Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 54812 |
|---|---|
| ensemblid | ENSG00000119844.17 |
| hgncid | 25951 |
| symbol | AFTPH |
| name | aftiphilin |
| refseq_nuc | NM_203437.4 |
| refseq_prot | NP_982261.2 |
| ensembl_nuc | ENST00000409933.6 |
| ensembl_prot | ENSP00000387071.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 64524328 |
| end | 64593005 |
| strand | + |
| ver | v1.2 |
| region | chr2:64524328-64593005 |
| region5000 | chr2:64519328-64598005 |
| regionname0 | AFTPH_chr2_64524328_64593005 |
| regionname5000 | AFTPH_chr2_64519328_64598005 |
| 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 | 936 | 267 | 41 | 57 | 125 | 11 | 31 | 104 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0002 | 0/0 | 936 | 85 | 36 | 0 | 45 | 1 | 3 | 35 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0003 | 0/0 | 936 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0004 | 0/0 | 936 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0005 | 0/0 | 936 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0006 | 0/0 | 936 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0007 | 0/0 | 936 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0008 | 0/0 | 936 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0009 | 0/0 | 936 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0010 | 0/0 | 936 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0011 | 0/0 | 936 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0012 | 0/0 | 936 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| 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 | 2811 | 262 | 41 | 56 | 124 | 9 | 30 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0002 | 0/0 | 2811 | 84 | 35 | 0 | 45 | 1 | 3 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0003 | 0/0 | 2811 | 5 | 5 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0004 | 0/0 | 2811 | 4 | 0 | 0 | 4 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0005 | 0/0 | 2811 | 3 | 0 | 0 | 0 | 2 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0006 | 0/0 | 2811 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0007 | 0/0 | 2811 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0008 | 0/0 | 2811 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0009 | 0/0 | 2811 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0010 | 0/0 | 2811 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0011 | 0/0 | 2811 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0012 | 0/0 | 2811 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0013 | 0/0 | 2811 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0014 | 0/0 | 2811 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0015 | 0/0 | 2811 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0016 | 0/0 | 2811 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| c0017 | 0/0 | 2811 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1288 | 149 | 25 | 34 | 64 | 8 | 16 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0002 | 0/0 | 1293 | 52 | 17 | 1 | 32 | 1 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0003 | 0/0 | 1294 | 45 | 8 | 3 | 30 | 1 | 3 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0004 | 0/0 | 1291 | 42 | 14 | 5 | 16 | 0 | 7 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0005 | 0/0 | 1291 | 38 | 3 | 12 | 14 | 2 | 7 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0006 | 0/0 | 1289 | 9 | 3 | 0 | 4 | 0 | 2 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0007 | 0/0 | 1287 | 8 | 1 | 2 | 5 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0008 | 0/0 | 1293 | 5 | 5 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0009 | 0/0 | 1292 | 4 | 3 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0010 | 0/0 | 1295 | 3 | 1 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0011 | 0/0 | 1290 | 3 | 0 | 1 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0012 | 0/0 | 1288 | 3 | 0 | 0 | 3 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0013 | 0/0 | 1288 | 3 | 0 | 0 | 3 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0014 | 0/0 | 1290 | 2 | 2 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0015 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0016 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0017 | 0/0 | 1290 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0018 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0019 | 0/0 | 1293 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| t0020 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| 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 | 2 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| 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 | 2811 | 262 | 41 | 56 | 124 | 9 | 30 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0005 | 0/0 | 2811 | 3 | 0 | 0 | 0 | 2 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0012 | 0/0 | 2811 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0016 | 0/0 | 2811 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0002c0002 | 0/0 | 2811 | 84 | 35 | 0 | 45 | 1 | 3 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0002c0010 | 0/0 | 2811 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0003c0003 | 0/0 | 2811 | 5 | 5 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0004c0004 | 0/0 | 2811 | 4 | 0 | 0 | 4 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0005c0007 | 0/0 | 2811 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0005c0008 | 0/0 | 2811 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0006c0006 | 0/0 | 2811 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0007c0009 | 0/0 | 2811 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0008c0017 | 0/0 | 2811 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0009c0015 | 0/0 | 2811 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0010c0013 | 0/0 | 2811 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0011c0014 | 0/0 | 2811 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0012c0011 | 0/0 | 2811 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4098 | 129 | 15 | 33 | 59 | 6 | 14 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0002 | 0/0 | 4103 | 3 | 1 | 1 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0003 | 0/0 | 4104 | 19 | 1 | 3 | 13 | 1 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0004 | 0/0 | 4101 | 40 | 14 | 4 | 16 | 0 | 6 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0005 | 0/0 | 4101 | 37 | 2 | 12 | 14 | 2 | 7 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0006 | 0/0 | 4099 | 9 | 3 | 0 | 4 | 0 | 2 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0007 | 0/0 | 4097 | 8 | 1 | 2 | 5 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0009 | 0/0 | 4102 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0010 | 0/0 | 4105 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0011 | 0/0 | 4100 | 3 | 0 | 1 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0012 | 0/0 | 4098 | 3 | 0 | 0 | 3 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0013 | 0/0 | 4098 | 3 | 0 | 0 | 3 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0014 | 0/0 | 4100 | 2 | 2 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0015 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0018 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0001t0020 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0005t0001 | 0/0 | 4098 | 3 | 0 | 0 | 0 | 2 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0012t0004 | 0/0 | 4101 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0001c0016t0001 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0002c0002t0001 | 0/0 | 4098 | 9 | 9 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0002c0002t0002 | 0/0 | 4103 | 46 | 16 | 0 | 28 | 1 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0002c0002t0003 | 0/0 | 4104 | 25 | 6 | 0 | 17 | 0 | 2 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0002c0002t0009 | 0/0 | 4102 | 2 | 2 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0002c0002t0010 | 0/0 | 4105 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0002c0002t0019 | 0/0 | 4103 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0002c0010t0016 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0003c0003t0008 | 0/0 | 4103 | 5 | 5 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0004c0004t0001 | 0/0 | 4098 | 4 | 0 | 0 | 4 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0005c0007t0002 | 0/0 | 4103 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0005c0007t0009 | 0/0 | 4102 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0005c0008t0005 | 0/0 | 4101 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0006c0006t0002 | 0/0 | 4103 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0007c0009t0004 | 0/0 | 4101 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0008c0017t0003 | 0/0 | 4104 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0009c0015t0001 | 0/0 | 4098 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0010c0013t0017 | 0/0 | 4100 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0011c0014t0001 | 0/0 | 4098 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| a0012c0011t0001 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | copy fasta | chr2 | 64519328 | 64598005 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0010g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0010g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0011g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0011g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0011g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0012g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0012g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0012g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0013g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0013g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0013g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0014g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0014g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0015g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0018g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0020g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0005t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0005t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0012t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0016t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0009g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0009g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0010g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0019g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0010t0016g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0003c0003t0008g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0003c0003t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0003c0003t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0003c0003t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0003c0003t0008g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0004c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0004c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0004c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0004c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0005c0007t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0005c0007t0009g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0005c0008t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0006c0006t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0006c0006t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0007c0009t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0008c0017t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0009c0015t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0010c0013t0017g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0011c0014t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0012c0011t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0078 | EUR | GBR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00099 | hp2 | a0001 | c0005 | t0001 | g0177 | EUR | GBR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0101 | EUR | GBR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | FIN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0020 | EUR | FIN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0366 | EUR | FIN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00408 | hp1 | a0002 | c0002 | t0003 | g0298 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00408 | hp2 | a0006 | c0006 | t0002 | g0343 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00438 | hp2 | a0001 | c0001 | t0006 | g0198 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00558 | hp1 | a0002 | c0002 | t0003 | g0305 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0363 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0057 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00673 | hp2 | a0002 | c0002 | t0003 | g0291 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0086 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0102 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0046 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01167 | hp1 | a0001 | c0001 | t0011 | g0034 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0093 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0099 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0200 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0202 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0035 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0105 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | IBS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0367 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01891 | hp2 | a0002 | c0002 | t0003 | g0324 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0079 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0076 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0065 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02004 | hp1 | a0009 | c0015 | t0001 | g0151 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02004 | hp2 | a0001 | c0012 | t0004 | g0073 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02027 | hp2 | a0001 | c0001 | t0012 | g0055 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0345 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0365 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02080 | hp1 | a0001 | c0001 | t0018 | g0157 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02083 | hp2 | a0002 | c0002 | t0003 | g0303 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02129 | hp2 | a0002 | c0002 | t0003 | g0290 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0088 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0335 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02145 | hp2 | a0002 | c0002 | t0010 | g0323 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0038 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0106 | EAS | CDX | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CDX | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0307 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0218 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0312 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0096 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0356 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0297 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02602 | hp1 | a0002 | c0002 | t0003 | g0329 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0054 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02622 | hp1 | a0002 | c0002 | t0003 | g0308 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0319 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0310 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0318 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02683 | hp1 | a0001 | c0005 | t0001 | g0122 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0121 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0285 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0286 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0255 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02723 | hp2 | a0002 | c0010 | t0016 | g0317 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0103 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0060 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0253 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0281 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0327 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02886 | hp2 | a0008 | c0017 | t0003 | g0326 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0284 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02896 | hp1 | a0003 | c0003 | t0008 | g0266 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0260 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02897 | hp2 | a0003 | c0003 | t0008 | g0263 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0314 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02970 | hp1 | a0003 | c0003 | t0008 | g0264 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02976 | hp2 | a0002 | c0002 | t0009 | g0325 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03017 | hp2 | a0007 | c0009 | t0004 | g0071 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03041 | hp1 | a0002 | c0002 | t0019 | g0360 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0267 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0213 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0283 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03130 | hp1 | a0002 | c0002 | t0003 | g0320 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0111 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0108 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0309 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03195 | hp2 | a0010 | c0013 | t0017 | g0268 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03209 | hp1 | a0001 | c0001 | t0014 | g0043 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0112 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03225 | hp2 | a0003 | c0003 | t0008 | g0265 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0066 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03453 | hp2 | a0003 | c0003 | t0008 | g0232 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03486 | hp1 | a0012 | c0011 | t0001 | g0233 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03486 | hp2 | a0005 | c0008 | t0005 | g0279 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0040 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03540 | hp1 | a0002 | c0002 | t0003 | g0322 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03540 | hp2 | a0001 | c0001 | t0014 | g0006 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0361 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0090 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0246 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03688 | hp1 | a0011 | c0014 | t0001 | g0241 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0077 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0037 | SAS | BEB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0033 | SAS | BEB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0091 | SAS | BEB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0058 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0100 | SAS | BEB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04204 | hp1 | a0002 | c0002 | t0003 | g0330 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0230 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0018 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | YRI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0333 | AFR | YRI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0346 | EAS | CHB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0313 | AFR | YRI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | YRI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18940 | hp1 | a0002 | c0002 | t0003 | g0296 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18941 | hp1 | a0001 | c0001 | t0011 | g0083 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18942 | hp1 | a0001 | c0001 | t0011 | g0059 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18946 | hp1 | a0001 | c0001 | t0013 | g0236 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18946 | hp2 | a0005 | c0007 | t0009 | g0331 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0339 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18950 | hp2 | a0001 | c0016 | t0001 | g0161 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0338 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18953 | hp2 | a0002 | c0002 | t0003 | g0304 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18956 | hp1 | a0001 | c0001 | t0012 | g0104 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18956 | hp2 | a0002 | c0002 | t0003 | g0294 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0125 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18959 | hp2 | a0002 | c0002 | t0003 | g0293 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0350 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0353 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18963 | hp1 | a0002 | c0002 | t0003 | g0300 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18967 | hp2 | a0001 | c0001 | t0012 | g0081 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18968 | hp1 | a0002 | c0002 | t0003 | g0289 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0347 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0359 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18972 | hp2 | a0001 | c0001 | t0007 | g0184 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0292 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18975 | hp2 | a0001 | c0001 | t0010 | g0029 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0085 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0336 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18979 | hp1 | a0001 | c0001 | t0010 | g0025 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0349 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0337 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18981 | hp2 | a0004 | c0004 | t0001 | g0225 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18982 | hp1 | a0001 | c0001 | t0007 | g0248 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0344 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18986 | hp2 | a0002 | c0002 | t0003 | g0287 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18992 | hp1 | a0001 | c0001 | t0006 | g0110 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0340 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18994 | hp2 | a0002 | c0002 | t0003 | g0301 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0185 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18997 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19001 | hp2 | a0001 | c0001 | t0007 | g0136 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19002 | hp1 | a0002 | c0002 | t0003 | g0295 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19002 | hp2 | a0001 | c0001 | t0007 | g0116 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19005 | hp1 | a0002 | c0002 | t0003 | g0288 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0355 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0357 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19011 | hp1 | a0001 | c0001 | t0013 | g0235 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19011 | hp2 | a0006 | c0006 | t0002 | g0354 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19012 | hp1 | a0002 | c0002 | t0003 | g0299 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | LWK | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0316 | AFR | LWK | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | LWK | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19043 | hp2 | a0002 | c0002 | t0009 | g0282 | AFR | LWK | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19055 | hp1 | a0002 | c0002 | t0003 | g0328 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19055 | hp2 | a0005 | c0007 | t0002 | g0351 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0342 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19058 | hp2 | a0001 | c0001 | t0007 | g0251 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19060 | hp1 | a0001 | c0001 | t0013 | g0269 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0348 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0341 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0362 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0302 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0364 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19077 | hp2 | a0004 | c0004 | t0001 | g0132 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0334 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19083 | hp1 | a0004 | c0004 | t0001 | g0221 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0352 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19085 | hp1 | a0001 | c0001 | t0020 | g0148 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19086 | hp2 | a0004 | c0004 | t0001 | g0223 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0087 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19240 | hp1 | a0002 | c0002 | t0003 | g0321 | AFR | YRI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0306 | AFR | YRI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0280 | AFR | ASW | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0358 | AFR | ASW | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA20752 | hp1 | a0001 | c0005 | t0001 | g0141 | EUR | TSI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | GIH | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | GIH | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0092 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0311 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0084 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | USA | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0315 | AFR | USA | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | LWK | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0211 | REF | REF | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0176 | REF | REF | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:64552061
|
G | A | 1 | a0007 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.587G>A | p.Gly196Glu | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 904/4098 | 587/2811 | 196/936 | chr2 | 64552061 | ||
| chr2:64552187
|
C | T | 1 | a0008 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.713C>T | p.Ser238Phe | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1030/4098 | 713/2811 | 238/936 | chr2 | 64552187 | ||
| chr2:64552318
|
G | A | 1 | a0004 | 4 | NA18981.hp2 NA19077.hp2 NA19083.hp1 others(1): Show |
missense_variant | MODERATE | c.844G>A | p.Gly282Ser | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1161/4098 | 844/2811 | 282/936 | chr2 | 64552318 | ||
| chr2:64552375
|
G | A | 4 | a0002a0005a0006others(1): Show | 91 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
missense_variant | MODERATE | c.901G>A | p.Glu301Lys | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1218/4098 | 901/2811 | 301/936 | chr2 | 64552375 | ||
| chr2:64552492
|
T | C | 1 | a0003 | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.1018T>C | p.Ser340Pro | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1335/4098 | 1018/2811 | 340/936 | chr2 | 64552492 | ||
| chr2:64552528
|
T | C | 1 | a0012 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1054T>C | p.Cys352Arg | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1371/4098 | 1054/2811 | 352/936 | chr2 | 64552528 | ||
| chr2:64553123
|
A | G | 1 | a0005 | 3 | HG03486.hp2 NA18946.hp2 NA19055.hp2 |
missense_variant | MODERATE | c.1649A>G | p.Asn550Ser | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1966/4098 | 1649/2811 | 550/936 | chr2 | 64553123 | ||
| chr2:64553225
|
C | G | 1 | a0009 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.1751C>G | p.Ser584Cys | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 2068/4098 | 1751/2811 | 584/936 | chr2 | 64553225 | ||
| chr2:64553337
|
C | G | 1 | a0011 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1863C>G | p.His621Gln | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 2180/4098 | 1863/2811 | 621/936 | chr2 | 64553337 | ||
| chr2:64581253
|
G | A | 1 | a0006 | 2 | HG00408.hp2 NA19011.hp2 |
missense_variant | MODERATE | c.2519G>A | p.Ser840Asn | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/10 | 2836/4098 | 2519/2811 | 840/936 | chr2 | 64581253 | ||
| chr2:64592009
|
A | C | 1 | a0010 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.2785A>C | p.Ser929Arg | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 3102/4098 | 2785/2811 | 929/936 | chr2 | 64592009 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:64551852
|
T | C | 1 | a0005c0008 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.378T>C | p.Asp126Asp | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 695/4098 | 378/2811 | 126/936 | chr2 | 64551852 | ||
| chr2:64552248
|
A | T | 1 | a0001c0016 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.774A>T | p.Ala258Ala | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1091/4098 | 774/2811 | 258/936 | chr2 | 64552248 | ||
| chr2:64553010
|
A | G | 2 | a0001c0005a0002c0010 | 4 | HG00099.hp2 HG02683.hp1 HG02723.hp2 others(1): Show |
synonymous_variant | LOW | c.1536A>G | p.Gln512Gln | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1853/4098 | 1536/2811 | 512/936 | chr2 | 64553010 | ||
| chr2:64592029
|
C | T | 1 | a0001c0012 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.2805C>T | p.Asp935Asp | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 3122/4098 | 2805/2811 | 935/936 | chr2 | 64592029 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:64524355
|
G | A | 1 | a0001c0001t0015 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-290G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/10 | 27120 | chr2 | 64524355 | |||||
| chr2:64524402
|
G | A | 1 | a0002c0010t0016 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-243G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/10 | 27073 | chr2 | 64524402 | |||||
| chr2:64524404
|
A | C | 1 | a0001c0001t0020 | 1 | NA19085.hp1 | 5_prime_UTR_variant | MODIFIER | c.-241A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/10 | 27071 | chr2 | 64524404 | |||||
| chr2:64524485
|
C | G | 1 | a0001c0001t0013 | 3 | NA18946.hp1 NA19011.hp1 NA19060.hp1 |
5_prime_UTR_variant | MODIFIER | c.-160C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/10 | 26990 | chr2 | 64524485 | |||||
| chr2:64524601
|
C | T | 1 | a0002c0002t0019 | 1 | HG03041.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-44C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/10 | chr2 | 64524601 | ||||||
| chr2:64592115
|
T | TA | 7 | a0001c0001t0002a0001c0001t0006a0002c0002t0002others(4): Show | 67 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*100dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 101 | INFO_REALIGN_3_PRIME | chr2 | 64592115 | ||||
| chr2:64592115
|
T | TAA | 6 | a0001c0001t0003a0001c0001t0011a0001c0001t0014others(3): Show | 51 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*99_*100dupAA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 101 | INFO_REALIGN_3_PRIME | chr2 | 64592115 | ||||
| chr2:64592115
|
T | TAAA | 7 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(4): Show | 83 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*98_*100dupAAA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 101 | INFO_REALIGN_3_PRIME | chr2 | 64592115 | ||||
| chr2:64592115
|
TA | T | 1 | a0001c0001t0007 | 8 | HG01168.hp2 HG01169.hp1 HG02896.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*100delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 100 | INFO_REALIGN_3_PRIME | chr2 | 64592115 | ||||
| chr2:64592246
|
G | A | 4 | a0001c0001t0005a0001c0001t0011a0001c0001t0012others(1): Show | 44 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*211G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 211 | chr2 | 64592246 | |||||
| chr2:64592381
|
G | A | 1 | a0001c0001t0018 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*346G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 346 | chr2 | 64592381 | |||||
| chr2:64592516
|
G | A | 1 | a0003c0003t0008 | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*481G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 481 | chr2 | 64592516 | |||||
| chr2:64592575
|
G | A | 1 | a0010c0013t0017 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*540G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 540 | chr2 | 64592575 | |||||
| chr2:64592605
|
T | TAATC | 14 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(11): Show | 110 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*573_*574insCAAT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 574 | INFO_REALIGN_3_PRIME | chr2 | 64592605 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:64524619
|
G | T | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | splice_region_variant&intron_variant | LOW | c.-33+7G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64524619 | ||||||
| chr2:64524881
|
C | T | 90 | a0001c0001t0001g0332a0001c0001t0004g0363a0001c0001t0004g0364others(87): Show | 92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-33+269C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64524881 | ||||||
| chr2:64524926
|
T | C | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+314T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64524926 | ||||||
| chr2:64524938
|
G | A | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-33+326G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64524938 | ||||||
| chr2:64524952
|
C | T | 1 | a0002c0002t0002g0366 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-33+340C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64524952 | ||||||
| chr2:64525009
|
C | T | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | NA18987.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-33+397C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525009 | ||||||
| chr2:64525088
|
A | G | 1 | a0001c0001t0004g0276 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-33+476A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525088 | ||||||
| chr2:64525160
|
T | C | 201 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(198): Show | 205 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.-33+548T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525160 | ||||||
| chr2:64525320
|
G | A | 1 | a0005c0008t0005g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-33+708G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525320 | ||||||
| chr2:64525320
|
G | T | 1 | a0001c0001t0005g0113 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-33+708G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525320 | ||||||
| chr2:64525346
|
A | G | 1 | a0002c0002t0002g0365 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-33+734A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525346 | ||||||
| chr2:64525359
|
A | G | 92 | a0001c0001t0001g0332a0001c0001t0004g0363a0001c0001t0004g0364others(89): Show | 94 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.-33+747A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525359 | ||||||
| chr2:64525506
|
A | G | 6 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | NA18954.hp2 NA18957.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+894A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525506 | ||||||
| chr2:64525507
|
A | C | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+895A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525507 | ||||||
| chr2:64525580
|
C | A | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-33+968C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525580 | ||||||
| chr2:64525738
|
A | G | 241 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(238): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-33+1126A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525738 | ||||||
| chr2:64525776
|
A | G | 89 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(86): Show | 91 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-33+1164A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525776 | ||||||
| chr2:64525807
|
C | A | 1 | a0003c0003t0008g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-33+1195C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525807 | ||||||
| chr2:64525959
|
T | C | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+1347T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525959 | ||||||
| chr2:64526065
|
T | G | 1 | a0012c0011t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-33+1453T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526065 | ||||||
| chr2:64526129
|
C | T | 90 | a0001c0001t0001g0332a0001c0001t0014g0006a0002c0002t0001g0004others(87): Show | 92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-33+1517C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526129 | ||||||
| chr2:64526196
|
T | A | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-33+1584T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526196 | ||||||
| chr2:64526315
|
A | G | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+1703A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526315 | ||||||
| chr2:64526542
|
T | C | 3 | a0001c0001t0001g0114a0001c0001t0003g0007a0001c0001t0003g0008 | 3 | HG00741.hp2 HG01496.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-33+1930T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526542 | ||||||
| chr2:64526595
|
C | T | 1 | a0001c0001t0013g0269 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-33+1983C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526595 | ||||||
| chr2:64526600
|
C | T | 108 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(105): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-33+1988C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526600 | ||||||
| chr2:64526645
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-33+2033T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526645 | ||||||
| chr2:64526701
|
A | T | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+2089A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526701 | ||||||
| chr2:64526714
|
A | T | 35 | a0001c0001t0001g0332a0002c0002t0002g0005a0002c0002t0002g0333others(32): Show | 36 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(33): Show |
intron_variant | MODIFIER | c.-33+2102A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526714 | ||||||
| chr2:64526721
|
A | G | 2 | a0001c0001t0009g0267a0010c0013t0017g0268 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-33+2109A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526721 | ||||||
| chr2:64526991
|
T | G | 2 | a0001c0001t0001g0115a0001c0001t0007g0116 | 2 | NA18952.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-33+2379T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526991 | ||||||
| chr2:64527212
|
T | C | 33 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(30): Show | 34 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.-33+2600T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527212 | ||||||
| chr2:64527242
|
G | A | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-33+2630G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527242 | ||||||
| chr2:64527441
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-33+2829G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527441 | ||||||
| chr2:64527489
|
G | A | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-33+2877G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527489 | ||||||
| chr2:64527495
|
G | A | 34 | a0001c0001t0001g0332a0002c0002t0002g0005a0002c0002t0002g0333others(31): Show | 35 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.-33+2883G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527495 | ||||||
| chr2:64527580
|
C | CA | 243 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(240): Show | 248 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.-33+2981dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64527580 | |||||
| chr2:64527627
|
A | G | 6 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+3015A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527627 | ||||||
| chr2:64527825
|
C | T | 1 | a0002c0002t0003g0329 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-33+3213C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527825 | ||||||
| chr2:64527829
|
C | G | 1 | a0002c0002t0003g0328 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-33+3217C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527829 | ||||||
| chr2:64527863
|
A | G | 2 | a0001c0001t0002g0109a0001c0001t0005g0108 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-33+3251A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527863 | ||||||
| chr2:64528162
|
C | A | 88 | a0001c0001t0001g0332a0001c0001t0014g0006a0002c0002t0001g0004others(85): Show | 90 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-33+3550C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528162 | ||||||
| chr2:64528381
|
C | A | 88 | a0001c0001t0001g0332a0001c0001t0014g0006a0002c0002t0001g0004others(85): Show | 90 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-33+3769C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528381 | ||||||
| chr2:64528657
|
G | C | 1 | a0001c0001t0004g0030 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-33+4045G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528657 | ||||||
| chr2:64528750
|
G | A | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-33+4138G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528750 | ||||||
| chr2:64528762
|
G | A | 1 | a0001c0001t0004g0031 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-33+4150G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528762 | ||||||
| chr2:64528800
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-33+4188G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528800 | ||||||
| chr2:64528842
|
G | A | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-33+4230G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528842 | ||||||
| chr2:64528920
|
T | C | 1 | a0002c0002t0003g0330 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-33+4308T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528920 | ||||||
| chr2:64529111
|
A | G | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-33+4499A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529111 | ||||||
| chr2:64529150
|
T | C | 1 | a0001c0001t0005g0032 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-33+4538T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529150 | ||||||
| chr2:64529315
|
G | GT | 88 | a0001c0001t0001g0231a0001c0001t0001g0332a0001c0001t0014g0006others(85): Show | 90 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-33+4715dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64529315 | |||||
| chr2:64529315
|
G | GTT | 111 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-33+4714_-33+4715d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64529315 | |||||
| chr2:64529347
|
A | G | 1 | a0002c0002t0002g0361 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-33+4735A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529347 | ||||||
| chr2:64529528
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-33+4916T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529528 | ||||||
| chr2:64529584
|
G | A | 201 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(198): Show | 205 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.-33+4972G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529584 | ||||||
| chr2:64529633
|
CT | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(149): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-33+5035delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64529633 | |||||
| chr2:64529758
|
T | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-33+5146T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529758 | ||||||
| chr2:64529775
|
G | A | 2 | a0001c0001t0005g0035a0001c0001t0011g0034 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-33+5163G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529775 | ||||||
| chr2:64529786
|
T | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(150): Show | 156 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.-33+5174T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529786 | ||||||
| chr2:64529891
|
C | T | 86 | a0001c0001t0001g0332a0002c0002t0001g0004a0002c0002t0001g0312others(83): Show | 88 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.-33+5279C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529891 | ||||||
| chr2:64529892
|
G | A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-33+5280G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529892 | ||||||
| chr2:64530087
|
T | C | 1 | a0002c0002t0002g0285 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-33+5475T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530087 | ||||||
| chr2:64530167
|
A | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-33+5555A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530167 | ||||||
| chr2:64530362
|
T | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(150): Show | 156 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.-33+5750T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530362 | ||||||
| chr2:64530693
|
T | G | 1 | a0001c0001t0003g0009 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-33+6081T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530693 | ||||||
| chr2:64530705
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-33+6093C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530705 | ||||||
| chr2:64530716
|
C | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(29): Show | 33 | HG01243.hp1 HG01261.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-33+6104C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530716 | ||||||
| chr2:64530780
|
G | A | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-33+6168G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530780 | ||||||
| chr2:64530797
|
C | T | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-33+6185C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530797 | ||||||
| chr2:64530830
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-33+6218G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530830 | ||||||
| chr2:64530832
|
C | T | 1 | a0001c0001t0004g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-33+6220C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530832 | ||||||
| chr2:64530891
|
G | A | 2 | a0002c0002t0002g0285a0002c0002t0002g0365 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-33+6279G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530891 | ||||||
| chr2:64530936
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-33+6324C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530936 | ||||||
| chr2:64530946
|
C | T | 1 | a0008c0017t0003g0326 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-33+6334C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530946 | ||||||
| chr2:64530987
|
G | A | 1 | a0001c0001t0004g0031 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-33+6375G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530987 | ||||||
| chr2:64530989
|
G | A | 3 | a0001c0001t0013g0235a0001c0001t0013g0236a0001c0001t0013g0269 | 3 | NA18946.hp1 NA19011.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-33+6377G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530989 | ||||||
| chr2:64531061
|
C | CA | 34 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0128others(31): Show | 35 | HG01261.hp1 HG01261.hp2 HG01993.hp1 others(32): Show |
intron_variant | MODIFIER | c.-33+6469dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64531061 | |||||
| chr2:64531061
|
C | CAA | 105 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(102): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-33+6468_-33+6469d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64531061 | |||||
| chr2:64531061
|
C | CAAA | 8 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0004g0036others(5): Show | 8 | HG00621.hp1 HG02135.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33+6467_-33+6469d others(5): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64531061 | |||||
| chr2:64531061
|
CA | C | 29 | a0001c0001t0001g0262a0001c0001t0014g0006a0002c0002t0001g0004others(26): Show | 30 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.-33+6469delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64531061 | |||||
| chr2:64531079
|
AAAC | A | 34 | a0001c0001t0001g0332a0002c0002t0002g0005a0002c0002t0002g0333others(31): Show | 35 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.-33+6469_-33+6471d others(5): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64531079 | |||||
| chr2:64531081
|
AC | A | 4 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0261others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+6470delC | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64531081 | ||||||
| chr2:64531082
|
C | A | 1 | a0001c0001t0001g0257 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-33+6470C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64531082 | ||||||
| chr2:64531276
|
G | A | 111 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-33+6664G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64531276 | ||||||
| chr2:64531546
|
A | G | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+6934A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64531546 | ||||||
| chr2:64531584
|
A | G | 1 | a0002c0002t0019g0360 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-33+6972A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64531584 | ||||||
| chr2:64532011
|
C | T | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-33+7399C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532011 | ||||||
| chr2:64532186
|
CTGTAAGT others(12): Show |
C | 9 | a0002c0002t0002g0281a0002c0002t0002g0285a0002c0002t0002g0286others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33+7577_-33+7595d others(21): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64532186 | |||||
| chr2:64532308
|
G | T | 199 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(196): Show | 203 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.-33+7696G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532308 | ||||||
| chr2:64532310
|
G | A | 88 | a0001c0001t0001g0332a0002c0002t0001g0004a0002c0002t0001g0312others(85): Show | 90 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-33+7698G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532310 | ||||||
| chr2:64532337
|
T | A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-33+7725T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532337 | ||||||
| chr2:64532344
|
A | T | 2 | a0001c0001t0001g0120a0001c0001t0004g0230 | 2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-33+7732A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532344 | ||||||
| chr2:64532750
|
G | C | 1 | a0001c0001t0006g0033 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-33+8138G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532750 | ||||||
| chr2:64532892
|
C | A | 1 | a0001c0001t0001g0257 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-33+8280C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532892 | ||||||
| chr2:64532914
|
G | C | 1 | a0001c0001t0006g0253 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-33+8302G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532914 | ||||||
| chr2:64532985
|
G | A | 240 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(237): Show | 245 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.-33+8373G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532985 | ||||||
| chr2:64533088
|
T | C | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-33+8476T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533088 | ||||||
| chr2:64533209
|
G | A | 35 | a0001c0001t0001g0332a0002c0002t0002g0005a0002c0002t0002g0333others(32): Show | 36 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(33): Show |
intron_variant | MODIFIER | c.-33+8597G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533209 | ||||||
| chr2:64533398
|
G | C | 1 | a0001c0001t0004g0103 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-33+8786G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533398 | ||||||
| chr2:64533487
|
T | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(146): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-33+8875T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533487 | ||||||
| chr2:64533607
|
G | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(146): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-33+8995G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533607 | ||||||
| chr2:64533611
|
A | G | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-33+8999A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533611 | ||||||
| chr2:64533669
|
A | G | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-33+9057A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533669 | ||||||
| chr2:64533990
|
A | G | 23 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(20): Show | 24 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.-33+9378A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533990 | ||||||
| chr2:64533996
|
T | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(146): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-33+9384T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533996 | ||||||
| chr2:64534075
|
T | C | 2 | a0001c0001t0002g0109a0001c0001t0005g0108 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-33+9463T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534075 | ||||||
| chr2:64534107
|
GT | G | 14 | a0001c0001t0001g0042a0001c0001t0004g0001a0001c0001t0004g0030others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-33+9499delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64534107 | |||||
| chr2:64534337
|
T | C | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-33+9725T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534337 | ||||||
| chr2:64534351
|
AT | A | 91 | a0001c0001t0001g0332a0001c0001t0014g0006a0002c0002t0001g0004others(88): Show | 93 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-33+9745delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64534351 | |||||
| chr2:64534419
|
C | T | 91 | a0001c0001t0001g0332a0001c0001t0014g0006a0002c0002t0001g0004others(88): Show | 93 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-33+9807C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534419 | ||||||
| chr2:64534580
|
A | G | 1 | a0002c0002t0002g0285 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-33+9968A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534580 | ||||||
| chr2:64534582
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-33+9970G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534582 | ||||||
| chr2:64534742
|
GT | G | 233 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(230): Show | 238 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.-33+10144delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64534742 | |||||
| chr2:64534764
|
T | G | 23 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(20): Show | 24 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.-33+10152T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534764 | ||||||
| chr2:64534906
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-33+10294C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534906 | ||||||
| chr2:64534996
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-33+10384C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534996 | ||||||
| chr2:64535206
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-33+10594C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535206 | ||||||
| chr2:64535229
|
A | G | 1 | a0002c0002t0002g0357 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-33+10617A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535229 | ||||||
| chr2:64535284
|
AGTATCAT others(5): Show |
A | 6 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+10673_-33+1068 others(16): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535284 | ||||||
| chr2:64535331
|
C | T | 107 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(104): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.-33+10719C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535331 | ||||||
| chr2:64535358
|
C | T | 2 | a0001c0001t0005g0101a0001c0001t0005g0102 | 2 | HG00140.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.-33+10746C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535358 | ||||||
| chr2:64535454
|
C | A | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+10842C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535454 | ||||||
| chr2:64535568
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-33+10956G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535568 | ||||||
| chr2:64535589
|
ATG | A | 91 | a0001c0001t0001g0332a0001c0001t0014g0006a0002c0002t0001g0004others(88): Show | 93 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-33+10979_-33+1098 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64535589 | |||||
| chr2:64535771
|
C | CAT | 199 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(196): Show | 203 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.-33+11159_-33+1116 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535771 | ||||||
| chr2:64536023
|
G | T | 1 | a0001c0001t0005g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-33+11411G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64536023 | ||||||
| chr2:64536102
|
T | C | 1 | a0001c0001t0004g0053 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-33+11490T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64536102 | ||||||
| chr2:64536404
|
T | TAAAAATA others(172): Show |
1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-33+11807_-33+1180 others(183): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536404 | |||||
| chr2:64536532
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-33+11920A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64536532 | ||||||
| chr2:64536537
|
G | A | 1 | a0001c0001t0004g0011 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-33+11925G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64536537 | ||||||
| chr2:64536566
|
TA | T | 17 | a0001c0001t0001g0222a0001c0001t0001g0224a0001c0001t0001g0226others(14): Show | 17 | HG01515.hp2 HG02027.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.-33+11977delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536566 | |||||
| chr2:64536566
|
TAA | T | 95 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(92): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-33+11976_-33+1197 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536566 | |||||
| chr2:64536566
|
TAAA | T | 6 | a0001c0001t0002g0109a0001c0001t0004g0052a0001c0001t0004g0097others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+11975_-33+1197 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536566 | |||||
| chr2:64536566
|
TAAAA | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(36): Show | 40 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.-33+11974_-33+1197 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536566 | |||||
| chr2:64536566
|
TAAAAAAA others(2): Show |
T | 85 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(82): Show | 87 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.-33+11969_-33+1197 others(13): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536566 | |||||
| chr2:64536566
|
TAAAAAAA others(3): Show |
T | 2 | a0002c0002t0003g0280a0002c0002t0003g0305 | 2 | HG00558.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-33+11968_-33+1197 others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536566 | |||||
| chr2:64536640
|
A | G | 23 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(20): Show | 24 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.-33+12028A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64536640 | ||||||
| chr2:64536720
|
A | G | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-33+12108A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64536720 | ||||||
| chr2:64536856
|
A | G | 38 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(35): Show | 39 | HG01243.hp1 HG01261.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.-33+12244A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64536856 | ||||||
| chr2:64536951
|
C | CA | 6 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0001g0271others(3): Show | 6 | HG02683.hp2 HG02738.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+12363dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536951 | |||||
| chr2:64536951
|
CA | C | 22 | a0001c0001t0001g0124a0001c0001t0001g0135a0001c0001t0001g0219others(19): Show | 23 | HG01106.hp2 HG01496.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-33+12363delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536951 | |||||
| chr2:64536951
|
CAA | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0238others(93): Show | 98 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-33+12362_-33+1236 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536951 | |||||
| chr2:64536951
|
CAAA | C | 82 | a0001c0001t0001g0042a0001c0001t0001g0107a0001c0001t0001g0254others(79): Show | 84 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-33+12361_-33+1236 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536951 | |||||
| chr2:64536951
|
CAAAA | C | 37 | a0001c0001t0001g0095a0001c0001t0002g0021a0001c0001t0002g0109others(34): Show | 37 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-33+12360_-33+1236 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536951 | |||||
| chr2:64537078
|
C | T | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-33+12466C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64537078 | ||||||
| chr2:64537107
|
T | C | 89 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(86): Show | 91 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-33+12495T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64537107 | ||||||
| chr2:64537111
|
C | T | 234 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(231): Show | 239 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.-33+12499C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64537111 | ||||||
| chr2:64537129
|
T | TA | 235 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(232): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.-33+12523dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64537129 | |||||
| chr2:64537268
|
A | G | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0015g0218 | 3 | HG02280.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-33+12656A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64537268 | ||||||
| chr2:64537369
|
C | T | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+12757C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64537369 | ||||||
| chr2:64537798
|
T | A | 1 | a0001c0001t0001g0258 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-33+13186T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64537798 | ||||||
| chr2:64538122
|
A | T | 9 | a0001c0001t0001g0214a0001c0001t0001g0215a0002c0002t0002g0283others(6): Show | 9 | HG00558.hp2 HG02145.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-32-13321A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538122 | ||||||
| chr2:64538207
|
C | T | 1 | a0001c0001t0006g0213 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-32-13236C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538207 | ||||||
| chr2:64538340
|
T | G | 238 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(235): Show | 243 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.-32-13103T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538340 | ||||||
| chr2:64538363
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-32-13080A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538363 | ||||||
| chr2:64538418
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-32-13025G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538418 | ||||||
| chr2:64538425
|
C | T | 143 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(140): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-32-13018C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538425 | ||||||
| chr2:64538457
|
C | T | 3 | a0001c0001t0004g0092a0001c0001t0004g0093a0001c0001t0004g0094 | 3 | HG01123.hp1 HG01167.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-32-12986C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538457 | ||||||
| chr2:64538608
|
G | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG00323.hp2 HG01433.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-12835G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538608 | ||||||
| chr2:64538620
|
C | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG00323.hp2 HG01433.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-12823C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538620 | ||||||
| chr2:64538644
|
T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-12799T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538644 | ||||||
| chr2:64538831
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-32-12612T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538831 | ||||||
| chr2:64538866
|
GCTT | G | 38 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(35): Show | 39 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.-32-12573_-32-1257 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64538866 | |||||
| chr2:64538984
|
A | AT | 235 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(232): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.-32-12453dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64538984 | |||||
| chr2:64539124
|
A | C | 9 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(6): Show | 10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-12319A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539124 | ||||||
| chr2:64539156
|
G | A | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-32-12287G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539156 | ||||||
| chr2:64539168
|
T | G | 1 | a0001c0001t0005g0056 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-32-12275T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539168 | ||||||
| chr2:64539191
|
G | A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-12252G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539191 | ||||||
| chr2:64539365
|
A | G | 22 | a0001c0001t0002g0021a0001c0001t0003g0007a0001c0001t0003g0008others(19): Show | 22 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-32-12078A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539365 | ||||||
| chr2:64539376
|
G | GT | 9 | a0002c0002t0002g0281a0002c0002t0002g0285a0002c0002t0002g0286others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-12061dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64539376 | |||||
| chr2:64539434
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-32-12009T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539434 | ||||||
| chr2:64539518
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-32-11925T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539518 | ||||||
| chr2:64539594
|
T | C | 3 | a0002c0002t0001g0312a0002c0002t0001g0313a0002c0002t0001g0314 | 3 | HG02280.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-32-11849T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539594 | ||||||
| chr2:64539676
|
G | C | 5 | a0002c0002t0002g0285a0002c0002t0002g0286a0002c0002t0002g0306others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-11767G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539676 | ||||||
| chr2:64539702
|
A | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(36): Show | 40 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.-32-11741A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539702 | ||||||
| chr2:64539779
|
A | T | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-32-11664A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539779 | ||||||
| chr2:64539785
|
G | T | 5 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(2): Show | 5 | HG02080.hp2 HG02155.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-11658G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539785 | ||||||
| chr2:64539844
|
G | A | 35 | a0002c0002t0002g0005a0002c0002t0002g0333a0002c0002t0002g0334others(32): Show | 36 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(33): Show |
intron_variant | MODIFIER | c.-32-11599G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539844 | ||||||
| chr2:64539891
|
TGAG | T | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-11545_-32-1154 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64539891 | |||||
| chr2:64540003
|
G | GTGATGGA others(2902): Show |
1 | a0002c0002t0003g0304 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-32-11425_-32-1142 others(2913): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64540003 | |||||
| chr2:64540128
|
C | T | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-32-11315C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540128 | ||||||
| chr2:64540163
|
A | C | 1 | a0001c0001t0005g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-32-11280A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540163 | ||||||
| chr2:64540321
|
A | G | 1 | a0005c0008t0005g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-32-11122A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540321 | ||||||
| chr2:64540340
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-32-11103A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540340 | ||||||
| chr2:64540546
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0133 | 2 | NA18998.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-32-10897G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540546 | ||||||
| chr2:64540629
|
A | G | 240 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(237): Show | 245 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.-32-10814A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540629 | ||||||
| chr2:64540646
|
T | C | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-10797T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540646 | ||||||
| chr2:64540656
|
A | T | 1 | a0001c0001t0001g0203 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-32-10787A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540656 | ||||||
| chr2:64540797
|
C | T | 3 | a0001c0001t0004g0092a0001c0001t0004g0093a0001c0001t0004g0094 | 3 | HG01123.hp1 HG01167.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-32-10646C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540797 | ||||||
| chr2:64540815
|
C | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-10628C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540815 | ||||||
| chr2:64540854
|
T | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-32-10589T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540854 | ||||||
| chr2:64540867
|
G | A | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-10576G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540867 | ||||||
| chr2:64540940
|
C | G | 2 | a0002c0002t0003g0324a0002c0002t0010g0323 | 2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-32-10503C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540940 | ||||||
| chr2:64540943
|
A | G | 1 | a0001c0001t0005g0102 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-32-10500A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540943 | ||||||
| chr2:64540957
|
A | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-10486A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540957 | ||||||
| chr2:64540992
|
AC | A | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-10450delC | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540992 | ||||||
| chr2:64540993
|
C | T | 21 | a0001c0001t0001g0129a0001c0001t0001g0188a0001c0001t0001g0189others(18): Show | 21 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.-32-10450C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540993 | ||||||
| chr2:64540994
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-32-10449G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540994 | ||||||
| chr2:64541061
|
T | C | 108 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(105): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-32-10382T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541061 | ||||||
| chr2:64541103
|
C | A | 38 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(35): Show | 39 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.-32-10340C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541103 | ||||||
| chr2:64541133
|
CAT | C | 14 | a0001c0001t0001g0042a0001c0001t0004g0001a0001c0001t0004g0030others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-32-10307_-32-1030 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64541133 | |||||
| chr2:64541254
|
C | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0226a0001c0001t0004g0121 | 3 | HG01515.hp2 HG01928.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-32-10189C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541254 | ||||||
| chr2:64541424
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-32-10019C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541424 | ||||||
| chr2:64541440
|
C | T | 1 | a0002c0002t0001g0319 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-32-10003C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541440 | ||||||
| chr2:64541490
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-32-9953A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541490 | ||||||
| chr2:64541576
|
G | T | 1 | a0012c0011t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-32-9867G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541576 | ||||||
| chr2:64541650
|
G | T | 1 | a0001c0001t0001g0187 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-32-9793G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541650 | ||||||
| chr2:64541829
|
A | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-9614A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541829 | ||||||
| chr2:64542018
|
C | T | 1 | a0002c0002t0003g0303 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-32-9425C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542018 | ||||||
| chr2:64542020
|
A | G | 2 | a0002c0002t0002g0285a0002c0002t0002g0365 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-32-9423A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542020 | ||||||
| chr2:64542034
|
A | T | 1 | a0001c0001t0002g0186 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-32-9409A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542034 | ||||||
| chr2:64542090
|
T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-9353T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542090 | ||||||
| chr2:64542234
|
G | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(36): Show | 40 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.-32-9209G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542234 | ||||||
| chr2:64542250
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-32-9193C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542250 | ||||||
| chr2:64542301
|
T | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-32-9142T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542301 | ||||||
| chr2:64542347
|
C | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-32-9096C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542347 | ||||||
| chr2:64542415
|
A | G | 1 | a0003c0003t0008g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-32-9028A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542415 | ||||||
| chr2:64542525
|
T | A | 9 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(6): Show | 10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-8918T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542525 | ||||||
| chr2:64542624
|
C | T | 2 | a0001c0001t0003g0016a0001c0001t0004g0090 | 2 | HG03669.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.-32-8819C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542624 | ||||||
| chr2:64542805
|
ATGTT | A | 106 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(103): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-32-8634_-32-8631d others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64542805 | |||||
| chr2:64542892
|
A | G | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-8551A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542892 | ||||||
| chr2:64542957
|
T | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-8486T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542957 | ||||||
| chr2:64543133
|
C | A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-8310C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543133 | ||||||
| chr2:64543253
|
T | C | 1 | a0001c0001t0001g0332 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-8190T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543253 | ||||||
| chr2:64543291
|
C | T | 5 | a0001c0001t0006g0125a0001c0001t0006g0185a0002c0002t0002g0285others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-8152C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543291 | ||||||
| chr2:64543391
|
A | G | 148 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(145): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.-32-8052A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543391 | ||||||
| chr2:64543419
|
T | C | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-32-8024T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543419 | ||||||
| chr2:64543645
|
A | G | 108 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(105): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-32-7798A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543645 | ||||||
| chr2:64543703
|
G | A | 1 | a0001c0005t0001g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-32-7740G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543703 | ||||||
| chr2:64543747
|
T | C | 108 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(105): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-32-7696T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543747 | ||||||
| chr2:64543773
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-32-7670T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543773 | ||||||
| chr2:64543847
|
C | G | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-7596C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543847 | ||||||
| chr2:64543865
|
C | T | 6 | a0001c0001t0009g0267a0003c0003t0008g0232a0003c0003t0008g0263others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-7578C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543865 | ||||||
| chr2:64543952
|
C | G | 2 | a0002c0002t0002g0281a0002c0002t0002g0327 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-32-7491C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543952 | ||||||
| chr2:64544006
|
T | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-32-7437T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544006 | ||||||
| chr2:64544137
|
A | G | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-32-7306A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544137 | ||||||
| chr2:64544141
|
C | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-32-7302C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544141 | ||||||
| chr2:64544311
|
G | C | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-32-7132G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544311 | ||||||
| chr2:64544366
|
C | T | 34 | a0002c0002t0002g0005a0002c0002t0002g0333a0002c0002t0002g0334others(31): Show | 35 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.-32-7077C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544366 | ||||||
| chr2:64544468
|
T | C | 237 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(234): Show | 242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.-32-6975T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544468 | ||||||
| chr2:64544505
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-32-6938G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544505 | ||||||
| chr2:64544594
|
CCT | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(28): Show | 32 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(29): Show |
intron_variant | MODIFIER | c.-32-6848_-32-6847d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544594 | ||||||
| chr2:64544650
|
T | TAGAAATG others(319): Show |
1 | a0001c0001t0001g0242 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-32-6777_-32-6776i others(328): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64544650 | |||||
| chr2:64544650
|
T | TAGAAATG others(318): Show |
20 | a0001c0001t0001g0003a0001c0001t0001g0237a0001c0001t0001g0238others(17): Show | 21 | HG01243.hp1 HG01993.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.-32-6777_-32-6776i others(327): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64544650 | |||||
| chr2:64544650
|
T | TAGAAATG others(317): Show |
11 | a0001c0001t0001g0234a0001c0001t0001g0256a0001c0001t0001g0257others(8): Show | 11 | HG01109.hp2 HG02486.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32-6777_-32-6776i others(326): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64544650 | |||||
| chr2:64544650
|
T | TAGAAATG others(315): Show |
5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-6777_-32-6776i others(324): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64544650 | |||||
| chr2:64544650
|
T | TAGAAATG others(314): Show |
1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-32-6777_-32-6776i others(323): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64544650 | |||||
| chr2:64544650
|
T | TAGAAATG others(317): Show |
1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-32-6777_-32-6776i others(326): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64544650 | |||||
| chr2:64544771
|
C | T | 9 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(6): Show | 10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-6672C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544771 | ||||||
| chr2:64544809
|
C | G | 7 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0089others(4): Show | 7 | HG02027.hp2 HG02132.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-6634C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544809 | ||||||
| chr2:64544874
|
C | T | 79 | a0002c0002t0002g0005a0002c0002t0002g0111a0002c0002t0002g0112others(76): Show | 80 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.-32-6569C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544874 | ||||||
| chr2:64544885
|
G | A | 227 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(224): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-32-6558G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544885 | ||||||
| chr2:64544892
|
A | G | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-32-6551A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544892 | ||||||
| chr2:64545012
|
C | T | 40 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(37): Show | 41 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.-32-6431C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545012 | ||||||
| chr2:64545089
|
G | T | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-32-6354G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545089 | ||||||
| chr2:64545122
|
A | G | 1 | a0001c0001t0001g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-32-6321A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545122 | ||||||
| chr2:64545137
|
A | T | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-6306A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545137 | ||||||
| chr2:64545319
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-32-6124C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545319 | ||||||
| chr2:64545475
|
T | C | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-5968T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545475 | ||||||
| chr2:64545570
|
T | TA | 28 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0124others(25): Show | 28 | HG00323.hp2 HG01071.hp1 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.-32-5831dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
T | TAA | 20 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0001g0137others(17): Show | 20 | HG00597.hp1 HG00621.hp2 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.-32-5832_-32-5831d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
T | TAAA | 10 | a0001c0001t0001g0150a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00280.hp1 HG00558.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-5833_-32-5831d others(5): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
T | TAAAAA | 7 | a0001c0001t0001g0126a0001c0001t0001g0149a0001c0001t0001g0189others(4): Show | 7 | HG00597.hp2 HG00642.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-5835_-32-5831d others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
T | TAAAAAAA | 9 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0144others(6): Show | 9 | HG00140.hp1 HG01175.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-32-5837_-32-5831d others(9): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
T | TAAAAAAA others(1): Show |
7 | a0001c0001t0001g0114a0001c0001t0001g0143a0001c0001t0001g0270others(4): Show | 7 | HG00741.hp2 HG03831.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-5838_-32-5831d others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0001g0220 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-32-5840_-32-5831d others(12): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
T | TAAAAAAA others(4): Show |
1 | a0001c0001t0001g0142 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-32-5841_-32-5831d others(13): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
T | TAAAAAAA others(7): Show |
1 | a0001c0001t0001g0188 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-32-5844_-32-5831d others(16): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAA | T | 17 | a0001c0001t0001g0178a0002c0002t0002g0292a0002c0002t0002g0327others(14): Show | 17 | HG00673.hp2 HG01074.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-32-5833_-32-5831d others(5): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAA | T | 18 | a0001c0001t0004g0037a0001c0001t0005g0087a0001c0001t0009g0267others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.-32-5834_-32-5831d others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAA | T | 10 | a0001c0001t0005g0088a0001c0001t0005g0089a0001c0001t0005g0100others(7): Show | 10 | HG02132.hp1 HG02135.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-5835_-32-5831d others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAA | T | 20 | a0001c0001t0001g0256a0001c0001t0003g0012a0001c0001t0005g0057others(17): Show | 20 | HG00408.hp2 HG00642.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-32-5836_-32-5831d others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA | T | 38 | a0001c0001t0002g0109a0001c0001t0004g0011a0001c0001t0004g0036others(35): Show | 38 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.-32-5837_-32-5831d others(9): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA others(1): Show |
T | 59 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(56): Show | 61 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-32-5838_-32-5831d others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA others(2): Show |
T | 40 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(37): Show | 41 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-32-5839_-32-5831d others(11): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA others(3): Show |
T | 6 | a0001c0001t0001g0180a0001c0001t0001g0242a0001c0001t0001g0254others(3): Show | 6 | HG00673.hp1 HG01261.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-5840_-32-5831d others(12): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA others(4): Show |
T | 6 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32-5841_-32-5831d others(13): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0001g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-32-5842_-32-5831d others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA others(9): Show |
T | 2 | a0001c0001t0001g0181a0001c0001t0001g0219 | 2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-32-5846_-32-5831d others(18): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA others(10): Show |
T | 4 | a0001c0001t0001g0182a0001c0001t0003g0008a0002c0002t0002g0309others(1): Show | 4 | HG01496.hp1 HG02735.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-5847_-32-5831d others(19): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA others(11): Show |
T | 6 | a0001c0001t0001g0199a0001c0001t0005g0098a0002c0002t0002g0111others(3): Show | 6 | HG01975.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-5848_-32-5831d others(20): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA others(12): Show |
T | 2 | a0001c0001t0001g0201a0001c0001t0007g0200 | 2 | HG01168.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.-32-5849_-32-5831d others(21): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA others(13): Show |
T | 3 | a0001c0001t0001g0252a0001c0001t0007g0202a0001c0001t0014g0006 | 3 | HG01169.hp1 HG01993.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-32-5850_-32-5831d others(22): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA others(14): Show |
T | 9 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(6): Show | 10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-5851_-32-5831d others(23): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA others(15): Show |
T | 2 | a0001c0001t0001g0183a0002c0002t0002g0005 | 3 | NA19009.hp1 NA19063.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-32-5852_-32-5831d others(24): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA others(16): Show |
T | 1 | a0001c0001t0007g0184 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-32-5853_-32-5831d others(25): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545570
|
TAAAAAAA others(17): Show |
T | 4 | a0001c0001t0004g0092a0001c0001t0004g0093a0001c0001t0004g0094others(1): Show | 4 | HG01123.hp1 HG01167.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-5854_-32-5831d others(26): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | |||||
| chr2:64545709
|
T | A | 241 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(238): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-32-5734T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545709 | ||||||
| chr2:64545710
|
C | T | 241 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(238): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-32-5733C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545710 | ||||||
| chr2:64545711
|
CT | C | 241 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(238): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-32-5729delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545711 | |||||
| chr2:64545715
|
C | G | 241 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(238): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-32-5728C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545715 | ||||||
| chr2:64545835
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-32-5608G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545835 | ||||||
| chr2:64545847
|
G | A | 237 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(234): Show | 242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.-32-5596G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545847 | ||||||
| chr2:64545894
|
C | T | 1 | a0001c0001t0006g0198 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-32-5549C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545894 | ||||||
| chr2:64545955
|
C | T | 4 | a0003c0003t0008g0263a0003c0003t0008g0264a0003c0003t0008g0265others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-5488C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545955 | ||||||
| chr2:64545956
|
G | A | 2 | a0001c0001t0002g0109a0001c0001t0005g0108 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-32-5487G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545956 | ||||||
| chr2:64546081
|
T | C | 237 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(234): Show | 242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.-32-5362T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546081 | ||||||
| chr2:64546117
|
T | A | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-5326T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546117 | ||||||
| chr2:64546133
|
T | C | 1 | a0001c0001t0006g0033 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-32-5310T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546133 | ||||||
| chr2:64546193
|
C | CT | 145 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(142): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.-32-5240dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64546193 | |||||
| chr2:64546289
|
A | G | 2 | a0001c0001t0001g0367a0001c0001t0003g0027 | 2 | HG01891.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.-32-5154A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546289 | ||||||
| chr2:64546439
|
T | G | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-32-5004T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546439 | ||||||
| chr2:64546468
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-32-4975A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546468 | ||||||
| chr2:64546526
|
A | G | 1 | a0002c0002t0001g0314 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-32-4917A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546526 | ||||||
| chr2:64546550
|
C | T | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-32-4893C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546550 | ||||||
| chr2:64546573
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-32-4870T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546573 | ||||||
| chr2:64546645
|
G | A | 236 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(233): Show | 241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.-32-4798G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546645 | ||||||
| chr2:64546799
|
C | T | 1 | a0001c0001t0005g0106 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-32-4644C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546799 | ||||||
| chr2:64546870
|
T | A | 1 | a0001c0001t0007g0136 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-32-4573T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546870 | ||||||
| chr2:64546870
|
TA | T | 145 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(142): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.-32-4562delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64546870 | |||||
| chr2:64546884
|
C | A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-4559C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546884 | ||||||
| chr2:64546887
|
A | G | 1 | a0001c0001t0007g0136 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-32-4556A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546887 | ||||||
| chr2:64546972
|
C | T | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-4471C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546972 | ||||||
| chr2:64546973
|
C | T | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-32-4470C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546973 | ||||||
| chr2:64547043
|
T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-4400T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547043 | ||||||
| chr2:64547056
|
T | C | 1 | a0001c0001t0005g0087 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-32-4387T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547056 | ||||||
| chr2:64547242
|
C | T | 1 | a0001c0001t0006g0213 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-32-4201C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547242 | ||||||
| chr2:64547247
|
A | G | 2 | a0002c0002t0003g0294a0002c0002t0003g0301 | 2 | NA18956.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-32-4196A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547247 | ||||||
| chr2:64547322
|
G | C | 238 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(235): Show | 243 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.-32-4121G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547322 | ||||||
| chr2:64547324
|
C | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(30): Show | 34 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.-32-4119C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547324 | ||||||
| chr2:64547372
|
A | G | 32 | a0001c0001t0004g0276a0002c0002t0002g0005a0002c0002t0002g0334others(29): Show | 33 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.-32-4071A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547372 | ||||||
| chr2:64547401
|
C | T | 2 | a0002c0002t0003g0300a0002c0002t0003g0303 | 2 | HG02083.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-32-4042C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547401 | ||||||
| chr2:64547412
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-32-4031T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547412 | ||||||
| chr2:64547450
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-32-3993A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547450 | ||||||
| chr2:64547671
|
A | G | 1 | a0001c0001t0004g0276 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-32-3772A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547671 | ||||||
| chr2:64547740
|
T | C | 9 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(6): Show | 10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-3703T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547740 | ||||||
| chr2:64547740
|
T | TGTATC | 227 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(224): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-32-3703_-32-3702i others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547740 | ||||||
| chr2:64547905
|
C | T | 1 | a0001c0001t0004g0031 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-32-3538C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547905 | ||||||
| chr2:64547907
|
T | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(36): Show | 40 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.-32-3536T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547907 | ||||||
| chr2:64548070
|
T | C | 1 | a0012c0011t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-32-3373T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548070 | ||||||
| chr2:64548083
|
G | A | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-32-3360G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548083 | ||||||
| chr2:64548119
|
C | T | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-32-3324C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548119 | ||||||
| chr2:64548310
|
G | T | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-3133G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548310 | ||||||
| chr2:64548322
|
A | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-3121A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548322 | ||||||
| chr2:64548348
|
G | CCGCCACT others(168): Show |
1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-3096_-32-3095i others(177): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548348 | ||||||
| chr2:64548363
|
G | A | 2 | a0002c0002t0003g0324a0002c0002t0010g0323 | 2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-32-3080G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548363 | ||||||
| chr2:64548407
|
G | GA | 28 | a0001c0001t0001g0114a0001c0001t0001g0129a0001c0001t0001g0140others(25): Show | 28 | HG00642.hp1 HG00741.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.-32-3008dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64548407 | |||||
| chr2:64548407
|
GA | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0134others(92): Show | 97 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.-32-3008delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64548407 | |||||
| chr2:64548407
|
GAAAAA | G | 8 | a0001c0001t0003g0010a0001c0001t0003g0017a0001c0001t0003g0022others(5): Show | 8 | NA18954.hp1 NA18964.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32-3012_-32-3008d others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64548407 | |||||
| chr2:64548407
|
GAAAAAAA others(8): Show |
G | 1 | a0002c0002t0002g0302 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-32-3022_-32-3008d others(17): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64548407 | |||||
| chr2:64548412
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-32-3031A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548412 | ||||||
| chr2:64548429
|
A | C | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-32-3014A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548429 | ||||||
| chr2:64548433
|
A | AAAAAC | 23 | a0001c0001t0001g0042a0001c0001t0002g0021a0001c0001t0003g0018others(20): Show | 23 | HG00280.hp2 HG00438.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.-32-3008_-32-3007i others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64548433 | |||||
| chr2:64548433
|
A | AAAAC | 69 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0002g0109others(66): Show | 71 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.-32-3008_-32-3007i others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64548433 | |||||
| chr2:64548433
|
A | C | 9 | a0001c0001t0003g0010a0001c0001t0003g0016a0001c0001t0003g0017others(6): Show | 9 | NA18954.hp1 NA18957.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.-32-3010A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548433 | ||||||
| chr2:64548615
|
G | A | 20 | a0001c0001t0002g0021a0001c0001t0003g0009a0001c0001t0003g0010others(17): Show | 20 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-32-2828G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548615 | ||||||
| chr2:64548656
|
CAA | C | 3 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0310 | 3 | HG02630.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-32-2786_-32-2785d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548656 | ||||||
| chr2:64548682
|
G | A | 34 | a0002c0002t0002g0005a0002c0002t0002g0333a0002c0002t0002g0334others(31): Show | 35 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.-32-2761G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548682 | ||||||
| chr2:64548983
|
G | A | 3 | a0001c0001t0001g0042a0001c0001t0004g0001a0001c0001t0014g0043 | 4 | HG01243.hp2 HG03209.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-2460G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548983 | ||||||
| chr2:64549250
|
G | A | 1 | a0001c0001t0006g0253 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-32-2193G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549250 | ||||||
| chr2:64549308
|
C | CTTTTTTT others(6): Show |
1 | a0002c0002t0002g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-32-2117_-32-2105d others(15): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | |||||
| chr2:64549308
|
CT | C | 128 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0114others(125): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.-32-2105delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | |||||
| chr2:64549308
|
CTT | C | 75 | a0001c0001t0001g0107a0001c0001t0001g0149a0001c0001t0001g0154others(72): Show | 76 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.-32-2106_-32-2105d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | |||||
| chr2:64549308
|
CTTTTT | C | 35 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.-32-2109_-32-2105d others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | |||||
| chr2:64549308
|
CTTTTTTT others(2): Show |
C | 31 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(28): Show | 32 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(29): Show |
intron_variant | MODIFIER | c.-32-2113_-32-2105d others(11): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | |||||
| chr2:64549308
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0245a0001c0001t0001g0367a0001c0001t0007g0251others(1): Show | 4 | HG01891.hp1 NA18948.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-2114_-32-2105d others(12): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | |||||
| chr2:64549308
|
CTTTTTTT others(4): Show |
C | 35 | a0001c0001t0014g0006a0002c0002t0002g0005a0002c0002t0002g0111others(32): Show | 36 | HG00323.hp1 HG00408.hp2 HG02135.hp1 others(33): Show |
intron_variant | MODIFIER | c.-32-2115_-32-2105d others(13): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | |||||
| chr2:64549308
|
CTTTTTTT others(5): Show |
C | 6 | a0002c0002t0002g0334a0002c0002t0002g0336a0002c0002t0002g0338others(3): Show | 6 | HG02040.hp2 NA18949.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-2116_-32-2105d others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | |||||
| chr2:64549308
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0153 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-32-2118_-32-2105d others(16): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | |||||
| chr2:64549308
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0004g0037 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-32-2119_-32-2105d others(17): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | |||||
| chr2:64549338
|
T | G | 1 | a0002c0002t0003g0295 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-32-2105T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549338 | ||||||
| chr2:64549446
|
A | C | 39 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(36): Show | 40 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-32-1997A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549446 | ||||||
| chr2:64549461
|
C | CTTAGGAA others(28): Show |
1 | a0001c0001t0001g0147 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-32-1982_-32-1981i others(37): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549461 | ||||||
| chr2:64549478
|
G | A | 1 | a0002c0002t0009g0325 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-32-1965G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549478 | ||||||
| chr2:64549482
|
G | T | 1 | a0002c0002t0002g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-32-1961G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549482 | ||||||
| chr2:64549513
|
G | T | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-1930G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549513 | ||||||
| chr2:64549601
|
G | A | 5 | a0002c0002t0002g0281a0002c0002t0002g0285a0002c0002t0002g0307others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-1842G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549601 | ||||||
| chr2:64549632
|
T | C | 1 | a0001c0001t0004g0037 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-32-1811T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549632 | ||||||
| chr2:64549639
|
C | A | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-1804C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549639 | ||||||
| chr2:64549663
|
A | G | 2 | a0002c0002t0002g0286a0002c0002t0002g0306 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-32-1780A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549663 | ||||||
| chr2:64549720
|
A | G | 49 | a0002c0002t0002g0005a0002c0002t0002g0111a0002c0002t0002g0112others(46): Show | 50 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(47): Show |
intron_variant | MODIFIER | c.-32-1723A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549720 | ||||||
| chr2:64549781
|
GA | G | 88 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(85): Show | 90 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-32-1652delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549781 | |||||
| chr2:64549959
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-32-1484C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549959 | ||||||
| chr2:64550009
|
C | G | 4 | a0001c0001t0001g0130a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG02280.hp1 HG02572.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-1434C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550009 | ||||||
| chr2:64550020
|
C | G | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-1423C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550020 | ||||||
| chr2:64550047
|
G | A | 3 | a0002c0002t0001g0312a0002c0002t0001g0313a0002c0002t0001g0314 | 3 | HG02280.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-32-1396G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550047 | ||||||
| chr2:64550127
|
A | C | 1 | a0001c0001t0001g0155 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-32-1316A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550127 | ||||||
| chr2:64550304
|
G | T | 1 | a0011c0014t0001g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-32-1139G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550304 | ||||||
| chr2:64550380
|
A | G | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-32-1063A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550380 | ||||||
| chr2:64550470
|
A | G | 1 | a0002c0002t0002g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-32-973A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550470 | ||||||
| chr2:64550598
|
T | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(36): Show | 40 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.-32-845T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550598 | ||||||
| chr2:64550677
|
G | GCA | 26 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0001g0129others(23): Show | 26 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.-32-713_-32-712dup others(2): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
G | GCACA | 31 | a0001c0001t0001g0003a0001c0001t0001g0115a0001c0001t0001g0134others(28): Show | 32 | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.-32-715_-32-712dup others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
G | GCACACA | 25 | a0001c0001t0001g0114a0001c0001t0001g0123a0001c0001t0001g0135others(22): Show | 25 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.-32-717_-32-712dup others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
G | GCACACAC others(1): Show |
7 | a0001c0001t0001g0180a0001c0001t0001g0188a0001c0001t0001g0227others(4): Show | 7 | HG00673.hp1 HG01978.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-719_-32-712dup others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
G | GCACACAC others(3): Show |
3 | a0001c0001t0001g0163a0001c0001t0001g0189a0002c0002t0003g0293 | 3 | HG00642.hp1 HG04115.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.-32-721_-32-712dup others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
G | GCACACAC others(7): Show |
1 | a0001c0001t0007g0136 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-32-725_-32-712dup others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
GCA | G | 40 | a0001c0001t0001g0118a0001c0001t0001g0130a0001c0001t0001g0139others(37): Show | 41 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.-32-713_-32-712del others(2): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
GCACA | G | 24 | a0001c0001t0001g0137a0001c0001t0001g0167a0001c0001t0001g0204others(21): Show | 24 | HG01168.hp2 HG01169.hp1 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.-32-715_-32-712del others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
GCACACA | G | 27 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0231others(24): Show | 27 | HG01891.hp1 HG02129.hp1 HG02135.hp1 others(24): Show |
intron_variant | MODIFIER | c.-32-717_-32-712del others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
GCACACAC others(1): Show |
G | 19 | a0001c0001t0001g0209a0001c0001t0001g0256a0001c0001t0006g0033others(16): Show | 20 | HG00408.hp2 HG01109.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-32-719_-32-712del others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
GCACACAC others(3): Show |
G | 7 | a0001c0001t0001g0126a0002c0002t0001g0316a0002c0002t0002g0286others(4): Show | 7 | HG00558.hp1 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-721_-32-712del others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
GCACACAC others(5): Show |
G | 6 | a0001c0001t0003g0028a0001c0001t0004g0036a0001c0001t0006g0246others(3): Show | 6 | HG01433.hp1 HG02083.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-723_-32-712del others(12): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
GCACACAC others(7): Show |
G | 22 | a0001c0001t0001g0042a0001c0001t0001g0222a0001c0001t0004g0001others(19): Show | 23 | HG01243.hp2 HG01943.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.-32-725_-32-712del others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
GCACACAC others(9): Show |
G | 77 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0120others(74): Show | 78 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-32-727_-32-712del others(16): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
GCACACAC others(11): Show |
G | 23 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(20): Show | 23 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.-32-729_-32-712del others(18): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550677
|
GCACACAC others(15): Show |
G | 1 | a0001c0001t0003g0016 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-32-733_-32-712del others(22): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | |||||
| chr2:64550679
|
A | ACG | 3 | a0002c0002t0002g0353a0005c0007t0009g0331a0006c0006t0002g0354 | 3 | NA18946.hp2 NA18962.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-32-763_-32-762ins others(2): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550679 | |||||
| chr2:64550681
|
A | G | 1 | a0002c0002t0002g0352 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-32-762A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550681 | ||||||
| chr2:64550683
|
A | G | 9 | a0002c0002t0002g0005a0002c0002t0002g0336a0002c0002t0002g0338others(6): Show | 10 | HG00323.hp1 HG02040.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-760A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550683 | ||||||
| chr2:64550685
|
A | G | 4 | a0002c0002t0002g0355a0002c0002t0002g0357a0002c0002t0002g0359others(1): Show | 4 | NA18972.hp1 NA19009.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-758A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550685 | ||||||
| chr2:64550687
|
A | G | 5 | a0001c0001t0001g0256a0002c0002t0002g0335a0002c0002t0002g0346others(2): Show | 5 | HG01109.hp2 HG02135.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-756A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550687 | ||||||
| chr2:64550689
|
A | G | 4 | a0001c0001t0001g0256a0002c0002t0002g0358a0002c0002t0019g0360others(1): Show | 4 | HG00408.hp2 HG01109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-754A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550689 | ||||||
| chr2:64550691
|
A | G | 1 | a0002c0002t0002g0333 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-32-752A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550691 | ||||||
| chr2:64550692
|
C | G | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-751C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550692 | ||||||
| chr2:64550697
|
A | G | 9 | a0002c0002t0002g0337a0002c0002t0002g0340a0002c0002t0002g0341others(6): Show | 9 | NA18961.hp1 NA18969.hp1 NA18979.hp2 others(6): Show |
intron_variant | MODIFIER | c.-32-746A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550697 | ||||||
| chr2:64550783
|
T | C | 1 | a0003c0003t0008g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-32-660T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550783 | ||||||
| chr2:64550984
|
T | C | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-459T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550984 | ||||||
| chr2:64551025
|
T | C | 5 | a0002c0002t0002g0285a0002c0002t0002g0286a0002c0002t0002g0306others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-418T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64551025 | ||||||
| chr2:64551308
|
C | A | 88 | a0001c0001t0014g0006a0002c0002t0001g0004a0002c0002t0001g0312others(85): Show | 90 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-32-135C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64551308 | ||||||
| chr2:64551338
|
A | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-105A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64551338 | ||||||
| chr2:64551388
|
G | A | 1 | a0012c0011t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-32-55G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64551388 | ||||||
| chr2:64553519
|
C | T | 1 | a0001c0001t0003g0020 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1935+110C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64553519 | ||||||
| chr2:64553641
|
G | A | 5 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0309others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1935+232G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64553641 | ||||||
| chr2:64553655
|
A | T | 40 | a0002c0002t0002g0005a0002c0002t0002g0111a0002c0002t0002g0112others(37): Show | 41 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(38): Show |
intron_variant | MODIFIER | c.1935+246A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64553655 | ||||||
| chr2:64553702
|
TA | T | 211 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(208): Show | 215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1935+310delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64553702 | |||||
| chr2:64553702
|
TAA | T | 40 | a0001c0001t0001g0237a0001c0001t0004g0011a0001c0001t0010g0025others(37): Show | 41 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.1935+309_1935+310d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64553702 | |||||
| chr2:64553714
|
A | C | 1 | a0001c0001t0001g0243 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1935+305A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64553714 | ||||||
| chr2:64553812
|
C | CT | 111 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1935+414dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64553812 | |||||
| chr2:64554264
|
G | T | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+855G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554264 | ||||||
| chr2:64554266
|
GGTGTAGC others(8): Show |
G | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+858_1935+872d others(17): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554266 | ||||||
| chr2:64554289
|
T | A | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+880T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554289 | ||||||
| chr2:64554291
|
C | T | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+882C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554291 | ||||||
| chr2:64554319
|
A | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+910A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554319 | ||||||
| chr2:64554324
|
T | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+915T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554324 | ||||||
| chr2:64554329
|
T | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+920T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554329 | ||||||
| chr2:64554330
|
T | TGTCTAAA others(9): Show |
1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+921_1935+922i others(18): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554330 | ||||||
| chr2:64554331
|
T | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+922T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554331 | ||||||
| chr2:64554334
|
C | G | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+925C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554334 | ||||||
| chr2:64554347
|
G | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+938G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554347 | ||||||
| chr2:64554383
|
T | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+974T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554383 | ||||||
| chr2:64554394
|
G | A | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+985G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554394 | ||||||
| chr2:64554395
|
A | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+986A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554395 | ||||||
| chr2:64554396
|
T | A | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+987T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554396 | ||||||
| chr2:64554405
|
C | A | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+996C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554405 | ||||||
| chr2:64554413
|
T | A | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+1004T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554413 | ||||||
| chr2:64554416
|
T | A | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+1007T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554416 | ||||||
| chr2:64554417
|
C | T | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+1008C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554417 | ||||||
| chr2:64554443
|
T | A | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+1034T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554443 | ||||||
| chr2:64554444
|
A | G | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+1035A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554444 | ||||||
| chr2:64554445
|
A | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+1036A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554445 | ||||||
| chr2:64554447
|
A | T | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+1038A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554447 | ||||||
| chr2:64554450
|
C | T | 5 | a0001c0001t0004g0061a0001c0001t0004g0074a0001c0001t0004g0080others(2): Show | 5 | HG02735.hp2 NA18949.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1935+1041C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554450 | ||||||
| chr2:64554479
|
T | G | 113 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(110): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1935+1070T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554479 | ||||||
| chr2:64554583
|
A | G | 1 | a0001c0005t0001g0122 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1935+1174A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554583 | ||||||
| chr2:64554650
|
A | T | 198 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(195): Show | 202 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1935+1241A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554650 | ||||||
| chr2:64554678
|
T | C | 1 | a0001c0001t0005g0077 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1935+1269T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554678 | ||||||
| chr2:64554829
|
C | T | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1935+1420C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554829 | ||||||
| chr2:64555289
|
A | G | 3 | a0001c0001t0004g0092a0001c0001t0004g0093a0001c0001t0004g0094 | 3 | HG01123.hp1 HG01167.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1935+1880A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64555289 | ||||||
| chr2:64555441
|
A | G | 1 | a0002c0002t0002g0284 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1935+2032A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64555441 | ||||||
| chr2:64555509
|
C | T | 1 | a0001c0001t0005g0106 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1935+2100C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64555509 | ||||||
| chr2:64555555
|
T | TCA | 73 | a0001c0001t0001g0003a0001c0001t0001g0123a0001c0001t0001g0131others(70): Show | 74 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1935+2189_1935+219 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | |||||
| chr2:64555555
|
T | TCACA | 17 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0219others(14): Show | 17 | HG01175.hp1 HG01175.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1935+2187_1935+219 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | |||||
| chr2:64555555
|
T | TCACACA | 7 | a0001c0001t0001g0124a0001c0001t0001g0160a0001c0001t0001g0258others(4): Show | 7 | HG01993.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1935+2185_1935+219 others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | |||||
| chr2:64555555
|
T | TCACACAC others(1): Show |
4 | a0001c0001t0001g0165a0001c0001t0001g0181a0001c0001t0001g0257others(1): Show | 4 | HG02486.hp2 HG03486.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1935+2183_1935+219 others(12): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | |||||
| chr2:64555555
|
TCA | T | 75 | a0001c0001t0001g0042a0001c0001t0001g0117a0001c0001t0001g0126others(72): Show | 78 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1935+2189_1935+219 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | |||||
| chr2:64555555
|
TCACA | T | 33 | a0001c0001t0001g0118a0001c0001t0001g0149a0001c0001t0001g0168others(30): Show | 33 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1935+2187_1935+219 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | |||||
| chr2:64555555
|
TCACACA | T | 28 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0004g0066others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1935+2185_1935+219 others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | |||||
| chr2:64555555
|
TCACACAC others(3): Show |
T | 2 | a0002c0002t0002g0353a0002c0002t0002g0366 | 2 | HG00323.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1935+2181_1935+219 others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | |||||
| chr2:64555835
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1935+2426A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64555835 | ||||||
| chr2:64555989
|
C | CTTTTTTT others(6): Show |
1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1935+2583_1935+259 others(17): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | |||||
| chr2:64555989
|
C | CTTTTTTT others(7): Show |
27 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(24): Show | 28 | HG00408.hp1 HG00558.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1935+2582_1935+259 others(18): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | |||||
| chr2:64555989
|
C | CTTTTTTT others(8): Show |
14 | a0002c0002t0001g0315a0002c0002t0001g0319a0002c0002t0002g0111others(11): Show | 14 | HG00673.hp2 HG02129.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1935+2581_1935+259 others(19): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | |||||
| chr2:64555989
|
C | CTTTTTTT others(9): Show |
5 | a0002c0002t0002g0112a0002c0002t0002g0310a0002c0002t0002g0311others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1935+2595_1935+259 others(20): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | |||||
| chr2:64555989
|
C | CTTTTTTT others(10): Show |
20 | a0001c0001t0004g0276a0002c0002t0002g0005a0002c0002t0002g0333others(17): Show | 21 | HG00323.hp1 HG00408.hp2 HG02523.hp1 others(18): Show |
intron_variant | MODIFIER | c.1935+2595_1935+259 others(21): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | |||||
| chr2:64555989
|
C | CTTTTTTT others(11): Show |
11 | a0002c0002t0002g0334a0002c0002t0002g0335a0002c0002t0002g0336others(8): Show | 11 | HG02040.hp2 HG02135.hp1 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.1935+2595_1935+259 others(22): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | |||||
| chr2:64555989
|
C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0186a0002c0002t0002g0339a0002c0002t0002g0357 | 3 | NA18949.hp2 NA18993.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1935+2595_1935+259 others(23): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | |||||
| chr2:64555989
|
C | CTTTTTTT others(13): Show |
1 | a0002c0002t0002g0346 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1935+2595_1935+259 others(24): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | |||||
| chr2:64555989
|
C | CTTTTTTT others(14): Show |
1 | a0002c0002t0002g0361 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1935+2595_1935+259 others(25): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | |||||
| chr2:64556068
|
G | A | 28 | a0002c0002t0002g0292a0002c0002t0002g0297a0002c0002t0002g0302others(25): Show | 28 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1935+2659G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556068 | ||||||
| chr2:64556435
|
G | A | 1 | a0001c0001t0003g0012 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1935+3026G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556435 | ||||||
| chr2:64556468
|
A | G | 90 | a0001c0001t0002g0186a0002c0002t0001g0004a0002c0002t0001g0312others(87): Show | 92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1935+3059A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556468 | ||||||
| chr2:64556736
|
G | T | 236 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(233): Show | 241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1935+3327G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556736 | ||||||
| chr2:64556746
|
A | G | 5 | a0001c0001t0004g0061a0001c0001t0004g0074a0001c0001t0004g0080others(2): Show | 5 | HG02735.hp2 NA18949.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1935+3337A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556746 | ||||||
| chr2:64556751
|
T | C | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1935+3342T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556751 | ||||||
| chr2:64556752
|
G | A | 1 | a0001c0001t0003g0008 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1935+3343G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556752 | ||||||
| chr2:64556860
|
G | A | 1 | a0001c0001t0003g0018 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1935+3451G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556860 | ||||||
| chr2:64556863
|
G | A | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1935+3454G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556863 | ||||||
| chr2:64557026
|
A | G | 5 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0309others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1935+3617A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64557026 | ||||||
| chr2:64557081
|
A | AT | 9 | a0002c0002t0002g0281a0002c0002t0002g0285a0002c0002t0002g0286others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1935+3681dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64557081 | |||||
| chr2:64557256
|
T | C | 1 | a0001c0001t0005g0086 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1935+3847T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64557256 | ||||||
| chr2:64557639
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1935+4230T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64557639 | ||||||
| chr2:64557662
|
C | T | 1 | a0001c0001t0004g0031 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1935+4253C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64557662 | ||||||
| chr2:64557684
|
T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1935+4275T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64557684 | ||||||
| chr2:64557977
|
ACT | A | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1935+4571_1935+457 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64557977 | |||||
| chr2:64558019
|
T | C | 108 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(105): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1935+4610T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64558019 | ||||||
| chr2:64558316
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1935+4907A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64558316 | ||||||
| chr2:64558480
|
C | T | 202 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(199): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1935+5071C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64558480 | ||||||
| chr2:64558764
|
A | G | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1935+5355A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64558764 | ||||||
| chr2:64559002
|
A | G | 9 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(6): Show | 10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1935+5593A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559002 | ||||||
| chr2:64559010
|
C | A | 105 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(102): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1935+5601C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559010 | ||||||
| chr2:64559025
|
C | T | 1 | a0002c0002t0003g0288 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1935+5616C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559025 | ||||||
| chr2:64559087
|
G | A | 1 | a0002c0002t0002g0333 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1935+5678G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559087 | ||||||
| chr2:64559212
|
T | A | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1935+5803T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559212 | ||||||
| chr2:64559233
|
A | ATTCG | 90 | a0001c0001t0002g0186a0001c0001t0004g0276a0002c0002t0001g0004others(87): Show | 92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1935+5826_1935+582 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64559233 | |||||
| chr2:64559277
|
G | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(20): Show | 24 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.1935+5868G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559277 | ||||||
| chr2:64559332
|
G | T | 2 | a0001c0001t0003g0017a0001c0001t0005g0070 | 2 | NA18989.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1935+5923G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559332 | ||||||
| chr2:64559333
|
A | T | 2 | a0001c0001t0003g0017a0001c0001t0005g0070 | 2 | NA18989.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1935+5924A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559333 | ||||||
| chr2:64559404
|
G | A | 38 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(35): Show | 39 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(36): Show |
intron_variant | MODIFIER | c.1935+5995G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559404 | ||||||
| chr2:64559468
|
G | A | 236 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(233): Show | 241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1935+6059G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559468 | ||||||
| chr2:64559558
|
C | A | 2 | a0001c0001t0004g0363a0001c0001t0004g0364 | 2 | HG00597.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1935+6149C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559558 | ||||||
| chr2:64559705
|
G | A | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1935+6296G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559705 | ||||||
| chr2:64559711
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1935+6302T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559711 | ||||||
| chr2:64559749
|
G | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1935+6340G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559749 | ||||||
| chr2:64560000
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1935+6591C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560000 | ||||||
| chr2:64560091
|
T | G | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1935+6682T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560091 | ||||||
| chr2:64560093
|
C | T | 106 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(103): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1935+6684C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560093 | ||||||
| chr2:64560133
|
C | G | 4 | a0001c0001t0005g0058a0001c0001t0005g0060a0001c0001t0005g0084others(1): Show | 4 | HG01261.hp1 HG02559.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1935+6724C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560133 | ||||||
| chr2:64560301
|
A | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1935+6892A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560301 | ||||||
| chr2:64560305
|
A | G | 1 | a0001c0001t0005g0069 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1935+6896A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560305 | ||||||
| chr2:64560316
|
C | T | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1935+6907C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560316 | ||||||
| chr2:64560643
|
C | T | 1 | a0001c0001t0006g0213 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1936-6919C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560643 | ||||||
| chr2:64560646
|
A | G | 1 | a0001c0001t0006g0213 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1936-6916A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560646 | ||||||
| chr2:64560718
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0018g0157 | 2 | HG02080.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1936-6844C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560718 | ||||||
| chr2:64560778
|
C | T | 1 | a0001c0005t0001g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1936-6784C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560778 | ||||||
| chr2:64560783
|
G | T | 107 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(104): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1936-6779G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560783 | ||||||
| chr2:64560948
|
G | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG02280.hp1 HG02572.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936-6614G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560948 | ||||||
| chr2:64561004
|
A | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0227a0001c0001t0001g0234others(112): Show | 118 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1936-6558A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561004 | ||||||
| chr2:64561049
|
C | G | 1 | a0005c0007t0002g0351 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1936-6513C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561049 | ||||||
| chr2:64561202
|
T | C | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1936-6360T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561202 | ||||||
| chr2:64561223
|
G | A | 5 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(2): Show | 5 | HG02080.hp2 HG02155.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.1936-6339G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561223 | ||||||
| chr2:64561274
|
G | A | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1936-6288G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561274 | ||||||
| chr2:64561410
|
C | T | 1 | a0002c0002t0003g0301 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1936-6152C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561410 | ||||||
| chr2:64561581
|
T | C | 1 | a0001c0001t0004g0066 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1936-5981T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561581 | ||||||
| chr2:64561712
|
C | A | 191 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(188): Show | 194 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1936-5850C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561712 | ||||||
| chr2:64561902
|
C | T | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1936-5660C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561902 | ||||||
| chr2:64561914
|
C | T | 1 | a0001c0001t0006g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1936-5648C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561914 | ||||||
| chr2:64562030
|
T | G | 1 | a0001c0001t0001g0208 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1936-5532T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64562030 | ||||||
| chr2:64562313
|
T | C | 38 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(35): Show | 39 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1936-5249T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64562313 | ||||||
| chr2:64562360
|
G | A | 187 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(184): Show | 190 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1936-5202G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64562360 | ||||||
| chr2:64562447
|
A | G | 1 | a0003c0003t0008g0265 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1936-5115A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64562447 | ||||||
| chr2:64562742
|
T | A | 188 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(185): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1936-4820T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64562742 | ||||||
| chr2:64562866
|
C | G | 2 | a0002c0002t0002g0285a0002c0002t0002g0365 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1936-4696C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64562866 | ||||||
| chr2:64562940
|
T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1936-4622T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64562940 | ||||||
| chr2:64563037
|
G | A | 226 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(223): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1936-4525G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563037 | ||||||
| chr2:64563108
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(29): Show | 33 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(30): Show |
intron_variant | MODIFIER | c.1936-4454C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563108 | ||||||
| chr2:64563190
|
A | G | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1936-4372A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563190 | ||||||
| chr2:64563300
|
CAG | C | 6 | a0001c0001t0009g0267a0003c0003t0008g0232a0003c0003t0008g0263others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1936-4260_1936-425 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64563300 | |||||
| chr2:64563305
|
G | T | 226 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(223): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1936-4257G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563305 | ||||||
| chr2:64563322
|
C | A | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1936-4240C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563322 | ||||||
| chr2:64563332
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1936-4230T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563332 | ||||||
| chr2:64563880
|
A | G | 81 | a0001c0001t0002g0186a0002c0002t0002g0005a0002c0002t0002g0111others(78): Show | 82 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1936-3682A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563880 | ||||||
| chr2:64563898
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1936-3664G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563898 | ||||||
| chr2:64564034
|
T | A | 23 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(20): Show | 24 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.1936-3528T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564034 | ||||||
| chr2:64564062
|
A | G | 41 | a0001c0001t0002g0186a0001c0001t0004g0276a0002c0002t0002g0005others(38): Show | 42 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(39): Show |
intron_variant | MODIFIER | c.1936-3500A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564062 | ||||||
| chr2:64564104
|
T | A | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1936-3458T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564104 | ||||||
| chr2:64564106
|
T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1936-3456T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564106 | ||||||
| chr2:64564283
|
A | G | 3 | a0001c0001t0004g0063a0001c0001t0004g0097a0001c0001t0004g0276 | 3 | NA18962.hp2 NA18966.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1936-3279A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564283 | ||||||
| chr2:64564310
|
C | A | 2 | a0002c0002t0002g0286a0002c0002t0002g0307 | 2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1936-3252C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564310 | ||||||
| chr2:64564381
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1936-3181G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564381 | ||||||
| chr2:64564583
|
C | T | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1936-2979C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564583 | ||||||
| chr2:64564589
|
C | T | 29 | a0002c0002t0002g0292a0002c0002t0002g0297a0002c0002t0002g0302others(26): Show | 29 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1936-2973C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564589 | ||||||
| chr2:64564616
|
AAAAATAA others(5): Show |
A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1936-2941_1936-293 others(16): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64564616 | |||||
| chr2:64564633
|
AAT | A | 77 | a0001c0001t0002g0186a0002c0002t0002g0005a0002c0002t0002g0111others(74): Show | 78 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.1936-2927_1936-292 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64564633 | |||||
| chr2:64564635
|
T | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(146): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1936-2927T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564635 | ||||||
| chr2:64564637
|
A | T | 110 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(107): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1936-2925A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564637 | ||||||
| chr2:64564638
|
A | G | 1 | a0001c0001t0004g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1936-2924A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564638 | ||||||
| chr2:64564640
|
T | A | 226 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(223): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1936-2922T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564640 | ||||||
| chr2:64564700
|
A | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1936-2862A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564700 | ||||||
| chr2:64564734
|
G | A | 24 | a0001c0001t0001g0120a0001c0001t0002g0021a0001c0001t0003g0007others(21): Show | 24 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1936-2828G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564734 | ||||||
| chr2:64564855
|
TA | T | 4 | a0001c0001t0001g0107a0001c0001t0004g0074a0001c0001t0005g0084others(1): Show | 4 | HG02559.hp2 HG03195.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936-2705delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64564855 | |||||
| chr2:64564856
|
A | T | 188 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0120others(185): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1936-2706A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564856 | ||||||
| chr2:64564861
|
C | A | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1936-2701C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564861 | ||||||
| chr2:64564997
|
C | A | 1 | a0001c0001t0004g0031 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1936-2565C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564997 | ||||||
| chr2:64565068
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1936-2494A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565068 | ||||||
| chr2:64565086
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1936-2476G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565086 | ||||||
| chr2:64565104
|
G | T | 80 | a0001c0001t0002g0186a0002c0002t0002g0005a0002c0002t0002g0111others(77): Show | 81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1936-2458G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565104 | ||||||
| chr2:64565111
|
T | C | 1 | a0001c0001t0004g0037 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1936-2451T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565111 | ||||||
| chr2:64565119
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1936-2443G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565119 | ||||||
| chr2:64565180
|
T | G | 40 | a0001c0001t0001g0003a0001c0001t0001g0188a0001c0001t0001g0189others(37): Show | 41 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1936-2382T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565180 | ||||||
| chr2:64565335
|
C | T | 5 | a0002c0002t0002g0281a0002c0002t0002g0285a0002c0002t0002g0307others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1936-2227C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565335 | ||||||
| chr2:64565446
|
A | G | 12 | a0001c0001t0005g0002a0001c0001t0005g0035a0001c0001t0005g0038others(9): Show | 13 | HG01167.hp1 HG01169.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1936-2116A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565446 | ||||||
| chr2:64565461
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1936-2101C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565461 | ||||||
| chr2:64565474
|
C | CA | 49 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0129others(46): Show | 50 | HG00673.hp1 HG00673.hp2 HG01123.hp2 others(47): Show |
intron_variant | MODIFIER | c.1936-2069dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64565474 | |||||
| chr2:64565474
|
C | CAA | 100 | a0001c0001t0001g0042a0001c0001t0001g0107a0001c0001t0001g0120others(97): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1936-2070_1936-206 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64565474 | |||||
| chr2:64565474
|
C | CAAA | 6 | a0001c0001t0001g0095a0001c0001t0003g0023a0001c0001t0004g0090others(3): Show | 6 | HG00642.hp2 HG03139.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1936-2071_1936-206 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64565474 | |||||
| chr2:64565474
|
CA | C | 49 | a0001c0001t0001g0275a0001c0001t0004g0276a0002c0002t0002g0005others(46): Show | 50 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1936-2069delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64565474 | |||||
| chr2:64565497
|
T | C | 81 | a0001c0001t0002g0186a0001c0001t0004g0276a0002c0002t0002g0005others(78): Show | 82 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1936-2065T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565497 | ||||||
| chr2:64566168
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1936-1394G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64566168 | ||||||
| chr2:64566278
|
TC | T | 80 | a0001c0001t0002g0186a0002c0002t0002g0005a0002c0002t0002g0111others(77): Show | 81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1936-1283delC | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64566278 | ||||||
| chr2:64566418
|
AT | A | 7 | a0001c0001t0001g0118a0001c0001t0001g0207a0001c0001t0005g0075others(4): Show | 7 | HG01069.hp1 HG02523.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1936-1133delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64566418 | |||||
| chr2:64566530
|
T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1936-1032T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64566530 | ||||||
| chr2:64566660
|
ATAGT | A | 4 | a0002c0002t0002g0285a0002c0002t0002g0307a0002c0002t0002g0365others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936-898_1936-895d others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64566660 | |||||
| chr2:64566693
|
G | T | 1 | a0002c0002t0003g0289 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1936-869G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64566693 | ||||||
| chr2:64566774
|
T | TA | 90 | a0001c0001t0001g0239a0001c0001t0002g0186a0002c0002t0001g0004others(87): Show | 92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1936-777dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64566774 | |||||
| chr2:64567303
|
T | C | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG00323.hp2 HG01433.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936-259T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64567303 | ||||||
| chr2:64567806
|
C | T | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2087+93C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64567806 | ||||||
| chr2:64567811
|
G | A | 107 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(104): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2087+98G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64567811 | ||||||
| chr2:64567897
|
CA | C | 107 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(104): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2087+185delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64567897 | ||||||
| chr2:64568009
|
C | A | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2087+296C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568009 | ||||||
| chr2:64568106
|
T | C | 4 | a0001c0001t0005g0067a0001c0001t0005g0069a0001c0001t0005g0098others(1): Show | 4 | NA18941.hp1 NA18952.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.2087+393T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568106 | ||||||
| chr2:64568139
|
A | C | 81 | a0001c0001t0002g0186a0001c0001t0004g0276a0002c0002t0002g0005others(78): Show | 82 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.2087+426A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568139 | ||||||
| chr2:64568143
|
A | T | 109 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(106): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.2087+430A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568143 | ||||||
| chr2:64568258
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2087+545T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568258 | ||||||
| chr2:64568286
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2087+573C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568286 | ||||||
| chr2:64568303
|
C | CTT | 189 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(186): Show | 192 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.2087+590_2087+591i others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568303 | ||||||
| chr2:64568444
|
G | A | 1 | a0002c0002t0003g0305 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2088-648G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568444 | ||||||
| chr2:64568650
|
C | T | 31 | a0001c0001t0005g0091a0002c0002t0002g0292a0002c0002t0002g0297others(28): Show | 31 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.2088-442C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568650 | ||||||
| chr2:64568792
|
A | G | 2 | a0002c0002t0002g0281a0002c0002t0002g0327 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2088-300A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568792 | ||||||
| chr2:64568798
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2088-294G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568798 | ||||||
| chr2:64568902
|
G | A | 1 | a0002c0002t0002g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2088-190G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568902 | ||||||
| chr2:64568965
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2088-127T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568965 | ||||||
| chr2:64568977
|
G | A | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2088-115G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568977 | ||||||
| chr2:64568978
|
T | C | 1 | a0002c0002t0002g0286 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2088-114T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568978 | ||||||
| chr2:64569015
|
A | C | 1 | a0002c0002t0003g0328 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2088-77A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64569015 | ||||||
| chr2:64569069
|
T | C | 1 | a0002c0002t0002g0366 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2088-23T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64569069 | ||||||
| chr2:64569345
|
C | T | 227 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(224): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.2214+127C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 4/9 | chr2 | 64569345 | ||||||
| chr2:64569510
|
A | G | 1 | a0002c0002t0002g0349 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2215-113A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 4/9 | chr2 | 64569510 | ||||||
| chr2:64569593
|
A | T | 5 | a0002c0002t0003g0308a0002c0002t0003g0320a0002c0002t0003g0321others(2): Show | 5 | HG02622.hp1 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2215-30A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 4/9 | chr2 | 64569593 | ||||||
| chr2:64569683
|
A | C | 29 | a0002c0002t0002g0292a0002c0002t0002g0297a0002c0002t0002g0302others(26): Show | 29 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(26): Show |
splice_region_variant&intron_variant | LOW | c.2271+4A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64569683 | ||||||
| chr2:64569713
|
A | G | 106 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(103): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.2271+34A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64569713 | ||||||
| chr2:64569754
|
C | T | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2271+75C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64569754 | ||||||
| chr2:64569766
|
A | G | 1 | a0002c0002t0003g0287 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2271+87A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64569766 | ||||||
| chr2:64569798
|
G | A | 106 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(103): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.2271+119G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64569798 | ||||||
| chr2:64570019
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2271+340T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570019 | ||||||
| chr2:64570058
|
G | A | 106 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(103): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.2271+379G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570058 | ||||||
| chr2:64570070
|
A | T | 1 | a0001c0001t0001g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2271+391A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570070 | ||||||
| chr2:64570071
|
C | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0237a0001c0001t0001g0238others(17): Show | 21 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(18): Show |
intron_variant | MODIFIER | c.2271+392C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570071 | ||||||
| chr2:64570199
|
C | T | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2271+520C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570199 | ||||||
| chr2:64570200
|
G | A | 105 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(102): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.2271+521G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570200 | ||||||
| chr2:64570293
|
T | C | 1 | a0002c0002t0003g0298 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2271+614T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570293 | ||||||
| chr2:64570381
|
G | T | 106 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(103): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.2271+702G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570381 | ||||||
| chr2:64570915
|
T | TC | 47 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0120others(44): Show | 48 | HG00673.hp1 HG00735.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.2271+1249dupC | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64570915 | |||||
| chr2:64570915
|
T | TCC | 50 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0123others(47): Show | 50 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2271+1248_2271+124 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64570915 | |||||
| chr2:64570915
|
T | TCCC | 16 | a0001c0001t0001g0160a0001c0001t0001g0170a0001c0001t0001g0172others(13): Show | 16 | HG00280.hp1 HG00597.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.2271+1247_2271+124 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64570915 | |||||
| chr2:64570915
|
TC | T | 28 | a0001c0001t0002g0186a0001c0001t0004g0276a0002c0002t0002g0111others(25): Show | 28 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.2271+1249delC | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64570915 | |||||
| chr2:64570915
|
TCC | T | 63 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0245others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.2271+1248_2271+124 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64570915 | |||||
| chr2:64570915
|
TCCC | T | 124 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0234others(121): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2271+1247_2271+124 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64570915 | |||||
| chr2:64570923
|
C | A | 1 | a0002c0002t0009g0325 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2271+1244C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570923 | ||||||
| chr2:64570950
|
A | G | 1 | a0001c0005t0001g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2271+1271A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570950 | ||||||
| chr2:64571155
|
C | T | 185 | a0001c0001t0001g0042a0001c0001t0002g0021a0001c0001t0002g0109others(182): Show | 188 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.2271+1476C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571155 | ||||||
| chr2:64571243
|
A | G | 6 | a0002c0002t0002g0327a0002c0002t0003g0308a0002c0002t0003g0320others(3): Show | 6 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2271+1564A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571243 | ||||||
| chr2:64571267
|
AC | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(28): Show | 32 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(29): Show |
intron_variant | MODIFIER | c.2271+1594delC | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64571267 | |||||
| chr2:64571272
|
CCT | C | 81 | a0001c0001t0002g0186a0001c0001t0004g0276a0002c0002t0002g0005others(78): Show | 82 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.2271+1594_2271+159 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571272 | ||||||
| chr2:64571318
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2272-1628G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571318 | ||||||
| chr2:64571362
|
C | G | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2272-1584C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571362 | ||||||
| chr2:64571397
|
A | C | 1 | a0002c0002t0003g0288 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2272-1549A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571397 | ||||||
| chr2:64571404
|
C | A | 225 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0234others(222): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2272-1542C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571404 | ||||||
| chr2:64571480
|
TA | T | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2272-1465delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571480 | ||||||
| chr2:64571483
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0244 | 2 | NA18967.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2272-1463A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571483 | ||||||
| chr2:64571741
|
G | A | 1 | a0002c0002t0002g0284 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2272-1205G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571741 | ||||||
| chr2:64571889
|
A | G | 2 | a0002c0002t0002g0333a0002c0002t0019g0360 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2272-1057A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571889 | ||||||
| chr2:64571934
|
G | A | 1 | a0002c0002t0003g0308 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2272-1012G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571934 | ||||||
| chr2:64571937
|
C | T | 1 | a0005c0007t0002g0351 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2272-1009C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571937 | ||||||
| chr2:64571953
|
C | T | 3 | a0001c0001t0001g0256a0002c0002t0009g0325a0010c0013t0017g0268 | 3 | HG01109.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2272-993C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571953 | ||||||
| chr2:64571987
|
G | T | 7 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0286others(4): Show | 7 | HG02559.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2272-959G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571987 | ||||||
| chr2:64572121
|
G | A | 3 | a0001c0001t0005g0068a0001c0001t0005g0085a0001c0001t0012g0081 | 3 | NA18967.hp2 NA18977.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2272-825G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64572121 | ||||||
| chr2:64572123
|
G | A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2272-823G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64572123 | ||||||
| chr2:64572201
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0220 | 2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2272-745C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64572201 | ||||||
| chr2:64572220
|
C | CA | 8 | a0001c0001t0001g0129a0001c0001t0001g0197a0001c0001t0001g0278others(5): Show | 8 | HG00741.hp1 HG02135.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.2272-710dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64572220 | |||||
| chr2:64572220
|
C | CAA | 84 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(81): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.2272-711_2272-710d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64572220 | |||||
| chr2:64572220
|
C | CAAA | 21 | a0001c0001t0004g0031a0001c0001t0004g0037a0001c0001t0004g0039others(18): Show | 21 | HG00438.hp1 HG00621.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.2272-712_2272-710d others(5): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64572220 | |||||
| chr2:64572220
|
CA | C | 25 | a0001c0001t0001g0164a0001c0001t0007g0136a0002c0002t0002g0284others(22): Show | 25 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.2272-710delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64572220 | |||||
| chr2:64572292
|
A | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(36): Show | 40 | HG01243.hp1 HG01261.hp2 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.2272-654A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64572292 | ||||||
| chr2:64572316
|
G | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0237a0001c0001t0001g0238others(17): Show | 21 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(18): Show |
intron_variant | MODIFIER | c.2272-630G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64572316 | ||||||
| chr2:64572394
|
T | C | 1 | a0002c0002t0003g0290 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2272-552T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64572394 | ||||||
| chr2:64572522
|
ATTG | A | 3 | a0001c0001t0001g0129a0001c0001t0007g0200a0001c0001t0007g0202 | 3 | HG01168.hp2 HG01169.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2272-419_2272-417d others(5): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64572522 | |||||
| chr2:64572803
|
T | TA | 11 | a0001c0001t0001g0222a0001c0001t0007g0136a0002c0002t0001g0004others(8): Show | 12 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.2272-130dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64572803 | |||||
| chr2:64572803
|
TAA | T | 224 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0234others(221): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2272-131_2272-130d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64572803 | |||||
| chr2:64573105
|
G | A | 47 | a0001c0001t0001g0115a0001c0001t0001g0127a0001c0001t0001g0128others(44): Show | 47 | HG00323.hp2 HG00597.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.2394+37G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64573105 | ||||||
| chr2:64573110
|
T | C | 6 | a0001c0001t0009g0267a0003c0003t0008g0232a0003c0003t0008g0263others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2394+42T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64573110 | ||||||
| chr2:64573318
|
C | T | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG00140.hp1 HG01074.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.2394+250C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64573318 | ||||||
| chr2:64573432
|
T | TA | 111 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2394+379dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64573432 | |||||
| chr2:64573432
|
TA | T | 11 | a0001c0001t0001g0142a0001c0001t0001g0273a0001c0001t0001g0332others(8): Show | 11 | HG02040.hp2 HG02280.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.2394+379delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64573432 | |||||
| chr2:64573631
|
C | G | 105 | a0001c0001t0001g0042a0001c0001t0001g0120a0001c0001t0002g0021others(102): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.2394+563C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64573631 | ||||||
| chr2:64573812
|
C | T | 4 | a0001c0001t0005g0058a0001c0001t0005g0060a0001c0001t0005g0084others(1): Show | 4 | HG01261.hp1 HG02559.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.2394+744C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64573812 | ||||||
| chr2:64573850
|
G | C | 81 | a0001c0001t0002g0186a0001c0001t0004g0276a0002c0002t0002g0005others(78): Show | 82 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.2394+782G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64573850 | ||||||
| chr2:64573953
|
C | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0192others(1): Show | 4 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2394+885C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64573953 | ||||||
| chr2:64574042
|
C | T | 1 | a0002c0002t0003g0304 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2394+974C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574042 | ||||||
| chr2:64574282
|
T | C | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2394+1214T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574282 | ||||||
| chr2:64574390
|
TCACAA | T | 9 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(6): Show | 10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2394+1327_2394+133 others(9): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64574390 | |||||
| chr2:64574519
|
G | A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2394+1451G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574519 | ||||||
| chr2:64574621
|
C | T | 4 | a0002c0002t0002g0337a0002c0002t0002g0342a0002c0002t0002g0349others(1): Show | 4 | NA18979.hp2 NA18981.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.2394+1553C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574621 | ||||||
| chr2:64574778
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2394+1710T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574778 | ||||||
| chr2:64574797
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2394+1729C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574797 | ||||||
| chr2:64574819
|
C | T | 14 | a0001c0001t0001g0042a0001c0001t0004g0001a0001c0001t0004g0030others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2394+1751C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574819 | ||||||
| chr2:64574902
|
T | G | 7 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0286others(4): Show | 7 | HG02559.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2394+1834T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574902 | ||||||
| chr2:64574928
|
C | G | 29 | a0002c0002t0002g0292a0002c0002t0002g0297a0002c0002t0002g0302others(26): Show | 29 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2394+1860C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574928 | ||||||
| chr2:64574964
|
C | CTACTTGG others(8): Show |
2 | a0002c0002t0002g0285a0002c0002t0002g0365 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2394+1912_2394+192 others(19): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64574964 | |||||
| chr2:64575043
|
T | TGCTTCCT others(13): Show |
2 | a0001c0001t0001g0128a0001c0001t0001g0133 | 2 | NA18998.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2394+1976_2394+199 others(24): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575043 | |||||
| chr2:64575064
|
A | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0133 | 2 | NA18998.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2394+1996A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575064 | ||||||
| chr2:64575123
|
AT | A | 103 | a0001c0001t0001g0042a0001c0001t0002g0021a0001c0001t0002g0109others(100): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2394+2061delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575123 | |||||
| chr2:64575313
|
A | C | 6 | a0002c0002t0002g0327a0002c0002t0003g0308a0002c0002t0003g0320others(3): Show | 6 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2394+2245A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575313 | ||||||
| chr2:64575344
|
G | A | 1 | a0002c0002t0002g0309 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2394+2276G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575344 | ||||||
| chr2:64575468
|
T | C | 1 | a0002c0002t0003g0293 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2394+2400T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575468 | ||||||
| chr2:64575516
|
C | G | 1 | a0001c0001t0004g0011 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2394+2448C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575516 | ||||||
| chr2:64575550
|
G | C | 105 | a0001c0001t0001g0042a0001c0001t0002g0021a0001c0001t0002g0109others(102): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.2394+2482G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575550 | ||||||
| chr2:64575679
|
T | A | 33 | a0001c0001t0002g0186a0001c0001t0004g0276a0002c0002t0002g0005others(30): Show | 34 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(31): Show |
intron_variant | MODIFIER | c.2394+2611T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575679 | ||||||
| chr2:64575679
|
T | TTA | 3 | a0001c0001t0005g0057a0001c0001t0005g0077a0001c0001t0005g0086 | 3 | HG00642.hp2 HG00735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2394+2621_2394+262 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575679 | |||||
| chr2:64575703
|
ATG | A | 11 | a0001c0001t0001g0154a0002c0002t0002g0281a0002c0002t0002g0283others(8): Show | 11 | HG02622.hp1 HG02818.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.2394+2673_2394+267 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | |||||
| chr2:64575703
|
ATGTG | A | 37 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0164others(34): Show | 37 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.2394+2671_2394+267 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | |||||
| chr2:64575703
|
ATGTGTG | A | 108 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0114others(105): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.2394+2669_2394+267 others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | |||||
| chr2:64575703
|
ATGTGTGT others(1): Show |
A | 6 | a0001c0001t0001g0130a0001c0001t0001g0216a0001c0001t0001g0217others(3): Show | 6 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2394+2667_2394+267 others(12): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | |||||
| chr2:64575703
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2394+2665_2394+267 others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | |||||
| chr2:64575703
|
ATGTGTGT others(5): Show |
A | 38 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(35): Show | 39 | HG01243.hp1 HG01261.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.2394+2663_2394+267 others(16): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | |||||
| chr2:64575703
|
ATGTGTGT others(11): Show |
A | 2 | a0001c0001t0004g0076a0001c0001t0004g0090 | 2 | HG01943.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2394+2657_2394+267 others(22): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | |||||
| chr2:64575703
|
ATGTGTGT others(13): Show |
A | 102 | a0001c0001t0001g0042a0001c0001t0002g0021a0001c0001t0002g0109others(99): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.2394+2655_2394+267 others(24): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | |||||
| chr2:64575705
|
G | A | 52 | a0001c0001t0002g0186a0001c0001t0004g0276a0002c0002t0001g0004others(49): Show | 54 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(51): Show |
intron_variant | MODIFIER | c.2394+2637G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575705 | ||||||
| chr2:64575707
|
G | A | 3 | a0002c0002t0002g0281a0002c0002t0002g0283a0002c0002t0002g0284 | 3 | HG02818.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2394+2639G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575707 | ||||||
| chr2:64575709
|
G | A | 5 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0309others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2394+2641G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575709 | ||||||
| chr2:64575711
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2394+2643G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575711 | ||||||
| chr2:64575737
|
G | A | 1 | a0002c0002t0009g0325 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2394+2669G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575737 | ||||||
| chr2:64575737
|
GTGTGTA | G | 4 | a0001c0001t0001g0150a0001c0001t0001g0155a0001c0001t0001g0166others(1): Show | 4 | HG00621.hp2 HG01106.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.2394+2671_2394+267 others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575737 | |||||
| chr2:64575739
|
G | A | 52 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(49): Show | 53 | HG00408.hp1 HG00673.hp2 HG01891.hp2 others(50): Show |
intron_variant | MODIFIER | c.2394+2671G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575739 | ||||||
| chr2:64575741
|
G | A | 215 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0160others(212): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.2394+2673G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575741 | ||||||
| chr2:64575746
|
TA | T | 3 | a0002c0002t0002g0286a0002c0002t0002g0306a0004c0004t0001g0221 | 3 | HG02717.hp2 NA19083.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2394+2679delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575746 | ||||||
| chr2:64575747
|
A | ATATT | 10 | a0001c0001t0004g0276a0002c0002t0002g0337a0002c0002t0002g0340others(7): Show | 10 | NA18961.hp1 NA18966.hp1 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.2394+2680_2394+268 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575747 | |||||
| chr2:64575747
|
A | ATT | 24 | a0001c0001t0002g0186a0002c0002t0002g0005a0002c0002t0002g0334others(21): Show | 25 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.2394+2686_2394+268 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575747 | |||||
| chr2:64575747
|
A | T | 52 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(49): Show | 53 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.2394+2679A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575747 | ||||||
| chr2:64575749
|
T | A | 103 | a0001c0001t0001g0042a0001c0001t0002g0021a0001c0001t0002g0109others(100): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2394+2681T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575749 | ||||||
| chr2:64575756
|
G | T | 233 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0234others(230): Show | 238 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2394+2688G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575756 | ||||||
| chr2:64575792
|
G | A | 1 | a0002c0002t0002g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2394+2724G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575792 | ||||||
| chr2:64575962
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2394+2894C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575962 | ||||||
| chr2:64576018
|
C | T | 1 | a0002c0002t0003g0287 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2394+2950C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576018 | ||||||
| chr2:64576033
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2394+2965C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576033 | ||||||
| chr2:64576074
|
T | TAC | 20 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(17): Show | 20 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.2394+3049_2394+305 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | |||||
| chr2:64576074
|
TAC | T | 24 | a0001c0001t0001g0120a0001c0001t0001g0130a0001c0001t0001g0135others(21): Show | 24 | HG00642.hp2 HG00735.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2394+3049_2394+305 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | |||||
| chr2:64576074
|
TACAC | T | 27 | a0001c0001t0001g0095a0001c0001t0001g0115a0001c0001t0001g0137others(24): Show | 27 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.2394+3047_2394+305 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | |||||
| chr2:64576074
|
TACACAC | T | 31 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0134others(28): Show | 31 | HG00323.hp2 HG01175.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.2394+3045_2394+305 others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | |||||
| chr2:64576074
|
TACACACA others(3): Show |
T | 16 | a0001c0001t0001g0367a0001c0001t0009g0267a0002c0002t0001g0004others(13): Show | 17 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2394+3041_2394+305 others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | |||||
| chr2:64576074
|
TACACACA others(5): Show |
T | 3 | a0001c0001t0001g0128a0001c0001t0001g0133a0002c0002t0009g0282 | 3 | NA18998.hp2 NA19043.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2394+3039_2394+305 others(16): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | |||||
| chr2:64576074
|
TACACACA others(7): Show |
T | 2 | a0001c0001t0003g0008a0001c0001t0004g0053 | 2 | HG01496.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.2394+3037_2394+305 others(18): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | |||||
| chr2:64576074
|
TACACACA others(9): Show |
T | 11 | a0002c0002t0002g0283a0002c0002t0002g0284a0002c0002t0002g0327others(8): Show | 11 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.2394+3035_2394+305 others(20): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | |||||
| chr2:64576074
|
TACACACA others(11): Show |
T | 1 | a0002c0002t0003g0290 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2394+3033_2394+305 others(22): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | |||||
| chr2:64576074
|
TACACACA others(13): Show |
T | 26 | a0001c0001t0001g0156a0002c0002t0002g0111a0002c0002t0002g0112others(23): Show | 26 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.2394+3031_2394+305 others(24): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | |||||
| chr2:64576074
|
TACACACA others(15): Show |
T | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2394+3029_2394+305 others(26): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | |||||
| chr2:64576074
|
TACACACA others(17): Show |
T | 42 | a0001c0001t0002g0186a0001c0001t0004g0276a0002c0002t0002g0005others(39): Show | 43 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(40): Show |
intron_variant | MODIFIER | c.2394+3027_2394+305 others(28): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | |||||
| chr2:64576074
|
TACACACA others(19): Show |
T | 40 | a0001c0001t0001g0003a0001c0001t0001g0188a0001c0001t0001g0189others(37): Show | 41 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.2394+3025_2394+305 others(30): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | |||||
| chr2:64576110
|
CACACACA others(14): Show |
C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2394+3044_2394+306 others(25): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576110 | |||||
| chr2:64576115
|
A | G | 9 | a0002c0002t0002g0327a0002c0002t0003g0280a0002c0002t0003g0287others(6): Show | 9 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.2394+3047A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576115 | ||||||
| chr2:64576116
|
C | T | 9 | a0002c0002t0002g0327a0002c0002t0003g0280a0002c0002t0003g0287others(6): Show | 9 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.2394+3048C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576116 | ||||||
| chr2:64576117
|
A | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0188others(140): Show | 146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.2394+3049A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576117 | ||||||
| chr2:64576118
|
C | CACACACA others(3): Show |
1 | a0001c0001t0005g0087 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2394+3050_2394+305 others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576118 | ||||||
| chr2:64576118
|
C | CACACGT | 4 | a0001c0001t0001g0042a0001c0001t0004g0001a0001c0001t0004g0094others(1): Show | 5 | HG01074.hp2 HG01243.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2394+3050_2394+305 others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576118 | ||||||
| chr2:64576118
|
C | CACGT | 30 | a0001c0001t0002g0109a0001c0001t0004g0011a0001c0001t0004g0030others(27): Show | 30 | HG00140.hp2 HG00621.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.2394+3050_2394+305 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576118 | ||||||
| chr2:64576118
|
C | CGT | 37 | a0001c0001t0002g0021a0001c0001t0003g0010a0001c0001t0003g0019others(34): Show | 38 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.2394+3055_2394+305 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576118 | |||||
| chr2:64576118
|
C | CGTGT | 26 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0292others(23): Show | 26 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.2394+3053_2394+305 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576118 | |||||
| chr2:64576118
|
C | T | 143 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0188others(140): Show | 146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.2394+3050C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576118 | ||||||
| chr2:64576135
|
A | T | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2394+3067A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576135 | ||||||
| chr2:64576140
|
CGT | C | 105 | a0001c0001t0001g0042a0001c0001t0001g0214a0001c0001t0002g0021others(102): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.2394+3087_2394+308 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576140 | |||||
| chr2:64576140
|
CGTGT | C | 7 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0309others(4): Show | 7 | HG02559.hp1 HG02630.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2394+3085_2394+308 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576140 | |||||
| chr2:64576157
|
A | G | 23 | a0002c0002t0002g0292a0002c0002t0002g0297a0002c0002t0002g0302others(20): Show | 23 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.2394+3089A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576157 | ||||||
| chr2:64576159
|
GTATATAT others(34): Show |
G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2394+3104_2394+314 others(45): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576159 | |||||
| chr2:64576172
|
G | T | 223 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0234others(220): Show | 227 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2394+3104G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576172 | ||||||
| chr2:64576184
|
C | CAT | 4 | a0001c0001t0005g0075a0001c0001t0009g0267a0001c0001t0011g0059others(1): Show | 4 | HG03041.hp2 NA18942.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.2394+3128_2394+312 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576184 | |||||
| chr2:64576216
|
A | G | 1 | a0005c0008t0005g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2394+3148A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576216 | ||||||
| chr2:64576496
|
T | G | 1 | a0005c0008t0005g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2395-2990T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576496 | ||||||
| chr2:64576551
|
T | C | 29 | a0002c0002t0002g0292a0002c0002t0002g0297a0002c0002t0002g0302others(26): Show | 29 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2395-2935T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576551 | ||||||
| chr2:64576640
|
G | A | 241 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0188others(238): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.2395-2846G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576640 | ||||||
| chr2:64576661
|
C | T | 1 | a0002c0002t0003g0294 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2395-2825C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576661 | ||||||
| chr2:64576671
|
T | C | 103 | a0001c0001t0001g0042a0001c0001t0002g0021a0001c0001t0002g0109others(100): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2395-2815T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576671 | ||||||
| chr2:64576815
|
A | G | 1 | a0001c0001t0003g0016 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2395-2671A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576815 | ||||||
| chr2:64576861
|
C | T | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2395-2625C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576861 | ||||||
| chr2:64576902
|
G | GCACCTGC | 89 | a0001c0001t0002g0186a0002c0002t0001g0004a0002c0002t0001g0312others(86): Show | 91 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.2395-2579_2395-257 others(11): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576902 | |||||
| chr2:64576979
|
A | C | 1 | a0001c0001t0004g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2395-2507A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576979 | ||||||
| chr2:64577042
|
AGCCACCG others(6): Show |
A | 29 | a0002c0002t0002g0292a0002c0002t0002g0297a0002c0002t0002g0302others(26): Show | 29 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2395-2437_2395-242 others(17): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64577042 | |||||
| chr2:64577051
|
G | A | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2395-2435G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577051 | ||||||
| chr2:64577051
|
G | T | 1 | a0001c0001t0005g0102 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2395-2435G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577051 | ||||||
| chr2:64577176
|
A | G | 1 | a0001c0001t0003g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2395-2310A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577176 | ||||||
| chr2:64577330
|
C | T | 1 | a0001c0001t0005g0078 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2395-2156C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577330 | ||||||
| chr2:64577332
|
G | GTATCCTG others(10): Show |
5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2395-2152_2395-213 others(21): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64577332 | |||||
| chr2:64577361
|
G | A | 243 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0126others(240): Show | 248 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.2395-2125G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577361 | ||||||
| chr2:64577376
|
G | A | 3 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0052 | 3 | HG02257.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2395-2110G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577376 | ||||||
| chr2:64577463
|
A | G | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2395-2023A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577463 | ||||||
| chr2:64577690
|
T | C | 2 | a0002c0002t0003g0287a0002c0002t0003g0295 | 2 | NA18986.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2395-1796T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577690 | ||||||
| chr2:64577946
|
ACCACCAC others(24): Show |
A | 1 | a0001c0001t0004g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2395-1527_2395-149 others(35): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64577946 | |||||
| chr2:64577966
|
T | TA | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG00140.hp1 HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2395-1519dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64577966 | |||||
| chr2:64578203
|
TAAC | T | 3 | a0002c0002t0002g0285a0002c0002t0002g0307a0002c0002t0002g0365 | 3 | HG02055.hp2 HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2395-1282_2395-128 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578203 | ||||||
| chr2:64578271
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2395-1215T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578271 | ||||||
| chr2:64578316
|
C | T | 115 | a0001c0001t0001g0042a0001c0001t0002g0021a0001c0001t0002g0109others(112): Show | 117 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2395-1170C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578316 | ||||||
| chr2:64578353
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2395-1133A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578353 | ||||||
| chr2:64578385
|
A | T | 41 | a0001c0001t0001g0003a0001c0001t0001g0188a0001c0001t0001g0189others(38): Show | 42 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.2395-1101A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578385 | ||||||
| chr2:64578465
|
A | C | 3 | a0001c0005t0001g0122a0001c0005t0001g0141a0001c0005t0001g0177 | 3 | HG00099.hp2 HG02683.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2395-1021A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578465 | ||||||
| chr2:64578485
|
T | C | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2395-1001T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578485 | ||||||
| chr2:64578516
|
A | T | 1 | a0007c0009t0004g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2395-970A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578516 | ||||||
| chr2:64578558
|
AT | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0118others(142): Show | 147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2395-911delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64578558 | |||||
| chr2:64578558
|
ATTT | A | 89 | a0001c0001t0001g0042a0001c0001t0002g0186a0001c0001t0004g0001others(86): Show | 91 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.2395-913_2395-911d others(5): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64578558 | |||||
| chr2:64578589
|
C | G | 7 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0204others(4): Show | 7 | HG02080.hp2 HG02132.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.2395-897C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578589 | ||||||
| chr2:64578611
|
G | C | 6 | a0002c0002t0002g0327a0002c0002t0003g0308a0002c0002t0003g0320others(3): Show | 6 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2395-875G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578611 | ||||||
| chr2:64578621
|
G | A | 2 | a0002c0002t0002g0283a0002c0002t0002g0284 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2395-865G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578621 | ||||||
| chr2:64578724
|
AT | A | 185 | a0001c0001t0001g0042a0001c0001t0001g0117a0001c0001t0001g0118others(182): Show | 188 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.2395-753delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64578724 | |||||
| chr2:64578752
|
G | T | 1 | a0001c0001t0003g0017 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2395-734G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578752 | ||||||
| chr2:64578846
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2395-640C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578846 | ||||||
| chr2:64578867
|
T | G | 1 | a0001c0001t0005g0056 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2395-619T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578867 | ||||||
| chr2:64578897
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2395-589C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578897 | ||||||
| chr2:64579060
|
TATTAGCC others(1): Show |
T | 35 | a0001c0001t0002g0186a0002c0002t0002g0005a0002c0002t0002g0333others(32): Show | 36 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(33): Show |
intron_variant | MODIFIER | c.2395-423_2395-416d others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64579060 | |||||
| chr2:64579091
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2395-395T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64579091 | ||||||
| chr2:64579117
|
C | T | 1 | a0001c0012t0004g0073 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2395-369C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64579117 | ||||||
| chr2:64579125
|
C | A | 1 | a0001c0001t0005g0099 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2395-361C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64579125 | ||||||
| chr2:64579410
|
A | AT | 10 | a0001c0001t0009g0267a0001c0005t0001g0122a0001c0005t0001g0141others(7): Show | 10 | HG00099.hp2 HG02622.hp1 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.2395-65dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64579410 | |||||
| chr2:64579652
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2455+106T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64579652 | ||||||
| chr2:64579713
|
G | A | 1 | a0002c0002t0009g0325 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2455+167G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64579713 | ||||||
| chr2:64579784
|
A | G | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2455+238A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64579784 | ||||||
| chr2:64579794
|
T | G | 87 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(84): Show | 89 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.2455+248T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64579794 | ||||||
| chr2:64579810
|
ATATCTAG others(4): Show |
A | 1 | a0001c0001t0005g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2455+266_2455+276d others(13): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 64579810 | |||||
| chr2:64579941
|
CAATT | C | 5 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0309others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2455+397_2455+400d others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 64579941 | |||||
| chr2:64580160
|
T | G | 86 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(83): Show | 88 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.2455+614T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580160 | ||||||
| chr2:64580191
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2455+645C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580191 | ||||||
| chr2:64580323
|
T | G | 38 | a0001c0001t0002g0109a0001c0001t0002g0186a0001c0001t0004g0276others(35): Show | 39 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.2455+777T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580323 | ||||||
| chr2:64580344
|
C | G | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2455+798C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580344 | ||||||
| chr2:64580430
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2456-760C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580430 | ||||||
| chr2:64580443
|
T | C | 1 | a0002c0002t0002g0285 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2456-747T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580443 | ||||||
| chr2:64580700
|
T | A | 7 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0089others(4): Show | 7 | HG02027.hp2 HG02132.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.2456-490T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580700 | ||||||
| chr2:64580706
|
C | G | 1 | a0001c0001t0001g0183 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2456-484C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580706 | ||||||
| chr2:64580710
|
G | T | 1 | a0001c0001t0004g0062 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2456-480G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580710 | ||||||
| chr2:64580725
|
C | T | 1 | a0001c0001t0007g0184 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2456-465C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580725 | ||||||
| chr2:64580990
|
T | C | 17 | a0002c0002t0001g0004a0002c0002t0001g0312a0002c0002t0001g0313others(14): Show | 18 | HG02055.hp1 HG02055.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2456-200T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580990 | ||||||
| chr2:64581526
|
G | GTTAA | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2539+254_2539+257d others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64581526 | |||||
| chr2:64581638
|
GAGAT | G | 93 | a0001c0001t0002g0109a0001c0001t0002g0186a0002c0002t0001g0004others(90): Show | 95 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.2539+373_2539+376d others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64581638 | |||||
| chr2:64581645
|
A | G | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2539+372A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64581645 | ||||||
| chr2:64581699
|
T | G | 91 | a0001c0001t0002g0109a0001c0001t0002g0186a0002c0002t0001g0004others(88): Show | 93 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.2539+426T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64581699 | ||||||
| chr2:64581884
|
G | T | 8 | a0001c0001t0003g0010a0001c0001t0003g0017a0001c0001t0003g0022others(5): Show | 8 | NA18954.hp1 NA18964.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2539+611G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64581884 | ||||||
| chr2:64581946
|
G | A | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG00323.hp2 HG01433.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2539+673G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64581946 | ||||||
| chr2:64581990
|
A | T | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2539+717A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64581990 | ||||||
| chr2:64582138
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2539+865G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582138 | ||||||
| chr2:64582144
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG00140.hp1 HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2539+871G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582144 | ||||||
| chr2:64582152
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2539+879G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582152 | ||||||
| chr2:64582262
|
A | G | 1 | a0005c0008t0005g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2539+989A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582262 | ||||||
| chr2:64582297
|
T | A | 11 | a0001c0001t0001g0128a0001c0001t0001g0131a0001c0001t0001g0133others(8): Show | 11 | HG02083.hp1 NA18950.hp2 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.2539+1024T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582297 | ||||||
| chr2:64582404
|
G | A | 80 | a0001c0001t0002g0109a0001c0001t0002g0186a0001c0001t0004g0276others(77): Show | 81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.2539+1131G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582404 | ||||||
| chr2:64582507
|
T | C | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2539+1234T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582507 | ||||||
| chr2:64582621
|
C | CG | 34 | a0001c0001t0002g0109a0001c0001t0002g0186a0001c0001t0004g0276others(31): Show | 35 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.2539+1355dupG | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64582621 | |||||
| chr2:64582674
|
C | A | 1 | a0002c0002t0003g0300 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2539+1401C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582674 | ||||||
| chr2:64582924
|
G | C | 2 | a0002c0002t0002g0361a0002c0002t0003g0330 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2539+1651G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582924 | ||||||
| chr2:64582987
|
C | T | 1 | a0001c0001t0004g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2539+1714C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582987 | ||||||
| chr2:64583316
|
T | TA | 40 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(37): Show | 41 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.2539+2057dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64583316 | |||||
| chr2:64583316
|
T | TAA | 6 | a0001c0001t0003g0012a0001c0001t0004g0076a0001c0001t0005g0075others(3): Show | 6 | HG00099.hp1 HG01943.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2539+2056_2539+205 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64583316 | |||||
| chr2:64583316
|
T | TAAA | 106 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(103): Show | 108 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.2539+2055_2539+205 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64583316 | |||||
| chr2:64583420
|
GTGGTGGT others(81): Show |
G | 1 | a0001c0001t0005g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2540-2000_2540-191 others(92): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64583420 | |||||
| chr2:64583633
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2540-1789G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64583633 | ||||||
| chr2:64583638
|
A | C | 1 | a0002c0002t0002g0286 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2540-1784A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64583638 | ||||||
| chr2:64583901
|
T | C | 87 | a0001c0001t0002g0109a0001c0001t0002g0186a0001c0001t0004g0276others(84): Show | 88 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2540-1521T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64583901 | ||||||
| chr2:64584308
|
G | A | 1 | a0001c0001t0005g0078 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2540-1114G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584308 | ||||||
| chr2:64584438
|
C | T | 88 | a0001c0001t0002g0109a0001c0001t0002g0186a0001c0001t0004g0093others(85): Show | 89 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.2540-984C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584438 | ||||||
| chr2:64584593
|
A | AT | 216 | a0001c0001t0001g0003a0001c0001t0001g0095a0001c0001t0001g0120others(213): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.2540-808dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64584593 | |||||
| chr2:64584593
|
A | ATT | 20 | a0001c0001t0001g0042a0001c0001t0001g0107a0001c0001t0001g0249others(17): Show | 20 | HG01109.hp1 HG01243.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.2540-809_2540-808d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64584593 | |||||
| chr2:64584621
|
C | G | 199 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(196): Show | 202 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.2540-801C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584621 | ||||||
| chr2:64584659
|
T | C | 1 | a0002c0002t0003g0293 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2540-763T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584659 | ||||||
| chr2:64584659
|
T | G | 82 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0163others(79): Show | 83 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.2540-763T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584659 | ||||||
| chr2:64584662
|
T | G | 1 | a0002c0002t0003g0298 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2540-760T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584662 | ||||||
| chr2:64584687
|
TC | T | 5 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0309others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2540-733delC | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64584687 | |||||
| chr2:64584697
|
T | C | 4 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0178others(1): Show | 4 | HG01074.hp1 HG03490.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.2540-725T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584697 | ||||||
| chr2:64584712
|
C | T | 1 | a0002c0002t0003g0298 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2540-710C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584712 | ||||||
| chr2:64584721
|
T | C | 2 | a0002c0002t0002g0281a0002c0002t0002g0327 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2540-701T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584721 | ||||||
| chr2:64584756
|
C | CCGGCTAA others(95): Show |
1 | a0004c0004t0001g0221 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2540-645_2540-644i others(104): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64584756 | |||||
| chr2:64584812
|
G | C | 1 | a0001c0001t0001g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2540-610G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584812 | ||||||
| chr2:64584838
|
T | C | 1 | a0001c0001t0001g0237 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2540-584T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584838 | ||||||
| chr2:64584843
|
G | A | 6 | a0002c0002t0002g0297a0002c0002t0003g0288a0002c0002t0003g0291others(3): Show | 6 | HG00673.hp2 HG02523.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.2540-579G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584843 | ||||||
| chr2:64584895
|
C | T | 2 | a0001c0001t0006g0253a0001c0001t0006g0255 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2540-527C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584895 | ||||||
| chr2:64584918
|
C | G | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2540-504C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584918 | ||||||
| chr2:64585068
|
T | A | 5 | a0002c0002t0002g0285a0002c0002t0002g0286a0002c0002t0002g0306others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2540-354T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64585068 | ||||||
| chr2:64585114
|
T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2540-308T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64585114 | ||||||
| chr2:64585133
|
C | G | 1 | a0001c0001t0003g0015 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2540-289C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64585133 | ||||||
| chr2:64585139
|
G | A | 80 | a0001c0001t0002g0109a0001c0001t0002g0186a0001c0001t0004g0276others(77): Show | 81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.2540-283G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64585139 | ||||||
| chr2:64585304
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2540-118T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64585304 | ||||||
| chr2:64585624
|
C | T | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2663+79C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64585624 | ||||||
| chr2:64585789
|
T | C | 1 | a0004c0004t0001g0221 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2663+244T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64585789 | ||||||
| chr2:64585790
|
G | T | 1 | a0004c0004t0001g0221 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2663+245G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64585790 | ||||||
| chr2:64585791
|
C | G | 1 | a0004c0004t0001g0221 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2663+246C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64585791 | ||||||
| chr2:64585803
|
A | T | 2 | a0002c0002t0002g0281a0002c0002t0002g0327 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2663+258A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64585803 | ||||||
| chr2:64585990
|
C | T | 110 | a0001c0001t0002g0021a0001c0001t0002g0109a0001c0001t0002g0186others(107): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2663+445C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64585990 | ||||||
| chr2:64586023
|
G | A | 230 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0173others(227): Show | 234 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.2663+478G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586023 | ||||||
| chr2:64586078
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2663+533C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586078 | ||||||
| chr2:64586162
|
A | G | 4 | a0001c0001t0005g0087a0001c0001t0005g0100a0001c0001t0005g0106others(1): Show | 4 | HG02027.hp2 HG02155.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.2663+617A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586162 | ||||||
| chr2:64586195
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2663+650A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586195 | ||||||
| chr2:64586201
|
C | G | 1 | a0007c0009t0004g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2663+656C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586201 | ||||||
| chr2:64586346
|
T | A | 3 | a0001c0001t0004g0093a0002c0002t0002g0283a0002c0002t0002g0284 | 3 | HG01167.hp2 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2663+801T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586346 | ||||||
| chr2:64586357
|
A | G | 232 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0095others(229): Show | 236 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2663+812A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586357 | ||||||
| chr2:64586369
|
A | T | 1 | a0002c0002t0002g0334 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2663+824A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586369 | ||||||
| chr2:64586718
|
T | A | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2663+1173T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586718 | ||||||
| chr2:64586774
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2663+1229A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586774 | ||||||
| chr2:64586788
|
A | T | 187 | a0001c0001t0001g0042a0001c0001t0001g0095a0001c0001t0001g0107others(184): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.2663+1243A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586788 | ||||||
| chr2:64587046
|
G | T | 2 | a0002c0002t0002g0285a0002c0002t0002g0365 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2663+1501G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587046 | ||||||
| chr2:64587109
|
C | T | 4 | a0001c0001t0005g0067a0001c0001t0005g0069a0001c0001t0005g0098others(1): Show | 4 | NA18941.hp1 NA18952.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.2663+1564C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587109 | ||||||
| chr2:64587132
|
C | G | 2 | a0006c0006t0002g0343a0006c0006t0002g0354 | 2 | HG00408.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2663+1587C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587132 | ||||||
| chr2:64587182
|
A | T | 1 | a0001c0001t0005g0101 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2663+1637A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587182 | ||||||
| chr2:64587415
|
C | A | 84 | a0001c0001t0001g0042a0001c0001t0001g0178a0001c0001t0004g0001others(81): Show | 86 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.2663+1870C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587415 | ||||||
| chr2:64587422
|
T | A | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2663+1877T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587422 | ||||||
| chr2:64587433
|
C | G | 84 | a0001c0001t0001g0042a0001c0001t0001g0178a0001c0001t0004g0001others(81): Show | 86 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.2663+1888C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587433 | ||||||
| chr2:64587570
|
C | A | 121 | a0001c0001t0001g0120a0001c0001t0002g0021a0001c0001t0002g0109others(118): Show | 123 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.2663+2025C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587570 | ||||||
| chr2:64587621
|
G | A | 23 | a0001c0001t0001g0003a0001c0001t0001g0234a0001c0001t0001g0237others(20): Show | 24 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.2663+2076G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587621 | ||||||
| chr2:64587631
|
A | G | 116 | a0001c0001t0001g0120a0001c0001t0002g0021a0001c0001t0002g0109others(113): Show | 118 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.2663+2086A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587631 | ||||||
| chr2:64587703
|
G | A | 205 | a0001c0001t0001g0042a0001c0001t0001g0120a0001c0001t0001g0178others(202): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.2663+2158G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587703 | ||||||
| chr2:64587799
|
G | A | 1 | a0001c0001t0005g0078 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2663+2254G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587799 | ||||||
| chr2:64587800
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2255T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587800 | ||||||
| chr2:64587801
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2256T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587801 | ||||||
| chr2:64587802
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2257T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587802 | ||||||
| chr2:64587803
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2258T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587803 | ||||||
| chr2:64587806
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2261A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587806 | ||||||
| chr2:64587809
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2264A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587809 | ||||||
| chr2:64587811
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2266T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587811 | ||||||
| chr2:64587812
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2267T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587812 | ||||||
| chr2:64587814
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2269C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587814 | ||||||
| chr2:64587820
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2275C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587820 | ||||||
| chr2:64587821
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2276T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587821 | ||||||
| chr2:64587822
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2277T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587822 | ||||||
| chr2:64587823
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2278G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587823 | ||||||
| chr2:64587824
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2279C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587824 | ||||||
| chr2:64587875
|
A | C | 2 | a0001c0001t0004g0063a0001c0001t0004g0097 | 2 | NA18962.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.2663+2330A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587875 | ||||||
| chr2:64587942
|
TTC | T | 38 | a0001c0001t0002g0109a0001c0001t0002g0186a0001c0001t0004g0276others(35): Show | 39 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.2663+2399_2663+240 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64587942 | |||||
| chr2:64588038
|
C | T | 1 | a0001c0001t0005g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2663+2493C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64588038 | ||||||
| chr2:64588205
|
A | G | 117 | a0001c0001t0001g0120a0001c0001t0002g0021a0001c0001t0002g0109others(114): Show | 119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2663+2660A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64588205 | ||||||
| chr2:64588385
|
G | A | 205 | a0001c0001t0001g0042a0001c0001t0001g0178a0001c0001t0002g0021others(202): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.2663+2840G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64588385 | ||||||
| chr2:64588730
|
C | T | 4 | a0001c0001t0001g0123a0001c0001t0001g0139a0001c0001t0001g0227others(1): Show | 4 | HG00438.hp2 HG01928.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2664-3158C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64588730 | ||||||
| chr2:64588932
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2664-2956G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64588932 | ||||||
| chr2:64589124
|
C | T | 1 | a0001c0001t0004g0001 | 2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2664-2764C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589124 | ||||||
| chr2:64589226
|
G | A | 117 | a0001c0001t0002g0021a0001c0001t0002g0109a0001c0001t0002g0186others(114): Show | 119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2664-2662G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589226 | ||||||
| chr2:64589293
|
T | C | 207 | a0001c0001t0001g0042a0001c0001t0001g0178a0001c0001t0002g0021others(204): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.2664-2595T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589293 | ||||||
| chr2:64589596
|
C | CTTG | 202 | a0001c0001t0001g0042a0001c0001t0002g0021a0001c0001t0002g0109others(199): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2664-2290_2664-228 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64589596 | |||||
| chr2:64589596
|
C | G | 2 | a0001c0001t0003g0018a0001c0001t0004g0031 | 2 | HG04228.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.2664-2292C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589596 | ||||||
| chr2:64589718
|
C | T | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2664-2170C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589718 | ||||||
| chr2:64589926
|
C | T | 8 | a0001c0001t0004g0093a0002c0002t0002g0283a0002c0002t0002g0284others(5): Show | 8 | HG01167.hp2 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2664-1962C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589926 | ||||||
| chr2:64589944
|
TG | T | 25 | a0001c0001t0001g0095a0001c0001t0001g0127a0001c0001t0001g0128others(22): Show | 25 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.2664-1928delG | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64589944 | |||||
| chr2:64589944
|
TGG | T | 59 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(56): Show | 59 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.2664-1929_2664-192 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64589944 | |||||
| chr2:64589944
|
TGGG | T | 27 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0152others(24): Show | 27 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.2664-1930_2664-192 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64589944 | |||||
| chr2:64589944
|
TGGGG | T | 40 | a0001c0001t0001g0129a0001c0001t0001g0194a0001c0001t0001g0205others(37): Show | 41 | HG00280.hp2 HG01069.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.2664-1931_2664-192 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64589944 | |||||
| chr2:64589944
|
TGGGGG | T | 147 | a0001c0001t0001g0042a0001c0001t0001g0123a0001c0001t0001g0139others(144): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.2664-1932_2664-192 others(9): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64589944 | |||||
| chr2:64589944
|
TGGGGGG | T | 37 | a0001c0001t0002g0186a0001c0001t0004g0276a0001c0001t0005g0060others(34): Show | 38 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(35): Show |
intron_variant | MODIFIER | c.2664-1933_2664-192 others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64589944 | |||||
| chr2:64589949
|
G | C | 12 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0163others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.2664-1939G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589949 | ||||||
| chr2:64589950
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2664-1938G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589950 | ||||||
| chr2:64590005
|
C | T | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2664-1883C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64590005 | ||||||
| chr2:64590041
|
C | A | 237 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0234others(234): Show | 242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.2664-1847C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64590041 | ||||||
| chr2:64590081
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2664-1807C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64590081 | ||||||
| chr2:64590122
|
G | A | 82 | a0001c0001t0001g0042a0001c0001t0004g0001a0001c0001t0004g0011others(79): Show | 84 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.2664-1766G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64590122 | ||||||
| chr2:64590129
|
A | G | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2664-1759A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64590129 | ||||||
| chr2:64590634
|
A | G | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2664-1254A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64590634 | ||||||
| chr2:64590748
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2664-1140C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64590748 | ||||||
| chr2:64591005
|
T | G | 3 | a0002c0002t0002g0333a0002c0002t0002g0358a0002c0002t0019g0360 | 3 | HG03041.hp1 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2664-883T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591005 | ||||||
| chr2:64591038
|
C | T | 5 | a0003c0003t0008g0232a0003c0003t0008g0263a0003c0003t0008g0264others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2664-850C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591038 | ||||||
| chr2:64591084
|
A | G | 2 | a0002c0002t0002g0355a0002c0002t0002g0359 | 2 | NA18972.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2664-804A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591084 | ||||||
| chr2:64591184
|
C | T | 3 | a0001c0001t0004g0093a0002c0002t0002g0283a0002c0002t0002g0284 | 3 | HG01167.hp2 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2664-704C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591184 | ||||||
| chr2:64591260
|
A | T | 108 | a0001c0001t0002g0021a0001c0001t0002g0109a0001c0001t0002g0186others(105): Show | 109 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.2664-628A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591260 | ||||||
| chr2:64591485
|
C | G | 108 | a0001c0001t0002g0021a0001c0001t0002g0109a0001c0001t0002g0186others(105): Show | 109 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.2664-403C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591485 | ||||||
| chr2:64591526
|
A | G | 1 | a0001c0001t0005g0108 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2664-362A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591526 | ||||||
| chr2:64591565
|
T | G | 1 | a0001c0001t0001g0231 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2664-323T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591565 | ||||||
| chr2:64591600
|
G | A | 1 | a0012c0011t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2664-288G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591600 | ||||||
| chr2:64591650
|
T | G | 1 | a0002c0002t0009g0325 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2664-238T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591650 | ||||||
| chr2:64591675
|
C | T | 3 | a0001c0001t0004g0093a0002c0002t0002g0283a0002c0002t0002g0284 | 3 | HG01167.hp2 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2664-213C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591675 | ||||||
| chr2:64591690
|
C | T | 194 | a0001c0001t0001g0042a0001c0001t0002g0021a0001c0001t0002g0109others(191): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.2664-198C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591690 | ||||||
| chr2:64591706
|
A | T | 41 | a0001c0001t0002g0109a0001c0001t0002g0186a0002c0002t0002g0005others(38): Show | 42 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(39): Show |
intron_variant | MODIFIER | c.2664-182A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591706 | ||||||
| chr2:64591730
|
T | C | 108 | a0001c0001t0002g0021a0001c0001t0002g0109a0001c0001t0002g0186others(105): Show | 109 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.2664-158T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591730 |