(83): Show | 86 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.2000-2152C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741493 | ||||||
| chr16:71741544
|
T | C | 2 | a0001c0001t0004g0300a0001c0001t0018g0314 | 2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2000-2203A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741544 | ||||||
| chr16:71741559
|
G | T | 3 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0006g0177 | 3 | NA18941.hp1 NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2000-2218C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741559 | ||||||
| chr16:71741629
|
T | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2000-2288A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741629 | ||||||
| chr16:71741742
|
T | C | 6 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2000-2401A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741742 | ||||||
| chr16:71741888
|
G | C | 4 | a0001c0001t0016g0041a0001c0001t0016g0042a0001c0001t0020g0064others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2000-2547C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741888 | ||||||
| chr16:71742069
|
A | G | 1 | a0001c0001t0024g0088 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2000-2728T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742069 | ||||||
| chr16:71742133
|
T | G | 1 | a0002c0002t0001g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2000-2792A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742133 | ||||||
| chr16:71742241
|
C | T | 122 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2000-2900G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742241 | ||||||
| chr16:71742407
|
T | G | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1999+2737A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742407 | ||||||
| chr16:71742439
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1999+2705G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742439 | ||||||
| chr16:71742532
|
A | T | 1 | a0001c0001t0036g0271 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1999+2612T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742532 | ||||||
| chr16:71742804
|
T | A | 58 | a0002c0002t0001g0048a0002c0002t0001g0095a0002c0002t0001g0096others(55): Show | 58 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1999+2340A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742804 | ||||||
| chr16:71742836
|
G | A | 2 | a0001c0001t0002g0249a0001c0001t0002g0258 | 2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1999+2308C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742836 | ||||||
| chr16:71742865
|
C | T | 5 | a0002c0002t0001g0107a0002c0002t0001g0108a0002c0002t0001g0109others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999+2279G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742865 | ||||||
| chr16:71742866
|
G | A | 122 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1999+2278C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742866 | ||||||
| chr16:71742981
|
C | CA | 18 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(15): Show | 18 | HG00738.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1999+2162dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742981 | ||||||
| chr16:71742998
|
C | G | 1 | a0001c0001t0002g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1999+2146G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742998 | ||||||
| chr16:71743165
|
T | C | 2 | a0001c0001t0016g0041a0001c0001t0016g0042 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1999+1979A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743165 | ||||||
| chr16:71743188
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1999+1956C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743188 | ||||||
| chr16:71743227
|
A | T | 1 | a0001c0001t0003g0277 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1999+1917T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743227 | ||||||
| chr16:71743300
|
GA | G | 62 | a0002c0002t0001g0048a0002c0002t0001g0095a0002c0002t0001g0096others(59): Show | 62 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1999+1843delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743300 | ||||||
| chr16:71743512
|
A | G | 1 | a0001c0001t0003g0277 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1999+1632T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743512 | ||||||
| chr16:71743540
|
T | C | 22 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(19): Show | 22 | HG00738.hp2 HG01515.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1999+1604A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743540 | ||||||
| chr16:71743545
|
G | C | 122 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1999+1599C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743545 | ||||||
| chr16:71743551
|
C | A | 1 | a0001c0001t0003g0277 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1999+1593G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743551 | ||||||
| chr16:71743602
|
C | CA | 29 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(26): Show | 29 | HG00738.hp2 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1999+1541dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743602 | ||||||
| chr16:71743602
|
CAAAAAAA | C | 121 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(118): Show | 121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1999+1535_1999+154 others(11): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743602 | ||||||
| chr16:71743604
|
A | G | 2 | a0001c0001t0005g0112a0001c0001t0005g0116 | 2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1999+1540T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743604 | ||||||
| chr16:71743807
|
G | A | 5 | a0001c0001t0004g0061a0001c0001t0016g0041a0001c0001t0016g0042others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1999+1337C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743807 | ||||||
| chr16:71743945
|
C | CA | 33 | a0001c0001t0004g0021a0001c0001t0004g0030a0001c0001t0005g0053others(30): Show | 33 | HG01123.hp1 HG01175.hp2 HG01258.hp1 others(30): Show |
intron_variant | MODIFIER | c.1999+1198dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743945 | ||||||
| chr16:71743945
|
C | T | 1 | a0001c0001t0007g0078 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1999+1199G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743945 | ||||||
| chr16:71743945
|
CA | C | 141 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1999+1198delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743945 | ||||||
| chr16:71743946
|
A | C | 1 | a0001c0001t0007g0078 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1999+1198T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743946 | ||||||
| chr16:71744131
|
C | G | 1 | a0001c0001t0010g0008 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1999+1013G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744131 | ||||||
| chr16:71744169
|
G | A | 152 | a0001c0001t0005g0043a0001c0001t0005g0050a0001c0001t0005g0051others(149): Show | 153 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.1999+975C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744169 | ||||||
| chr16:71744176
|
G | A | 6 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(3): Show | 6 | HG00733.hp1 HG02602.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1999+968C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744176 | ||||||
| chr16:71744262
|
G | T | 1 | a0002c0002t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1999+882C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744262 | ||||||
| chr16:71744426
|
G | A | 4 | a0002c0002t0006g0099a0002c0002t0006g0101a0002c0002t0006g0127others(1): Show | 4 | HG00741.hp1 HG01071.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1999+718C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744426 | ||||||
| chr16:71744571
|
G | GT | 181 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(178): Show | 182 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.1999+572dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744571 | ||||||
| chr16:71744571
|
G | GTT | 37 | a0001c0001t0002g0262a0001c0001t0002g0281a0001c0001t0002g0285others(34): Show | 37 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1999+571_1999+572d others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744571 | ||||||
| chr16:71744571
|
G | GTTT | 47 | a0001c0001t0002g0312a0001c0001t0005g0043a0001c0001t0005g0093others(44): Show | 47 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1999+570_1999+572d others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744571 | ||||||
| chr16:71744571
|
G | GTTTT | 16 | a0002c0002t0001g0048a0002c0002t0001g0095a0002c0002t0001g0111others(13): Show | 16 | HG00741.hp2 HG01168.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1999+569_1999+572d others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744571 | ||||||
| chr16:71744644
|
C | T | 1 | a0001c0001t0040g0238 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1999+500G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744644 | ||||||
| chr16:71744737
|
G | A | 122 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1999+407C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744737 | ||||||
| chr16:71744975
|
T | C | 3 | a0001c0001t0002g0245a0001c0001t0002g0299a0001c0001t0028g0251 | 3 | HG02129.hp1 NA18962.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1999+169A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744975 | ||||||
| chr16:71745059
|
C | T | 1 | a0001c0001t0004g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1999+85G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71745059 | ||||||
| chr16:71745062
|
G | A | 1 | a0001c0001t0004g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1999+82C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71745062 | ||||||
| chr16:71745407
|
G | T | 26 | a0001c0001t0007g0066a0001c0001t0007g0071a0001c0001t0007g0072others(23): Show | 27 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1872+66C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 18/22 | chr16 | 71745407 | ||||||
| chr16:71745839
|
C | A | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1731-225G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71745839 | ||||||
| chr16:71745845
|
GCATATAT others(2): Show |
G | 150 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(147): Show | 151 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1731-240_1731-232d others(11): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71745845 | ||||||
| chr16:71745922
|
A | G | 1 | a0001c0001t0009g0067 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1731-308T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71745922 | ||||||
| chr16:71746076
|
C | G | 6 | a0002c0002t0001g0096a0002c0002t0001g0136a0002c0002t0001g0137others(3): Show | 6 | NA18957.hp2 NA18965.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.1731-462G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71746076 | ||||||
| chr16:71746187
|
T | A | 3 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0054 | 3 | HG02602.hp2 HG02683.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1730+401A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71746187 | ||||||
| chr16:71746355
|
A | G | 1 | a0001c0001t0007g0075 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1730+233T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71746355 | ||||||
| chr16:71746374
|
T | G | 281 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.1730+214A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71746374 | ||||||
| chr16:71746385
|
G | C | 1 | a0001c0001t0004g0025 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1730+203C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71746385 | ||||||
| chr16:71746467
|
C | T | 1 | a0002c0002t0001g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1730+121G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71746467 | ||||||
| chr16:71746582
|
G | A | 122 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
splice_region_variant&intron_variant | LOW | c.1730+6C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71746582 | ||||||
| chr16:71746696
|
T | C | 123 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(120): Show | 123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
splice_region_variant&intron_variant | LOW | c.1626-4A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71746696 | ||||||
| chr16:71746983
|
T | C | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1626-291A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71746983 | ||||||
| chr16:71746993
|
A | G | 1 | a0001c0001t0003g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1626-301T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71746993 | ||||||
| chr16:71747078
|
A | G | 1 | a0001c0001t0028g0251 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1626-386T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747078 | ||||||
| chr16:71747127
|
AT | A | 7 | a0001c0001t0002g0133a0001c0001t0002g0301a0001c0001t0002g0305others(4): Show | 7 | HG02280.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1626-436delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747127 | ||||||
| chr16:71747199
|
C | T | 24 | a0002c0002t0001g0092a0002c0002t0001g0107a0002c0002t0001g0108others(21): Show | 24 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1626-507G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747199 | ||||||
| chr16:71747267
|
G | A | 1 | a0001c0001t0004g0032 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1626-575C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747267 | ||||||
| chr16:71747348
|
C | G | 1 | a0002c0002t0001g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1626-656G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747348 | ||||||
| chr16:71747435
|
C | G | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1626-743G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747435 | ||||||
| chr16:71747618
|
C | T | 7 | a0001c0001t0003g0205a0001c0001t0003g0236a0001c0001t0003g0255others(4): Show | 7 | NA18957.hp1 NA18964.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.1625+633G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747618 | ||||||
| chr16:71747676
|
C | A | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1625+575G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747676 | ||||||
| chr16:71747769
|
C | T | 1 | a0001c0001t0009g0001 | 2 | HG00609.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1625+482G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747769 | ||||||
| chr16:71747978
|
G | A | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1625+273C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747978 | ||||||
| chr16:71748000
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1625+251G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71748000 | ||||||
| chr16:71748429
|
A | G | 1 | a0001c0001t0036g0271 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1498-51T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71748429 | ||||||
| chr16:71748444
|
T | C | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1498-66A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71748444 | ||||||
| chr16:71748541
|
A | G | 124 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(121): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1498-163T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71748541 | ||||||
| chr16:71748911
|
G | T | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1498-533C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71748911 | ||||||
| chr16:71749043
|
A | C | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1498-665T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749043 | ||||||
| chr16:71749050
|
G | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1498-672C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749050 | ||||||
| chr16:71749173
|
T | G | 139 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(136): Show | 140 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1497+721A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749173 | ||||||
| chr16:71749218
|
T | C | 286 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(283): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1497+676A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749218 | ||||||
| chr16:71749260
|
T | C | 3 | a0001c0001t0009g0001a0001c0001t0009g0067a0001c0001t0009g0070 | 4 | HG00609.hp2 NA18968.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+634A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749260 | ||||||
| chr16:71749279
|
C | T | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1497+615G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749279 | ||||||
| chr16:71749470
|
T | A | 121 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(118): Show | 121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1497+424A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749470 | ||||||
| chr16:71749471
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1497+423C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749471 | ||||||
| chr16:71749481
|
T | TA | 7 | a0001c0001t0010g0003a0001c0001t0010g0004a0001c0001t0010g0005others(4): Show | 7 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1497+412dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749481 | ||||||
| chr16:71749481
|
TA | T | 140 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(137): Show | 140 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1497+412delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749481 | ||||||
| chr16:71749495
|
C | A | 1 | a0001c0001t0010g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1497+399G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749495 | ||||||
| chr16:71749592
|
T | A | 5 | a0001c0001t0009g0065a0001c0001t0009g0069a0001c0001t0009g0079others(2): Show | 5 | HG01358.hp2 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1497+302A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749592 | ||||||
| chr16:71749755
|
C | T | 33 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0002g0240others(30): Show | 33 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1497+139G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749755 | ||||||
| chr16:71749826
|
T | A | 3 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030 | 3 | HG00099.hp1 HG02257.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1497+68A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749826 | ||||||
| chr16:71750097
|
A | T | 139 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(136): Show | 140 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1407+113T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 14/22 | chr16 | 71750097 | ||||||
| chr16:71750389
|
T | C | 1 | a0001c0001t0010g0005 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1285-57A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750389 | ||||||
| chr16:71750445
|
C | T | 24 | a0002c0002t0001g0092a0002c0002t0001g0107a0002c0002t0001g0108others(21): Show | 24 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1285-113G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750445 | ||||||
| chr16:71750466
|
G | C | 2 | a0001c0001t0002g0301a0001c0001t0002g0305 | 2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1285-134C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750466 | ||||||
| chr16:71750467
|
T | A | 2 | a0001c0001t0004g0300a0001c0001t0018g0314 | 2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1285-135A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750467 | ||||||
| chr16:71750470
|
G | A | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1285-138C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750470 | ||||||
| chr16:71750476
|
G | A | 4 | a0001c0001t0002g0198a0001c0001t0002g0215a0001c0001t0002g0270others(1): Show | 4 | HG02080.hp1 NA18955.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.1285-144C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750476 | ||||||
| chr16:71750653
|
T | A | 1 | a0001c0001t0010g0004 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1285-321A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750653 | ||||||
| chr16:71750882
|
T | C | 4 | a0001c0004t0007g0068a0001c0004t0007g0074a0001c0004t0007g0076others(1): Show | 4 | HG01106.hp1 HG01192.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1285-550A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750882 | ||||||
| chr16:71751149
|
C | T | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1285-817G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751149 | ||||||
| chr16:71751154
|
C | CA | 13 | a0001c0001t0003g0211a0001c0001t0003g0213a0001c0001t0004g0013others(10): Show | 13 | HG00140.hp1 HG00733.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1285-823dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751154 | ||||||
| chr16:71751154
|
CA | C | 52 | a0001c0001t0002g0201a0001c0001t0002g0215a0001c0001t0002g0291others(49): Show | 52 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.1285-823delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751154 | ||||||
| chr16:71751324
|
C | CAAT | 4 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(1): Show | 4 | HG01258.hp1 HG02257.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1285-995_1285-993d others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751324 | ||||||
| chr16:71751401
|
T | C | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1285-1069A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751401 | ||||||
| chr16:71751432
|
A | G | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1285-1100T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751432 | ||||||
| chr16:71751471
|
GA | G | 29 | a0001c0001t0007g0066a0001c0001t0007g0071a0001c0001t0007g0072others(26): Show | 30 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1285-1140delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751471 | ||||||
| chr16:71751914
|
A | C | 107 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(104): Show | 107 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1285-1582T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751914 | ||||||
| chr16:71752163
|
T | C | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1284+1670A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71752163 | ||||||
| chr16:71752175
|
A | G | 1 | a0001c0001t0004g0020 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1284+1658T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71752175 | ||||||
| chr16:71752634
|
T | C | 55 | a0001c0001t0002g0044a0001c0001t0002g0198a0001c0001t0002g0210others(52): Show | 55 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1284+1199A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71752634 | ||||||
| chr16:71752797
|
T | TA | 5 | a0001c0001t0015g0035a0001c0001t0015g0036a0001c0001t0015g0037others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284+1035dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71752797 | ||||||
| chr16:71752890
|
T | C | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1284+943A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71752890 | ||||||
| chr16:71752950
|
A | G | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1284+883T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71752950 | ||||||
| chr16:71753015
|
T | C | 1 | a0001c0001t0004g0033 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1284+818A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753015 | ||||||
| chr16:71753091
|
G | A | 26 | a0001c0001t0007g0066a0001c0001t0007g0071a0001c0001t0007g0072others(23): Show | 27 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1284+742C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753091 | ||||||
| chr16:71753121
|
G | A | 2 | a0001c0001t0020g0064a0001c0009t0019g0010 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1284+712C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753121 | ||||||
| chr16:71753235
|
G | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1284+598C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753235 | ||||||
| chr16:71753535
|
C | A | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1284+298G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753535 | ||||||
| chr16:71753685
|
G | A | 13 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(10): Show | 13 | HG00733.hp1 HG01361.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1284+148C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753685 | ||||||
| chr16:71753785
|
C | T | 18 | a0001c0001t0002g0194a0001c0001t0002g0201a0001c0001t0002g0239others(15): Show | 18 | HG00408.hp2 HG00741.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.1284+48G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753785 | ||||||
| chr16:71753809
|
T | C | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1284+24A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753809 | ||||||
| chr16:71754015
|
G | C | 65 | a0001c0001t0002g0133a0001c0001t0005g0050a0001c0001t0005g0051others(62): Show | 65 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1230-128C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71754015 | ||||||
| chr16:71754340
|
AAAAG | A | 45 | a0001c0001t0005g0043a0001c0001t0005g0050a0001c0001t0005g0051others(42): Show | 46 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.1230-457_1230-454d others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71754340 | ||||||
| chr16:71754498
|
T | C | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1230-611A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71754498 | ||||||
| chr16:71754927
|
G | C | 121 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(118): Show | 121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1230-1040C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71754927 | ||||||
| chr16:71754941
|
C | T | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1230-1054G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71754941 | ||||||
| chr16:71755024
|
G | T | 1 | a0001c0001t0002g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1229+995C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755024 | ||||||
| chr16:71755128
|
T | C | 2 | a0001c0001t0004g0300a0001c0001t0018g0314 | 2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1229+891A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755128 | ||||||
| chr16:71755190
|
C | G | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1229+829G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755190 | ||||||
| chr16:71755331
|
G | T | 2 | a0001c0001t0002g0133a0002c0002t0001g0109 | 2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1229+688C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755331 | ||||||
| chr16:71755460
|
C | A | 1 | a0001c0001t0002g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1229+559G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755460 | ||||||
| chr16:71755559
|
T | C | 35 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233others(32): Show | 35 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1229+460A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755559 | ||||||
| chr16:71755590
|
G | T | 1 | a0002c0002t0001g0135 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1229+429C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755590 | ||||||
| chr16:71755626
|
A | C | 281 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.1229+393T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755626 | ||||||
| chr16:71755639
|
AT | A | 9 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0212others(6): Show | 9 | HG01099.hp1 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1229+379delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755639 | ||||||
| chr16:71755647
|
T | G | 154 | a0001c0001t0002g0133a0001c0001t0004g0300a0001c0001t0005g0050others(151): Show | 155 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1229+372A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755647 | ||||||
| chr16:71755650
|
T | G | 281 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.1229+369A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755650 | ||||||
| chr16:71755707
|
A | G | 27 | a0001c0001t0007g0066a0001c0001t0007g0071a0001c0001t0007g0072others(24): Show | 28 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1229+312T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755707 | ||||||
| chr16:71755770
|
C | T | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1229+249G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755770 | ||||||
| chr16:71755771
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1229+248C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755771 | ||||||
| chr16:71755933
|
C | T | 1 | a0002c0002t0006g0100 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1229+86G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755933 | ||||||
| chr16:71756181
|
A | G | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1089-22T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756181 | ||||||
| chr16:71756182
|
AAC | A | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1089-25_1089-24del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756182 | ||||||
| chr16:71756263
|
G | A | 286 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(283): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1089-104C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756263 | ||||||
| chr16:71756300
|
C | A | 1 | a0001c0001t0002g0224 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1089-141G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756300 | ||||||
| chr16:71756318
|
A | G | 281 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.1089-159T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756318 | ||||||
| chr16:71756454
|
G | T | 1 | a0002c0002t0006g0100 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1089-295C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756454 | ||||||
| chr16:71756664
|
G | A | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1089-505C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756664 | ||||||
| chr16:71756770
|
C | T | 122 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1089-611G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756770 | ||||||
| chr16:71756850
|
G | A | 3 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022 | 3 | HG00099.hp2 HG00639.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1089-691C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756850 | ||||||
| chr16:71756855
|
T | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1089-696A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756855 | ||||||
| chr16:71756879
|
T | C | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1089-720A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756879 | ||||||
| chr16:71756909
|
A | C | 286 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(283): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1089-750T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756909 | ||||||
| chr16:71756930
|
C | CA | 58 | a0001c0001t0002g0264a0001c0001t0003g0275a0001c0001t0004g0011others(55): Show | 58 | HG00642.hp2 HG00738.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.1089-772dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756930 | ||||||
| chr16:71756930
|
CA | C | 18 | a0001c0001t0002g0215a0001c0001t0002g0240a0001c0001t0002g0279others(15): Show | 18 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1089-772delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756930 | ||||||
| chr16:71757123
|
A | G | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1089-964T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71757123 | ||||||
| chr16:71757370
|
G | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1089-1211C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71757370 | ||||||
| chr16:71757401
|
A | AGGTCG | 122 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1089-1247_1089-124 others(9): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71757401 | ||||||
| chr16:71757525
|
G | A | 1 | a0001c0001t0005g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1088+1283C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71757525 | ||||||
| chr16:71757526
|
A | T | 151 | a0001c0001t0002g0133a0001c0001t0005g0050a0001c0001t0005g0051others(148): Show | 152 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1088+1282T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71757526 | ||||||
| chr16:71757895
|
C | T | 121 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(118): Show | 121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1088+913G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71757895 | ||||||
| chr16:71757950
|
GCT | G | 5 | a0001c0001t0007g0087a0001c0001t0007g0090a0001c0001t0009g0073others(2): Show | 5 | HG01256.hp2 HG03942.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088+856_1088+857d others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71757950 | ||||||
| chr16:71758029
|
T | C | 1 | a0001c0001t0004g0033 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1088+779A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758029 | ||||||
| chr16:71758086
|
G | C | 1 | a0002c0002t0001g0141 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1088+722C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758086 | ||||||
| chr16:71758266
|
C | A | 1 | a0001c0001t0003g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1088+542G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758266 | ||||||
| chr16:71758287
|
G | A | 97 | a0001c0001t0002g0133a0001c0001t0005g0093a0001c0001t0005g0112others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1088+521C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758287 | ||||||
| chr16:71758305
|
T | C | 122 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1088+503A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758305 | ||||||
| chr16:71758496
|
T | C | 1 | a0001c0001t0005g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1088+312A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758496 | ||||||
| chr16:71758502
|
C | T | 1 | a0001c0001t0007g0087 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1088+306G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758502 | ||||||
| chr16:71758516
|
T | C | 1 | a0002c0002t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1088+292A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758516 | ||||||
| chr16:71758579
|
T | TAAAAAAA others(18): Show |
1 | a0001c0001t0013g0282 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1088+228_1088+229i others(27): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758579 | ||||||
| chr16:71758692
|
T | C | 1 | a0002c0002t0001g0167 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1088+116A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758692 | ||||||
| chr16:71758793
|
C | A | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.1088+15G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758793 | ||||||
| chr16:71759147
|
T | C | 3 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0080 | 3 | HG01168.hp1 HG01169.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.975-226A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759147 | ||||||
| chr16:71759422
|
C | T | 1 | a0001c0001t0015g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.975-501G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759422 | ||||||
| chr16:71759621
|
G | A | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.975-700C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759621 | ||||||
| chr16:71759637
|
G | A | 1 | a0001c0003t0008g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.975-716C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759637 | ||||||
| chr16:71759714
|
C | T | 1 | a0001c0001t0005g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.975-793G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759714 | ||||||
| chr16:71759746
|
C | T | 2 | a0001c0001t0002g0232a0001c0001t0003g0277 | 2 | HG02698.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.975-825G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759746 | ||||||
| chr16:71759759
|
C | CA | 10 | a0001c0001t0004g0032a0001c0001t0004g0040a0001c0001t0010g0002others(7): Show | 10 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.975-839dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759759 | ||||||
| chr16:71759770
|
A | T | 279 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(276): Show | 280 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.975-849T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759770 | ||||||
| chr16:71759771
|
A | T | 2 | a0001c0001t0004g0300a0001c0001t0018g0314 | 2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.975-850T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759771 | ||||||
| chr16:71760101
|
G | A | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.975-1180C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760101 | ||||||
| chr16:71760158
|
C | T | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.975-1237G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760158 | ||||||
| chr16:71760165
|
C | A | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.975-1244G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760165 | ||||||
| chr16:71760230
|
CT | C | 270 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(267): Show | 271 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.974+1281delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760230 | ||||||
| chr16:71760230
|
CTT | C | 11 | a0001c0001t0004g0061a0001c0001t0004g0300a0001c0001t0007g0078others(8): Show | 11 | HG01168.hp1 HG01256.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.974+1280_974+1281d others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760230 | ||||||
| chr16:71760336
|
A | C | 1 | a0002c0002t0001g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.974+1176T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760336 | ||||||
| chr16:71760376
|
C | T | 5 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.974+1136G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760376 | ||||||
| chr16:71760545
|
C | CA | 29 | a0001c0001t0002g0044a0001c0001t0004g0014a0001c0001t0016g0041others(26): Show | 29 | HG00642.hp2 HG00738.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.974+966dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760545 | ||||||
| chr16:71760579
|
G | C | 2 | a0001c0001t0004g0300a0001c0001t0018g0314 | 2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.974+933C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760579 | ||||||
| chr16:71760620
|
C | T | 1 | a0001c0003t0008g0186 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.974+892G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760620 | ||||||
| chr16:71760768
|
C | A | 1 | a0002c0002t0001g0130 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.974+744G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760768 | ||||||
| chr16:71760769
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.974+743C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760769 | ||||||
| chr16:71760831
|
A | G | 303 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(300): Show | 304 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.974+681T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760831 | ||||||
| chr16:71760839
|
G | A | 1 | a0002c0002t0001g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.974+673C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760839 | ||||||
| chr16:71760884
|
C | G | 1 | a0002c0002t0001g0130 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.974+628G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760884 | ||||||
| chr16:71760987
|
G | A | 1 | a0002c0002t0006g0173 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.974+525C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760987 | ||||||
| chr16:71761063
|
A | G | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.974+449T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71761063 | ||||||
| chr16:71761072
|
G | A | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.974+440C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71761072 | ||||||
| chr16:71761098
|
G | A | 1 | a0001c0001t0003g0268 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.974+414C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71761098 | ||||||
| chr16:71761226
|
T | C | 1 | a0002c0002t0001g0111 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.974+286A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71761226 | ||||||
| chr16:71761366
|
A | G | 1 | a0001c0001t0007g0090 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.974+146T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71761366 | ||||||
| chr16:71761645
|
A | G | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.919-78T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761645 | ||||||
| chr16:71761675
|
A | G | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.919-108T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761675 | ||||||
| chr16:71761742
|
G | A | 1 | a0001c0001t0003g0274 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.919-175C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761742 | ||||||
| chr16:71761800
|
G | C | 2 | a0001c0001t0020g0064a0001c0009t0019g0010 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.919-233C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761800 | ||||||
| chr16:71761816
|
C | CA | 17 | a0001c0001t0002g0291a0001c0001t0004g0013a0001c0001t0004g0018others(14): Show | 17 | HG00642.hp2 HG01123.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.919-250dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761816 | ||||||
| chr16:71761816
|
C | CAA | 12 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(9): Show | 12 | HG00738.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.919-251_919-250dup others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761816 | ||||||
| chr16:71761816
|
CA | C | 20 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0257others(17): Show | 20 | HG00738.hp2 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.919-250delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761816 | ||||||
| chr16:71761816
|
CAA | C | 32 | a0001c0001t0002g0044a0001c0001t0002g0198a0001c0001t0002g0210others(29): Show | 32 | HG00733.hp2 HG01099.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.919-251_919-250del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761816 | ||||||
| chr16:71761882
|
G | T | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.919-315C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761882 | ||||||
| chr16:71762225
|
A | G | 1 | a0002c0002t0001g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.919-658T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71762225 | ||||||
| chr16:71762244
|
G | C | 2 | a0001c0001t0004g0014a0001c0001t0004g0018 | 2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.919-677C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71762244 | ||||||
| chr16:71762501
|
C | T | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.919-934G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71762501 | ||||||
| chr16:71762700
|
C | T | 1 | a0002c0002t0001g0126 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.919-1133G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71762700 | ||||||
| chr16:71762840
|
CCTGA | C | 26 | a0001c0001t0007g0066a0001c0001t0007g0071a0001c0001t0007g0072others(23): Show | 27 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.919-1277_919-1274d others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71762840 | ||||||
| chr16:71762911
|
C | G | 5 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.919-1344G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71762911 | ||||||
| chr16:71762914
|
C | T | 3 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022 | 3 | HG00099.hp2 HG00639.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.919-1347G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71762914 | ||||||
| chr16:71763060
|
C | A | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.918+1290G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763060 | ||||||
| chr16:71763088
|
C | T | 318 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(315): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.918+1262G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763088 | ||||||
| chr16:71763121
|
G | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.918+1229C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763121 | ||||||
| chr16:71763242
|
T | C | 3 | a0001c0001t0002g0210a0001c0001t0002g0220a0001c0001t0002g0224 | 3 | HG02071.hp1 HG02165.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.918+1108A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763242 | ||||||
| chr16:71763334
|
G | A | 1 | a0001c0001t0007g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.918+1016C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763334 | ||||||
| chr16:71763500
|
T | A | 1 | a0001c0001t0003g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.918+850A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763500 | ||||||
| chr16:71763571
|
T | C | 4 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0040g0238others(1): Show | 4 | HG00408.hp2 HG02523.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+779A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763571 | ||||||
| chr16:71763652
|
G | A | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.918+698C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763652 | ||||||
| chr16:71763653
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.918+697C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763653 | ||||||
| chr16:71763689
|
G | C | 8 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(5): Show | 8 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+661C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763689 | ||||||
| chr16:71764047
|
T | C | 12 | a0001c0001t0002g0278a0001c0001t0002g0279a0001c0001t0002g0281others(9): Show | 12 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.918+303A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71764047 | ||||||
| chr16:71764140
|
C | T | 5 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+210G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71764140 | ||||||
| chr16:71764264
|
G | A | 2 | a0001c0001t0037g0082a0001c0001t0038g0083 | 2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.918+86C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71764264 | ||||||
| chr16:71764321
|
G | T | 5 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+29C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71764321 | ||||||
| chr16:71764551
|
G | C | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.819+95C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 8/22 | chr16 | 71764551 | ||||||
| chr16:71764573
|
C | A | 1 | a0001c0001t0003g0255 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.819+73G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 8/22 | chr16 | 71764573 | ||||||
| chr16:71764628
|
T | C | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.819+18A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 8/22 | chr16 | 71764628 | ||||||
| chr16:71764642
|
T | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | splice_region_variant&intron_variant | LOW | c.819+4A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 8/22 | chr16 | 71764642 | ||||||
| chr16:71764918
|
C | G | 24 | a0002c0002t0001g0092a0002c0002t0001g0107a0002c0002t0001g0108others(21): Show | 24 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.739-192G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 7/22 | chr16 | 71764918 | ||||||
| chr16:71765197
|
G | A | 23 | a0002c0002t0001g0092a0002c0002t0001g0107a0002c0002t0001g0108others(20): Show | 23 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.738+292C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 7/22 | chr16 | 71765197 | ||||||
| chr16:71765444
|
A | G | 139 | a0001c0001t0002g0133a0001c0001t0005g0043a0001c0001t0005g0050others(136): Show | 140 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.738+45T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 7/22 | chr16 | 71765444 | ||||||
| chr16:71765455
|
A | G | 7 | a0001c0001t0002g0201a0001c0001t0012g0197a0001c0001t0012g0200others(4): Show | 7 | NA18952.hp2 NA18954.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.738+34T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 7/22 | chr16 | 71765455 | ||||||
| chr16:71765468
|
A | G | 2 | a0001c0001t0037g0082a0001c0001t0038g0083 | 2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.738+21T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 7/22 | chr16 | 71765468 | ||||||
| chr16:71765732
|
G | C | 2 | a0001c0001t0002g0230a0001c0001t0002g0290 | 2 | NA18977.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.643-148C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71765732 | ||||||
| chr16:71765829
|
A | T | 1 | a0001c0001t0003g0268 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.643-245T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71765829 | ||||||
| chr16:71765856
|
G | C | 29 | a0001c0001t0007g0066a0001c0001t0007g0071a0001c0001t0007g0072others(26): Show | 30 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.643-272C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71765856 | ||||||
| chr16:71766091
|
T | C | 21 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0006g0099others(18): Show | 21 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.643-507A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766091 | ||||||
| chr16:71766095
|
C | T | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.643-511G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766095 | ||||||
| chr16:71766133
|
T | C | 125 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(122): Show | 125 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.643-549A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766133 | ||||||
| chr16:71766142
|
G | A | 38 | a0001c0001t0005g0052a0001c0001t0005g0053a0001c0001t0005g0055others(35): Show | 39 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.643-558C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766142 | ||||||
| chr16:71766339
|
T | C | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.643-755A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766339 | ||||||
| chr16:71766481
|
T | A | 108 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(105): Show | 108 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.643-897A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766481 | ||||||
| chr16:71766547
|
T | C | 1 | a0001c0001t0005g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.643-963A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766547 | ||||||
| chr16:71766569
|
A | T | 1 | a0001c0001t0002g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.643-985T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766569 | ||||||
| chr16:71766577
|
C | T | 2 | a0001c0001t0020g0064a0001c0009t0019g0010 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.643-993G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766577 | ||||||
| chr16:71766633
|
A | AAT | 27 | a0002c0002t0001g0092a0002c0002t0001g0107a0002c0002t0001g0108others(24): Show | 27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.643-1050_643-1049i others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766633 | ||||||
| chr16:71766635
|
C | G | 27 | a0002c0002t0001g0092a0002c0002t0001g0107a0002c0002t0001g0108others(24): Show | 27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.643-1051G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766635 | ||||||
| chr16:71766637
|
C | G | 27 | a0002c0002t0001g0092a0002c0002t0001g0107a0002c0002t0001g0108others(24): Show | 27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.643-1053G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766637 | ||||||
| chr16:71766697
|
G | T | 1 | a0002c0002t0001g0157 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.643-1113C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766697 | ||||||
| chr16:71766756
|
A | G | 1 | a0002c0002t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.643-1172T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766756 | ||||||
| chr16:71766796
|
G | T | 1 | a0001c0001t0004g0033 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.643-1212C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766796 | ||||||
| chr16:71766846
|
T | C | 1 | a0001c0001t0014g0266 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.643-1262A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766846 | ||||||
| chr16:71767039
|
A | G | 304 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(301): Show | 305 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.643-1455T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767039 | ||||||
| chr16:71767059
|
T | G | 151 | a0001c0001t0002g0133a0001c0001t0004g0032a0001c0001t0005g0050others(148): Show | 152 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.643-1475A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767059 | ||||||
| chr16:71767081
|
C | A | 2 | a0001c0001t0020g0064a0001c0009t0019g0010 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.643-1497G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767081 | ||||||
| chr16:71767189
|
C | G | 282 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(279): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.643-1605G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767189 | ||||||
| chr16:71767200
|
G | A | 1 | a0001c0001t0004g0025 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.643-1616C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767200 | ||||||
| chr16:71767204
|
C | T | 1 | a0001c0001t0004g0025 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.643-1620G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767204 | ||||||
| chr16:71767356
|
C | A | 20 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0006g0099others(17): Show | 20 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.643-1772G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767356 | ||||||
| chr16:71767467
|
G | A | 1 | a0001c0001t0004g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.643-1883C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767467 | ||||||
| chr16:71767501
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.643-1917C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767501 | ||||||
| chr16:71767533
|
A | G | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.643-1949T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767533 | ||||||
| chr16:71767691
|
G | C | 124 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(121): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.642+1932C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767691 | ||||||
| chr16:71767955
|
C | T | 1 | a0002c0002t0006g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.642+1668G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767955 | ||||||
| chr16:71768043
|
C | T | 12 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(9): Show | 12 | HG00733.hp1 HG01884.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.642+1580G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768043 | ||||||
| chr16:71768055
|
T | C | 152 | a0001c0001t0002g0133a0001c0001t0004g0032a0001c0001t0005g0050others(149): Show | 153 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.642+1568A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768055 | ||||||
| chr16:71768090
|
C | T | 5 | a0001c0001t0009g0065a0001c0001t0009g0069a0001c0001t0009g0079others(2): Show | 5 | HG01358.hp2 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+1533G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768090 | ||||||
| chr16:71768192
|
TA | T | 180 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0201others(177): Show | 181 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.642+1430delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768192 | ||||||
| chr16:71768192
|
TAA | T | 44 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0310others(41): Show | 44 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.642+1429_642+1430d others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768192 | ||||||
| chr16:71768192
|
TAAA | T | 68 | a0001c0001t0002g0133a0001c0001t0004g0032a0001c0001t0005g0093others(65): Show | 68 | HG00423.hp2 HG01071.hp2 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.642+1428_642+1430d others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768192 | ||||||
| chr16:71768220
|
G | A | 2 | a0001c0001t0009g0069a0001c0001t0009g0079 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.642+1403C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768220 | ||||||
| chr16:71768231
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.642+1392G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768231 | ||||||
| chr16:71768358
|
G | A | 124 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(121): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.642+1265C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768358 | ||||||
| chr16:71768479
|
C | T | 98 | a0001c0001t0002g0133a0001c0001t0004g0032a0001c0001t0005g0093others(95): Show | 98 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.642+1144G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768479 | ||||||
| chr16:71768500
|
C | CAAAAAAA others(1): Show |
17 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0006g0099others(14): Show | 17 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.642+1115_642+1122d others(10): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768500 | ||||||
| chr16:71768500
|
C | CAAAAAAA others(2): Show |
19 | a0001c0001t0002g0298a0001c0001t0005g0043a0001c0001t0016g0041others(16): Show | 19 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.642+1114_642+1122d others(11): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768500 | ||||||
| chr16:71768500
|
C | CAAAAAAA others(3): Show |
216 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(213): Show | 217 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.642+1113_642+1122d others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768500 | ||||||
| chr16:71768500
|
C | CAAAAAAA others(4): Show |
29 | a0001c0001t0002g0264a0001c0001t0002g0306a0001c0001t0002g0316others(26): Show | 29 | HG01175.hp2 HG01358.hp2 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.642+1112_642+1122d others(13): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768500 | ||||||
| chr16:71768500
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0002g0302a0002c0002t0001g0154 | 2 | HG01433.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.642+1111_642+1122d others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768500 | ||||||
| chr16:71768500
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.642+1110_642+1122d others(15): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768500 | ||||||
| chr16:71768500
|
C | CCAAAAAA others(3): Show |
2 | a0002c0002t0001g0156a0002c0002t0001g0157 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.642+1122_642+1123i others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768500 | ||||||
| chr16:71768512
|
A | AAAAAAAA others(3): Show |
1 | a0002c0002t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.642+1110_642+1111i others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768512 | ||||||
| chr16:71768558
|
G | A | 1 | a0002c0002t0031g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.642+1065C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768558 | ||||||
| chr16:71768595
|
A | G | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.642+1028T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768595 | ||||||
| chr16:71768626
|
T | C | 1 | a0001c0001t0016g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.642+997A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768626 | ||||||
| chr16:71768655
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.642+968G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768655 | ||||||
| chr16:71768664
|
A | C | 282 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(279): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.642+959T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768664 | ||||||
| chr16:71768759
|
C | CA | 74 | a0001c0001t0002g0133a0001c0001t0004g0032a0001c0001t0005g0093others(71): Show | 74 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.642+863dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768759 | ||||||
| chr16:71768776
|
G | A | 1 | a0001c0001t0002g0270 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.642+847C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768776 | ||||||
| chr16:71768810
|
G | A | 1 | a0001c0001t0004g0017 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.642+813C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768810 | ||||||
| chr16:71768843
|
G | A | 1 | a0002c0002t0006g0173 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.642+780C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768843 | ||||||
| chr16:71768904
|
C | A | 123 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(120): Show | 123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.642+719G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768904 | ||||||
| chr16:71768910
|
T | C | 1 | a0001c0001t0002g0283 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.642+713A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768910 | ||||||
| chr16:71768917
|
C | CA | 51 | a0001c0001t0004g0011a0001c0001t0004g0013a0001c0001t0004g0014others(48): Show | 51 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.642+705dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768917 | ||||||
| chr16:71768917
|
C | CAA | 8 | a0001c0001t0004g0012a0001c0001t0004g0016a0001c0001t0004g0026others(5): Show | 8 | HG01123.hp2 HG01981.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+704_642+705dup others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768917 | ||||||
| chr16:71768917
|
CA | C | 10 | a0001c0001t0002g0269a0001c0001t0002g0276a0001c0001t0002g0284others(7): Show | 10 | HG00642.hp1 HG00733.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.642+705delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768917 | ||||||
| chr16:71768917
|
CAA | C | 109 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(106): Show | 109 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.642+704_642+705del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768917 | ||||||
| chr16:71768917
|
CAAA | C | 8 | a0001c0001t0002g0233a0001c0001t0002g0240a0001c0001t0002g0241others(5): Show | 8 | HG00639.hp2 HG00735.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+703_642+705del others(3): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768917 | ||||||
| chr16:71768934
|
A | G | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.642+689T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768934 | ||||||
| chr16:71768936
|
A | G | 23 | a0001c0001t0002g0249a0001c0001t0002g0258a0001c0001t0002g0301others(20): Show | 23 | HG00621.hp1 HG00733.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.642+687T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768936 | ||||||
| chr16:71768965
|
T | TA | 273 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(270): Show | 274 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.642+657dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768965 | ||||||
| chr16:71768978
|
C | CA | 93 | a0001c0001t0002g0133a0001c0001t0002g0242a0001c0001t0002g0244others(90): Show | 93 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.642+644dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768978 | ||||||
| chr16:71768978
|
C | CAA | 101 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(98): Show | 101 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.642+643_642+644dup others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768978 | ||||||
| chr16:71768978
|
C | CAAA | 13 | a0001c0001t0002g0231a0001c0001t0002g0233a0001c0001t0002g0241others(10): Show | 13 | HG00735.hp1 HG01192.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.642+642_642+644dup others(3): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768978 | ||||||
| chr16:71768978
|
CA | C | 43 | a0001c0001t0004g0031a0001c0001t0005g0051a0001c0001t0005g0052others(40): Show | 44 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.642+644delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768978 | ||||||
| chr16:71768988
|
A | AC | 3 | a0001c0001t0002g0302a0001c0001t0003g0308a0002c0002t0001g0109 | 3 | HG01433.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.642+634_642+635ins others(1): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768988 | ||||||
| chr16:71769121
|
A | G | 1 | a0001c0001t0036g0271 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.642+502T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71769121 | ||||||
| chr16:71769212
|
GGA | G | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.642+409_642+410del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71769212 | ||||||
| chr16:71769232
|
G | A | 8 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(5): Show | 8 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.642+391C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71769232 | ||||||
| chr16:71769364
|
T | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.642+259A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71769364 | ||||||
| chr16:71769926
|
G | T | 17 | a0001c0001t0002g0210a0001c0001t0002g0220a0001c0001t0002g0224others(14): Show | 17 | HG01099.hp1 HG01256.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.566-227C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71769926 | ||||||
| chr16:71769964
|
T | C | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.566-265A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71769964 | ||||||
| chr16:71770011
|
G | T | 107 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(104): Show | 107 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.566-312C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770011 | ||||||
| chr16:71770070
|
A | C | 1 | a0002c0002t0006g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-371T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770070 | ||||||
| chr16:71770071
|
G | A | 124 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(121): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.566-372C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770071 | ||||||
| chr16:71770191
|
C | T | 4 | a0002c0002t0001g0111a0002c0002t0001g0123a0002c0002t0001g0124others(1): Show | 4 | HG02083.hp1 HG02523.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-492G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770191 | ||||||
| chr16:71770212
|
C | T | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.566-513G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770212 | ||||||
| chr16:71770384
|
A | G | 286 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(283): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.566-685T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770384 | ||||||
| chr16:71770811
|
T | C | 1 | a0001c0001t0016g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.565+345A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770811 | ||||||
| chr16:71770899
|
C | T | 281 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.565+257G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770899 | ||||||
| chr16:71771015
|
C | G | 3 | a0001c0001t0002g0233a0001c0001t0002g0240a0001c0001t0002g0241 | 3 | HG00735.hp1 HG01169.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.565+141G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71771015 | ||||||
| chr16:71771053
|
C | G | 281 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.565+103G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71771053 | ||||||
| chr16:71771257
|
G | A | 287 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(284): Show | 288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
splice_region_variant&intron_variant | LOW | c.469-5C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71771257 | ||||||
| chr16:71771302
|
G | A | 1 | a0002c0002t0001g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.469-50C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71771302 | ||||||
| chr16:71771496
|
G | A | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.469-244C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71771496 | ||||||
| chr16:71771715
|
T | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.469-463A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71771715 | ||||||
| chr16:71771839
|
T | C | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.469-587A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71771839 | ||||||
| chr16:71771909
|
T | C | 1 | a0002c0002t0001g0150 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.469-657A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71771909 | ||||||
| chr16:71772006
|
C | T | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.469-754G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772006 | ||||||
| chr16:71772017
|
A | G | 2 | a0001c0001t0020g0064a0001c0008t0008g0181 | 2 | HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.469-765T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772017 | ||||||
| chr16:71772024
|
C | T | 5 | a0001c0001t0015g0035a0001c0001t0015g0036a0001c0001t0015g0037others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-772G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772024 | ||||||
| chr16:71772036
|
G | C | 3 | a0002c0002t0006g0171a0002c0002t0006g0172a0002c0002t0006g0173 | 3 | HG00642.hp2 HG00738.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.469-784C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772036 | ||||||
| chr16:71772138
|
C | CT | 286 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(283): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.469-887dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772138 | ||||||
| chr16:71772153
|
C | T | 1 | a0002c0002t0001g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.469-901G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772153 | ||||||
| chr16:71772162
|
G | T | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.469-910C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772162 | ||||||
| chr16:71772303
|
G | T | 1 | a0002c0002t0001g0048 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.468+918C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772303 | ||||||
| chr16:71772350
|
T | C | 1 | a0002c0002t0001g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.468+871A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772350 | ||||||
| chr16:71772411
|
G | A | 150 | a0001c0001t0002g0133a0001c0001t0005g0050a0001c0001t0005g0051others(147): Show | 151 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.468+810C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772411 | ||||||
| chr16:71772496
|
A | G | 1 | a0001c0001t0002g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.468+725T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772496 | ||||||
| chr16:71772588
|
G | A | 1 | a0002c0002t0001g0180 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.468+633C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772588 | ||||||
| chr16:71772673
|
T | G | 1 | a0001c0001t0002g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.468+548A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772673 | ||||||
| chr16:71772862
|
T | C | 1 | a0001c0001t0011g0248 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.468+359A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772862 | ||||||
| chr16:71772966
|
G | A | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+255C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772966 | ||||||
| chr16:71773053
|
C | G | 2 | a0001c0001t0005g0119a0001c0001t0005g0122 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.468+168G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71773053 | ||||||
| chr16:71773128
|
A | G | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.468+93T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71773128 | ||||||
| chr16:71773388
|
A | G | 3 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0080 | 3 | HG01168.hp1 HG01169.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.327-26T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773388 | ||||||
| chr16:71773501
|
T | C | 1 | a0001c0001t0004g0034 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.327-139A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773501 | ||||||
| chr16:71773546
|
T | A | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.327-184A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773546 | ||||||
| chr16:71773651
|
A | G | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.327-289T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773651 | ||||||
| chr16:71773733
|
A | C | 1 | a0001c0001t0007g0090 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.327-371T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773733 | ||||||
| chr16:71773738
|
T | A | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.327-376A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773738 | ||||||
| chr16:71773812
|
G | A | 1 | a0002c0002t0001g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.327-450C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773812 | ||||||
| chr16:71773846
|
G | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.327-484C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773846 | ||||||
| chr16:71773868
|
T | G | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.327-506A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773868 | ||||||
| chr16:71773907
|
C | T | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.327-545G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773907 | ||||||
| chr16:71773920
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.326+548C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773920 | ||||||
| chr16:71774067
|
G | GA | 9 | a0001c0001t0002g0198a0001c0001t0002g0281a0001c0001t0003g0212others(6): Show | 9 | HG01106.hp2 HG01978.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.326+400dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71774067 | ||||||
| chr16:71774103
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.326+365G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71774103 | ||||||
| chr16:71774244
|
G | A | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.326+224C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71774244 | ||||||
| chr16:71774285
|
G | A | 2 | a0001c0001t0020g0064a0001c0008t0008g0181 | 2 | HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.326+183C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71774285 | ||||||
| chr16:71774332
|
C | T | 146 | a0001c0001t0002g0133a0001c0001t0005g0050a0001c0001t0005g0051others(143): Show | 147 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.326+136G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71774332 | ||||||
| chr16:71774919
|
CCATGTTG others(304): Show |
C | 2 | a0001c0001t0002g0249a0001c0001t0002g0258 | 2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.202-638_202-328del | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71774919 | ||||||
| chr16:71775019
|
C | CT | 39 | a0001c0001t0002g0194a0001c0001t0002g0201a0001c0001t0002g0210others(36): Show | 39 | HG00408.hp1 HG00408.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.202-428dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775019 | ||||||
| chr16:71775019
|
CT | C | 18 | a0001c0001t0004g0315a0001c0001t0005g0050a0001c0001t0005g0114others(15): Show | 18 | HG00423.hp2 HG00741.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.202-428delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775019 | ||||||
| chr16:71775019
|
CTT | C | 134 | a0001c0001t0002g0133a0001c0001t0005g0043a0001c0001t0005g0051others(131): Show | 135 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.202-429_202-428del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775019 | ||||||
| chr16:71775120
|
G | T | 1 | a0001c0001t0003g0205 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.202-528C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775120 | ||||||
| chr16:71775125
|
C | T | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.202-533G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775125 | ||||||
| chr16:71775185
|
C | T | 119 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(116): Show | 119 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.202-593G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775185 | ||||||
| chr16:71775233
|
T | C | 6 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-641A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775233 | ||||||
| chr16:71775294
|
A | G | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-702T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775294 | ||||||
| chr16:71775335
|
C | T | 27 | a0002c0002t0001g0092a0002c0002t0001g0107a0002c0002t0001g0108others(24): Show | 27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.202-743G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775335 | ||||||
| chr16:71775495
|
A | G | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.202-903T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775495 | ||||||
| chr16:71775566
|
C | T | 1 | a0001c0001t0005g0112 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.202-974G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775566 | ||||||
| chr16:71775631
|
C | T | 124 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(121): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.202-1039G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775631 | ||||||
| chr16:71775758
|
C | T | 1 | a0002c0002t0001g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.202-1166G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775758 | ||||||
| chr16:71776058
|
C | A | 2 | a0001c0001t0009g0069a0001c0001t0009g0079 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.202-1466G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776058 | ||||||
| chr16:71776061
|
T | G | 1 | a0001c0003t0008g0192 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.202-1469A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776061 | ||||||
| chr16:71776085
|
C | T | 1 | a0001c0001t0002g0278 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.202-1493G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776085 | ||||||
| chr16:71776113
|
G | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-1521C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776113 | ||||||
| chr16:71776182
|
G | A | 1 | a0002c0002t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.202-1590C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776182 | ||||||
| chr16:71776297
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.202-1705C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776297 | ||||||
| chr16:71776431
|
A | G | 1 | a0002c0002t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.202-1839T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776431 | ||||||
| chr16:71776591
|
T | C | 2 | a0002c0002t0001g0319a0002c0002t0039g0318 | 2 | HG02071.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.202-1999A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776591 | ||||||
| chr16:71776685
|
T | C | 3 | a0002c0002t0001g0134a0002c0002t0001g0162a0002c0002t0033g0152 | 3 | NA18951.hp2 NA19003.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.202-2093A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776685 | ||||||
| chr16:71776725
|
C | A | 1 | a0001c0001t0002g0228 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.202-2133G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776725 | ||||||
| chr16:71776778
|
T | C | 4 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-2186A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776778 | ||||||
| chr16:71776793
|
C | T | 1 | a0001c0001t0002g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.202-2201G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776793 | ||||||
| chr16:71776850
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.202-2258G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776850 | ||||||
| chr16:71776860
|
A | G | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.202-2268T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776860 | ||||||
| chr16:71777101
|
T | C | 2 | a0002c0002t0001g0048a0002c0002t0001g0144 | 2 | NA18966.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.202-2509A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777101 | ||||||
| chr16:71777106
|
C | CA | 43 | a0001c0001t0002g0198a0001c0001t0002g0224a0001c0001t0002g0226others(40): Show | 43 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.202-2515dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777106 | ||||||
| chr16:71777106
|
C | CAA | 11 | a0001c0001t0002g0228a0001c0001t0002g0233a0001c0001t0002g0241others(8): Show | 11 | HG00735.hp1 HG01192.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.202-2516_202-2515d others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777106 | ||||||
| chr16:71777106
|
CA | C | 89 | a0001c0001t0002g0133a0001c0001t0004g0014a0001c0001t0004g0017others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.202-2515delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777106 | ||||||
| chr16:71777106
|
CAA | C | 59 | a0001c0001t0004g0012a0001c0001t0004g0013a0001c0001t0004g0015others(56): Show | 60 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.202-2516_202-2515d others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777106 | ||||||
| chr16:71777195
|
C | A | 152 | a0001c0001t0002g0133a0001c0001t0005g0050a0001c0001t0005g0051others(149): Show | 153 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.202-2603G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777195 | ||||||
| chr16:71777272
|
C | A | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.202-2680G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777272 | ||||||
| chr16:71777371
|
G | A | 4 | a0002c0002t0001g0111a0002c0002t0001g0123a0002c0002t0001g0124others(1): Show | 4 | HG02083.hp1 HG02523.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-2779C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777371 | ||||||
| chr16:71777471
|
G | C | 27 | a0002c0002t0001g0092a0002c0002t0001g0107a0002c0002t0001g0108others(24): Show | 27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.202-2879C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777471 | ||||||
| chr16:71777791
|
T | C | 4 | a0001c0001t0002g0233a0001c0001t0002g0240a0001c0001t0002g0241others(1): Show | 4 | HG00735.hp1 HG01169.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-3199A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777791 | ||||||
| chr16:71777891
|
C | G | 1 | a0002c0002t0001g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.202-3299G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777891 | ||||||
| chr16:71777982
|
T | C | 4 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-3390A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777982 | ||||||
| chr16:71778092
|
G | A | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.202-3500C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778092 | ||||||
| chr16:71778280
|
C | A | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.202-3688G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778280 | ||||||
| chr16:71778393
|
A | G | 303 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(300): Show | 304 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.202-3801T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778393 | ||||||
| chr16:71778493
|
C | T | 3 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022 | 3 | HG00099.hp2 HG00639.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.202-3901G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778493 | ||||||
| chr16:71778500
|
C | T | 1 | a0001c0001t0004g0032 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.202-3908G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778500 | ||||||
| chr16:71778543
|
C | T | 2 | a0001c0001t0013g0287a0001c0001t0013g0288 | 2 | NA18612.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.202-3951G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778543 | ||||||
| chr16:71778576
|
G | A | 1 | a0001c0001t0004g0032 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.202-3984C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778576 | ||||||
| chr16:71778637
|
C | T | 2 | a0001c0001t0009g0069a0001c0001t0009g0079 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.202-4045G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778637 | ||||||
| chr16:71778640
|
G | A | 1 | a0002c0002t0001g0156 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.202-4048C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778640 | ||||||
| chr16:71778682
|
TA | T | 285 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(282): Show | 286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.202-4091delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778682 | ||||||
| chr16:71778768
|
G | A | 295 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(292): Show | 296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.202-4176C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778768 | ||||||
| chr16:71778965
|
C | T | 1 | a0002c0002t0033g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.202-4373G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778965 | ||||||
| chr16:71778988
|
C | T | 1 | a0001c0001t0005g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.202-4396G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778988 | ||||||
| chr16:71779073
|
G | T | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-4481C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779073 | ||||||
| chr16:71779098
|
T | A | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.202-4506A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779098 | ||||||
| chr16:71779177
|
T | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.202-4585A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779177 | ||||||
| chr16:71779180
|
C | G | 4 | a0001c0001t0002g0233a0001c0001t0002g0240a0001c0001t0002g0241others(1): Show | 4 | HG00735.hp1 HG01169.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-4588G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779180 | ||||||
| chr16:71779377
|
AC | A | 4 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-4786delG | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779377 | ||||||
| chr16:71779456
|
T | C | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.202-4864A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779456 | ||||||
| chr16:71779623
|
A | G | 1 | a0001c0001t0004g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.202-5031T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779623 | ||||||
| chr16:71779773
|
T | C | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.202-5181A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779773 | ||||||
| chr16:71779848
|
T | C | 123 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(120): Show | 123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.202-5256A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779848 | ||||||
| chr16:71779877
|
G | T | 13 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(10): Show | 13 | HG00733.hp1 HG01361.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.202-5285C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779877 | ||||||
| chr16:71779973
|
A | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-5381T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779973 | ||||||
| chr16:71779984
|
AGTTTTTT others(3): Show |
A | 1 | a0001c0001t0004g0300 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.202-5402_202-5393d others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779984 | ||||||
| chr16:71779995
|
G | GT | 38 | a0001c0001t0002g0307a0001c0001t0003g0211a0001c0001t0004g0315others(35): Show | 38 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.202-5404dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779995 | ||||||
| chr16:71779995
|
G | T | 12 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-5403C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779995 | ||||||
| chr16:71780017
|
G | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-5425C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780017 | ||||||
| chr16:71780056
|
C | T | 124 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(121): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.202-5464G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780056 | ||||||
| chr16:71780141
|
G | A | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.202-5549C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780141 | ||||||
| chr16:71780154
|
C | T | 152 | a0001c0001t0002g0133a0001c0001t0005g0050a0001c0001t0005g0051others(149): Show | 153 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.202-5562G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780154 | ||||||
| chr16:71780178
|
G | A | 1 | a0001c0001t0005g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.202-5586C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780178 | ||||||
| chr16:71780228
|
A | T | 1 | a0002c0002t0001g0144 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.202-5636T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780228 | ||||||
| chr16:71780241
|
G | A | 1 | a0001c0001t0014g0266 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.202-5649C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780241 | ||||||
| chr16:71780271
|
G | A | 1 | a0001c0001t0002g0316 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.202-5679C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780271 | ||||||
| chr16:71780463
|
C | T | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.202-5871G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780463 | ||||||
| chr16:71780497
|
T | A | 2 | a0001c0001t0020g0064a0001c0008t0008g0181 | 2 | HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.202-5905A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780497 | ||||||
| chr16:71780497
|
T | TA | 120 | a0001c0001t0002g0133a0001c0001t0003g0277a0001c0001t0004g0040others(117): Show | 121 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.202-5906dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780497 | ||||||
| chr16:71780497
|
T | TAA | 10 | a0001c0001t0005g0093a0001c0001t0005g0114a0001c0001t0005g0115others(7): Show | 10 | HG01358.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.202-5907_202-5906d others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780497 | ||||||
| chr16:71780497
|
TA | T | 14 | a0001c0001t0002g0244a0001c0001t0002g0306a0001c0001t0002g0310others(11): Show | 14 | HG00323.hp1 HG01496.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.202-5906delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780497 | ||||||
| chr16:71780757
|
T | G | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-6165A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780757 | ||||||
| chr16:71780820
|
C | CT | 6 | a0001c0001t0004g0034a0001c0001t0015g0035a0001c0001t0015g0036others(3): Show | 6 | HG01515.hp1 HG01934.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-6229dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780820 | ||||||
| chr16:71780925
|
C | T | 1 | a0002c0002t0017g0129 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.202-6333G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780925 | ||||||
| chr16:71780951
|
G | A | 1 | a0002c0002t0001g0147 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.202-6359C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780951 | ||||||
| chr16:71781231
|
C | A | 1 | a0001c0001t0002g0312 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.202-6639G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71781231 | ||||||
| chr16:71781275
|
T | C | 1 | a0002c0002t0001g0095 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.202-6683A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71781275 | ||||||
| chr16:71781380
|
C | G | 2 | a0001c0001t0002g0249a0001c0001t0002g0258 | 2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.202-6788G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71781380 | ||||||
| chr16:71781381
|
T | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.202-6789A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71781381 | ||||||
| chr16:71781423
|
C | T | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.202-6831G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71781423 | ||||||
| chr16:71781487
|
T | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.202-6895A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71781487 | ||||||
| chr16:71781799
|
T | C | 60 | a0001c0001t0002g0133a0002c0002t0001g0048a0002c0002t0001g0095others(57): Show | 60 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.202-7207A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71781799 | ||||||
| chr16:71782010
|
C | T | 286 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(283): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.201+7269G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782010 | ||||||
| chr16:71782208
|
G | C | 1 | a0001c0001t0010g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.201+7071C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782208 | ||||||
| chr16:71782250
|
G | A | 1 | a0001c0001t0015g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.201+7029C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782250 | ||||||
| chr16:71782288
|
G | A | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.201+6991C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782288 | ||||||
| chr16:71782466
|
A | AATT | 59 | a0001c0001t0002g0133a0002c0002t0001g0048a0002c0002t0001g0095others(56): Show | 59 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.201+6810_201+6812d others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782466 | ||||||
| chr16:71782466
|
A | AATTATTA others(2): Show |
11 | a0001c0001t0005g0093a0001c0001t0005g0112a0001c0001t0005g0114others(8): Show | 11 | HG02109.hp1 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+6804_201+6812d others(11): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782466 | ||||||
| chr16:71782466
|
A | AATTATTA others(5): Show |
1 | a0001c0001t0005g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.201+6801_201+6812d others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782466 | ||||||
| chr16:71782479
|
ATTATTAT others(5): Show |
A | 1 | a0002c0002t0022g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.201+6788_201+6799d others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782479 | ||||||
| chr16:71782488
|
A | T | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.201+6791T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782488 | ||||||
| chr16:71782491
|
T | A | 1 | a0002c0002t0039g0318 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.201+6788A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782491 | ||||||
| chr16:71782762
|
AG | A | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+6516delC | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782762 | ||||||
| chr16:71782996
|
G | A | 281 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.201+6283C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782996 | ||||||
| chr16:71783068
|
G | C | 2 | a0002c0002t0001g0096a0002c0002t0001g0137 | 2 | NA19002.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.201+6211C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783068 | ||||||
| chr16:71783077
|
CTTTAT | C | 3 | a0001c0001t0002g0301a0001c0001t0002g0305a0001c0001t0002g0309 | 3 | HG02280.hp1 HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.201+6197_201+6201d others(7): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783077 | ||||||
| chr16:71783104
|
T | C | 1 | a0001c0001t0009g0067 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.201+6175A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783104 | ||||||
| chr16:71783115
|
G | A | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.201+6164C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783115 | ||||||
| chr16:71783230
|
T | A | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.201+6049A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783230 | ||||||
| chr16:71783267
|
A | C | 139 | a0001c0001t0002g0133a0001c0001t0005g0050a0001c0001t0005g0051others(136): Show | 140 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.201+6012T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783267 | ||||||
| chr16:71783270
|
A | G | 2 | a0001c0001t0004g0300a0001c0001t0018g0314 | 2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.201+6009T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783270 | ||||||
| chr16:71783309
|
T | C | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+5970A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783309 | ||||||
| chr16:71783396
|
A | G | 1 | a0001c0003t0008g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.201+5883T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783396 | ||||||
| chr16:71783574
|
T | G | 1 | a0002c0002t0001g0131 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.201+5705A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783574 | ||||||
| chr16:71783682
|
G | A | 1 | a0001c0001t0011g0248 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.201+5597C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783682 | ||||||
| chr16:71783831
|
T | G | 1 | a0002c0002t0001g0138 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.201+5448A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783831 | ||||||
| chr16:71784018
|
C | A | 3 | a0002c0002t0001g0095a0002c0002t0001g0125a0005c0006t0001g0132 | 3 | HG01168.hp2 HG02074.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.201+5261G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784018 | ||||||
| chr16:71784246
|
T | C | 2 | a0001c0001t0004g0031a0001c0001t0004g0032 | 2 | NA18954.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.201+5033A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784246 | ||||||
| chr16:71784281
|
A | T | 1 | a0002c0002t0006g0172 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.201+4998T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784281 | ||||||
| chr16:71784528
|
C | G | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.201+4751G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784528 | ||||||
| chr16:71784597
|
C | T | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+4682G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784597 | ||||||
| chr16:71784643
|
C | T | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.201+4636G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784643 | ||||||
| chr16:71784725
|
A | C | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.201+4554T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784725 | ||||||
| chr16:71784787
|
G | T | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.201+4492C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784787 | ||||||
| chr16:71784928
|
T | G | 1 | a0001c0001t0002g0302 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.201+4351A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784928 | ||||||
| chr16:71785135
|
G | T | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.201+4144C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785135 | ||||||
| chr16:71785243
|
G | T | 2 | a0001c0001t0020g0064a0001c0009t0019g0010 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.201+4036C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785243 | ||||||
| chr16:71785348
|
G | A | 1 | a0001c0001t0014g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.201+3931C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785348 | ||||||
| chr16:71785384
|
T | C | 2 | a0001c0001t0002g0230a0001c0001t0002g0290 | 2 | NA18977.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.201+3895A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785384 | ||||||
| chr16:71785425
|
A | C | 1 | a0002c0002t0001g0048 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.201+3854T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785425 | ||||||
| chr16:71785575
|
C | CA | 27 | a0001c0001t0002g0231a0001c0001t0002g0239a0001c0001t0002g0241others(24): Show | 27 | HG00735.hp1 HG00741.hp2 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.201+3703dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785575 | ||||||
| chr16:71785575
|
CA | C | 128 | a0001c0001t0002g0133a0001c0001t0002g0228a0001c0001t0002g0232others(125): Show | 129 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.201+3703delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785575 | ||||||
| chr16:71785575
|
CAAA | C | 24 | a0002c0002t0001g0092a0002c0002t0001g0107a0002c0002t0001g0108others(21): Show | 24 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.201+3701_201+3703d others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785575 | ||||||
| chr16:71785577
|
A | G | 3 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0040g0238 | 3 | HG00408.hp2 HG02523.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.201+3702T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785577 | ||||||
| chr16:71785678
|
G | A | 41 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(38): Show | 42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.201+3601C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785678 | ||||||
| chr16:71785744
|
T | C | 5 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+3535A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785744 | ||||||
| chr16:71785787
|
A | C | 1 | a0001c0001t0013g0287 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.201+3492T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785787 | ||||||
| chr16:71786006
|
G | A | 1 | a0001c0001t0009g0067 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.201+3273C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786006 | ||||||
| chr16:71786008
|
G | C | 1 | a0002c0002t0001g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.201+3271C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786008 | ||||||
| chr16:71786045
|
T | C | 6 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(3): Show | 6 | HG02074.hp1 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+3234A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786045 | ||||||
| chr16:71786139
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.201+3140C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786139 | ||||||
| chr16:71786172
|
C | T | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+3107G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786172 | ||||||
| chr16:71786202
|
T | C | 1 | a0001c0001t0023g0121 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.201+3077A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786202 | ||||||
| chr16:71786301
|
GTCTTAAA others(5): Show |
G | 2 | a0001c0001t0016g0041a0001c0001t0016g0042 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.201+2966_201+2977d others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786301 | ||||||
| chr16:71786390
|
T | C | 1 | a0001c0001t0004g0025 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.201+2889A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786390 | ||||||
| chr16:71786608
|
G | A | 3 | a0001c0001t0009g0065a0001c0001t0009g0085a0001c0001t0009g0086 | 3 | HG01358.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.201+2671C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786608 | ||||||
| chr16:71786633
|
G | C | 1 | a0001c0001t0004g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.201+2646C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786633 | ||||||
| chr16:71786724
|
T | G | 286 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(283): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.201+2555A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786724 | ||||||
| chr16:71786748
|
C | T | 11 | a0002c0002t0001g0111a0002c0002t0001g0123a0002c0002t0001g0124others(8): Show | 11 | HG00323.hp1 HG00323.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+2531G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786748 | ||||||
| chr16:71786893
|
T | C | 1 | a0001c0001t0015g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.201+2386A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786893 | ||||||
| chr16:71786940
|
C | T | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.201+2339G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786940 | ||||||
| chr16:71787175
|
C | T | 1 | a0001c0001t0004g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.201+2104G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787175 | ||||||
| chr16:71787224
|
C | A | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.201+2055G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787224 | ||||||
| chr16:71787245
|
G | C | 1 | a0002c0002t0031g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.201+2034C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787245 | ||||||
| chr16:71787267
|
C | T | 3 | a0002c0002t0001g0139a0002c0002t0001g0148a0002c0002t0031g0160 | 3 | HG03017.hp1 HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.201+2012G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787267 | ||||||
| chr16:71787318
|
CA | C | 15 | a0001c0001t0004g0040a0001c0001t0010g0002a0001c0001t0010g0003others(12): Show | 15 | HG00738.hp2 HG01515.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.201+1960delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787318 | ||||||
| chr16:71787318
|
CAAAA | C | 25 | a0001c0001t0002g0233a0001c0001t0002g0264a0001c0001t0002g0265others(22): Show | 25 | HG00140.hp1 HG00408.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.201+1957_201+1960d others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787318 | ||||||
| chr16:71787318
|
CAAAAA | C | 215 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(212): Show | 216 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.201+1956_201+1960d others(7): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787318 | ||||||
| chr16:71787318
|
CAAAAAA | C | 37 | a0001c0001t0002g0316a0001c0003t0008g0183a0001c0003t0008g0184others(34): Show | 37 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.201+1955_201+1960d others(8): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787318 | ||||||
| chr16:71787356
|
T | C | 6 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+1923A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787356 | ||||||
| chr16:71787392
|
G | T | 1 | a0001c0001t0003g0214 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.201+1887C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787392 | ||||||
| chr16:71787474
|
C | T | 124 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(121): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.201+1805G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787474 | ||||||
| chr16:71787656
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.201+1623A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787656 | ||||||
| chr16:71787897
|
A | T | 12 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(9): Show | 12 | HG00733.hp1 HG01884.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+1382T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787897 | ||||||
| chr16:71788075
|
C | G | 1 | a0002c0002t0031g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.201+1204G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788075 | ||||||
| chr16:71788119
|
T | A | 1 | a0002c0002t0001g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.201+1160A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788119 | ||||||
| chr16:71788120
|
A | C | 1 | a0002c0002t0001g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.201+1159T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788120 | ||||||
| chr16:71788198
|
T | A | 281 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.201+1081A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788198 | ||||||
| chr16:71788328
|
C | T | 124 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(121): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.201+951G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788328 | ||||||
| chr16:71788347
|
A | C | 281 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.201+932T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788347 | ||||||
| chr16:71788616
|
C | T | 1 | a0001c0001t0002g0278 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.201+663G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788616 | ||||||
| chr16:71788638
|
T | C | 1 | a0001c0001t0002g0269 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.201+641A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788638 | ||||||
| chr16:71788657
|
CTT | C | 268 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(265): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.201+620_201+621del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788657 | ||||||
| chr16:71788667
|
T | A | 100 | a0001c0001t0002g0133a0001c0001t0002g0228a0001c0001t0002g0310others(97): Show | 100 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.201+612A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788667 | ||||||
| chr16:71788667
|
TA | T | 5 | a0001c0001t0015g0035a0001c0001t0015g0036a0001c0001t0015g0037others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+611delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788667 | ||||||
| chr16:71788686
|
A | C | 3 | a0002c0002t0001g0096a0002c0002t0001g0136a0002c0002t0001g0137 | 3 | NA18965.hp2 NA19002.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.201+593T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788686 | ||||||
| chr16:71788765
|
A | C | 2 | a0001c0001t0009g0001a0001c0001t0009g0070 | 3 | HG00609.hp2 NA18968.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.201+514T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788765 | ||||||
| chr16:71788771
|
C | G | 3 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0080 | 3 | HG01168.hp1 HG01169.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.201+508G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788771 | ||||||
| chr16:71788825
|
CT | C | 269 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(266): Show | 270 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.201+453delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788825 | ||||||
| chr16:71789100
|
T | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.201+179A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71789100 | ||||||
| chr16:71789214
|
T | C | 18 | a0001c0001t0002g0194a0001c0001t0002g0201a0001c0001t0002g0239others(15): Show | 18 | HG00408.hp2 HG00741.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.201+65A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71789214 | ||||||
| chr16:71789541
|
A | T | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-59T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71789541 | ||||||
| chr16:71789787
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-3-305A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71789787 | ||||||
| chr16:71789944
|
A | G | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-3-462T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71789944 | ||||||
| chr16:71790051
|
A | G | 5 | a0001c0001t0015g0035a0001c0001t0015g0036a0001c0001t0015g0037others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-569T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790051 | ||||||
| chr16:71790100
|
TA | T | 283 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(280): Show | 284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.-3-619delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790100 | ||||||
| chr16:71790130
|
A | G | 1 | a0001c0001t0012g0292 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-3-648T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790130 | ||||||
| chr16:71790210
|
G | C | 1 | a0001c0001t0010g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-3-728C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790210 | ||||||
| chr16:71790268
|
C | T | 124 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(121): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-3-786G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790268 | ||||||
| chr16:71790293
|
C | A | 4 | a0001c0003t0008g0184a0001c0003t0008g0189a0001c0003t0008g0190others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-811G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790293 | ||||||
| chr16:71790339
|
G | A | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-3-857C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790339 | ||||||
| chr16:71790359
|
G | A | 1 | a0002c0002t0033g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-3-877C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790359 | ||||||
| chr16:71790480
|
T | C | 1 | a0001c0001t0002g0244 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-3-998A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790480 | ||||||
| chr16:71790527
|
C | CA | 123 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(120): Show | 123 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.-3-1046dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790527 | ||||||
| chr16:71790664
|
C | A | 8 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(5): Show | 8 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-1182G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790664 | ||||||
| chr16:71790682
|
G | A | 5 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-1200C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790682 | ||||||
| chr16:71790769
|
A | G | 12 | a0002c0002t0001g0111a0002c0002t0001g0123a0002c0002t0001g0124others(9): Show | 12 | HG00323.hp1 HG00323.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3-1287T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790769 | ||||||
| chr16:71790811
|
C | T | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.-3-1329G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790811 | ||||||
| chr16:71791010
|
C | G | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-3-1528G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791010 | ||||||
| chr16:71791040
|
G | C | 1 | a0001c0001t0003g0229 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-3-1558C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791040 | ||||||
| chr16:71791225
|
C | CA | 12 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3-1744dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791225 | ||||||
| chr16:71791238
|
C | CA | 6 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-1757dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791238 | ||||||
| chr16:71791247
|
C | A | 1 | a0001c0001t0005g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-3-1765G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791247 | ||||||
| chr16:71791400
|
T | C | 2 | a0001c0001t0013g0287a0001c0001t0013g0288 | 2 | NA18612.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-3-1918A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791400 | ||||||
| chr16:71791424
|
C | T | 2 | a0001c0001t0009g0069a0001c0001t0009g0079 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-3-1942G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791424 | ||||||
| chr16:71791539
|
G | T | 1 | a0001c0001t0007g0080 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-3-2057C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791539 | ||||||
| chr16:71791542
|
A | G | 281 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.-3-2060T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791542 | ||||||
| chr16:71791673
|
CA | C | 268 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(265): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.-3-2192delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791673 | ||||||
| chr16:71791728
|
C | T | 7 | a0001c0001t0004g0017a0001c0001t0004g0026a0001c0001t0004g0027others(4): Show | 7 | HG00099.hp1 HG01123.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3-2246G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791728 | ||||||
| chr16:71791763
|
C | CT | 171 | a0001c0001t0002g0044a0001c0001t0002g0198a0001c0001t0002g0201others(168): Show | 172 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.-3-2282dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791763 | ||||||
| chr16:71791763
|
C | CTT | 16 | a0001c0001t0002g0194a0001c0001t0002g0244a0001c0001t0002g0245others(13): Show | 16 | HG00741.hp2 HG01175.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.-3-2283_-3-2282dup others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791763 | ||||||
| chr16:71791763
|
CT | C | 11 | a0001c0001t0005g0093a0001c0001t0005g0112a0001c0001t0005g0113others(8): Show | 11 | HG02109.hp1 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-2282delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791763 | ||||||
| chr16:71791876
|
C | T | 5 | a0001c0001t0015g0035a0001c0001t0015g0036a0001c0001t0015g0037others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-2394G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791876 | ||||||
| chr16:71791948
|
G | C | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.-3-2466C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791948 | ||||||
| chr16:71791990
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-2508C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791990 | ||||||
| chr16:71792095
|
G | A | 124 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(121): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-3-2613C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792095 | ||||||
| chr16:71792122
|
T | C | 7 | a0001c0001t0004g0017a0001c0001t0004g0026a0001c0001t0004g0027others(4): Show | 7 | HG00099.hp1 HG01123.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3-2640A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792122 | ||||||
| chr16:71792162
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-2680C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792162 | ||||||
| chr16:71792185
|
T | A | 1 | a0002c0002t0001g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-3-2703A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792185 | ||||||
| chr16:71792425
|
T | G | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-2943A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792425 | ||||||
| chr16:71792618
|
T | C | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-3-3136A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792618 | ||||||
| chr16:71792704
|
A | C | 3 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0017g0047 | 3 | NA18941.hp2 NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-3-3222T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792704 | ||||||
| chr16:71792708
|
G | T | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.-3-3226C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792708 | ||||||
| chr16:71792773
|
T | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-3-3291A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792773 | ||||||
| chr16:71792833
|
G | A | 1 | a0002c0002t0001g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-3-3351C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792833 | ||||||
| chr16:71792980
|
C | T | 43 | a0001c0001t0002g0242a0001c0001t0005g0050a0001c0001t0005g0051others(40): Show | 44 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.-3-3498G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792980 | ||||||
| chr16:71793086
|
C | A | 5 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-3604G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793086 | ||||||
| chr16:71793162
|
G | C | 1 | a0001c0001t0010g0004 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-3-3680C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793162 | ||||||
| chr16:71793291
|
T | C | 3 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0080 | 3 | HG01168.hp1 HG01169.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.-3-3809A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793291 | ||||||
| chr16:71793357
|
A | G | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-3875T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793357 | ||||||
| chr16:71793747
|
C | G | 1 | a0002c0002t0001g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-3-4265G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793747 | ||||||
| chr16:71793753
|
CGGCTCAC others(18): Show |
C | 5 | a0001c0001t0015g0035a0001c0001t0015g0036a0001c0001t0015g0037others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-4296_-3-4272del others(25): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793753 | ||||||
| chr16:71793847
|
C | T | 4 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0054others(1): Show | 4 | HG02602.hp2 HG02683.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-4365G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793847 | ||||||
| chr16:71793870
|
A | C | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-4388T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793870 | ||||||
| chr16:71793889
|
T | C | 27 | a0002c0002t0001g0092a0002c0002t0001g0107a0002c0002t0001g0108others(24): Show | 27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.-3-4407A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793889 | ||||||
| chr16:71793896
|
T | C | 71 | a0001c0001t0002g0133a0001c0001t0005g0093a0001c0001t0005g0112others(68): Show | 71 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-3-4414A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793896 | ||||||
| chr16:71794025
|
T | G | 3 | a0001c0001t0009g0065a0001c0001t0009g0085a0001c0001t0009g0086 | 3 | HG01358.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-3-4543A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794025 | ||||||
| chr16:71794298
|
G | T | 1 | a0002c0002t0001g0169 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-3-4816C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794298 | ||||||
| chr16:71794494
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-5012C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794494 | ||||||
| chr16:71794574
|
C | G | 1 | a0001c0001t0002g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-3-5092G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794574 | ||||||
| chr16:71794630
|
T | C | 3 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030 | 3 | HG00099.hp1 HG02257.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-3-5148A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794630 | ||||||
| chr16:71794671
|
A | G | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-5189T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794671 | ||||||
| chr16:71794713
|
C | T | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.-3-5231G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794713 | ||||||
| chr16:71794835
|
C | CT | 7 | a0001c0001t0002g0233a0001c0001t0004g0013a0001c0001t0004g0030others(4): Show | 7 | HG01192.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-5354dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
C | CTTT | 7 | a0001c0001t0004g0061a0001c0008t0008g0181a0002c0002t0001g0092others(4): Show | 7 | HG02055.hp2 HG02165.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-5356_-3-5354dup others(3): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
C | CTTTT | 8 | a0001c0001t0004g0040a0002c0002t0006g0104a0002c0002t0006g0105others(5): Show | 8 | HG00738.hp1 HG01123.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-5357_-3-5354dup others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
C | CTTTTCTT others(4): Show |
2 | a0001c0003t0008g0191a0001c0003t0008g0192 | 2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-3-5354_-3-5353ins others(11): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
C | CTTTTCTT others(5): Show |
8 | a0001c0003t0008g0183a0001c0003t0008g0185a0001c0003t0008g0186others(5): Show | 8 | HG01891.hp1 HG02258.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3-5354_-3-5353ins others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
C | CTTTTCTT others(6): Show |
1 | a0001c0003t0008g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-3-5354_-3-5353ins others(13): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
C | CTTTTT | 13 | a0001c0001t0009g0065a0001c0001t0009g0086a0002c0002t0001g0153others(10): Show | 13 | HG00642.hp2 HG00741.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-3-5358_-3-5354dup others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
C | CTTTTTT | 14 | a0001c0001t0009g0085a0002c0002t0001g0048a0002c0002t0001g0126others(11): Show | 14 | HG00323.hp1 HG00323.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3-5359_-3-5354dup others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
C | CTTTTTTT | 33 | a0002c0002t0001g0095a0002c0002t0001g0096a0002c0002t0001g0111others(30): Show | 33 | HG00423.hp2 HG01168.hp2 HG02071.hp2 others(30): Show |
intron_variant | MODIFIER | c.-3-5360_-3-5354dup others(7): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0007g0080a0001c0001t0007g0087a0001c0001t0009g0001others(5): Show | 9 | HG00609.hp2 HG01257.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-5361_-3-5354dup others(8): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
C | CTTTTTTT others(2): Show |
18 | a0001c0001t0005g0122a0001c0001t0007g0071a0001c0001t0007g0072others(15): Show | 18 | HG00140.hp1 HG01168.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-3-5362_-3-5354dup others(9): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
C | CTTTTTTT others(3): Show |
8 | a0001c0001t0002g0133a0001c0001t0005g0060a0001c0001t0005g0118others(5): Show | 8 | HG01106.hp1 HG02486.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3-5363_-3-5354dup others(10): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
C | CTTTTTTT others(4): Show |
9 | a0001c0001t0005g0058a0001c0001t0005g0059a0001c0001t0005g0093others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3-5364_-3-5354dup others(11): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
C | CTTTTTTT others(5): Show |
9 | a0001c0001t0005g0051a0001c0001t0005g0054a0001c0001t0005g0055others(6): Show | 9 | HG02683.hp2 HG02970.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-5365_-3-5354dup others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0005g0050a0002c0002t0001g0167a0005c0006t0001g0132 | 3 | HG02074.hp2 HG02602.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-3-5366_-3-5354dup others(13): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
CT | C | 99 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(96): Show | 99 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.-3-5354delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0001g0089 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-3-5365_-3-5354del others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
CTTTTTTT others(7): Show |
C | 1 | a0002c0002t0001g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-3-5367_-3-5354del others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-3-5368_-3-5354del others(15): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794835
|
CTTTTTTT others(11): Show |
C | 1 | a0002c0002t0006g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-3-5371_-3-5354del others(18): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | ||||||
| chr16:71794916
|
C | A | 1 | a0001c0001t0004g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-3-5434G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794916 | ||||||
| chr16:71794958
|
C | T | 2 | a0002c0002t0001g0126a0002c0002t0001g0131 | 2 | HG00323.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-3-5476G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794958 | ||||||
| chr16:71795426
|
T | C | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.-3-5944A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71795426 | ||||||
| chr16:71795962
|
C | T | 1 | a0001c0001t0004g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-3-6480G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71795962 | ||||||
| chr16:71796007
|
C | G | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-3-6525G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796007 | ||||||
| chr16:71796093
|
T | C | 2 | a0001c0001t0004g0300a0001c0001t0018g0314 | 2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-3-6611A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796093 | ||||||
| chr16:71796485
|
G | A | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-3-7003C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796485 | ||||||
| chr16:71796530
|
A | G | 1 | a0001c0001t0015g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-3-7048T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796530 | ||||||
| chr16:71796636
|
C | T | 1 | a0001c0001t0003g0205 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-3-7154G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796636 | ||||||
| chr16:71796744
|
T | C | 1 | a0001c0001t0029g0267 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-3-7262A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796744 | ||||||
| chr16:71796768
|
T | C | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-3-7286A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796768 | ||||||
| chr16:71796785
|
T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-3-7303A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796785 | ||||||
| chr16:71796855
|
A | G | 4 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0017g0047others(1): Show | 4 | HG03017.hp1 NA18941.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-7373T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796855 | ||||||
| chr16:71796893
|
G | A | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-7411C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796893 | ||||||
| chr16:71797016
|
T | TTA | 10 | a0001c0001t0004g0023a0001c0001t0004g0040a0001c0001t0010g0002others(7): Show | 10 | HG00738.hp2 HG01361.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3-7536_-3-7535dup others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797016 | ||||||
| chr16:71797016
|
TTA | T | 125 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(122): Show | 125 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-3-7536_-3-7535del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797016 | ||||||
| chr16:71797018
|
A | T | 1 | a0001c0001t0003g0272 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-3-7536T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797018 | ||||||
| chr16:71797019
|
T | C | 138 | a0001c0001t0002g0133a0001c0001t0005g0050a0001c0001t0005g0051others(135): Show | 139 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-3-7537A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797019 | ||||||
| chr16:71797101
|
C | T | 1 | a0002c0002t0001g0130 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-3-7619G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797101 | ||||||
| chr16:71797440
|
T | A | 124 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(121): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-3-7958A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797440 | ||||||
| chr16:71797538
|
C | T | 5 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-8056G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797538 | ||||||
| chr16:71797629
|
T | A | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-8147A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797629 | ||||||
| chr16:71797656
|
G | A | 5 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-8174C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797656 | ||||||
| chr16:71797674
|
C | T | 2 | a0001c0001t0003g0208a0001c0001t0003g0209 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-3-8192G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797674 | ||||||
| chr16:71797696
|
G | A | 1 | a0001c0001t0002g0296 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-3-8214C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797696 | ||||||
| chr16:71797736
|
T | C | 1 | a0001c0001t0003g0275 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-3-8254A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797736 | ||||||
| chr16:71797810
|
G | T | 6 | a0001c0001t0005g0055a0001c0001t0005g0056a0001c0001t0005g0057others(3): Show | 6 | HG01884.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-8328C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797810 | ||||||
| chr16:71797828
|
G | C | 1 | a0002c0002t0001g0159 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-3-8346C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797828 | ||||||
| chr16:71797850
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-3-8368G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797850 | ||||||
| chr16:71797947
|
A | C | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-3-8465T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797947 | ||||||
| chr16:71797974
|
T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-3-8492A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797974 | ||||||
| chr16:71798052
|
C | A | 1 | a0001c0001t0038g0083 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-3-8570G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798052 | ||||||
| chr16:71798120
|
G | T | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-8638C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798120 | ||||||
| chr16:71798145
|
TATC | T | 4 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022others(1): Show | 4 | HG00099.hp2 HG00639.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-8666_-3-8664del others(3): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798145 | ||||||
| chr16:71798173
|
C | T | 5 | a0001c0001t0015g0035a0001c0001t0015g0036a0001c0001t0015g0037others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-8691G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798173 | ||||||
| chr16:71798211
|
A | G | 5 | a0001c0001t0015g0035a0001c0001t0015g0036a0001c0001t0015g0037others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-8729T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798211 | ||||||
| chr16:71798313
|
C | T | 8 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-8831G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798313 | ||||||
| chr16:71798339
|
T | C | 1 | a0001c0001t0004g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-3-8857A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798339 | ||||||
| chr16:71798439
|
T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-3-8957A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798439 | ||||||
| chr16:71798451
|
G | A | 2 | a0001c0001t0037g0082a0001c0001t0038g0083 | 2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-3-8969C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798451 | ||||||
| chr16:71798849
|
C | T | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-9367G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798849 | ||||||
| chr16:71798878
|
G | C | 2 | a0001c0001t0020g0064a0001c0009t0019g0010 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-3-9396C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798878 | ||||||
| chr16:71799429
|
C | T | 282 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(279): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.-4+9334G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799429 | ||||||
| chr16:71799606
|
T | TAAAAAAC others(344): Show |
1 | a0001c0001t0004g0031 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-4+9156_-4+9157ins others(351): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799606 | ||||||
| chr16:71799606
|
T | TAAAAAAC others(349): Show |
1 | a0001c0001t0004g0032 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-4+9156_-4+9157ins others(356): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799606 | ||||||
| chr16:71799625
|
G | A | 2 | a0001c0001t0004g0061a0001c0008t0008g0181 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-4+9138C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799625 | ||||||
| chr16:71799754
|
C | G | 1 | a0002c0002t0001g0111 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-4+9009G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799754 | ||||||
| chr16:71799755
|
G | C | 287 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(284): Show | 288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-4+9008C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799755 | ||||||
| chr16:71799772
|
G | A | 1 | a0001c0001t0003g0268 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-4+8991C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799772 | ||||||
| chr16:71799816
|
G | A | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-4+8947C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799816 | ||||||
| chr16:71799901
|
AAAT | A | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.-4+8859_-4+8861del others(3): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799901 | ||||||
| chr16:71799928
|
A | T | 128 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(125): Show | 128 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.-4+8835T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799928 | ||||||
| chr16:71799959
|
G | A | 2 | a0003c0005t0001g0165a0003c0005t0001g0166 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-4+8804C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799959 | ||||||
| chr16:71799990
|
G | A | 1 | a0002c0002t0006g0172 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-4+8773C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799990 | ||||||
| chr16:71800080
|
T | C | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-4+8683A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800080 | ||||||
| chr16:71800137
|
G | A | 1 | a0001c0001t0007g0084 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-4+8626C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800137 | ||||||
| chr16:71800139
|
T | G | 6 | a0001c0001t0005g0055a0001c0001t0005g0056a0001c0001t0005g0057others(3): Show | 6 | HG01884.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+8624A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800139 | ||||||
| chr16:71800200
|
T | TA | 7 | a0001c0001t0004g0033a0001c0001t0005g0043a0001c0001t0009g0065others(4): Show | 7 | HG01358.hp2 HG01516.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+8562dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800200 | ||||||
| chr16:71800224
|
AG | A | 152 | a0001c0001t0002g0133a0001c0001t0004g0061a0001c0001t0005g0050others(149): Show | 153 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.-4+8538delC | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800224 | ||||||
| chr16:71800228
|
G | A | 2 | a0001c0001t0007g0087a0001c0001t0007g0090 | 2 | NA18971.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-4+8535C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800228 | ||||||
| chr16:71800243
|
CGCCTGTA others(423): Show |
C | 6 | a0001c0001t0005g0055a0001c0001t0005g0056a0001c0001t0005g0057others(3): Show | 6 | HG01884.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+8090_-4+8519del | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800243 | ||||||
| chr16:71800319
|
C | T | 5 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+8444G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800319 | ||||||
| chr16:71800372
|
C | CA | 18 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0003t0008g0183others(15): Show | 18 | HG01891.hp1 HG02109.hp2 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.-4+8390dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800372 | ||||||
| chr16:71800372
|
CA | C | 18 | a0001c0001t0002g0301a0001c0001t0002g0302a0001c0001t0002g0305others(15): Show | 18 | HG01433.hp1 HG02280.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.-4+8390delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800372 | ||||||
| chr16:71800508
|
C | A | 144 | a0001c0001t0002g0133a0001c0001t0005g0050a0001c0001t0005g0051others(141): Show | 145 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.-4+8255G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800508 | ||||||
| chr16:71800530
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4+8233C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800530 | ||||||
| chr16:71800540
|
G | A | 1 | a0001c0001t0005g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-4+8223C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800540 | ||||||
| chr16:71800551
|
T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4+8212A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800551 | ||||||
| chr16:71800756
|
G | A | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+8007C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800756 | ||||||
| chr16:71800780
|
A | G | 6 | a0001c0001t0005g0055a0001c0001t0005g0056a0001c0001t0005g0057others(3): Show | 6 | HG01884.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+7983T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800780 | ||||||
| chr16:71800788
|
G | C | 1 | a0002c0002t0001g0319 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-4+7975C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800788 | ||||||
| chr16:71800833
|
T | C | 1 | a0001c0001t0005g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-4+7930A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800833 | ||||||
| chr16:71800861
|
G | A | 1 | a0001c0001t0036g0271 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-4+7902C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800861 | ||||||
| chr16:71800939
|
G | A | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4+7824C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800939 | ||||||
| chr16:71801031
|
G | A | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-4+7732C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801031 | ||||||
| chr16:71801050
|
T | C | 152 | a0001c0001t0002g0133a0001c0001t0004g0061a0001c0001t0005g0050others(149): Show | 153 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.-4+7713A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801050 | ||||||
| chr16:71801128
|
G | A | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-4+7635C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801128 | ||||||
| chr16:71801174
|
G | A | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+7589C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801174 | ||||||
| chr16:71801274
|
C | T | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+7489G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801274 | ||||||
| chr16:71801284
|
A | C | 32 | a0001c0001t0002g0198a0001c0001t0002g0210a0001c0001t0002g0215others(29): Show | 32 | HG00733.hp2 HG01099.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.-4+7479T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801284 | ||||||
| chr16:71801300
|
A | C | 1 | a0002c0002t0021g0097 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-4+7463T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801300 | ||||||
| chr16:71801330
|
T | C | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+7433A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801330 | ||||||
| chr16:71801333
|
T | TA | 12 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4+7429dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801333 | ||||||
| chr16:71801333
|
TA | T | 187 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(184): Show | 187 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.-4+7429delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801333 | ||||||
| chr16:71801340
|
A | C | 42 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(39): Show | 43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.-4+7423T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801340 | ||||||
| chr16:71801419
|
G | A | 2 | a0001c0001t0024g0088a0002c0002t0001g0089 | 2 | HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-4+7344C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801419 | ||||||
| chr16:71801510
|
A | T | 1 | a0002c0002t0001g0175 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-4+7253T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801510 | ||||||
| chr16:71801608
|
G | T | 6 | a0001c0001t0005g0043a0001c0001t0012g0207a0001c0001t0016g0041others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+7155C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801608 | ||||||
| chr16:71801707
|
G | A | 124 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(121): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-4+7056C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801707 | ||||||
| chr16:71801781
|
G | C | 6 | a0001c0001t0005g0055a0001c0001t0005g0056a0001c0001t0005g0057others(3): Show | 6 | HG01884.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+6982C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801781 | ||||||
| chr16:71801853
|
C | T | 1 | a0001c0001t0003g0206 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-4+6910G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801853 | ||||||
| chr16:71801858
|
C | G | 1 | a0001c0001t0003g0206 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-4+6905G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801858 | ||||||
| chr16:71801878
|
C | CGCCACTG others(7): Show |
1 | a0001c0001t0003g0196 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-4+6871_-4+6884dup others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801878 | ||||||
| chr16:71801922
|
C | CA | 14 | a0001c0001t0002g0276a0001c0001t0002g0278a0001c0001t0002g0312others(11): Show | 14 | HG00621.hp2 HG01175.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.-4+6840dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801922 | ||||||
| chr16:71801936
|
A | G | 5 | a0001c0001t0015g0035a0001c0001t0015g0036a0001c0001t0015g0037others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+6827T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801936 | ||||||
| chr16:71801961
|
C | T | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4+6802G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801961 | ||||||
| chr16:71802045
|
T | C | 11 | a0001c0001t0002g0279a0001c0001t0002g0281a0001c0001t0002g0283others(8): Show | 11 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4+6718A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802045 | ||||||
| chr16:71802403
|
G | C | 1 | a0001c0001t0014g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-4+6360C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802403 | ||||||
| chr16:71802479
|
C | T | 1 | a0001c0001t0003g0205 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-4+6284G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802479 | ||||||
| chr16:71802488
|
G | A | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-4+6275C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802488 | ||||||
| chr16:71802524
|
G | A | 5 | a0001c0001t0015g0035a0001c0001t0015g0036a0001c0001t0015g0037others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+6239C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802524 | ||||||
| chr16:71802541
|
C | G | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4+6222G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802541 | ||||||
| chr16:71802569
|
A | G | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-4+6194T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802569 | ||||||
| chr16:71802671
|
G | T | 1 | a0001c0001t0030g0049 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-4+6092C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802671 | ||||||
| chr16:71802842
|
A | G | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-4+5921T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802842 | ||||||
| chr16:71803108
|
G | A | 1 | a0002c0002t0001g0167 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-4+5655C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803108 | ||||||
| chr16:71803177
|
G | C | 1 | a0002c0002t0001g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-4+5586C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803177 | ||||||
| chr16:71803390
|
T | A | 1 | a0001c0001t0002g0291 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-4+5373A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803390 | ||||||
| chr16:71803514
|
T | G | 1 | a0001c0001t0014g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-4+5249A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803514 | ||||||
| chr16:71803574
|
T | G | 150 | a0001c0001t0002g0133a0001c0001t0005g0050a0001c0001t0005g0051others(147): Show | 151 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.-4+5189A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803574 | ||||||
| chr16:71803634
|
CT | C | 3 | a0002c0002t0001g0164a0003c0005t0001g0165a0003c0005t0001g0166 | 3 | HG03491.hp1 HG03492.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-4+5128delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803634 | ||||||
| chr16:71803789
|
G | C | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-4+4974C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803789 | ||||||
| chr16:71803794
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4+4969C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803794 | ||||||
| chr16:71803800
|
C | A | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-4+4963G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803800 | ||||||
| chr16:71803883
|
C | T | 1 | a0002c0002t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-4+4880G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803883 | ||||||
| chr16:71803923
|
C | CA | 23 | a0001c0001t0002g0290a0001c0001t0002g0298a0001c0001t0005g0093others(20): Show | 23 | HG01071.hp1 HG01071.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-4+4839dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803923 | ||||||
| chr16:71803923
|
C | CAA | 49 | a0001c0001t0002g0133a0002c0002t0001g0048a0002c0002t0001g0095others(46): Show | 49 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.-4+4838_-4+4839dup others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803923 | ||||||
| chr16:71803923
|
CA | C | 13 | a0001c0001t0002g0198a0001c0001t0004g0011a0001c0001t0004g0012others(10): Show | 13 | HG01496.hp2 HG02055.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.-4+4839delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803923 | ||||||
| chr16:71803946
|
C | T | 1 | a0002c0002t0001g0095 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-4+4817G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803946 | ||||||
| chr16:71803977
|
T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4+4786A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803977 | ||||||
| chr16:71804053
|
A | AT | 6 | a0001c0001t0002g0201a0001c0001t0012g0197a0001c0001t0012g0200others(3): Show | 6 | NA18952.hp2 NA18954.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+4709dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804053 | ||||||
| chr16:71804053
|
A | T | 4 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+4710T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804053 | ||||||
| chr16:71804057
|
T | A | 1 | a0002c0002t0001g0167 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-4+4706A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804057 | ||||||
| chr16:71804087
|
C | G | 1 | a0001c0001t0011g0199 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-4+4676G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804087 | ||||||
| chr16:71804172
|
G | A | 5 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+4591C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804172 | ||||||
| chr16:71804274
|
C | T | 1 | a0002c0002t0022g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-4+4489G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804274 | ||||||
| chr16:71804298
|
G | A | 1 | a0001c0001t0002g0291 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-4+4465C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804298 | ||||||
| chr16:71804408
|
A | AT | 7 | a0001c0001t0002g0294a0001c0001t0002g0295a0001c0001t0002g0296others(4): Show | 7 | HG00639.hp2 HG01515.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+4354dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804408 | ||||||
| chr16:71804408
|
A | ATT | 117 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(114): Show | 117 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-4+4353_-4+4354dup others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804408 | ||||||
| chr16:71804408
|
AT | A | 50 | a0001c0001t0004g0040a0001c0001t0005g0050a0001c0001t0005g0051others(47): Show | 51 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.-4+4354delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804408 | ||||||
| chr16:71804555
|
A | G | 286 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(283): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.-4+4208T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804555 | ||||||
| chr16:71804568
|
C | T | 14 | a0001c0001t0002g0301a0001c0001t0002g0302a0001c0001t0002g0305others(11): Show | 14 | HG01433.hp1 HG02280.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-4+4195G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804568 | ||||||
| chr16:71804578
|
T | C | 150 | a0001c0001t0002g0133a0001c0001t0005g0050a0001c0001t0005g0051others(147): Show | 151 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.-4+4185A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804578 | ||||||
| chr16:71804678
|
G | T | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+4085C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804678 | ||||||
| chr16:71804756
|
C | A | 1 | a0001c0001t0007g0090 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-4+4007G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804756 | ||||||
| chr16:71804778
|
A | G | 1 | a0001c0001t0002g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-4+3985T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804778 | ||||||
| chr16:71804874
|
G | A | 1 | a0001c0004t0007g0091 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-4+3889C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804874 | ||||||
| chr16:71804965
|
T | C | 97 | a0001c0001t0002g0133a0001c0001t0005g0093a0001c0001t0005g0112others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.-4+3798A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804965 | ||||||
| chr16:71805014
|
C | A | 3 | a0002c0002t0006g0171a0002c0002t0006g0172a0002c0002t0006g0173 | 3 | HG00642.hp2 HG00738.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-4+3749G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805014 | ||||||
| chr16:71805060
|
G | A | 1 | a0001c0001t0012g0197 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-4+3703C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805060 | ||||||
| chr16:71805061
|
G | T | 1 | a0001c0001t0012g0197 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-4+3702C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805061 | ||||||
| chr16:71805171
|
G | A | 2 | a0001c0001t0020g0064a0001c0009t0019g0010 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-4+3592C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805171 | ||||||
| chr16:71805207
|
G | A | 1 | a0002c0002t0006g0173 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-4+3556C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805207 | ||||||
| chr16:71805312
|
G | T | 5 | a0001c0001t0015g0035a0001c0001t0015g0036a0001c0001t0015g0037others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+3451C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805312 | ||||||
| chr16:71805341
|
G | A | 3 | a0001c0001t0002g0316a0001c0001t0020g0064a0001c0009t0019g0010 | 3 | HG02451.hp2 HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-4+3422C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805341 | ||||||
| chr16:71805387
|
T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4+3376A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805387 | ||||||
| chr16:71805571
|
T | C | 1 | a0002c0002t0001g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-4+3192A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805571 | ||||||
| chr16:71805709
|
A | T | 1 | a0002c0002t0001g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-4+3054T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805709 | ||||||
| chr16:71805734
|
T | G | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4+3029A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805734 | ||||||
| chr16:71805792
|
T | C | 6 | a0001c0001t0005g0055a0001c0001t0005g0056a0001c0001t0005g0057others(3): Show | 6 | HG01884.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+2971A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805792 | ||||||
| chr16:71805794
|
C | T | 1 | a0001c0001t0003g0196 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-4+2969G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805794 | ||||||
| chr16:71805821
|
G | A | 5 | a0001c0001t0015g0035a0001c0001t0015g0036a0001c0001t0015g0037others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+2942C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805821 | ||||||
| chr16:71805899
|
T | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4+2864A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805899 | ||||||
| chr16:71806007
|
C | A | 28 | a0001c0001t0007g0066a0001c0001t0007g0071a0001c0001t0007g0072others(25): Show | 29 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-4+2756G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806007 | ||||||
| chr16:71806012
|
T | C | 124 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(121): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-4+2751A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806012 | ||||||
| chr16:71806031
|
T | A | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-4+2732A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806031 | ||||||
| chr16:71806031
|
TA | T | 7 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0008t0008g0181others(4): Show | 7 | HG00733.hp2 HG02809.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+2731delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806031 | ||||||
| chr16:71806031
|
TAA | T | 272 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(269): Show | 273 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.-4+2730_-4+2731del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806031 | ||||||
| chr16:71806034
|
A | T | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4+2729T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806034 | ||||||
| chr16:71806035
|
A | T | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | HG00733.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-4+2728T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806035 | ||||||
| chr16:71806036
|
A | T | 122 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-4+2727T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806036 | ||||||
| chr16:71806160
|
C | A | 97 | a0001c0001t0002g0133a0001c0001t0005g0093a0001c0001t0005g0112others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.-4+2603G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806160 | ||||||
| chr16:71806170
|
A | T | 281 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.-4+2593T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806170 | ||||||
| chr16:71806476
|
T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4+2287A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806476 | ||||||
| chr16:71806623
|
C | T | 1 | a0001c0001t0014g0195 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-4+2140G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806623 | ||||||
| chr16:71806775
|
C | T | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4+1988G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806775 | ||||||
| chr16:71806936
|
A | T | 8 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(5): Show | 8 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4+1827T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806936 | ||||||
| chr16:71806982
|
T | C | 1 | a0002c0002t0001g0182 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-4+1781A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806982 | ||||||
| chr16:71807032
|
T | C | 1 | a0001c0001t0002g0299 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-4+1731A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807032 | ||||||
| chr16:71807105
|
C | A | 11 | a0001c0003t0008g0183a0001c0003t0008g0184a0001c0003t0008g0185others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+1658G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807105 | ||||||
| chr16:71807125
|
A | G | 1 | a0001c0001t0004g0300 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-4+1638T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807125 | ||||||
| chr16:71807185
|
GGAGGCC | G | 107 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(104): Show | 107 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-4+1572_-4+1577del others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807185 | ||||||
| chr16:71807196
|
C | G | 1 | a0001c0001t0002g0194 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-4+1567G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807196 | ||||||
| chr16:71807354
|
C | T | 12 | a0001c0001t0005g0050a0001c0001t0005g0051a0001c0001t0005g0052others(9): Show | 12 | HG00733.hp1 HG01884.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4+1409G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807354 | ||||||
| chr16:71807381
|
G | A | 124 | a0001c0001t0002g0044a0001c0001t0002g0194a0001c0001t0002g0198others(121): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-4+1382C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807381 | ||||||
| chr16:71807386
|
C | T | 1 | a0002c0002t0001g0048 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-4+1377G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807386 | ||||||
| chr16:71807433
|
A | C | 3 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0017g0047 | 3 | NA18941.hp2 NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-4+1330T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807433 | ||||||
| chr16:71807471
|
A | C | 1 | a0001c0001t0002g0044 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-4+1292T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807471 | ||||||
| chr16:71807598
|
G | C | 1 | a0002c0002t0001g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-4+1165C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807598 | ||||||
| chr16:71807919
|
G | A | 2 | a0002c0002t0001g0319a0002c0002t0039g0318 | 2 | HG02071.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-4+844C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807919 | ||||||
| chr16:71808104
|
G | A | 3 | a0001c0001t0005g0043a0001c0001t0016g0041a0001c0001t0016g0042 | 3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-4+659C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71808104 | ||||||
| chr16:71808204
|
C | CAACA | 277 | a0001c0001t0002g0044a0001c0001t0002g0133a0001c0001t0002g0194others(274): Show | 278 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.-4+555_-4+558dupTG others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71808204 |