Search by Gene
| geneid | 9870 |
|---|---|
| ensemblid | ENSG00000119682.18 |
| hgncid | 20363 |
| symbol | AREL1 |
| name | apoptosis resistant E3 ubiquitin protein ligase 1 |
| refseq_nuc | NM_001039479.2 |
| refseq_prot | NP_001034568.1 |
| ensembl_nuc | ENST00000356357.9 |
| ensembl_prot | ENSP00000348714.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 74661256 |
| end | 74713080 |
| strand | - |
| ver | v1.2 |
| region | chr14:74661256-74713080 |
| region5000 | chr14:74656256-74718080 |
| regionname0 | AREL1_chr14_74661256_74713080 |
| regionname5000 | AREL1_chr14_74656256_74718080 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 823 | 361 | 89 | 67 | 161 | 12 | 30 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0002 | 0/0 | 823 | 7 | 0 | 0 | 7 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0003 | 0/0 | 823 | 4 | 4 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0004 | 0/0 | 823 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0005 | 0/0 | 823 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2472 | 346 | 81 | 64 | 158 | 12 | 29 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| c0002 | 0/0 | 2472 | 7 | 0 | 0 | 7 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| c0003 | 0/0 | 2472 | 4 | 4 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| c0004 | 0/0 | 2472 | 4 | 4 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| c0005 | 0/0 | 2472 | 4 | 3 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| c0006 | 0/0 | 2472 | 2 | 0 | 1 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| c0007 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| c0008 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| c0009 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| c0010 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| c0011 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| c0012 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| c0013 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2944 | 93 | 24 | 15 | 36 | 3 | 15 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0002 | 1/0 | 2946 | 85 | 26 | 14 | 37 | 2 | 5 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0003 | 0/1 | 2946 | 83 | 1 | 22 | 46 | 6 | 7 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0004 | 0/0 | 2944 | 26 | 9 | 9 | 8 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0005 | 0/0 | 2946 | 21 | 0 | 3 | 18 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0006 | 0/0 | 2944 | 9 | 0 | 0 | 7 | 0 | 2 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0007 | 0/0 | 2944 | 8 | 7 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0008 | 0/0 | 2946 | 7 | 0 | 0 | 7 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0009 | 0/0 | 2944 | 6 | 5 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0010 | 0/0 | 2944 | 5 | 5 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0011 | 0/0 | 2944 | 4 | 4 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0012 | 0/0 | 2944 | 3 | 3 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0013 | 0/0 | 2946 | 3 | 3 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0014 | 0/0 | 2944 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0015 | 0/0 | 2946 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0016 | 0/0 | 2946 | 2 | 0 | 2 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0017 | 0/0 | 2946 | 2 | 0 | 0 | 1 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0018 | 0/0 | 2946 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0019 | 0/0 | 2944 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0020 | 0/0 | 2944 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0021 | 0/0 | 2944 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0022 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0023 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0024 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0025 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0026 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0027 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0028 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| t0029 | 0/0 | 2944 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/1 | 8 | 0 | 4 | 0 | 2 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0018 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 346 | 81 | 64 | 158 | 12 | 29 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0007 | a0001 | c0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0008 | a0001 | c0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0009 | a0001 | c0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0012 | a0001 | c0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0013 | a0001 | c0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0003c0003 | a0003 | c0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0004c0010 | a0004 | c0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0005c0011 | a0005 | c0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 91 | 24 | 14 | 35 | 3 | 15 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 1/0 | 81 | 25 | 14 | 35 | 2 | 4 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/1 | 82 | 1 | 21 | 46 | 6 | 7 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 25 | 8 | 9 | 8 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 21 | 0 | 3 | 18 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0020 | a0001 | c0001 | t0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0021 | a0001 | c0001 | t0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0022 | a0001 | c0001 | t0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0023 | a0001 | c0001 | t0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0025 | a0001 | c0001 | t0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0026 | a0001 | c0001 | t0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0027 | a0001 | c0001 | t0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0028 | a0001 | c0001 | t0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0001t0029 | a0001 | c0001 | t0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0004t0013 | a0001 | c0004 | t0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0004t0015 | a0001 | c0004 | t0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0005t0009 | a0001 | c0005 | t0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0006t0002 | a0001 | c0006 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0006t0024 | a0001 | c0006 | t0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0007t0002 | a0001 | c0007 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0008t0003 | a0001 | c0008 | t0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0009t0004 | a0001 | c0009 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0012t0002 | a0001 | c0012 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0001c0013t0001 | a0001 | c0013 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0002c0002t0006 | a0002 | c0002 | t0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0003c0003t0011 | a0003 | c0003 | t0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0004c0010t0002 | a0004 | c0010 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| a0005c0011t0001 | a0005 | c0011 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0003 | a0001 | c0001 | t0002 | g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0004 | a0001 | c0001 | t0002 | g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0016 | a0001 | c0001 | t0002 | g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0017 | a0001 | c0001 | t0002 | g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0018 | a0001 | c0001 | t0002 | g0018 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0019 | a0001 | c0001 | t0002 | g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0155 | a0001 | c0001 | t0002 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0156 | a0001 | c0001 | t0002 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0157 | a0001 | c0001 | t0002 | g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0158 | a0001 | c0001 | t0002 | g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0159 | a0001 | c0001 | t0002 | g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0160 | a0001 | c0001 | t0002 | g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0161 | a0001 | c0001 | t0002 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0163 | a0001 | c0001 | t0002 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0168 | a0001 | c0001 | t0002 | g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0170 | a0001 | c0001 | t0002 | g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0172 | a0001 | c0001 | t0002 | g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0173 | a0001 | c0001 | t0002 | g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0174 | a0001 | c0001 | t0002 | g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0175 | a0001 | c0001 | t0002 | g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0176 | a0001 | c0001 | t0002 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0177 | a0001 | c0001 | t0002 | g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0178 | a0001 | c0001 | t0002 | g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0179 | a0001 | c0001 | t0002 | g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0180 | a0001 | c0001 | t0002 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0181 | a0001 | c0001 | t0002 | g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0182 | a0001 | c0001 | t0002 | g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0184 | a0001 | c0001 | t0002 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0185 | a0001 | c0001 | t0002 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0186 | a0001 | c0001 | t0002 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0187 | a0001 | c0001 | t0002 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0188 | a0001 | c0001 | t0002 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0189 | a0001 | c0001 | t0002 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0190 | a0001 | c0001 | t0002 | g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0191 | a0001 | c0001 | t0002 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0192 | a0001 | c0001 | t0002 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0193 | a0001 | c0001 | t0002 | g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0194 | a0001 | c0001 | t0002 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0195 | a0001 | c0001 | t0002 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0196 | a0001 | c0001 | t0002 | g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0198 | a0001 | c0001 | t0002 | g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0199 | a0001 | c0001 | t0002 | g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0200 | a0001 | c0001 | t0002 | g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0202 | a0001 | c0001 | t0002 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0203 | a0001 | c0001 | t0002 | g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0205 | a0001 | c0001 | t0002 | g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0206 | a0001 | c0001 | t0002 | g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0209 | a0001 | c0001 | t0002 | g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0210 | a0001 | c0001 | t0002 | g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0211 | a0001 | c0001 | t0002 | g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0214 | a0001 | c0001 | t0002 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0216 | a0001 | c0001 | t0002 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0217 | a0001 | c0001 | t0002 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0218 | a0001 | c0001 | t0002 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0219 | a0001 | c0001 | t0002 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0221 | a0001 | c0001 | t0002 | g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0222 | a0001 | c0001 | t0002 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0223 | a0001 | c0001 | t0002 | g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0224 | a0001 | c0001 | t0002 | g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0225 | a0001 | c0001 | t0002 | g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0226 | a0001 | c0001 | t0002 | g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0227 | a0001 | c0001 | t0002 | g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0228 | a0001 | c0001 | t0002 | g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0229 | a0001 | c0001 | t0002 | g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0230 | a0001 | c0001 | t0002 | g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0231 | a0001 | c0001 | t0002 | g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0232 | a0001 | c0001 | t0002 | g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0233 | a0001 | c0001 | t0002 | g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0235 | a0001 | c0001 | t0002 | g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0238 | a0001 | c0001 | t0002 | g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0239 | a0001 | c0001 | t0002 | g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0240 | a0001 | c0001 | t0002 | g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0002g0336 | a0001 | c0001 | t0002 | g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0001 | a0001 | c0001 | t0003 | g0001 | 0/1 | 8 | 0 | 4 | 0 | 2 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0020 | a0001 | c0001 | t0003 | g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0242 | a0001 | c0001 | t0003 | g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0243 | a0001 | c0001 | t0003 | g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0244 | a0001 | c0001 | t0003 | g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0246 | a0001 | c0001 | t0003 | g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0247 | a0001 | c0001 | t0003 | g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0248 | a0001 | c0001 | t0003 | g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0249 | a0001 | c0001 | t0003 | g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0250 | a0001 | c0001 | t0003 | g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0251 | a0001 | c0001 | t0003 | g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0252 | a0001 | c0001 | t0003 | g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0253 | a0001 | c0001 | t0003 | g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0254 | a0001 | c0001 | t0003 | g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0255 | a0001 | c0001 | t0003 | g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0257 | a0001 | c0001 | t0003 | g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0259 | a0001 | c0001 | t0003 | g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0260 | a0001 | c0001 | t0003 | g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0261 | a0001 | c0001 | t0003 | g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0263 | a0001 | c0001 | t0003 | g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0264 | a0001 | c0001 | t0003 | g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0265 | a0001 | c0001 | t0003 | g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0266 | a0001 | c0001 | t0003 | g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0267 | a0001 | c0001 | t0003 | g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0274 | a0001 | c0001 | t0003 | g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0275 | a0001 | c0001 | t0003 | g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0277 | a0001 | c0001 | t0003 | g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0278 | a0001 | c0001 | t0003 | g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0282 | a0001 | c0001 | t0003 | g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0283 | a0001 | c0001 | t0003 | g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0284 | a0001 | c0001 | t0003 | g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0288 | a0001 | c0001 | t0003 | g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0289 | a0001 | c0001 | t0003 | g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0290 | a0001 | c0001 | t0003 | g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0291 | a0001 | c0001 | t0003 | g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0292 | a0001 | c0001 | t0003 | g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0293 | a0001 | c0001 | t0003 | g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0294 | a0001 | c0001 | t0003 | g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0295 | a0001 | c0001 | t0003 | g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0296 | a0001 | c0001 | t0003 | g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0297 | a0001 | c0001 | t0003 | g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0299 | a0001 | c0001 | t0003 | g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0300 | a0001 | c0001 | t0003 | g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0301 | a0001 | c0001 | t0003 | g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0302 | a0001 | c0001 | t0003 | g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0303 | a0001 | c0001 | t0003 | g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0304 | a0001 | c0001 | t0003 | g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0305 | a0001 | c0001 | t0003 | g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0306 | a0001 | c0001 | t0003 | g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0307 | a0001 | c0001 | t0003 | g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0308 | a0001 | c0001 | t0003 | g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0309 | a0001 | c0001 | t0003 | g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0310 | a0001 | c0001 | t0003 | g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0311 | a0001 | c0001 | t0003 | g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0312 | a0001 | c0001 | t0003 | g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0313 | a0001 | c0001 | t0003 | g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0314 | a0001 | c0001 | t0003 | g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0315 | a0001 | c0001 | t0003 | g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0316 | a0001 | c0001 | t0003 | g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0318 | a0001 | c0001 | t0003 | g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0319 | a0001 | c0001 | t0003 | g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0320 | a0001 | c0001 | t0003 | g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0321 | a0001 | c0001 | t0003 | g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0322 | a0001 | c0001 | t0003 | g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0323 | a0001 | c0001 | t0003 | g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0324 | a0001 | c0001 | t0003 | g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0326 | a0001 | c0001 | t0003 | g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0328 | a0001 | c0001 | t0003 | g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0329 | a0001 | c0001 | t0003 | g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0330 | a0001 | c0001 | t0003 | g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0331 | a0001 | c0001 | t0003 | g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0332 | a0001 | c0001 | t0003 | g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0333 | a0001 | c0001 | t0003 | g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0003g0334 | a0001 | c0001 | t0003 | g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0005 | a0001 | c0001 | t0004 | g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0006 | a0001 | c0001 | t0004 | g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0008 | a0001 | c0001 | t0004 | g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0023 | a0001 | c0001 | t0004 | g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0032 | a0001 | c0001 | t0004 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0033 | a0001 | c0001 | t0004 | g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0034 | a0001 | c0001 | t0004 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0035 | a0001 | c0001 | t0004 | g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0036 | a0001 | c0001 | t0004 | g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0037 | a0001 | c0001 | t0004 | g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0038 | a0001 | c0001 | t0004 | g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0039 | a0001 | c0001 | t0004 | g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0040 | a0001 | c0001 | t0004 | g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0041 | a0001 | c0001 | t0004 | g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0042 | a0001 | c0001 | t0004 | g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0053 | a0001 | c0001 | t0004 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0055 | a0001 | c0001 | t0004 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0056 | a0001 | c0001 | t0004 | g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0057 | a0001 | c0001 | t0004 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0059 | a0001 | c0001 | t0004 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0066 | a0001 | c0001 | t0004 | g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0004g0154 | a0001 | c0001 | t0004 | g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0021 | a0001 | c0001 | t0005 | g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0245 | a0001 | c0001 | t0005 | g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0258 | a0001 | c0001 | t0005 | g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0268 | a0001 | c0001 | t0005 | g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0269 | a0001 | c0001 | t0005 | g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0270 | a0001 | c0001 | t0005 | g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0271 | a0001 | c0001 | t0005 | g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0272 | a0001 | c0001 | t0005 | g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0273 | a0001 | c0001 | t0005 | g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0276 | a0001 | c0001 | t0005 | g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0279 | a0001 | c0001 | t0005 | g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0280 | a0001 | c0001 | t0005 | g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0281 | a0001 | c0001 | t0005 | g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0285 | a0001 | c0001 | t0005 | g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0286 | a0001 | c0001 | t0005 | g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0287 | a0001 | c0001 | t0005 | g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0298 | a0001 | c0001 | t0005 | g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0317 | a0001 | c0001 | t0005 | g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0325 | a0001 | c0001 | t0005 | g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0005g0335 | a0001 | c0001 | t0005 | g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0006g0026 | a0001 | c0001 | t0006 | g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0006g0031 | a0001 | c0001 | t0006 | g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0007g0045 | a0001 | c0001 | t0007 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0007g0047 | a0001 | c0001 | t0007 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0007g0048 | a0001 | c0001 | t0007 | g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0007g0049 | a0001 | c0001 | t0007 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0007g0050 | a0001 | c0001 | t0007 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0007g0051 | a0001 | c0001 | t0007 | g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0007g0062 | a0001 | c0001 | t0007 | g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0007g0064 | a0001 | c0001 | t0007 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0008g0164 | a0001 | c0001 | t0008 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0008g0208 | a0001 | c0001 | t0008 | g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0008g0212 | a0001 | c0001 | t0008 | g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0008g0213 | a0001 | c0001 | t0008 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0008g0220 | a0001 | c0001 | t0008 | g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0008g0236 | a0001 | c0001 | t0008 | g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0008g0337 | a0001 | c0001 | t0008 | g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0009g0043 | a0001 | c0001 | t0009 | g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0009g0061 | a0001 | c0001 | t0009 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0010g0052 | a0001 | c0001 | t0010 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0010g0054 | a0001 | c0001 | t0010 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0010g0060 | a0001 | c0001 | t0010 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0010g0063 | a0001 | c0001 | t0010 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0010g0065 | a0001 | c0001 | t0010 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0012g0007 | a0001 | c0001 | t0012 | g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0012g0046 | a0001 | c0001 | t0012 | g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0013g0338 | a0001 | c0001 | t0013 | g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0014g0126 | a0001 | c0001 | t0014 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0014g0143 | a0001 | c0001 | t0014 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0016g0197 | a0001 | c0001 | t0016 | g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0016g0234 | a0001 | c0001 | t0016 | g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0017g0215 | a0001 | c0001 | t0017 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0017g0237 | a0001 | c0001 | t0017 | g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0018g0341 | a0001 | c0001 | t0018 | g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0018g0342 | a0001 | c0001 | t0018 | g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0019g0044 | a0001 | c0001 | t0019 | g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0020g0144 | a0001 | c0001 | t0020 | g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0021g0097 | a0001 | c0001 | t0021 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0022g0132 | a0001 | c0001 | t0022 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0023g0256 | a0001 | c0001 | t0023 | g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0025g0201 | a0001 | c0001 | t0025 | g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0026g0207 | a0001 | c0001 | t0026 | g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0027g0339 | a0001 | c0001 | t0027 | g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0028g0327 | a0001 | c0001 | t0028 | g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0001t0029g0340 | a0001 | c0001 | t0029 | g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0004t0013g0165 | a0001 | c0004 | t0013 | g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0004t0013g0167 | a0001 | c0004 | t0013 | g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0004t0015g0162 | a0001 | c0004 | t0015 | g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0004t0015g0166 | a0001 | c0004 | t0015 | g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0005t0009g0027 | a0001 | c0005 | t0009 | g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0005t0009g0028 | a0001 | c0005 | t0009 | g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0005t0009g0029 | a0001 | c0005 | t0009 | g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0005t0009g0030 | a0001 | c0005 | t0009 | g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0006t0002g0171 | a0001 | c0006 | t0002 | g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0006t0024g0169 | a0001 | c0006 | t0024 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0007t0002g0183 | a0001 | c0007 | t0002 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0008t0003g0262 | a0001 | c0008 | t0003 | g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0009t0004g0058 | a0001 | c0009 | t0004 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0012t0002g0204 | a0001 | c0012 | t0002 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0001c0013t0001g0098 | a0001 | c0013 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0002c0002t0006g0009 | a0002 | c0002 | t0006 | g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0002c0002t0006g0024 | a0002 | c0002 | t0006 | g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0002c0002t0006g0025 | a0002 | c0002 | t0006 | g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0002c0002t0006g0067 | a0002 | c0002 | t0006 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0002c0002t0006g0068 | a0002 | c0002 | t0006 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0002c0002t0006g0069 | a0002 | c0002 | t0006 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0003c0003t0011g0015 | a0003 | c0003 | t0011 | g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0003c0003t0011g0152 | a0003 | c0003 | t0011 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0003c0003t0011g0153 | a0003 | c0003 | t0011 | g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0004c0010t0002g0241 | a0004 | c0010 | t0002 | g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| a0005c0011t0001g0147 | a0005 | c0011 | t0001 | g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AREL1_chr14_74656256_74718080 | AREL1 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0205 | EUR | GBR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | GBR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0279 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00609 | hp2 | a0001 | c0001 | t0022 | g0132 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00621 | hp1 | a0001 | c0001 | t0017 | g0215 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00735 | hp2 | a0005 | c0011 | t0001 | g0147 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0311 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01074 | hp1 | a0001 | c0006 | t0024 | g0169 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0332 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01081 | hp2 | a0001 | c0005 | t0009 | g0027 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0326 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0062 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0315 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0309 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0297 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0285 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01361 | hp1 | a0001 | c0001 | t0016 | g0234 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0331 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0302 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0301 | EUR | IBS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01516 | hp1 | a0001 | c0001 | t0017 | g0237 | EUR | IBS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0295 | EUR | IBS | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01884 | hp1 | a0001 | c0001 | t0010 | g0060 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0269 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0330 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0299 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0038 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01943 | hp2 | a0001 | c0001 | t0016 | g0197 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0036 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0248 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0039 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0310 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0042 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0281 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0273 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02145 | hp1 | a0001 | c0004 | t0015 | g0162 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02145 | hp2 | a0003 | c0003 | t0011 | g0153 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0296 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02165 | hp1 | a0001 | c0001 | t0023 | g0256 | EAS | CDX | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | CDX | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0054 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02293 | hp1 | a0001 | c0008 | t0003 | g0262 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | PEL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02451 | hp1 | a0001 | c0009 | t0004 | g0058 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02451 | hp2 | a0001 | c0005 | t0009 | g0029 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0047 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02630 | hp2 | a0003 | c0003 | t0011 | g0152 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02647 | hp2 | a0001 | c0005 | t0009 | g0030 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0251 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02717 | hp1 | a0004 | c0010 | t0002 | g0241 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02717 | hp2 | a0001 | c0001 | t0018 | g0341 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02723 | hp1 | a0001 | c0001 | t0012 | g0007 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0031 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02818 | hp2 | a0001 | c0001 | t0019 | g0044 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02895 | hp1 | a0001 | c0001 | t0013 | g0338 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02922 | hp2 | a0001 | c0005 | t0009 | g0028 | AFR | ESN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ESN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | ESN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ESN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0045 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03041 | hp2 | a0001 | c0001 | t0018 | g0342 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0043 | AFR | MSL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0052 | AFR | ESN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0063 | AFR | ESN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | ESN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | MSL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | MSL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0048 | AFR | MSL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0061 | AFR | MSL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03490 | hp2 | a0001 | c0006 | t0002 | g0171 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0050 | AFR | ESN | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03540 | hp1 | a0001 | c0001 | t0027 | g0339 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | MSL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03579 | hp2 | a0001 | c0001 | t0010 | g0065 | AFR | MSL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0320 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0246 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0312 | SAS | BEB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | STU | AREL1_chr14_74656256_74718080 | AREL1 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | AREL1_chr14_74656256_74718080 | AREL1 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0247 | SAS | BEB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG04199 | hp1 | a0001 | c0001 | t0020 | g0144 | SAS | STU | AREL1_chr14_74656256_74718080 | AREL1 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | STU | AREL1_chr14_74656256_74718080 | AREL1 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0321 | SAS | STU | AREL1_chr14_74656256_74718080 | AREL1 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | STU | AREL1_chr14_74656256_74718080 | AREL1 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0026 | SAS | STU | AREL1_chr14_74656256_74718080 | AREL1 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18522 | hp1 | a0001 | c0004 | t0013 | g0165 | AFR | YRI | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18522 | hp2 | a0001 | c0001 | t0012 | g0046 | AFR | YRI | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18939 | hp2 | a0001 | c0001 | t0014 | g0126 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0333 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18946 | hp2 | a0001 | c0001 | t0021 | g0097 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18949 | hp1 | a0002 | c0002 | t0006 | g0024 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0325 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18963 | hp1 | a0001 | c0001 | t0005 | g0286 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18964 | hp1 | a0002 | c0002 | t0006 | g0025 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18967 | hp1 | a0001 | c0001 | t0008 | g0236 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18972 | hp2 | a0001 | c0001 | t0008 | g0213 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0271 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18973 | hp2 | a0002 | c0002 | t0006 | g0069 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18986 | hp1 | a0002 | c0002 | t0006 | g0068 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0258 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18993 | hp1 | a0001 | c0001 | t0008 | g0212 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18997 | hp1 | a0001 | c0001 | t0005 | g0335 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18997 | hp2 | a0001 | c0001 | t0008 | g0220 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18998 | hp1 | a0001 | c0012 | t0002 | g0204 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19000 | hp2 | a0001 | c0001 | t0028 | g0327 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19003 | hp2 | a0001 | c0001 | t0008 | g0164 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0280 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19009 | hp1 | a0001 | c0013 | t0001 | g0098 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19011 | hp1 | a0001 | c0001 | t0025 | g0201 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19011 | hp2 | a0002 | c0002 | t0006 | g0067 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0268 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19030 | hp1 | a0003 | c0003 | t0011 | g0015 | AFR | LWK | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | LWK | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | LWK | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19043 | hp2 | a0003 | c0003 | t0011 | g0015 | AFR | LWK | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19054 | hp1 | a0001 | c0001 | t0026 | g0207 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0298 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19066 | hp1 | a0001 | c0007 | t0002 | g0183 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19070 | hp1 | a0002 | c0002 | t0006 | g0009 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19075 | hp1 | a0001 | c0001 | t0005 | g0287 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19075 | hp2 | a0001 | c0001 | t0008 | g0337 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19079 | hp1 | a0002 | c0002 | t0006 | g0009 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19083 | hp1 | a0001 | c0001 | t0014 | g0143 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19083 | hp2 | a0001 | c0001 | t0005 | g0270 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0049 | AFR | YRI | AREL1_chr14_74656256_74718080 | AREL1 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0007 | AFR | YRI | AREL1_chr14_74656256_74718080 | AREL1 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ASW | AREL1_chr14_74656256_74718080 | AREL1 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0306 | AFR | ASW | AREL1_chr14_74656256_74718080 | AREL1 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | AREL1_chr14_74656256_74718080 | AREL1 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0300 | EUR | TSI | AREL1_chr14_74656256_74718080 | AREL1 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0316 | EUR | TSI | AREL1_chr14_74656256_74718080 | AREL1 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0200 | EUR | TSI | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0245 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0336 | AMR | CLM | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02109 | hp1 | a0001 | c0004 | t0015 | g0166 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG02559 | hp2 | a0001 | c0001 | t0029 | g0340 | AFR | ACB | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0051 | AFR | MSL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | AREL1_chr14_74656256_74718080 | AREL1 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0064 | AFR | USA | AREL1_chr14_74656256_74718080 | AREL1 |
| HG06807 | hp2 | a0001 | c0004 | t0013 | g0167 | AFR | USA | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18955 | hp1 | a0001 | c0001 | t0008 | g0208 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | AREL1_chr14_74656256_74718080 | AREL1 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | USA | AREL1_chr14_74656256_74718080 | AREL1 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | USA | AREL1_chr14_74656256_74718080 | AREL1 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0001 | REF | REF | AREL1_chr14_74656256_74718080 | AREL1 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0178 | REF | REF | AREL1_chr14_74656256_74718080 | AREL1 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74669719
|
T | C | 1 | a0004 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1844A>G | p.Asn615Ser | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/20 | 2325/5417 | 1844/2472 | 615/823 | chr14 | 74669719 | ||
| chr14:74670102
|
C | T | 1 | a0003 | 4 | HG02145.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
missense_variant | MODERATE | c.1633G>A | p.Ala545Thr | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 14/20 | 2114/5417 | 1633/2472 | 545/823 | chr14 | 74670102 | ||
| chr14:74670788
|
G | A | 1 | a0005 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1582C>T | p.Arg528Trp | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 13/20 | 2063/5417 | 1582/2472 | 528/823 | chr14 | 74670788 | ||
| chr14:74676206
|
T | C | 1 | a0002 | 7 | NA18949.hp1 NA18964.hp1 NA18973.hp2 others(4): Show |
missense_variant | MODERATE | c.767A>G | p.His256Arg | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 7/20 | 1248/5417 | 767/2472 | 256/823 | chr14 | 74676206 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74663958
|
A | G | 1 | a0001c0008 | 1 | HG02293.hp1 | synonymous_variant | LOW | c.2310T>C | p.Cys770Cys | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 19/20 | 2791/5417 | 2310/2472 | 770/823 | chr14 | 74663958 | ||
| chr14:74663967
|
G | A | 1 | a0001c0009 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.2301C>T | p.Ala767Ala | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 19/20 | 2782/5417 | 2301/2472 | 767/823 | chr14 | 74663967 | ||
| chr14:74667346
|
C | T | 1 | a0001c0007 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.2076G>A | p.Leu692Leu | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/20 | 2557/5417 | 2076/2472 | 692/823 | chr14 | 74667346 | ||
| chr14:74672864
|
G | A | 1 | a0001c0004 | 4 | HG02109.hp1 HG02145.hp1 HG06807.hp2 others(1): Show |
synonymous_variant | LOW | c.1389C>T | p.Thr463Thr | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 11/20 | 1870/5417 | 1389/2472 | 463/823 | chr14 | 74672864 | ||
| chr14:74673108
|
G | A | 1 | a0001c0012 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.1269C>T | p.Ala423Ala | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 10/20 | 1750/5417 | 1269/2472 | 423/823 | chr14 | 74673108 | ||
| chr14:74675846
|
T | C | 1 | a0001c0013 | 1 | NA19009.hp1 | synonymous_variant | LOW | c.933A>G | p.Pro311Pro | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/20 | 1414/5417 | 933/2472 | 311/823 | chr14 | 74675846 | ||
| chr14:74675903
|
G | A | 1 | a0001c0006 | 2 | HG01074.hp1 HG03490.hp2 |
synonymous_variant | LOW | c.876C>T | p.Gly292Gly | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/20 | 1357/5417 | 876/2472 | 292/823 | chr14 | 74675903 | ||
| chr14:74683458
|
G | A | 1 | a0001c0005 | 4 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
synonymous_variant | LOW | c.319C>T | p.Leu107Leu | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/20 | 800/5417 | 319/2472 | 107/823 | chr14 | 74683458 |
| chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74661576
|
C | T | 2 | a0001c0001t0006a0002c0002t0006 | 9 | HG02738.hp1 HG04228.hp1 NA18949.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2144G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 2144 | chr14 | 74661576 | |||||
| chr14:74661605
|
GAA | G | 18 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(15): Show | 160 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*2113_*2114delTT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 2113 | chr14 | 74661605 | |||||
| chr14:74661613
|
A | C | 11 | a0001c0001t0003a0001c0001t0005a0001c0001t0013others(8): Show | 115 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*2107T>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 2107 | chr14 | 74661613 | |||||
| chr14:74661716
|
A | C | 2 | a0001c0001t0006a0002c0002t0006 | 9 | HG02738.hp1 HG04228.hp1 NA18949.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2004T>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 2004 | chr14 | 74661716 | |||||
| chr14:74661722
|
G | A | 5 | a0001c0001t0003a0001c0001t0018a0001c0001t0022others(2): Show | 87 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1998C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 1998 | chr14 | 74661722 | |||||
| chr14:74661788
|
G | C | 1 | a0001c0001t0019 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1932C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 1932 | chr14 | 74661788 | |||||
| chr14:74662004
|
C | T | 1 | a0001c0006t0024 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1716G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 1716 | chr14 | 74662004 | |||||
| chr14:74662137
|
A | T | 1 | a0001c0001t0026 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1583T>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 1583 | chr14 | 74662137 | |||||
| chr14:74662230
|
T | C | 1 | a0001c0001t0012 | 3 | HG02723.hp1 NA18522.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1490A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 1490 | chr14 | 74662230 | |||||
| chr14:74662232
|
T | C | 1 | a0001c0001t0025 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1488A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 1488 | chr14 | 74662232 | |||||
| chr14:74662286
|
G | C | 1 | a0001c0001t0014 | 2 | NA18939.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1434C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 1434 | chr14 | 74662286 | |||||
| chr14:74662356
|
A | C | 1 | a0001c0001t0018 | 2 | HG02717.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1364T>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 1364 | chr14 | 74662356 | |||||
| chr14:74662440
|
G | A | 1 | a0001c0001t0020 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1280C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 1280 | chr14 | 74662440 | |||||
| chr14:74662455
|
A | C | 1 | a0001c0001t0028 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1265T>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 1265 | chr14 | 74662455 | |||||
| chr14:74662668
|
G | A | 1 | a0001c0004t0015 | 2 | HG02109.hp1 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1052C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 1052 | chr14 | 74662668 | |||||
| chr14:74662671
|
G | A | 1 | a0001c0001t0007 | 8 | HG01109.hp2 HG02572.hp2 HG03041.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1049C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 1049 | chr14 | 74662671 | |||||
| chr14:74662951
|
G | A | 2 | a0001c0001t0008a0001c0001t0026 | 8 | NA18955.hp1 NA18967.hp1 NA18972.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*769C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 769 | chr14 | 74662951 | |||||
| chr14:74663089
|
G | A | 1 | a0001c0001t0016 | 2 | HG01361.hp1 HG01943.hp2 |
3_prime_UTR_variant | MODIFIER | c.*631C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 631 | chr14 | 74663089 | |||||
| chr14:74663161
|
A | G | 2 | a0001c0001t0004a0001c0009t0004 | 26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*559T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 559 | chr14 | 74663161 | |||||
| chr14:74663235
|
C | A | 3 | a0001c0001t0009a0001c0001t0019a0001c0005t0009 | 7 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*485G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 485 | chr14 | 74663235 | |||||
| chr14:74663307
|
G | A | 1 | a0001c0001t0021 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*413C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 413 | chr14 | 74663307 | |||||
| chr14:74663411
|
G | A | 1 | a0001c0001t0027 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*309C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 309 | chr14 | 74663411 | |||||
| chr14:74663532
|
T | G | 7 | a0001c0001t0003a0001c0001t0005a0001c0001t0017others(4): Show | 109 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*188A>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 188 | chr14 | 74663532 | |||||
| chr14:74663656
|
T | C | 1 | a0001c0001t0018 | 2 | HG02717.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*64A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 20/20 | 64 | chr14 | 74663656 | |||||
| chr14:74685644
|
G | A | 2 | a0001c0001t0006a0002c0002t0006 | 9 | HG02738.hp1 HG04228.hp1 NA18949.hp1 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-29C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 3/20 | chr14 | 74685644 | ||||||
| chr14:74692185
|
A | G | 1 | a0001c0001t0023 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-190T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/20 | 6570 | chr14 | 74692185 | |||||
| chr14:74692287
|
T | C | 1 | a0001c0001t0010 | 5 | HG01884.hp1 HG02280.hp2 HG03130.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-292A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/20 | chr14 | 74692287 | ||||||
| chr14:74692304
|
G | A | 8 | a0001c0001t0001a0001c0001t0014a0001c0001t0020others(5): Show | 99 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-309C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/20 | chr14 | 74692304 | ||||||
| chr14:74712972
|
C | A | 1 | a0001c0001t0018 | 2 | HG02717.hp2 HG03041.hp2 |
5_prime_UTR_variant | MODIFIER | c.-373G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/20 | 27357 | chr14 | 74712972 | |||||
| chr14:74713031
|
C | G | 18 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(15): Show | 160 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(157): Show |
5_prime_UTR_variant | MODIFIER | c.-432G>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/20 | 27416 | chr14 | 74713031 |
| chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74663851
|
T | C | 2 | a0001c0001t0002g0181a0001c0001t0002g0224 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2370-29A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 19/19 | chr14 | 74663851 | ||||||
| chr14:74664241
|
C | T | 89 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0243others(86): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.2194-167G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 18/19 | chr14 | 74664241 | ||||||
| chr14:74664448
|
C | CT | 13 | a0001c0001t0002g0163a0001c0001t0002g0199a0001c0001t0002g0202others(10): Show | 13 | HG01884.hp2 HG01978.hp1 HG03516.hp1 others(10): Show |
intron_variant | MODIFIER | c.2194-375dupA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 18/19 | chr14 | 74664448 | ||||||
| chr14:74664448
|
CT | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(192): Show | 215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.2194-375delA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 18/19 | chr14 | 74664448 | ||||||
| chr14:74664613
|
A | AT | 102 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(99): Show | 112 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.2193+222dupA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 18/19 | chr14 | 74664613 | ||||||
| chr14:74664613
|
A | ATT | 9 | a0001c0001t0001g0110a0001c0001t0001g0117a0001c0001t0006g0026others(6): Show | 10 | HG00673.hp2 HG02738.hp1 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.2193+221_2193+222d others(4): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 18/19 | chr14 | 74664613 | ||||||
| chr14:74664650
|
G | C | 4 | a0001c0004t0013g0165a0001c0004t0013g0167a0001c0004t0015g0162others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2193+186C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 18/19 | chr14 | 74664650 | ||||||
| chr14:74665099
|
C | T | 1 | a0001c0001t0010g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2104-174G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74665099 | ||||||
| chr14:74665270
|
C | CT | 8 | a0001c0001t0001g0072a0001c0001t0005g0021a0001c0001t0005g0286others(5): Show | 9 | HG02717.hp1 HG02738.hp2 HG04228.hp1 others(6): Show |
intron_variant | MODIFIER | c.2104-346dupA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74665270 | ||||||
| chr14:74665325
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2104-400G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74665325 | ||||||
| chr14:74665396
|
G | C | 1 | a0001c0001t0002g0231 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2104-471C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74665396 | ||||||
| chr14:74665452
|
A | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(62): Show | 73 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.2104-527T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74665452 | ||||||
| chr14:74665473
|
A | G | 23 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0008others(20): Show | 26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.2104-548T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74665473 | ||||||
| chr14:74665808
|
C | T | 3 | a0003c0003t0011g0015a0003c0003t0011g0152a0003c0003t0011g0153 | 4 | HG02145.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2104-883G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74665808 | ||||||
| chr14:74665983
|
C | T | 3 | a0003c0003t0011g0015a0003c0003t0011g0152a0003c0003t0011g0153 | 4 | HG02145.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2104-1058G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74665983 | ||||||
| chr14:74666201
|
T | TC | 7 | a0001c0001t0002g0222a0001c0001t0013g0338a0001c0001t0027g0339others(4): Show | 7 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2103+1117dupG | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74666201 | ||||||
| chr14:74666204
|
C | T | 2 | a0001c0001t0009g0043a0001c0001t0009g0061 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2103+1115G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74666204 | ||||||
| chr14:74666531
|
G | A | 1 | a0001c0001t0003g0330 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2103+788C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74666531 | ||||||
| chr14:74666562
|
C | T | 6 | a0001c0001t0013g0338a0001c0001t0027g0339a0001c0004t0013g0165others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2103+757G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74666562 | ||||||
| chr14:74666657
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2103+662G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74666657 | ||||||
| chr14:74666683
|
C | T | 1 | a0001c0001t0027g0339 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2103+636G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74666683 | ||||||
| chr14:74666718
|
A | AT | 18 | a0001c0001t0002g0158a0001c0001t0002g0194a0001c0001t0002g0209others(15): Show | 18 | HG00408.hp1 HG01081.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2103+600dupA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74666718 | ||||||
| chr14:74666718
|
AT | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(87): Show | 100 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2103+600delA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74666718 | ||||||
| chr14:74666760
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2103+559G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 17/19 | chr14 | 74666760 | ||||||
| chr14:74667930
|
T | C | 1 | a0003c0003t0011g0153 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1915-336A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/19 | chr14 | 74667930 | ||||||
| chr14:74667956
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1915-362C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/19 | chr14 | 74667956 | ||||||
| chr14:74667987
|
T | C | 1 | a0001c0001t0003g0302 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1915-393A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/19 | chr14 | 74667987 | ||||||
| chr14:74668108
|
T | A | 1 | a0001c0001t0005g0269 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1915-514A>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/19 | chr14 | 74668108 | ||||||
| chr14:74668239
|
C | A | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1915-645G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/19 | chr14 | 74668239 | ||||||
| chr14:74668300
|
C | A | 6 | a0001c0001t0013g0338a0001c0001t0027g0339a0001c0004t0013g0165others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1915-706G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/19 | chr14 | 74668300 | ||||||
| chr14:74668301
|
A | G | 1 | a0001c0001t0005g0281 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1915-707T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/19 | chr14 | 74668301 | ||||||
| chr14:74668439
|
A | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(107): Show | 122 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1915-845T>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/19 | chr14 | 74668439 | ||||||
| chr14:74668468
|
AT | A | 8 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0023others(5): Show | 10 | HG01243.hp1 HG01496.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1915-875delA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/19 | chr14 | 74668468 | ||||||
| chr14:74668693
|
A | C | 1 | a0001c0001t0004g0041 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1914+956T>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/19 | chr14 | 74668693 | ||||||
| chr14:74668784
|
G | A | 1 | a0001c0001t0003g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1914+865C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/19 | chr14 | 74668784 | ||||||
| chr14:74668876
|
A | G | 2 | a0001c0001t0002g0003a0001c0001t0002g0221 | 4 | HG02622.hp2 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1914+773T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/19 | chr14 | 74668876 | ||||||
| chr14:74669246
|
T | C | 1 | a0001c0001t0004g0034 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1914+403A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/19 | chr14 | 74669246 | ||||||
| chr14:74669363
|
G | C | 2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1914+286C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 15/19 | chr14 | 74669363 | ||||||
| chr14:74670297
|
T | C | 19 | a0001c0001t0003g0242a0001c0001t0003g0257a0001c0001t0003g0288others(16): Show | 20 | HG00438.hp1 HG02015.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1609-171A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 13/19 | chr14 | 74670297 | ||||||
| chr14:74670459
|
A | G | 1 | a0001c0001t0007g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1608+303T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 13/19 | chr14 | 74670459 | ||||||
| chr14:74670580
|
AC | A | 23 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0008others(20): Show | 26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.1608+181delG | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 13/19 | chr14 | 74670580 | ||||||
| chr14:74670961
|
T | C | 101 | a0001c0001t0002g0336a0001c0001t0003g0001a0001c0001t0003g0020others(98): Show | 110 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1499-90A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 12/19 | chr14 | 74670961 | ||||||
| chr14:74671194
|
CA | C | 4 | a0001c0001t0004g0008a0001c0001t0004g0055a0001c0001t0004g0056others(1): Show | 5 | HG02451.hp1 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498+213delT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 12/19 | chr14 | 74671194 | ||||||
| chr14:74671268
|
G | GA | 6 | a0001c0001t0002g0239a0001c0001t0010g0052a0001c0001t0010g0054others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498+139dupT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 12/19 | chr14 | 74671268 | ||||||
| chr14:74671283
|
GT | G | 7 | a0001c0001t0006g0031a0002c0002t0006g0009a0002c0002t0006g0024others(4): Show | 8 | HG02738.hp1 NA18949.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.1498+124delA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 12/19 | chr14 | 74671283 | ||||||
| chr14:74671321
|
C | CT | 34 | a0001c0001t0002g0170a0001c0001t0002g0172a0001c0001t0002g0173others(31): Show | 34 | HG00642.hp2 HG00735.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1498+86dupA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 12/19 | chr14 | 74671321 | ||||||
| chr14:74671321
|
CT | C | 28 | a0001c0001t0001g0011a0001c0001t0001g0070a0001c0001t0001g0072others(25): Show | 31 | HG00438.hp2 HG00544.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1498+86delA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 12/19 | chr14 | 74671321 | ||||||
| chr14:74671321
|
CTT | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(65): Show | 76 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1498+85_1498+86del others(2): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 12/19 | chr14 | 74671321 | ||||||
| chr14:74671321
|
CTTT | C | 39 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0091others(36): Show | 43 | HG00423.hp1 HG01109.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.1498+84_1498+86del others(3): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 12/19 | chr14 | 74671321 | ||||||
| chr14:74671321
|
CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159others(2): Show | 5 | HG02723.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+76_1498+86del others(11): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 12/19 | chr14 | 74671321 | ||||||
| chr14:74671321
|
CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0010g0052a0001c0001t0010g0054a0001c0001t0010g0060others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498+75_1498+86del others(12): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 12/19 | chr14 | 74671321 | ||||||
| chr14:74671627
|
A | G | 2 | a0001c0001t0008g0164a0001c0001t0008g0236 | 2 | NA18967.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1423-144T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 11/19 | chr14 | 74671627 | ||||||
| chr14:74671934
|
T | C | 23 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0008others(20): Show | 26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.1423-451A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 11/19 | chr14 | 74671934 | ||||||
| chr14:74672138
|
G | A | 1 | a0001c0001t0003g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1423-655C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 11/19 | chr14 | 74672138 | ||||||
| chr14:74672207
|
A | C | 1 | a0001c0001t0002g0194 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1422+624T>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 11/19 | chr14 | 74672207 | ||||||
| chr14:74672252
|
C | A | 5 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159others(2): Show | 5 | HG02723.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1422+579G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 11/19 | chr14 | 74672252 | ||||||
| chr14:74672406
|
A | G | 2 | a0001c0001t0003g0242a0001c0001t0003g0257 | 2 | HG00438.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1422+425T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 11/19 | chr14 | 74672406 | ||||||
| chr14:74672496
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1422+335C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 11/19 | chr14 | 74672496 | ||||||
| chr14:74672716
|
T | C | 7 | a0001c0001t0009g0043a0001c0001t0009g0061a0001c0001t0019g0044others(4): Show | 7 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1422+115A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 11/19 | chr14 | 74672716 | ||||||
| chr14:74672736
|
CAAACAAA others(5): Show |
C | 4 | a0001c0005t0009g0027a0001c0005t0009g0028a0001c0005t0009g0029others(1): Show | 4 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1422+83_1422+94del others(12): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 11/19 | chr14 | 74672736 | ||||||
| chr14:74672822
|
T | C | 2 | a0001c0001t0012g0007a0001c0001t0012g0046 | 3 | HG02723.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1422+9A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 11/19 | chr14 | 74672822 | ||||||
| chr14:74673233
|
C | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(142): Show | 160 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.1159-15G>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 9/19 | chr14 | 74673233 | ||||||
| chr14:74673409
|
GT | G | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0021g0097 | 3 | NA18942.hp2 NA18946.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1159-192delA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 9/19 | chr14 | 74673409 | ||||||
| chr14:74673414
|
A | C | 2 | a0001c0001t0012g0007a0001c0001t0012g0046 | 3 | HG02723.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1159-196T>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 9/19 | chr14 | 74673414 | ||||||
| chr14:74673478
|
G | A | 2 | a0001c0001t0012g0007a0001c0001t0012g0046 | 3 | HG02723.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1159-260C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 9/19 | chr14 | 74673478 | ||||||
| chr14:74673511
|
G | A | 1 | a0001c0001t0004g0042 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1159-293C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 9/19 | chr14 | 74673511 | ||||||
| chr14:74673891
|
T | C | 1 | a0001c0001t0005g0279 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1158+143A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 9/19 | chr14 | 74673891 | ||||||
| chr14:74674151
|
T | C | 1 | a0001c0001t0018g0342 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1081-40A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/19 | chr14 | 74674151 | ||||||
| chr14:74674239
|
A | G | 2 | a0001c0001t0002g0170a0001c0001t0002g0174 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1081-128T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/19 | chr14 | 74674239 | ||||||
| chr14:74674458
|
T | C | 5 | a0001c0001t0003g0259a0001c0001t0003g0260a0001c0001t0003g0274others(2): Show | 5 | HG00544.hp2 HG02523.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1081-347A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/19 | chr14 | 74674458 | ||||||
| chr14:74674617
|
T | A | 8 | a0001c0001t0007g0045a0001c0001t0007g0047a0001c0001t0007g0048others(5): Show | 8 | HG01109.hp2 HG02572.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1081-506A>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/19 | chr14 | 74674617 | ||||||
| chr14:74674628
|
T | G | 60 | a0001c0001t0003g0242a0001c0001t0003g0244a0001c0001t0003g0247others(57): Show | 61 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1081-517A>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/19 | chr14 | 74674628 | ||||||
| chr14:74675090
|
T | C | 19 | a0001c0001t0003g0242a0001c0001t0003g0257a0001c0001t0003g0288others(16): Show | 20 | HG00438.hp1 HG02015.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1080+609A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/19 | chr14 | 74675090 | ||||||
| chr14:74675222
|
C | T | 3 | a0001c0001t0003g0288a0001c0001t0003g0289a0001c0001t0003g0290 | 3 | NA18969.hp1 NA19058.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1080+477G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/19 | chr14 | 74675222 | ||||||
| chr14:74675409
|
C | T | 10 | a0001c0001t0006g0026a0001c0001t0006g0031a0001c0001t0018g0341others(7): Show | 11 | HG02717.hp2 HG02738.hp1 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.1080+290G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/19 | chr14 | 74675409 | ||||||
| chr14:74675511
|
A | G | 1 | a0001c0001t0003g0253 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1080+188T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/19 | chr14 | 74675511 | ||||||
| chr14:74675513
|
C | T | 3 | a0003c0003t0011g0015a0003c0003t0011g0152a0003c0003t0011g0153 | 4 | HG02145.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080+186G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/19 | chr14 | 74675513 | ||||||
| chr14:74675547
|
G | T | 1 | a0001c0001t0005g0271 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1080+152C>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/19 | chr14 | 74675547 | ||||||
| chr14:74675570
|
G | T | 23 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0008others(20): Show | 26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.1080+129C>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/19 | chr14 | 74675570 | ||||||
| chr14:74675643
|
C | A | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1080+56G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 8/19 | chr14 | 74675643 | ||||||
| chr14:74676848
|
G | C | 1 | a0001c0001t0001g0099 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.482-96C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74676848 | ||||||
| chr14:74676897
|
T | C | 241 | a0001c0001t0001g0093a0001c0001t0001g0099a0001c0001t0001g0102others(238): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.482-145A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74676897 | ||||||
| chr14:74676985
|
G | A | 1 | a0001c0001t0005g0273 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.482-233C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74676985 | ||||||
| chr14:74676990
|
G | T | 226 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(223): Show | 249 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.482-238C>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74676990 | ||||||
| chr14:74677000
|
T | C | 1 | a0001c0001t0003g0306 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.482-248A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677000 | ||||||
| chr14:74677001
|
G | A | 1 | a0001c0001t0003g0306 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.482-249C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677001 | ||||||
| chr14:74677005
|
T | C | 1 | a0001c0001t0003g0263 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.482-253A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677005 | ||||||
| chr14:74677006
|
A | G | 4 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0161others(1): Show | 4 | HG02723.hp2 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-254T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677006 | ||||||
| chr14:74677015
|
A | G | 10 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0161others(7): Show | 10 | HG01346.hp1 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.482-263T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677015 | ||||||
| chr14:74677079
|
G | C | 2 | a0001c0001t0013g0338a0001c0001t0027g0339 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.482-327C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677079 | ||||||
| chr14:74677087
|
C | T | 1 | a0001c0001t0004g0033 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.482-335G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677087 | ||||||
| chr14:74677095
|
G | A | 1 | a0001c0001t0003g0257 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.482-343C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677095 | ||||||
| chr14:74677237
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.482-485C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677237 | ||||||
| chr14:74677500
|
C | CT | 16 | a0001c0001t0002g0004a0001c0001t0002g0184a0001c0001t0002g0186others(13): Show | 18 | HG01261.hp1 HG01361.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.482-749dupA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677500 | ||||||
| chr14:74677500
|
CT | C | 189 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(186): Show | 210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.482-749delA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677500 | ||||||
| chr14:74677500
|
CTT | C | 20 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0003g0248others(17): Show | 21 | HG00738.hp1 HG01070.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.482-750_482-749del others(2): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677500 | ||||||
| chr14:74677585
|
C | T | 15 | a0001c0001t0007g0045a0001c0001t0007g0047a0001c0001t0007g0048others(12): Show | 16 | HG01109.hp2 HG01884.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.482-833G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677585 | ||||||
| chr14:74677597
|
G | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(107): Show | 121 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.482-845C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677597 | ||||||
| chr14:74677693
|
G | A | 6 | a0001c0001t0013g0338a0001c0001t0027g0339a0001c0004t0013g0165others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-941C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677693 | ||||||
| chr14:74677832
|
G | A | 1 | a0001c0001t0003g0299 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.482-1080C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677832 | ||||||
| chr14:74677915
|
T | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(248): Show | 275 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.482-1163A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74677915 | ||||||
| chr14:74678018
|
T | C | 1 | a0001c0001t0003g0274 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.482-1266A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74678018 | ||||||
| chr14:74678360
|
C | T | 1 | a0001c0001t0003g0257 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.482-1608G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74678360 | ||||||
| chr14:74678493
|
C | A | 4 | a0001c0005t0009g0027a0001c0005t0009g0028a0001c0005t0009g0029others(1): Show | 4 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1741G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74678493 | ||||||
| chr14:74678496
|
C | CA | 39 | a0001c0001t0003g0300a0001c0001t0004g0005a0001c0001t0004g0006others(36): Show | 43 | HG00423.hp1 HG01109.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.482-1745dupT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74678496 | ||||||
| chr14:74678695
|
CA | C | 138 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(135): Show | 149 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.482-1944delT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74678695 | ||||||
| chr14:74678695
|
CAA | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(95): Show | 110 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.482-1945_482-1944d others(4): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74678695 | ||||||
| chr14:74678809
|
G | A | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.482-2057C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74678809 | ||||||
| chr14:74678811
|
G | A | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.482-2059C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74678811 | ||||||
| chr14:74678825
|
T | A | 97 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0242others(94): Show | 106 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.482-2073A>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74678825 | ||||||
| chr14:74678953
|
A | T | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(105): Show | 119 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.482-2201T>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74678953 | ||||||
| chr14:74679554
|
C | T | 1 | a0003c0003t0011g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.482-2802G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74679554 | ||||||
| chr14:74679797
|
T | C | 255 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(252): Show | 279 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.482-3045A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74679797 | ||||||
| chr14:74679844
|
TAATA | T | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(105): Show | 119 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.482-3096_482-3093d others(6): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74679844 | ||||||
| chr14:74680135
|
G | T | 1 | a0001c0001t0002g0216 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.481+3161C>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74680135 | ||||||
| chr14:74680204
|
AAGAAAAG others(5): Show |
A | 4 | a0001c0004t0013g0165a0001c0004t0013g0167a0001c0004t0015g0162others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+3080_481+3091d others(14): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74680204 | ||||||
| chr14:74680339
|
T | C | 6 | a0001c0001t0013g0338a0001c0001t0027g0339a0001c0004t0013g0165others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.481+2957A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74680339 | ||||||
| chr14:74680450
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.481+2846C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74680450 | ||||||
| chr14:74680488
|
A | C | 2 | a0001c0001t0003g0323a0001c0001t0028g0327 | 2 | NA18946.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.481+2808T>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74680488 | ||||||
| chr14:74680821
|
G | T | 1 | a0001c0001t0002g0216 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.481+2475C>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74680821 | ||||||
| chr14:74680949
|
A | G | 2 | a0001c0001t0013g0338a0001c0001t0027g0339 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.481+2347T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74680949 | ||||||
| chr14:74681030
|
C | G | 1 | a0001c0001t0005g0325 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.481+2266G>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74681030 | ||||||
| chr14:74681047
|
G | A | 4 | a0001c0001t0002g0160a0001c0001t0002g0193a0001c0001t0002g0232others(1): Show | 4 | HG02559.hp1 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+2249C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74681047 | ||||||
| chr14:74681176
|
G | A | 1 | a0001c0001t0005g0269 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.481+2120C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74681176 | ||||||
| chr14:74681229
|
A | C | 8 | a0001c0001t0006g0026a0001c0001t0006g0031a0002c0002t0006g0009others(5): Show | 9 | HG02738.hp1 HG04228.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+2067T>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74681229 | ||||||
| chr14:74681248
|
G | C | 10 | a0001c0001t0007g0045a0001c0001t0007g0047a0001c0001t0007g0048others(7): Show | 11 | HG01109.hp2 HG02572.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.481+2048C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74681248 | ||||||
| chr14:74681545
|
C | T | 3 | a0001c0001t0010g0052a0001c0001t0010g0054a0001c0001t0010g0063 | 3 | HG02280.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.481+1751G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74681545 | ||||||
| chr14:74681739
|
C | T | 5 | a0001c0001t0010g0052a0001c0001t0010g0054a0001c0001t0010g0060others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+1557G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74681739 | ||||||
| chr14:74681756
|
G | A | 23 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0008others(20): Show | 26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.481+1540C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74681756 | ||||||
| chr14:74681805
|
T | TG | 91 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 100 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.481+1490dupC | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74681805 | ||||||
| chr14:74681825
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.481+1471C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74681825 | ||||||
| chr14:74682237
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.481+1059G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74682237 | ||||||
| chr14:74682275
|
C | A | 1 | a0001c0001t0012g0046 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.481+1021G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74682275 | ||||||
| chr14:74682314
|
A | G | 1 | a0001c0001t0002g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.481+982T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74682314 | ||||||
| chr14:74682436
|
G | A | 7 | a0001c0001t0007g0045a0001c0001t0007g0047a0001c0001t0007g0048others(4): Show | 7 | HG01109.hp2 HG02572.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+860C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74682436 | ||||||
| chr14:74682567
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.481+729G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74682567 | ||||||
| chr14:74683027
|
G | A | 2 | a0001c0001t0002g0181a0001c0001t0002g0224 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.481+269C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74683027 | ||||||
| chr14:74683096
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.481+200A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 5/19 | chr14 | 74683096 | ||||||
| chr14:74683987
|
G | A | 4 | a0001c0005t0009g0027a0001c0005t0009g0028a0001c0005t0009g0029others(1): Show | 4 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-454C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 4/19 | chr14 | 74683987 | ||||||
| chr14:74684021
|
A | T | 1 | a0001c0001t0004g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.243+433T>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 4/19 | chr14 | 74684021 | ||||||
| chr14:74684058
|
G | A | 4 | a0001c0001t0010g0052a0001c0001t0010g0054a0001c0001t0010g0063others(1): Show | 4 | HG02280.hp2 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+396C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 4/19 | chr14 | 74684058 | ||||||
| chr14:74684201
|
T | C | 1 | a0001c0001t0002g0187 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.243+253A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 4/19 | chr14 | 74684201 | ||||||
| chr14:74684344
|
G | A | 252 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(249): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.243+110C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 4/19 | chr14 | 74684344 | ||||||
| chr14:74684708
|
G | A | 4 | a0001c0001t0003g0244a0001c0001t0003g0264a0001c0001t0003g0265others(1): Show | 4 | HG00423.hp2 NA18944.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-28C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 3/19 | chr14 | 74684708 | ||||||
| chr14:74684784
|
G | A | 3 | a0001c0001t0009g0043a0001c0001t0009g0061a0001c0001t0019g0044 | 3 | HG02818.hp2 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.17-104C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 3/19 | chr14 | 74684784 | ||||||
| chr14:74684802
|
A | C | 1 | a0003c0003t0011g0153 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.17-122T>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 3/19 | chr14 | 74684802 | ||||||
| chr14:74685254
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.16+346A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 3/19 | chr14 | 74685254 | ||||||
| chr14:74685365
|
G | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(121): Show | 136 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.16+235C>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 3/19 | chr14 | 74685365 | ||||||
| chr14:74685446
|
T | C | 4 | a0002c0002t0006g0009a0002c0002t0006g0067a0002c0002t0006g0068others(1): Show | 5 | NA18973.hp2 NA18986.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+154A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 3/19 | chr14 | 74685446 | ||||||
| chr14:74685689
|
G | A | 1 | a0001c0001t0005g0276 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-45-29C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74685689 | ||||||
| chr14:74685709
|
G | A | 1 | a0001c0001t0007g0062 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-45-49C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74685709 | ||||||
| chr14:74685758
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-45-98A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74685758 | ||||||
| chr14:74685765
|
A | G | 3 | a0003c0003t0011g0015a0003c0003t0011g0152a0003c0003t0011g0153 | 4 | HG02145.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45-105T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74685765 | ||||||
| chr14:74685960
|
C | T | 1 | a0001c0006t0024g0169 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-45-300G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74685960 | ||||||
| chr14:74686068
|
T | G | 1 | a0001c0001t0002g0188 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-45-408A>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74686068 | ||||||
| chr14:74686172
|
T | C | 38 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0008others(35): Show | 42 | HG00423.hp1 HG01109.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.-45-512A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74686172 | ||||||
| chr14:74686223
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-45-563T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74686223 | ||||||
| chr14:74686237
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-45-577A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74686237 | ||||||
| chr14:74686391
|
A | G | 2 | a0001c0001t0008g0164a0001c0001t0008g0236 | 2 | NA18967.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-45-731T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74686391 | ||||||
| chr14:74686749
|
T | A | 1 | a0001c0001t0001g0149 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-45-1089A>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74686749 | ||||||
| chr14:74686781
|
C | A | 1 | a0001c0001t0007g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-45-1121G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74686781 | ||||||
| chr14:74686788
|
T | C | 1 | a0001c0001t0003g0303 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-45-1128A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74686788 | ||||||
| chr14:74686901
|
A | G | 22 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0008others(19): Show | 25 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.-45-1241T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74686901 | ||||||
| chr14:74687018
|
G | C | 2 | a0001c0001t0014g0126a0001c0001t0014g0143 | 2 | NA18939.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-45-1358C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74687018 | ||||||
| chr14:74687115
|
C | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(87): Show | 99 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-45-1455G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74687115 | ||||||
| chr14:74687247
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(87): Show | 99 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-45-1587C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74687247 | ||||||
| chr14:74687293
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-45-1633T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74687293 | ||||||
| chr14:74687396
|
C | A | 23 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0008others(20): Show | 26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.-45-1736G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74687396 | ||||||
| chr14:74687643
|
G | A | 4 | a0001c0004t0013g0165a0001c0004t0013g0167a0001c0004t0015g0162others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-45-1983C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74687643 | ||||||
| chr14:74687754
|
A | G | 38 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0008others(35): Show | 42 | HG00423.hp1 HG01109.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.-45-2094T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74687754 | ||||||
| chr14:74687816
|
G | A | 8 | a0001c0001t0006g0026a0001c0001t0006g0031a0002c0002t0006g0009others(5): Show | 9 | HG02738.hp1 HG04228.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.-45-2156C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74687816 | ||||||
| chr14:74687842
|
A | G | 1 | a0001c0001t0003g0291 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-45-2182T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74687842 | ||||||
| chr14:74688019
|
C | CT | 55 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0072others(52): Show | 58 | HG00673.hp1 HG00735.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.-45-2360dupA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688019 | ||||||
| chr14:74688019
|
CT | C | 8 | a0001c0001t0001g0086a0001c0001t0002g0186a0001c0001t0008g0164others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.-45-2360delA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688019 | ||||||
| chr14:74688020
|
T | A | 5 | a0001c0001t0006g0026a0001c0001t0006g0031a0002c0002t0006g0009others(2): Show | 6 | HG02738.hp1 HG04228.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45-2360A>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688020 | ||||||
| chr14:74688021
|
T | A | 1 | a0002c0002t0006g0025 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-45-2361A>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688021 | ||||||
| chr14:74688094
|
C | T | 14 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(11): Show | 15 | HG00423.hp1 HG01934.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.-45-2434G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688094 | ||||||
| chr14:74688119
|
G | A | 1 | a0001c0001t0003g0277 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-45-2459C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688119 | ||||||
| chr14:74688182
|
T | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(67): Show | 78 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.-45-2522A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688182 | ||||||
| chr14:74688320
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-45-2660G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688320 | ||||||
| chr14:74688336
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-45-2676G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688336 | ||||||
| chr14:74688680
|
C | T | 6 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0191others(3): Show | 6 | HG02071.hp1 NA18940.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45-3020G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688680 | ||||||
| chr14:74688685
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-45-3025G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688685 | ||||||
| chr14:74688774
|
A | G | 4 | a0001c0004t0013g0165a0001c0004t0013g0167a0001c0004t0015g0162others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-45-3114T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688774 | ||||||
| chr14:74688776
|
A | T | 1 | a0001c0001t0001g0085 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-45-3116T>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688776 | ||||||
| chr14:74688823
|
ATTTTAT | A | 23 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0008others(20): Show | 26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.-45-3169_-45-3164d others(8): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688823 | ||||||
| chr14:74688993
|
C | T | 1 | a0003c0003t0011g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-46+3048G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74688993 | ||||||
| chr14:74689028
|
A | T | 1 | a0001c0001t0001g0075 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-46+3013T>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689028 | ||||||
| chr14:74689034
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-46+3007C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689034 | ||||||
| chr14:74689065
|
C | A | 1 | a0001c0001t0014g0143 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-46+2976G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689065 | ||||||
| chr14:74689215
|
T | C | 23 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0008others(20): Show | 26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.-46+2826A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689215 | ||||||
| chr14:74689587
|
C | CT | 18 | a0001c0001t0003g0247a0001c0001t0003g0249a0001c0001t0003g0252others(15): Show | 18 | HG01123.hp1 HG01192.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.-46+2453dupA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689587 | ||||||
| chr14:74689591
|
TC | T | 4 | a0001c0001t0003g0278a0001c0001t0003g0301a0001c0001t0003g0333others(1): Show | 4 | HG00408.hp2 HG00558.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46+2449delG | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689591 | ||||||
| chr14:74689592
|
C | CT | 10 | a0001c0001t0002g0189a0001c0001t0002g0210a0001c0001t0002g0222others(7): Show | 11 | HG02145.hp2 HG02897.hp1 HG04228.hp1 others(8): Show |
intron_variant | MODIFIER | c.-46+2448dupA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689592 | ||||||
| chr14:74689592
|
C | T | 93 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0242others(90): Show | 102 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-46+2449G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689592 | ||||||
| chr14:74689592
|
CT | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(80): Show | 92 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.-46+2448delA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689592 | ||||||
| chr14:74689597
|
T | C | 1 | a0001c0001t0002g0200 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-46+2444A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689597 | ||||||
| chr14:74689620
|
G | A | 1 | a0001c0001t0005g0281 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-46+2421C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689620 | ||||||
| chr14:74689753
|
C | T | 1 | a0001c0001t0003g0283 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-46+2288G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689753 | ||||||
| chr14:74689825
|
A | G | 1 | a0001c0001t0007g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-46+2216T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689825 | ||||||
| chr14:74689839
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(95): Show | 107 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.-46+2202C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689839 | ||||||
| chr14:74689844
|
C | T | 3 | a0003c0003t0011g0015a0003c0003t0011g0152a0003c0003t0011g0153 | 4 | HG02145.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46+2197G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689844 | ||||||
| chr14:74689892
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0104 | 3 | HG01978.hp2 HG02273.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.-46+2149C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74689892 | ||||||
| chr14:74690111
|
C | T | 14 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(11): Show | 15 | HG00423.hp1 HG01934.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.-46+1930G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74690111 | ||||||
| chr14:74690112
|
G | A | 2 | a0001c0001t0012g0007a0001c0001t0012g0046 | 3 | HG02723.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-46+1929C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74690112 | ||||||
| chr14:74690264
|
C | CA | 27 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0123others(24): Show | 27 | HG00673.hp2 HG00741.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.-46+1776dupT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74690264 | ||||||
| chr14:74690264
|
CA | C | 109 | a0001c0001t0001g0074a0001c0001t0002g0216a0001c0001t0002g0227others(106): Show | 119 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-46+1776delT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74690264 | ||||||
| chr14:74690264
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0007g0048 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-46+1766_-46+1776d others(13): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74690264 | ||||||
| chr14:74690267
|
A | C | 9 | a0001c0001t0003g0244a0001c0001t0003g0264a0001c0001t0003g0265others(6): Show | 9 | HG00423.hp2 HG02027.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46+1774T>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74690267 | ||||||
| chr14:74690310
|
C | T | 7 | a0001c0001t0002g0017a0001c0001t0002g0189a0001c0001t0002g0190others(4): Show | 8 | HG02071.hp1 NA18940.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46+1731G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74690310 | ||||||
| chr14:74690428
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-46+1613C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74690428 | ||||||
| chr14:74690478
|
C | T | 2 | a0002c0002t0006g0024a0002c0002t0006g0025 | 2 | NA18949.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-46+1563G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74690478 | ||||||
| chr14:74690587
|
C | A | 1 | a0001c0001t0013g0338 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-46+1454G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74690587 | ||||||
| chr14:74690595
|
T | C | 1 | a0001c0001t0007g0064 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-46+1446A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74690595 | ||||||
| chr14:74690797
|
T | C | 3 | a0001c0001t0010g0052a0001c0001t0010g0054a0001c0001t0010g0063 | 3 | HG02280.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-46+1244A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74690797 | ||||||
| chr14:74690846
|
A | G | 1 | a0001c0001t0029g0340 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-46+1195T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74690846 | ||||||
| chr14:74690934
|
T | A | 1 | a0001c0001t0027g0339 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-46+1107A>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74690934 | ||||||
| chr14:74691010
|
G | T | 100 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0242others(97): Show | 109 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.-46+1031C>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74691010 | ||||||
| chr14:74691021
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-46+1020G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74691021 | ||||||
| chr14:74691087
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-46+954C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74691087 | ||||||
| chr14:74691264
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(87): Show | 99 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-46+777C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74691264 | ||||||
| chr14:74691320
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0139a0001c0001t0029g0340 | 4 | HG01891.hp2 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46+721G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74691320 | ||||||
| chr14:74691324
|
T | TA | 214 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(211): Show | 236 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.-46+716dupT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74691324 | ||||||
| chr14:74691324
|
T | TAA | 24 | a0001c0001t0001g0078a0001c0001t0001g0127a0001c0001t0001g0133others(21): Show | 25 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.-46+715_-46+716dup others(2): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74691324 | ||||||
| chr14:74691355
|
G | A | 8 | a0001c0001t0006g0026a0001c0001t0006g0031a0002c0002t0006g0009others(5): Show | 9 | HG02738.hp1 HG04228.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.-46+686C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74691355 | ||||||
| chr14:74691365
|
G | A | 1 | a0001c0001t0007g0064 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-46+676C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74691365 | ||||||
| chr14:74691390
|
A | G | 1 | a0001c0001t0002g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-46+651T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74691390 | ||||||
| chr14:74691712
|
C | A | 1 | a0001c0001t0004g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-46+329G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74691712 | ||||||
| chr14:74691784
|
C | T | 2 | a0001c0001t0002g0181a0001c0001t0002g0224 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-46+257G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 2/19 | chr14 | 74691784 | ||||||
| chr14:74692600
|
T | G | 6 | a0001c0001t0013g0338a0001c0001t0027g0339a0001c0004t0013g0165others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-333-272A>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74692600 | ||||||
| chr14:74692772
|
C | T | 11 | a0001c0001t0006g0026a0001c0001t0006g0031a0002c0002t0006g0009others(8): Show | 13 | HG02145.hp2 HG02630.hp2 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.-333-444G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74692772 | ||||||
| chr14:74693098
|
A | T | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-333-770T>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74693098 | ||||||
| chr14:74693246
|
T | C | 2 | a0003c0003t0011g0015a0003c0003t0011g0153 | 3 | HG02145.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-333-918A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74693246 | ||||||
| chr14:74693408
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-333-1080G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74693408 | ||||||
| chr14:74693420
|
T | G | 12 | a0001c0001t0004g0032a0001c0001t0004g0034a0001c0001t0004g0035others(9): Show | 12 | HG01934.hp2 HG01943.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-333-1092A>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74693420 | ||||||
| chr14:74693475
|
C | T | 4 | a0001c0001t0003g0261a0001c0001t0003g0263a0001c0001t0003g0283others(1): Show | 4 | HG01256.hp1 HG02293.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-333-1147G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74693475 | ||||||
| chr14:74693645
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-333-1317T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74693645 | ||||||
| chr14:74694175
|
A | AAAAT | 12 | a0001c0001t0003g0242a0001c0001t0003g0257a0001c0001t0003g0288others(9): Show | 12 | HG00438.hp1 HG02015.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-333-1851_-333-184 others(8): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74694175 | ||||||
| chr14:74694175
|
AAAAT | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 161 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-333-1851_-333-184 others(8): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74694175 | ||||||
| chr14:74694305
|
A | G | 3 | a0001c0001t0002g0216a0001c0001t0002g0218a0001c0001t0002g0240 | 3 | NA18948.hp2 NA18960.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-333-1977T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74694305 | ||||||
| chr14:74694699
|
G | A | 8 | a0001c0001t0006g0026a0001c0001t0006g0031a0002c0002t0006g0009others(5): Show | 9 | HG02738.hp1 HG04228.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.-333-2371C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74694699 | ||||||
| chr14:74694748
|
GGGA | G | 23 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0008others(20): Show | 26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.-333-2423_-333-242 others(7): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74694748 | ||||||
| chr14:74694764
|
C | A | 5 | a0001c0001t0007g0048a0001c0001t0007g0049a0001c0001t0007g0050others(2): Show | 5 | HG01109.hp2 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-333-2436G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74694764 | ||||||
| chr14:74694954
|
A | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(87): Show | 99 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-333-2626T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74694954 | ||||||
| chr14:74694990
|
G | GA | 35 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0187others(32): Show | 37 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.-333-2663dupT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74694990 | ||||||
| chr14:74694990
|
GA | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 99 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-333-2663delT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74694990 | ||||||
| chr14:74695029
|
A | G | 1 | a0001c0001t0002g0176 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-333-2701T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74695029 | ||||||
| chr14:74695072
|
C | CT | 16 | a0001c0001t0001g0073a0001c0001t0001g0113a0001c0001t0001g0142others(13): Show | 16 | HG01081.hp2 HG02615.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.-333-2745dupA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74695072 | ||||||
| chr14:74695204
|
C | A | 1 | a0001c0001t0003g0324 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-333-2876G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74695204 | ||||||
| chr14:74695227
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-333-2899C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74695227 | ||||||
| chr14:74695238
|
C | T | 8 | a0001c0001t0006g0026a0001c0001t0006g0031a0002c0002t0006g0009others(5): Show | 9 | HG02738.hp1 HG04228.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.-333-2910G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74695238 | ||||||
| chr14:74695281
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 158 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.-333-2953G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74695281 | ||||||
| chr14:74695318
|
G | A | 100 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0242others(97): Show | 109 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.-333-2990C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74695318 | ||||||
| chr14:74695381
|
G | C | 2 | a0001c0001t0012g0007a0001c0001t0012g0046 | 3 | HG02723.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-333-3053C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74695381 | ||||||
| chr14:74695546
|
C | T | 8 | a0001c0001t0006g0026a0001c0001t0006g0031a0002c0002t0006g0009others(5): Show | 9 | HG02738.hp1 HG04228.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.-333-3218G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74695546 | ||||||
| chr14:74695610
|
C | G | 3 | a0001c0001t0002g0016a0001c0001t0002g0194a0001c0001t0002g0214 | 4 | HG00408.hp1 HG00558.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.-333-3282G>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74695610 | ||||||
| chr14:74695653
|
T | C | 5 | a0001c0001t0003g0303a0001c0001t0003g0304a0001c0001t0003g0305others(2): Show | 5 | NA18964.hp2 NA18974.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.-333-3325A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74695653 | ||||||
| chr14:74695947
|
T | C | 2 | a0001c0001t0007g0045a0001c0001t0007g0047 | 2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-333-3619A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74695947 | ||||||
| chr14:74696012
|
T | A | 23 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0008others(20): Show | 26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.-333-3684A>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74696012 | ||||||
| chr14:74696109
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-333-3781C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74696109 | ||||||
| chr14:74696207
|
T | C | 1 | a0001c0001t0003g0250 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-333-3879A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74696207 | ||||||
| chr14:74696352
|
C | T | 8 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0023others(5): Show | 10 | HG01243.hp1 HG01496.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-333-4024G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74696352 | ||||||
| chr14:74696462
|
T | C | 4 | a0001c0005t0009g0027a0001c0005t0009g0028a0001c0005t0009g0029others(1): Show | 4 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-333-4134A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74696462 | ||||||
| chr14:74696466
|
G | A | 1 | a0001c0001t0004g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-333-4138C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74696466 | ||||||
| chr14:74696499
|
T | G | 1 | a0001c0001t0002g0206 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-333-4171A>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74696499 | ||||||
| chr14:74696847
|
C | A | 1 | a0001c0001t0002g0176 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-333-4519G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74696847 | ||||||
| chr14:74697118
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-333-4790G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74697118 | ||||||
| chr14:74697155
|
T | TAC | 2 | a0003c0003t0011g0015a0003c0003t0011g0153 | 3 | HG02145.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-333-4829_-333-482 others(6): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74697155 | ||||||
| chr14:74697155
|
T | TACAC | 5 | a0001c0001t0008g0164a0001c0001t0008g0208a0001c0001t0008g0236others(2): Show | 5 | NA18955.hp1 NA18967.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.-333-4831_-333-482 others(8): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74697155 | ||||||
| chr14:74697155
|
TAC | T | 31 | a0001c0001t0002g0226a0001c0001t0006g0026a0001c0001t0006g0031others(28): Show | 33 | HG01081.hp2 HG01109.hp2 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.-333-4829_-333-482 others(6): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74697155 | ||||||
| chr14:74697305
|
T | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 161 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-333-4977A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74697305 | ||||||
| chr14:74697404
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-333-5076A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74697404 | ||||||
| chr14:74697438
|
C | T | 105 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0242others(102): Show | 114 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-333-5110G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74697438 | ||||||
| chr14:74697505
|
A | T | 1 | a0001c0001t0009g0043 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-333-5177T>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74697505 | ||||||
| chr14:74697531
|
TAA | T | 2 | a0001c0001t0012g0007a0001c0001t0012g0046 | 3 | HG02723.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-333-5205_-333-520 others(6): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74697531 | ||||||
| chr14:74697729
|
T | C | 1 | a0001c0001t0003g0306 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-333-5401A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74697729 | ||||||
| chr14:74697851
|
T | C | 1 | a0001c0001t0002g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-333-5523A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74697851 | ||||||
| chr14:74697982
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-333-5654A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74697982 | ||||||
| chr14:74698142
|
C | T | 3 | a0001c0001t0010g0052a0001c0001t0010g0054a0001c0001t0010g0063 | 3 | HG02280.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-333-5814G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74698142 | ||||||
| chr14:74698286
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-333-5958A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74698286 | ||||||
| chr14:74698414
|
G | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0127 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-333-6086C>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74698414 | ||||||
| chr14:74698424
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-333-6096A>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74698424 | ||||||
| chr14:74698505
|
G | C | 1 | a0001c0001t0001g0127 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-333-6177C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74698505 | ||||||
| chr14:74698614
|
A | G | 4 | a0001c0004t0013g0165a0001c0004t0013g0167a0001c0004t0015g0162others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-333-6286T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74698614 | ||||||
| chr14:74698678
|
G | T | 3 | a0001c0001t0002g0216a0001c0001t0002g0218a0001c0001t0002g0240 | 3 | NA18948.hp2 NA18960.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-333-6350C>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74698678 | ||||||
| chr14:74698858
|
T | TA | 21 | a0001c0001t0001g0077a0001c0001t0001g0085a0001c0001t0002g0003others(18): Show | 24 | HG01109.hp2 HG01358.hp2 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.-333-6531dupT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74698858 | ||||||
| chr14:74698858
|
T | TAA | 84 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(81): Show | 94 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-333-6532_-333-653 others(6): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74698858 | ||||||
| chr14:74698858
|
TA | T | 7 | a0001c0001t0002g0179a0001c0001t0002g0189a0001c0001t0002g0190others(4): Show | 7 | HG02071.hp1 HG03491.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.-333-6531delT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74698858 | ||||||
| chr14:74698884
|
TGTG | T | 10 | a0001c0001t0002g0004a0001c0001t0002g0163a0001c0001t0002g0184others(7): Show | 12 | HG02027.hp2 HG02040.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.-333-6559_-333-655 others(7): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74698884 | ||||||
| chr14:74698948
|
C | A | 1 | a0001c0001t0003g0329 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-333-6620G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74698948 | ||||||
| chr14:74699122
|
A | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 161 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-333-6794T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699122 | ||||||
| chr14:74699348
|
G | GGT | 25 | a0001c0001t0002g0155a0001c0001t0002g0181a0001c0001t0002g0182others(22): Show | 26 | HG00438.hp1 HG00544.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-333-7022_-333-702 others(6): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699348 | ||||||
| chr14:74699348
|
G | GGTGT | 14 | a0001c0001t0004g0036a0001c0001t0004g0037a0001c0001t0004g0038others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-333-7024_-333-702 others(8): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699348 | ||||||
| chr14:74699348
|
G | GGTGTGT | 13 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(10): Show | 14 | HG00423.hp1 HG01081.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-333-7026_-333-702 others(10): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699348 | ||||||
| chr14:74699348
|
G | GGTGTGTG others(1): Show |
8 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0023others(5): Show | 10 | HG01243.hp1 HG01496.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-333-7028_-333-702 others(12): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699348 | ||||||
| chr14:74699348
|
G | GGTGTGTG others(3): Show |
3 | a0001c0001t0004g0055a0003c0003t0011g0152a0003c0003t0011g0153 | 3 | HG02145.hp2 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-333-7030_-333-702 others(14): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699348 | ||||||
| chr14:74699348
|
G | GGTGTGTG others(7): Show |
1 | a0003c0003t0011g0015 | 2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-333-7034_-333-702 others(18): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699348 | ||||||
| chr14:74699364
|
TGTGTGTG others(9): Show |
T | 7 | a0001c0001t0001g0074a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 7 | HG00280.hp2 HG00741.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-333-7052_-333-703 others(20): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699364 | ||||||
| chr14:74699376
|
TGA | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(79): Show | 92 | HG00438.hp2 HG00544.hp1 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.-333-7050_-333-704 others(6): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699376 | ||||||
| chr14:74699376
|
TGAGA | T | 4 | a0001c0001t0001g0113a0001c0001t0002g0216a0001c0001t0002g0218others(1): Show | 4 | HG02647.hp1 NA18948.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.-333-7052_-333-704 others(8): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699376 | ||||||
| chr14:74699378
|
A | T | 244 | a0001c0001t0001g0022a0001c0001t0001g0071a0001c0001t0001g0072others(241): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-333-7050T>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699378 | ||||||
| chr14:74699380
|
A | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(102): Show | 116 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.-333-7052T>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699380 | ||||||
| chr14:74699382
|
A | T | 6 | a0001c0001t0002g0216a0001c0001t0002g0218a0001c0001t0002g0240others(3): Show | 6 | HG03098.hp2 HG03486.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-333-7054T>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699382 | ||||||
| chr14:74699385
|
G | C | 100 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0242others(97): Show | 109 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.-333-7057C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699385 | ||||||
| chr14:74699521
|
A | G | 8 | a0001c0001t0009g0043a0001c0001t0009g0061a0001c0001t0010g0052others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-333-7193T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699521 | ||||||
| chr14:74699687
|
A | C | 15 | a0001c0001t0006g0026a0001c0001t0006g0031a0001c0005t0009g0027others(12): Show | 17 | HG01081.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-333-7359T>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699687 | ||||||
| chr14:74699790
|
T | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 161 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-333-7462A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699790 | ||||||
| chr14:74699842
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-333-7514C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699842 | ||||||
| chr14:74699900
|
G | A | 1 | a0001c0001t0014g0126 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-333-7572C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74699900 | ||||||
| chr14:74700148
|
A | G | 3 | a0001c0001t0009g0043a0001c0001t0009g0061a0001c0001t0019g0044 | 3 | HG02818.hp2 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-333-7820T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74700148 | ||||||
| chr14:74700312
|
G | A | 251 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(248): Show | 275 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.-333-7984C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74700312 | ||||||
| chr14:74700505
|
G | A | 4 | a0001c0004t0013g0165a0001c0004t0013g0167a0001c0004t0015g0162others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-333-8177C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74700505 | ||||||
| chr14:74700634
|
G | T | 1 | a0001c0001t0002g0223 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-333-8306C>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74700634 | ||||||
| chr14:74700655
|
C | T | 3 | a0001c0001t0009g0043a0001c0001t0009g0061a0001c0001t0019g0044 | 3 | HG02818.hp2 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-333-8327G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74700655 | ||||||
| chr14:74700853
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-333-8525G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74700853 | ||||||
| chr14:74701003
|
A | G | 93 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0242others(90): Show | 102 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.-333-8675T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74701003 | ||||||
| chr14:74701022
|
G | C | 1 | a0001c0001t0007g0050 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-333-8694C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74701022 | ||||||
| chr14:74701316
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-333-8988C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74701316 | ||||||
| chr14:74701387
|
C | T | 1 | a0001c0004t0013g0165 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-333-9059G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74701387 | ||||||
| chr14:74701513
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-333-9185A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74701513 | ||||||
| chr14:74701529
|
C | T | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-333-9201G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74701529 | ||||||
| chr14:74701545
|
C | A | 1 | a0003c0003t0011g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-333-9217G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74701545 | ||||||
| chr14:74701627
|
A | G | 1 | a0001c0001t0003g0294 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-333-9299T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74701627 | ||||||
| chr14:74701812
|
C | T | 3 | a0001c0005t0009g0027a0001c0005t0009g0028a0001c0005t0009g0029 | 3 | HG01081.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-333-9484G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74701812 | ||||||
| chr14:74701820
|
G | A | 1 | a0001c0001t0002g0156 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-333-9492C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74701820 | ||||||
| chr14:74701982
|
A | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 161 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-333-9654T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74701982 | ||||||
| chr14:74702065
|
G | T | 1 | a0001c0001t0002g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-333-9737C>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74702065 | ||||||
| chr14:74702149
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-333-9821C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74702149 | ||||||
| chr14:74702224
|
C | T | 146 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 161 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-333-9896G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74702224 | ||||||
| chr14:74702233
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(87): Show | 99 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-333-9905C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74702233 | ||||||
| chr14:74702238
|
A | G | 1 | a0001c0001t0003g0247 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-333-9910T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74702238 | ||||||
| chr14:74702365
|
C | A | 3 | a0003c0003t0011g0015a0003c0003t0011g0152a0003c0003t0011g0153 | 4 | HG02145.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-333-10037G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74702365 | ||||||
| chr14:74702432
|
T | C | 8 | a0001c0001t0009g0043a0001c0001t0009g0061a0001c0001t0010g0052others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-333-10104A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74702432 | ||||||
| chr14:74702764
|
G | C | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-334+10169C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74702764 | ||||||
| chr14:74702985
|
T | C | 1 | a0001c0001t0010g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-334+9948A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74702985 | ||||||
| chr14:74703297
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-334+9636G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74703297 | ||||||
| chr14:74703298
|
G | A | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-334+9635C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74703298 | ||||||
| chr14:74703477
|
T | C | 2 | a0001c0001t0013g0338a0001c0001t0027g0339 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-334+9456A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74703477 | ||||||
| chr14:74703583
|
C | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(87): Show | 99 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-334+9350G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74703583 | ||||||
| chr14:74703712
|
T | C | 4 | a0001c0004t0013g0165a0001c0004t0013g0167a0001c0004t0015g0162others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-334+9221A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74703712 | ||||||
| chr14:74704099
|
A | C | 1 | a0001c0001t0010g0052 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-334+8834T>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74704099 | ||||||
| chr14:74704222
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-334+8711C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74704222 | ||||||
| chr14:74704290
|
T | C | 341 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(338): Show | 373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.-334+8643A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74704290 | ||||||
| chr14:74704322
|
C | T | 1 | a0001c0001t0003g0243 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-334+8611G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74704322 | ||||||
| chr14:74704691
|
T | A | 1 | a0001c0001t0001g0129 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-334+8242A>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74704691 | ||||||
| chr14:74704810
|
T | C | 1 | a0001c0001t0003g0255 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-334+8123A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74704810 | ||||||
| chr14:74704871
|
G | A | 1 | a0001c0001t0003g0307 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-334+8062C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74704871 | ||||||
| chr14:74704980
|
C | T | 252 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(249): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.-334+7953G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74704980 | ||||||
| chr14:74705003
|
T | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 162 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.-334+7930A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74705003 | ||||||
| chr14:74705043
|
G | GT | 77 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0003others(74): Show | 80 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-334+7889dupA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74705043 | ||||||
| chr14:74705043
|
GT | G | 5 | a0001c0001t0003g0312a0001c0001t0007g0051a0003c0003t0011g0015others(2): Show | 6 | HG02145.hp2 HG02630.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-334+7889delA | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74705043 | ||||||
| chr14:74705069
|
C | T | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-334+7864G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74705069 | ||||||
| chr14:74705156
|
C | T | 4 | a0001c0005t0009g0027a0001c0005t0009g0028a0001c0005t0009g0029others(1): Show | 4 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-334+7777G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74705156 | ||||||
| chr14:74705186
|
T | C | 2 | a0001c0001t0013g0338a0001c0001t0027g0339 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-334+7747A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74705186 | ||||||
| chr14:74705501
|
AAAC | A | 4 | a0001c0005t0009g0027a0001c0005t0009g0028a0001c0005t0009g0029others(1): Show | 4 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-334+7429_-334+743 others(7): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74705501 | ||||||
| chr14:74705747
|
T | C | 1 | a0001c0001t0003g0308 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-334+7186A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74705747 | ||||||
| chr14:74705989
|
G | C | 2 | a0001c0001t0008g0164a0001c0001t0008g0236 | 2 | NA18967.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-334+6944C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74705989 | ||||||
| chr14:74706144
|
C | T | 1 | a0001c0001t0023g0256 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-334+6789G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74706144 | ||||||
| chr14:74706296
|
G | A | 99 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0242others(96): Show | 108 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-334+6637C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74706296 | ||||||
| chr14:74706626
|
G | A | 6 | a0001c0001t0003g0248a0001c0001t0003g0309a0001c0001t0003g0310others(3): Show | 6 | HG00738.hp1 HG01257.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.-334+6307C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74706626 | ||||||
| chr14:74706689
|
T | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(87): Show | 99 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-334+6244A>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74706689 | ||||||
| chr14:74706773
|
G | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0133others(1): Show | 4 | HG00609.hp2 HG00621.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-334+6160C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74706773 | ||||||
| chr14:74706787
|
G | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 161 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-334+6146C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74706787 | ||||||
| chr14:74706810
|
G | A | 1 | a0001c0001t0003g0312 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-334+6123C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74706810 | ||||||
| chr14:74706854
|
G | A | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-334+6079C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74706854 | ||||||
| chr14:74706971
|
C | A | 7 | a0001c0001t0007g0045a0001c0001t0007g0047a0001c0001t0007g0048others(4): Show | 7 | HG01109.hp2 HG02572.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-334+5962G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74706971 | ||||||
| chr14:74707089
|
C | T | 1 | a0001c0001t0010g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-334+5844G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74707089 | ||||||
| chr14:74707126
|
G | A | 1 | a0001c0001t0007g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-334+5807C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74707126 | ||||||
| chr14:74707429
|
A | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(255): Show | 282 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.-334+5504T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74707429 | ||||||
| chr14:74707743
|
G | A | 2 | a0001c0001t0008g0212a0001c0001t0008g0213 | 2 | NA18972.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-334+5190C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74707743 | ||||||
| chr14:74707773
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-334+5160C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74707773 | ||||||
| chr14:74707792
|
C | CA | 231 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(228): Show | 254 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.-334+5140dupT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74707792 | ||||||
| chr14:74707813
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-334+5120G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74707813 | ||||||
| chr14:74707862
|
C | T | 2 | a0001c0001t0004g0032a0001c0001t0004g0059 | 2 | NA18970.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-334+5071G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74707862 | ||||||
| chr14:74707863
|
G | A | 5 | a0001c0001t0004g0008a0001c0001t0004g0055a0001c0001t0004g0056others(2): Show | 6 | HG02451.hp1 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-334+5070C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74707863 | ||||||
| chr14:74707889
|
G | A | 1 | a0001c0001t0003g0332 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-334+5044C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74707889 | ||||||
| chr14:74707891
|
A | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(87): Show | 99 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-334+5042T>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74707891 | ||||||
| chr14:74707914
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-334+5019C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74707914 | ||||||
| chr14:74707959
|
G | GA | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(9): Show | 12 | HG00438.hp1 HG01175.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-334+4973dupT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74707959 | ||||||
| chr14:74708020
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 5 | HG01891.hp2 HG02109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-334+4913C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74708020 | ||||||
| chr14:74708048
|
G | C | 1 | a0001c0004t0013g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-334+4885C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74708048 | ||||||
| chr14:74708403
|
T | C | 4 | a0001c0005t0009g0027a0001c0005t0009g0028a0001c0005t0009g0029others(1): Show | 4 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-334+4530A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74708403 | ||||||
| chr14:74708502
|
C | T | 10 | a0001c0001t0007g0045a0001c0001t0007g0047a0001c0001t0007g0048others(7): Show | 11 | HG01109.hp2 HG02572.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.-334+4431G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74708502 | ||||||
| chr14:74708661
|
AG | A | 14 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(11): Show | 15 | HG00423.hp1 HG01934.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.-334+4271delC | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74708661 | ||||||
| chr14:74708664
|
T | A | 6 | a0001c0001t0013g0338a0001c0001t0027g0339a0001c0004t0013g0165others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-334+4269A>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74708664 | ||||||
| chr14:74708716
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-334+4217G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74708716 | ||||||
| chr14:74708903
|
G | C | 1 | a0001c0001t0003g0332 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-334+4030C>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74708903 | ||||||
| chr14:74709121
|
T | C | 8 | a0001c0001t0006g0026a0001c0001t0006g0031a0002c0002t0006g0009others(5): Show | 9 | HG02738.hp1 HG04228.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.-334+3812A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74709121 | ||||||
| chr14:74709322
|
C | T | 3 | a0001c0001t0003g0249a0001c0001t0003g0250a0001c0001t0003g0251 | 3 | HG01070.hp2 HG01192.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-334+3611G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74709322 | ||||||
| chr14:74709470
|
C | G | 1 | a0001c0001t0003g0248 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-334+3463G>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74709470 | ||||||
| chr14:74709535
|
T | G | 1 | a0001c0001t0002g0239 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-334+3398A>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74709535 | ||||||
| chr14:74709573
|
C | T | 1 | a0001c0001t0007g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-334+3360G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74709573 | ||||||
| chr14:74709971
|
T | C | 1 | a0001c0001t0004g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-334+2962A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74709971 | ||||||
| chr14:74710186
|
C | T | 1 | a0001c0001t0003g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-334+2747G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74710186 | ||||||
| chr14:74710518
|
TAAG | T | 6 | a0001c0001t0013g0338a0001c0001t0027g0339a0001c0004t0013g0165others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-334+2412_-334+241 others(7): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74710518 | ||||||
| chr14:74710730
|
T | G | 41 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0008others(38): Show | 45 | HG00423.hp1 HG01109.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.-334+2203A>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74710730 | ||||||
| chr14:74710874
|
C | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG02258.hp2 HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-334+2059G>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74710874 | ||||||
| chr14:74711007
|
G | A | 14 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(11): Show | 15 | HG00423.hp1 HG01934.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.-334+1926C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74711007 | ||||||
| chr14:74711099
|
C | T | 1 | a0001c0001t0003g0247 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-334+1834G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74711099 | ||||||
| chr14:74711179
|
C | T | 1 | a0001c0001t0003g0246 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-334+1754G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74711179 | ||||||
| chr14:74711231
|
G | A | 15 | a0001c0001t0006g0026a0001c0001t0006g0031a0001c0005t0009g0027others(12): Show | 17 | HG01081.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-334+1702C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74711231 | ||||||
| chr14:74711233
|
C | T | 1 | a0001c0001t0005g0245 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-334+1700G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74711233 | ||||||
| chr14:74711235
|
CA | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(91): Show | 103 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.-334+1697delT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74711235 | ||||||
| chr14:74711318
|
T | A | 1 | a0001c0001t0002g0240 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-334+1615A>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74711318 | ||||||
| chr14:74711357
|
T | C | 1 | a0001c0001t0003g0316 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-334+1576A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74711357 | ||||||
| chr14:74711760
|
TAAAG | T | 3 | a0001c0001t0009g0043a0001c0001t0009g0061a0001c0001t0019g0044 | 3 | HG02818.hp2 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-334+1169_-334+117 others(8): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74711760 | ||||||
| chr14:74711792
|
C | T | 1 | a0003c0003t0011g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-334+1141G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74711792 | ||||||
| chr14:74711850
|
C | G | 1 | a0001c0001t0010g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-334+1083G>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74711850 | ||||||
| chr14:74711990
|
C | T | 97 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0242others(94): Show | 106 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-334+943G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74711990 | ||||||
| chr14:74712038
|
C | CA | 23 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0221others(20): Show | 23 | HG01106.hp1 HG01261.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.-334+894dupT | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712038 | ||||||
| chr14:74712038
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0013g0338 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-334+884_-334+894d others(13): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712038 | ||||||
| chr14:74712038
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0018g0341a0001c0001t0027g0339 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-334+882_-334+894d others(15): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712038 | ||||||
| chr14:74712038
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0029g0340 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-334+881_-334+894d others(16): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712038 | ||||||
| chr14:74712038
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0004g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-334+880_-334+894d others(17): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712038 | ||||||
| chr14:74712038
|
C | CAAAAAAA others(11): Show |
1 | a0004c0010t0002g0241 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-334+877_-334+894d others(20): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712038 | ||||||
| chr14:74712038
|
CAA | C | 16 | a0001c0001t0003g0318a0001c0001t0003g0319a0001c0001t0003g0320others(13): Show | 16 | HG01081.hp1 HG01106.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.-334+893_-334+894d others(4): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712038 | ||||||
| chr14:74712038
|
CAAA | C | 77 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0242others(74): Show | 86 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.-334+892_-334+894d others(5): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712038 | ||||||
| chr14:74712038
|
CAAAAA | C | 6 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159others(3): Show | 6 | HG02145.hp1 HG02723.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-334+890_-334+894d others(7): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712038 | ||||||
| chr14:74712047
|
AAAAAAAA others(14): Show |
A | 6 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0072others(3): Show | 7 | HG01496.hp1 HG02683.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.-334+865_-334+885d others(23): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712047 | ||||||
| chr14:74712048
|
AAAAAAAA others(13): Show |
A | 76 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(73): Show | 84 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.-334+865_-334+884d others(22): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712048 | ||||||
| chr14:74712049
|
AAAAAAAA others(12): Show |
A | 8 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0148others(5): Show | 8 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.-334+865_-334+883d others(21): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712049 | ||||||
| chr14:74712050
|
AAAAAAAA others(11): Show |
A | 7 | a0001c0001t0006g0026a0002c0002t0006g0009a0002c0002t0006g0024others(4): Show | 8 | HG04228.hp1 NA18949.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.-334+865_-334+882d others(20): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712050 | ||||||
| chr14:74712051
|
AAAAAAAA others(10): Show |
A | 5 | a0001c0001t0006g0031a0001c0005t0009g0027a0001c0005t0009g0028others(2): Show | 5 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-334+865_-334+881d others(19): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712051 | ||||||
| chr14:74712053
|
AAAAAAAA others(8): Show |
A | 13 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(10): Show | 14 | HG00423.hp1 HG01934.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.-334+865_-334+879d others(17): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712053 | ||||||
| chr14:74712054
|
AAAAAAAA others(7): Show |
A | 21 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0053others(18): Show | 24 | HG01496.hp2 HG02280.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.-334+865_-334+878d others(16): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712054 | ||||||
| chr14:74712055
|
AAAAAAAA others(6): Show |
A | 5 | a0001c0001t0004g0023a0001c0001t0007g0062a0001c0001t0009g0061others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-334+865_-334+877d others(15): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712055 | ||||||
| chr14:74712056
|
AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0007g0064a0001c0001t0010g0065 | 2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-334+865_-334+876d others(14): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712056 | ||||||
| chr14:74712057
|
A | G | 5 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159others(2): Show | 5 | HG02723.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-334+876T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712057 | ||||||
| chr14:74712058
|
A | G | 1 | a0001c0001t0003g0244 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-334+875T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712058 | ||||||
| chr14:74712059
|
AAAAAAAA others(12): Show |
A | 1 | a0003c0003t0011g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-334+855_-334+873d others(21): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712059 | ||||||
| chr14:74712061
|
A | G | 1 | a0001c0001t0003g0243 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-334+872T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712061 | ||||||
| chr14:74712062
|
AAAAAAGA others(9): Show |
A | 2 | a0003c0003t0011g0015a0003c0003t0011g0153 | 3 | HG02145.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-334+855_-334+870d others(18): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712062 | ||||||
| chr14:74712064
|
A | G | 1 | a0001c0001t0003g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-334+869T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712064 | ||||||
| chr14:74712064
|
AAAAGAAA others(15): Show |
A | 1 | a0001c0001t0003g0244 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-334+847_-334+868d others(24): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712064 | ||||||
| chr14:74712068
|
G | A | 1 | a0001c0001t0004g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-334+865C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712068 | ||||||
| chr14:74712069
|
A | G | 2 | a0001c0001t0004g0005a0001c0001t0004g0023 | 3 | HG01243.hp1 HG01496.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-334+864T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712069 | ||||||
| chr14:74712074
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-334+859T>C | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712074 | ||||||
| chr14:74712074
|
AAAAGAAA others(5): Show |
A | 96 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0242others(93): Show | 105 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.-334+847_-334+858d others(14): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712074 | ||||||
| chr14:74712094
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-334+839C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712094 | ||||||
| chr14:74712204
|
T | A | 1 | a0001c0001t0002g0336 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-334+729A>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712204 | ||||||
| chr14:74712388
|
T | C | 4 | a0002c0002t0006g0009a0002c0002t0006g0067a0002c0002t0006g0068others(1): Show | 5 | NA18973.hp2 NA18986.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.-334+545A>G | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712388 | ||||||
| chr14:74712399
|
T | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(87): Show | 99 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-334+534A>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712399 | ||||||
| chr14:74712587
|
C | T | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG00673.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-334+346G>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712587 | ||||||
| chr14:74712864
|
CCT | C | 3 | a0003c0003t0011g0015a0003c0003t0011g0152a0003c0003t0011g0153 | 4 | HG02145.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-334+67_-334+68del others(2): Show |
AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712864 | ||||||
| chr14:74712894
|
G | A | 3 | a0001c0001t0013g0338a0001c0001t0027g0339a0001c0001t0029g0340 | 3 | HG02559.hp2 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-334+39C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712894 | ||||||
| chr14:74712902
|
G | A | 1 | a0001c0001t0004g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-334+31C>T | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712902 | ||||||
| chr14:74712908
|
G | T | 1 | a0001c0001t0001g0022 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-334+25C>A | AREL1 | ENSG00000119682.18 | transcript | ENST00000356357.9 | protein_coding | 1/19 | chr14 | 74712908 |