Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 121536 |
|---|---|
| ensemblid | ENSG00000139154.16 |
| hgncid | 24051 |
| symbol | AEBP2 |
| name | AE binding protein 2 |
| refseq_nuc | NM_153207.5 |
| refseq_prot | NP_694939.2 |
| ensembl_nuc | ENST00000266508.14 |
| ensembl_prot | ENSP00000266508.9 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 19439492 |
| end | 19522227 |
| strand | + |
| ver | v1.2 |
| region | chr12:19439492-19522227 |
| region5000 | chr12:19434492-19527227 |
| regionname0 | AEBP2_chr12_19439492_19522227 |
| regionname5000 | AEBP2_chr12_19434492_19527227 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 503 | 403 | 96 | 74 | 181 | 10 | 40 | 139 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0002 | 0/0 | 495 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1512 | 343 | 81 | 69 | 142 | 10 | 39 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| c0002 | 0/0 | 1512 | 53 | 13 | 3 | 37 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| c0003 | 0/0 | 1512 | 3 | 2 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| c0004 | 0/0 | 1512 | 2 | 0 | 0 | 2 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| c0005 | 0/0 | 1512 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| c0006 | 0/0 | 1512 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| c0007 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4322 | 78 | 33 | 8 | 35 | 0 | 2 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0002 | 1/0 | 4319 | 71 | 2 | 20 | 39 | 1 | 8 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0003 | 0/1 | 4317 | 52 | 1 | 12 | 30 | 4 | 4 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0004 | 0/0 | 4316 | 41 | 10 | 3 | 21 | 0 | 7 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0005 | 0/0 | 4319 | 28 | 7 | 11 | 9 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0006 | 0/0 | 4321 | 20 | 3 | 5 | 1 | 1 | 10 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0007 | 0/0 | 4317 | 14 | 11 | 0 | 1 | 1 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0008 | 0/0 | 4316 | 10 | 0 | 3 | 4 | 1 | 2 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0009 | 0/0 | 4318 | 8 | 0 | 4 | 4 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0010 | 0/0 | 4321 | 8 | 1 | 0 | 7 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0011 | 0/0 | 4315 | 7 | 1 | 0 | 5 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0012 | 0/0 | 4318 | 6 | 0 | 1 | 5 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0013 | 0/0 | 4319 | 5 | 5 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0014 | 0/0 | 4320 | 5 | 0 | 4 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0015 | 0/0 | 4318 | 4 | 4 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0016 | 0/0 | 4320 | 4 | 0 | 0 | 4 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0017 | 0/0 | 4318 | 3 | 3 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0018 | 0/0 | 4319 | 3 | 3 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0019 | 0/0 | 4320 | 3 | 0 | 0 | 3 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0020 | 0/0 | 4323 | 3 | 3 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0021 | 0/0 | 4316 | 2 | 0 | 0 | 2 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0022 | 0/0 | 4318 | 2 | 1 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0023 | 0/0 | 4323 | 2 | 0 | 0 | 1 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0024 | 0/0 | 4315 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0025 | 0/0 | 4317 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0026 | 0/0 | 4323 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0027 | 0/0 | 4317 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0028 | 0/0 | 4317 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0029 | 0/0 | 4317 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0030 | 0/0 | 4317 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0031 | 0/0 | 4317 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0032 | 0/0 | 4318 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0033 | 0/0 | 4319 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0034 | 0/0 | 4319 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0035 | 0/0 | 4319 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0036 | 0/0 | 4320 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0037 | 0/0 | 4319 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0038 | 0/0 | 4321 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0039 | 0/0 | 4321 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0040 | 0/0 | 4322 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0041 | 0/0 | 4322 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0042 | 0/0 | 4322 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0043 | 0/0 | 4322 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0044 | 0/0 | 4322 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0045 | 0/0 | 4322 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0046 | 0/0 | 4323 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0047 | 0/0 | 4322 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| t0048 | 0/0 | 4317 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0217 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0350 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0372 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0383 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0389 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0399 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1512 | 343 | 81 | 69 | 142 | 10 | 39 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0002 | 0/0 | 1512 | 53 | 13 | 3 | 37 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0003 | 0/0 | 1512 | 3 | 2 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0004 | 0/0 | 1512 | 2 | 0 | 0 | 2 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0005 | 0/0 | 1512 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0006 | 0/0 | 1512 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0002c0007 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5833 | 41 | 20 | 4 | 15 | 0 | 2 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0002 | 1/0 | 5830 | 59 | 2 | 20 | 27 | 1 | 8 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0003 | 0/1 | 5828 | 52 | 1 | 12 | 30 | 4 | 4 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0004 | 0/0 | 5827 | 41 | 10 | 3 | 21 | 0 | 7 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0005 | 0/0 | 5830 | 28 | 7 | 11 | 9 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0006 | 0/0 | 5832 | 20 | 3 | 5 | 1 | 1 | 10 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0007 | 0/0 | 5828 | 14 | 11 | 0 | 1 | 1 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0008 | 0/0 | 5827 | 10 | 0 | 3 | 4 | 1 | 2 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0009 | 0/0 | 5829 | 7 | 0 | 4 | 3 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0010 | 0/0 | 5832 | 4 | 1 | 0 | 3 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0011 | 0/0 | 5826 | 7 | 1 | 0 | 5 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0012 | 0/0 | 5829 | 6 | 0 | 1 | 5 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0013 | 0/0 | 5830 | 5 | 5 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0014 | 0/0 | 5831 | 5 | 0 | 4 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0015 | 0/0 | 5829 | 4 | 4 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0016 | 0/0 | 5831 | 4 | 0 | 0 | 4 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0017 | 0/0 | 5829 | 3 | 3 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0018 | 0/0 | 5830 | 3 | 3 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0019 | 0/0 | 5831 | 3 | 0 | 0 | 3 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0020 | 0/0 | 5834 | 3 | 3 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0021 | 0/0 | 5827 | 2 | 0 | 0 | 2 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0022 | 0/0 | 5829 | 2 | 1 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0023 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0024 | 0/0 | 5826 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0025 | 0/0 | 5828 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0026 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0027 | 0/0 | 5828 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0028 | 0/0 | 5828 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0029 | 0/0 | 5828 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0030 | 0/0 | 5828 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0031 | 0/0 | 5828 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0032 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0034 | 0/0 | 5830 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0035 | 0/0 | 5830 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0036 | 0/0 | 5831 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0037 | 0/0 | 5830 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0039 | 0/0 | 5832 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0041 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0042 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0046 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0047 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0001t0048 | 0/0 | 5828 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0002t0001 | 0/0 | 5833 | 35 | 12 | 3 | 20 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0002t0002 | 0/0 | 5830 | 10 | 0 | 0 | 10 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0002t0010 | 0/0 | 5832 | 4 | 0 | 0 | 4 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0002t0038 | 0/0 | 5832 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0002t0040 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0002t0043 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0002t0045 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0003t0001 | 0/0 | 5833 | 2 | 1 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0003t0044 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0004t0002 | 0/0 | 5830 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0004t0009 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0005t0023 | 0/0 | 5834 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0001c0006t0033 | 0/0 | 5830 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| a0002c0007t0002 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | copy fasta | chr12 | 19434492 | 19527227 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0217 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0350 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0383 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0003g0399 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0004g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0006g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0007g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0007g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0007g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0007g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0007g0389 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0007g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0007g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0007g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0007g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0007g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0007g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0008g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0008g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0008g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0008g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0008g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0008g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0008g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0008g0372 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0008g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0008g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0009g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0009g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0009g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0009g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0009g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0009g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0009g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0010g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0010g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0011g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0011g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0011g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0011g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0011g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0011g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0011g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0012g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0012g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0012g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0012g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0012g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0012g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0013g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0013g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0013g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0013g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0013g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0014g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0014g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0014g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0014g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0014g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0015g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0015g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0015g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0015g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0016g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0016g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0016g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0016g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0017g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0017g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0017g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0018g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0018g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0018g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0019g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0019g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0019g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0020g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0020g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0020g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0021g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0021g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0022g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0022g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0023g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0024g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0025g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0026g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0027g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0028g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0029g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0030g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0031g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0032g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0034g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0035g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0036g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0037g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0039g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0041g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0042g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0046g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0047g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0001t0048g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0010g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0010g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0010g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0010g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0038g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0040g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0043g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0002t0045g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0003t0044g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0004t0009g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0005t0023g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0001c0006t0033g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| a0002c0007t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0168 | EUR | GBR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0338 | EUR | GBR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0383 | EUR | FIN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00323 | hp2 | a0001 | c0001 | t0014 | g0027 | EUR | FIN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00438 | hp1 | a0001 | c0001 | t0030 | g0349 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0298 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00558 | hp2 | a0001 | c0002 | t0010 | g0107 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0144 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00639 | hp1 | a0001 | c0001 | t0014 | g0020 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0151 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0339 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0181 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01069 | hp2 | a0001 | c0001 | t0014 | g0025 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0026 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0145 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01074 | hp1 | a0001 | c0001 | t0008 | g0360 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0250 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01099 | hp1 | a0001 | c0001 | t0008 | g0325 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0280 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0022 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0274 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0323 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0152 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01167 | hp2 | a0001 | c0001 | t0014 | g0030 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0399 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01168 | hp2 | a0001 | c0001 | t0009 | g0162 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0398 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01169 | hp2 | a0001 | c0001 | t0014 | g0031 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0311 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0279 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0150 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01243 | hp2 | a0001 | c0001 | t0025 | g0288 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01256 | hp2 | a0001 | c0001 | t0009 | g0167 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0307 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0379 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0238 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0355 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0314 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0147 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0209 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0019 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01496 | hp2 | a0001 | c0001 | t0012 | g0337 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0373 | EUR | IBS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0010 | EUR | IBS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01884 | hp1 | a0001 | c0001 | t0041 | g0251 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01891 | hp1 | a0001 | c0001 | t0013 | g0161 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0252 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0149 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0014 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01934 | hp2 | a0001 | c0006 | t0033 | g0041 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0136 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0135 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01975 | hp1 | a0001 | c0001 | t0022 | g0128 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0146 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0341 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0134 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02015 | hp2 | a0001 | c0002 | t0040 | g0050 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02027 | hp1 | a0001 | c0001 | t0012 | g0362 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02040 | hp1 | a0001 | c0002 | t0010 | g0062 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0347 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02055 | hp1 | a0001 | c0001 | t0017 | g0044 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02071 | hp1 | a0001 | c0002 | t0043 | g0064 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02074 | hp1 | a0001 | c0001 | t0027 | g0352 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02083 | hp1 | a0001 | c0002 | t0010 | g0067 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02132 | hp2 | a0001 | c0001 | t0007 | g0348 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02145 | hp2 | a0001 | c0001 | t0013 | g0160 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0132 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CDX | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | CDX | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | CDX | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0397 | EAS | CDX | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0236 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02258 | hp1 | a0001 | c0003 | t0044 | g0249 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02258 | hp2 | a0001 | c0001 | t0020 | g0263 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02280 | hp2 | a0001 | c0001 | t0015 | g0231 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0376 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0378 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02523 | hp1 | a0001 | c0001 | t0011 | g0293 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02572 | hp2 | a0001 | c0001 | t0017 | g0042 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02602 | hp2 | a0001 | c0001 | t0006 | g0011 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0400 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02622 | hp2 | a0001 | c0001 | t0015 | g0233 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0317 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0154 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0316 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02735 | hp1 | a0001 | c0001 | t0036 | g0262 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02735 | hp2 | a0001 | c0005 | t0023 | g0033 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0277 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02809 | hp1 | a0001 | c0001 | t0035 | g0159 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02818 | hp1 | a0001 | c0001 | t0015 | g0234 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02818 | hp2 | a0001 | c0001 | t0024 | g0232 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02886 | hp1 | a0001 | c0001 | t0042 | g0243 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02886 | hp2 | a0001 | c0001 | t0015 | g0235 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0315 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02922 | hp1 | a0001 | c0001 | t0018 | g0230 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02922 | hp2 | a0001 | c0001 | t0020 | g0264 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0385 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02965 | hp2 | a0001 | c0001 | t0022 | g0237 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02970 | hp1 | a0001 | c0001 | t0018 | g0229 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0155 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02976 | hp1 | a0001 | c0001 | t0020 | g0227 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0254 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0272 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0015 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0306 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0396 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03098 | hp1 | a0001 | c0001 | t0034 | g0046 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0319 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0116 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03195 | hp1 | a0001 | c0002 | t0045 | g0120 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0386 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0303 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0017 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0313 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0318 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0125 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03486 | hp1 | a0001 | c0001 | t0013 | g0157 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03490 | hp1 | a0001 | c0001 | t0008 | g0331 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0012 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03492 | hp1 | a0001 | c0001 | t0011 | g0301 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0013 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0391 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03579 | hp1 | a0001 | c0001 | t0018 | g0228 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0278 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03654 | hp2 | a0001 | c0001 | t0006 | g0021 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0365 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0016 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0305 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03834 | hp2 | a0001 | c0001 | t0007 | g0387 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0137 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03942 | hp1 | a0001 | c0001 | t0028 | g0308 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG04115 | hp1 | a0001 | c0001 | t0006 | g0028 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0321 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG04184 | hp1 | a0001 | c0001 | t0006 | g0024 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0381 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0284 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0282 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0018 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG04228 | hp2 | a0001 | c0001 | t0039 | g0023 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0394 | AFR | YRI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18612 | hp1 | a0001 | c0001 | t0008 | g0367 | EAS | CHB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0294 | EAS | CHB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | CHB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | CHB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | YRI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0156 | AFR | YRI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18942 | hp1 | a0001 | c0001 | t0009 | g0186 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0368 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0345 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18946 | hp1 | a0001 | c0001 | t0026 | g0344 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18948 | hp1 | a0001 | c0001 | t0029 | g0326 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18948 | hp2 | a0001 | c0001 | t0021 | g0270 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18949 | hp2 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18950 | hp2 | a0001 | c0001 | t0012 | g0324 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18953 | hp2 | a0001 | c0001 | t0019 | g0034 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18954 | hp1 | a0001 | c0001 | t0005 | g0139 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0353 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18957 | hp1 | a0001 | c0002 | t0038 | g0059 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18959 | hp2 | a0001 | c0001 | t0011 | g0295 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18960 | hp1 | a0001 | c0001 | t0011 | g0299 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18960 | hp2 | a0001 | c0001 | t0010 | g0060 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18962 | hp2 | a0002 | c0007 | t0002 | g0200 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18963 | hp1 | a0001 | c0001 | t0021 | g0269 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0380 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18965 | hp2 | a0001 | c0001 | t0011 | g0275 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18966 | hp2 | a0001 | c0004 | t0009 | g0223 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0390 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18968 | hp1 | a0001 | c0001 | t0008 | g0384 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18972 | hp1 | a0001 | c0001 | t0019 | g0037 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18974 | hp1 | a0001 | c0001 | t0032 | g0178 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18974 | hp2 | a0001 | c0001 | t0008 | g0382 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0375 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18979 | hp2 | a0001 | c0004 | t0002 | g0224 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0364 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18982 | hp1 | a0001 | c0001 | t0046 | g0032 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18983 | hp1 | a0001 | c0001 | t0009 | g0258 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18988 | hp1 | a0001 | c0001 | t0048 | g0377 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18988 | hp2 | a0001 | c0002 | t0010 | g0110 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18989 | hp1 | a0001 | c0001 | t0012 | g0335 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0359 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18992 | hp1 | a0001 | c0001 | t0010 | g0103 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0358 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0374 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18998 | hp1 | a0001 | c0001 | t0016 | g0035 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0133 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0370 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19004 | hp2 | a0001 | c0001 | t0016 | g0038 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19005 | hp1 | a0001 | c0001 | t0008 | g0332 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19006 | hp2 | a0001 | c0001 | t0047 | g0123 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0343 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0140 | AFR | LWK | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19054 | hp2 | a0001 | c0001 | t0016 | g0039 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0131 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0346 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19057 | hp2 | a0001 | c0001 | t0011 | g0286 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0142 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19066 | hp1 | a0001 | c0001 | t0016 | g0036 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19068 | hp2 | a0001 | c0001 | t0010 | g0100 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19070 | hp2 | a0001 | c0001 | t0012 | g0333 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0297 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0369 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19079 | hp1 | a0001 | c0001 | t0019 | g0040 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19081 | hp2 | a0001 | c0001 | t0012 | g0366 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19085 | hp2 | a0001 | c0001 | t0009 | g0173 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0361 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19240 | hp1 | a0001 | c0001 | t0017 | g0043 | AFR | YRI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0003 | AFR | YRI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ASW | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ASW | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0371 | EUR | TSI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA20752 | hp2 | a0001 | c0001 | t0037 | g0203 | EUR | TSI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA20805 | hp1 | a0001 | c0001 | t0007 | g0389 | EUR | TSI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA20805 | hp2 | a0001 | c0001 | t0008 | g0372 | EUR | TSI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0388 | SAS | GIH | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA20905 | hp2 | a0001 | c0001 | t0008 | g0327 | SAS | GIH | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG01123 | hp2 | a0001 | c0001 | t0008 | g0351 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02109 | hp1 | a0001 | c0001 | t0013 | g0158 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0266 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0363 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0395 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0392 | AFR | USA | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| HG06807 | hp2 | a0001 | c0001 | t0031 | g0029 | AFR | USA | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA18955 | hp2 | a0001 | c0001 | t0023 | g0309 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0320 | AFR | USA | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0393 | AFR | USA | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | LWK | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | LWK | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0350 | REF | REF | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0217 | REF | REF | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:19439879
|
CGGCGGCA others(17): Show |
C | 1 | a0002 | 1 | NA18962.hp2 | conservative_inframe_deletion | MODERATE | c.187_210delAGCGGTGG others(16): Show |
p.Ser63_Gly70del | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/8 | 395/5830 | 187/1512 | 63/503 | INFO_REALIGN_3_PRIME | chr12 | 19439879 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:19439864
|
G | C | 1 | a0001c0004 | 2 | NA18966.hp2 NA18979.hp2 |
synonymous_variant | LOW | c.165G>C | p.Ala55Ala | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/8 | 373/5830 | 165/1512 | 55/503 | chr12 | 19439864 | ||
| chr12:19439966
|
C | T | 1 | a0001c0006 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.267C>T | p.Ser89Ser | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/8 | 475/5830 | 267/1512 | 89/503 | chr12 | 19439966 | ||
| chr12:19440158
|
C | T | 1 | a0001c0003 | 3 | HG01081.hp2 HG01891.hp2 HG02258.hp1 |
synonymous_variant | LOW | c.459C>T | p.Asp153Asp | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/8 | 667/5830 | 459/1512 | 153/503 | chr12 | 19440158 | ||
| chr12:19473271
|
T | C | 1 | a0001c0002 | 53 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(50): Show |
synonymous_variant | LOW | c.903T>C | p.Gly301Gly | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/8 | 1111/5830 | 903/1512 | 301/503 | chr12 | 19473271 | ||
| chr12:19500128
|
A | G | 1 | a0001c0005 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.1206A>G | p.Thr402Thr | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/8 | 1414/5830 | 1206/1512 | 402/503 | chr12 | 19500128 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:19439507
|
G | T | 1 | a0001c0001t0048 | 1 | NA18988.hp1 | 5_prime_UTR_variant | MODIFIER | c.-193G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/8 | 193 | chr12 | 19439507 | |||||
| chr12:19439666
|
G | GGGA | 22 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(19): Show | 133 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(130): Show |
5_prime_UTR_variant | MODIFIER | c.-14_-12dupGAG | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/8 | 11 | INFO_REALIGN_3_PRIME | chr12 | 19439666 | ||||
| chr12:19439666
|
GGGA | G | 15 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(12): Show | 140 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
5_prime_UTR_variant | MODIFIER | c.-14_-12delGAG | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/8 | 12 | INFO_REALIGN_3_PRIME | chr12 | 19439666 | ||||
| chr12:19518206
|
A | T | 1 | a0001c0001t0037 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 89 | chr12 | 19518206 | |||||
| chr12:19518218
|
C | CT | 12 | a0001c0001t0003a0001c0001t0007a0001c0001t0020others(9): Show | 78 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*121dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 122 | INFO_REALIGN_3_PRIME | chr12 | 19518218 | ||||
| chr12:19518218
|
C | CTT | 1 | a0001c0001t0012 | 6 | HG01496.hp2 HG02027.hp1 NA18950.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*120_*121dupTT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 122 | INFO_REALIGN_3_PRIME | chr12 | 19518218 | ||||
| chr12:19518218
|
CT | C | 13 | a0001c0001t0006a0001c0001t0009a0001c0001t0010others(10): Show | 56 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*121delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 121 | INFO_REALIGN_3_PRIME | chr12 | 19518218 | ||||
| chr12:19518218
|
CTT | C | 2 | a0001c0001t0014a0001c0001t0031 | 6 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*120_*121delTT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 120 | INFO_REALIGN_3_PRIME | chr12 | 19518218 | ||||
| chr12:19518218
|
CTTT | C | 2 | a0001c0001t0016a0001c0001t0019 | 7 | NA18953.hp2 NA18972.hp1 NA18998.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*119_*121delTTT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 119 | INFO_REALIGN_3_PRIME | chr12 | 19518218 | ||||
| chr12:19518878
|
C | T | 1 | a0001c0001t0035 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*761C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 761 | chr12 | 19518878 | |||||
| chr12:19518967
|
T | C | 1 | a0001c0001t0019 | 3 | NA18953.hp2 NA18972.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*850T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 850 | chr12 | 19518967 | |||||
| chr12:19519518
|
A | G | 1 | a0001c0001t0047 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1401A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 1401 | chr12 | 19519518 | |||||
| chr12:19519651
|
C | T | 1 | a0001c0001t0030 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1534C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 1534 | chr12 | 19519651 | |||||
| chr12:19519830
|
A | C | 3 | a0001c0001t0016a0001c0001t0019a0001c0001t0046 | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1713A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 1713 | chr12 | 19519830 | |||||
| chr12:19519884
|
A | T | 1 | a0001c0001t0021 | 2 | NA18948.hp2 NA18963.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1767A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 1767 | chr12 | 19519884 | |||||
| chr12:19519973
|
T | G | 1 | a0001c0001t0032 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1856T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 1856 | chr12 | 19519973 | |||||
| chr12:19520427
|
T | G | 1 | a0001c0001t0017 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2310T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 2310 | chr12 | 19520427 | |||||
| chr12:19520644
|
T | A | 1 | a0001c0002t0040 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2527T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 2527 | chr12 | 19520644 | |||||
| chr12:19520678
|
ACAAGCAT others(19): Show |
A | 1 | a0001c0001t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2562_*2587delCAAG others(22): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 2562 | chr12 | 19520678 | |||||
| chr12:19520740
|
G | A | 1 | a0001c0001t0041 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2623G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 2623 | chr12 | 19520740 | |||||
| chr12:19520764
|
C | T | 2 | a0001c0001t0013a0001c0001t0035 | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2647C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 2647 | chr12 | 19520764 | |||||
| chr12:19521067
|
T | A | 1 | a0001c0001t0042 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2950T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 2950 | chr12 | 19521067 | |||||
| chr12:19521164
|
T | C | 3 | a0001c0001t0016a0001c0001t0019a0001c0001t0046 | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3047T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3047 | chr12 | 19521164 | |||||
| chr12:19521228
|
T | A | 1 | a0001c0001t0017 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3111T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3111 | chr12 | 19521228 | |||||
| chr12:19521235
|
A | T | 2 | a0001c0001t0015a0001c0001t0024 | 5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3118A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3118 | chr12 | 19521235 | |||||
| chr12:19521247
|
G | C | 11 | a0001c0001t0003a0001c0001t0008a0001c0001t0012others(8): Show | 76 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*3130G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3130 | chr12 | 19521247 | |||||
| chr12:19521284
|
T | C | 1 | a0001c0002t0038 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3167T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3167 | chr12 | 19521284 | |||||
| chr12:19521301
|
A | G | 1 | a0001c0001t0018 | 3 | HG02922.hp1 HG02970.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3184A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3184 | chr12 | 19521301 | |||||
| chr12:19521310
|
C | T | 1 | a0001c0001t0034 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3193C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3193 | chr12 | 19521310 | |||||
| chr12:19521354
|
C | T | 5 | a0001c0001t0005a0001c0001t0013a0001c0001t0022others(2): Show | 37 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3237C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3237 | chr12 | 19521354 | |||||
| chr12:19521407
|
T | G | 1 | a0001c0002t0043 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3290T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3290 | chr12 | 19521407 | |||||
| chr12:19521462
|
G | A | 1 | a0001c0001t0027 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3345G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3345 | chr12 | 19521462 | |||||
| chr12:19521558
|
G | A | 1 | a0001c0003t0044 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3441G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3441 | chr12 | 19521558 | |||||
| chr12:19521577
|
T | C | 3 | a0001c0001t0016a0001c0001t0019a0001c0001t0046 | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3460T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3460 | chr12 | 19521577 | |||||
| chr12:19521821
|
A | G | 2 | a0001c0001t0034a0001c0006t0033 | 2 | HG01934.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3704A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3704 | chr12 | 19521821 | |||||
| chr12:19521831
|
T | A | 1 | a0001c0002t0045 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3714T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3714 | chr12 | 19521831 | |||||
| chr12:19521873
|
T | C | 6 | a0001c0001t0006a0001c0001t0014a0001c0001t0015others(3): Show | 32 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3756T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3756 | chr12 | 19521873 | |||||
| chr12:19521950
|
T | G | 1 | a0001c0001t0028 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3833T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3833 | chr12 | 19521950 | |||||
| chr12:19522067
|
A | AT | 4 | a0001c0001t0016a0001c0001t0019a0001c0001t0025others(1): Show | 9 | HG01243.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3962dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3963 | INFO_REALIGN_3_PRIME | chr12 | 19522067 | ||||
| chr12:19522067
|
A | T | 2 | a0001c0001t0034a0001c0006t0033 | 2 | HG01934.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3950A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3950 | chr12 | 19522067 | |||||
| chr12:19522079
|
T | G | 6 | a0001c0001t0006a0001c0001t0014a0001c0001t0015others(3): Show | 32 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3962T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3962 | chr12 | 19522079 | |||||
| chr12:19522092
|
C | A | 1 | a0001c0001t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3975C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3975 | chr12 | 19522092 | |||||
| chr12:19522094
|
T | A | 1 | a0001c0001t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3977T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3977 | chr12 | 19522094 | |||||
| chr12:19522101
|
G | A | 1 | a0001c0001t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3984G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3984 | chr12 | 19522101 | |||||
| chr12:19522103
|
T | TCTGTTAA others(25): Show |
1 | a0001c0001t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3986_*3987insCTGT others(28): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3987 | chr12 | 19522103 | |||||
| chr12:19522122
|
C | A | 1 | a0001c0001t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4005C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 4005 | chr12 | 19522122 | |||||
| chr12:19522190
|
C | T | 3 | a0001c0001t0013a0001c0001t0035a0001c0001t0039 | 7 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4073C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 4073 | chr12 | 19522190 | |||||
| chr12:19522191
|
G | A | 3 | a0001c0001t0016a0001c0001t0019a0001c0001t0046 | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4074G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 4074 | chr12 | 19522191 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:19440394
|
C | T | 1 | a0001c0001t0007g0400 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.671+24C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440394 | ||||||
| chr12:19440405
|
C | T | 2 | a0001c0001t0003g0398a0001c0001t0003g0399 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.671+35C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440405 | ||||||
| chr12:19440539
|
C | T | 96 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(93): Show | 97 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.671+169C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440539 | ||||||
| chr12:19440579
|
C | A | 1 | a0001c0001t0004g0004 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.671+209C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440579 | ||||||
| chr12:19440582
|
A | G | 42 | a0001c0001t0004g0004a0001c0001t0004g0265a0001c0001t0004g0266others(39): Show | 42 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.671+212A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440582 | ||||||
| chr12:19440631
|
C | T | 2 | a0001c0001t0020g0263a0001c0001t0020g0264 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.671+261C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440631 | ||||||
| chr12:19440779
|
A | T | 1 | a0001c0001t0004g0305 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.671+409A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440779 | ||||||
| chr12:19440818
|
G | C | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.671+448G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440818 | ||||||
| chr12:19440861
|
C | G | 1 | a0001c0001t0004g0304 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.671+491C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440861 | ||||||
| chr12:19441021
|
G | A | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+651G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441021 | ||||||
| chr12:19441045
|
G | A | 1 | a0001c0001t0004g0265 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.671+675G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441045 | ||||||
| chr12:19441089
|
CAA | C | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0036g0262 | 3 | HG00735.hp2 HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.671+722_671+723del others(2): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19441089 | |||||
| chr12:19441208
|
T | G | 100 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(97): Show | 101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.671+838T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441208 | ||||||
| chr12:19441212
|
T | C | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+842T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441212 | ||||||
| chr12:19441262
|
A | G | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.671+892A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441262 | ||||||
| chr12:19441317
|
TATC | T | 3 | a0001c0001t0002g0259a0001c0001t0003g0397a0001c0001t0009g0258 | 3 | HG02165.hp2 NA18983.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.671+950_671+952del others(3): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19441317 | |||||
| chr12:19441377
|
A | G | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+1007A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441377 | ||||||
| chr12:19441443
|
A | G | 6 | a0001c0001t0004g0396a0001c0001t0007g0003a0001c0001t0007g0392others(3): Show | 7 | HG02559.hp1 HG03041.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.671+1073A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441443 | ||||||
| chr12:19441580
|
A | T | 1 | a0001c0001t0005g0257 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.671+1210A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441580 | ||||||
| chr12:19441605
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.671+1235G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441605 | ||||||
| chr12:19441687
|
G | T | 2 | a0001c0001t0004g0302a0001c0001t0004g0303 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.671+1317G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441687 | ||||||
| chr12:19441840
|
A | G | 18 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(15): Show | 18 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.671+1470A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441840 | ||||||
| chr12:19441897
|
A | T | 1 | a0001c0002t0001g0238 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.671+1527A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441897 | ||||||
| chr12:19442306
|
G | C | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.671+1936G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442306 | ||||||
| chr12:19442322
|
C | T | 2 | a0001c0001t0005g0236a0001c0001t0022g0237 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.671+1952C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442322 | ||||||
| chr12:19442455
|
T | C | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+2085T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442455 | ||||||
| chr12:19442509
|
G | A | 104 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(101): Show | 104 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.671+2139G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442509 | ||||||
| chr12:19442538
|
T | G | 1 | a0001c0001t0017g0042 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.671+2168T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442538 | ||||||
| chr12:19442674
|
C | T | 136 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(133): Show | 136 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.671+2304C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442674 | ||||||
| chr12:19442679
|
G | A | 325 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(322): Show | 326 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.671+2309G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442679 | ||||||
| chr12:19442685
|
T | A | 37 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(34): Show | 37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.671+2315T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442685 | ||||||
| chr12:19442696
|
T | G | 42 | a0001c0001t0004g0004a0001c0001t0004g0265a0001c0001t0004g0266others(39): Show | 42 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.671+2326T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442696 | ||||||
| chr12:19442726
|
T | G | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049 | 3 | HG01109.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.671+2356T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442726 | ||||||
| chr12:19442785
|
A | G | 3 | a0001c0001t0018g0228a0001c0001t0018g0229a0001c0001t0018g0230 | 3 | HG02922.hp1 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.671+2415A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442785 | ||||||
| chr12:19443026
|
G | A | 1 | a0001c0002t0040g0050 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.671+2656G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443026 | ||||||
| chr12:19443037
|
G | A | 1 | a0001c0006t0033g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.671+2667G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443037 | ||||||
| chr12:19443103
|
CT | C | 325 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(322): Show | 326 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.671+2745delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19443103 | |||||
| chr12:19443133
|
A | G | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+2763A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443133 | ||||||
| chr12:19443190
|
GGGTT | G | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+2821_671+2824d others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443190 | ||||||
| chr12:19443266
|
T | G | 31 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(28): Show | 31 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+2896T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443266 | ||||||
| chr12:19443332
|
A | G | 148 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(145): Show | 148 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.671+2962A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443332 | ||||||
| chr12:19443416
|
C | G | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+3046C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443416 | ||||||
| chr12:19443438
|
G | T | 6 | a0001c0001t0013g0156a0001c0001t0013g0157a0001c0001t0013g0158others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.671+3068G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443438 | ||||||
| chr12:19443448
|
G | T | 1 | a0001c0001t0002g0226 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.671+3078G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443448 | ||||||
| chr12:19443485
|
G | A | 3 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG01346.hp1 HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.671+3115G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443485 | ||||||
| chr12:19443553
|
T | C | 6 | a0001c0001t0013g0156a0001c0001t0013g0157a0001c0001t0013g0158others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.671+3183T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443553 | ||||||
| chr12:19443669
|
G | A | 37 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(34): Show | 37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.671+3299G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443669 | ||||||
| chr12:19443813
|
T | C | 1 | a0001c0001t0006g0008 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.671+3443T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443813 | ||||||
| chr12:19443839
|
C | G | 4 | a0001c0002t0001g0124a0001c0002t0001g0125a0001c0002t0001g0126others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+3469C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443839 | ||||||
| chr12:19443859
|
AT | A | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+3496delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19443859 | |||||
| chr12:19443866
|
T | C | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+3496T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443866 | ||||||
| chr12:19443868
|
C | A | 1 | a0001c0001t0034g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.671+3498C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443868 | ||||||
| chr12:19443893
|
C | G | 3 | a0001c0001t0015g0233a0001c0001t0015g0234a0001c0001t0015g0235 | 3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.671+3523C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443893 | ||||||
| chr12:19443966
|
CTTTGGTT others(23): Show |
C | 1 | a0001c0001t0004g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.671+3629_671+3658d others(32): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19443966 | |||||
| chr12:19444043
|
G | A | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+3673G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444043 | ||||||
| chr12:19444144
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.671+3774G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444144 | ||||||
| chr12:19444160
|
A | T | 3 | a0001c0001t0005g0153a0001c0001t0005g0154a0001c0001t0005g0155 | 3 | HG02647.hp1 HG02717.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.671+3790A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444160 | ||||||
| chr12:19444162
|
T | A | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+3792T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444162 | ||||||
| chr12:19444163
|
T | A | 147 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(144): Show | 148 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.671+3793T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444163 | ||||||
| chr12:19444421
|
A | G | 32 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(29): Show | 32 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.671+4051A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444421 | ||||||
| chr12:19444559
|
G | C | 324 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(321): Show | 325 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.671+4189G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444559 | ||||||
| chr12:19444587
|
C | A | 3 | a0001c0001t0015g0233a0001c0001t0015g0234a0001c0001t0015g0235 | 3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.671+4217C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444587 | ||||||
| chr12:19444626
|
A | G | 1 | a0001c0001t0004g0305 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.671+4256A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444626 | ||||||
| chr12:19444736
|
C | T | 104 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(101): Show | 104 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.671+4366C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444736 | ||||||
| chr12:19444933
|
C | T | 1 | a0001c0001t0011g0301 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.671+4563C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444933 | ||||||
| chr12:19444936
|
G | A | 1 | a0001c0001t0003g0307 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.671+4566G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444936 | ||||||
| chr12:19445013
|
G | A | 37 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(34): Show | 37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.671+4643G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445013 | ||||||
| chr12:19445168
|
A | G | 1 | a0001c0002t0002g0122 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.671+4798A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445168 | ||||||
| chr12:19445201
|
A | G | 325 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(322): Show | 326 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.671+4831A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445201 | ||||||
| chr12:19445303
|
A | G | 1 | a0001c0001t0007g0391 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.671+4933A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445303 | ||||||
| chr12:19445308
|
C | T | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.671+4938C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445308 | ||||||
| chr12:19445337
|
T | A | 1 | a0001c0001t0003g0307 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.671+4967T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445337 | ||||||
| chr12:19445354
|
G | A | 325 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(322): Show | 326 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.671+4984G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445354 | ||||||
| chr12:19445364
|
C | T | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+4994C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445364 | ||||||
| chr12:19445370
|
C | CT | 17 | a0001c0001t0002g0219a0001c0001t0002g0220a0001c0001t0002g0221others(14): Show | 17 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.671+5017dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19445370 | |||||
| chr12:19445370
|
CT | C | 28 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0003g0390others(25): Show | 28 | HG00438.hp2 HG00621.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.671+5017delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19445370 | |||||
| chr12:19445370
|
CTT | C | 108 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(105): Show | 109 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.671+5016_671+5017d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19445370 | |||||
| chr12:19445525
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.671+5155A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445525 | ||||||
| chr12:19445798
|
C | A | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+5428C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445798 | ||||||
| chr12:19445887
|
ATAAC | A | 28 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(25): Show | 28 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.671+5520_671+5523d others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19445887 | |||||
| chr12:19445967
|
A | G | 1 | a0001c0001t0019g0040 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.671+5597A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445967 | ||||||
| chr12:19445970
|
A | C | 1 | a0001c0001t0015g0235 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.671+5600A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445970 | ||||||
| chr12:19446004
|
C | T | 1 | a0001c0006t0033g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.671+5634C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446004 | ||||||
| chr12:19446011
|
T | A | 2 | a0001c0001t0015g0231a0001c0001t0024g0232 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.671+5641T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446011 | ||||||
| chr12:19446022
|
C | A | 96 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(93): Show | 97 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.671+5652C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446022 | ||||||
| chr12:19446067
|
A | G | 40 | a0001c0001t0004g0004a0001c0001t0004g0265a0001c0001t0004g0268others(37): Show | 40 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.671+5697A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446067 | ||||||
| chr12:19446100
|
A | AATGGCTA others(3): Show |
109 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(106): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.671+5735_671+5736i others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19446100 | |||||
| chr12:19446151
|
T | C | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+5781T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446151 | ||||||
| chr12:19446194
|
C | T | 1 | a0001c0001t0004g0284 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.671+5824C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446194 | ||||||
| chr12:19446457
|
C | T | 5 | a0001c0001t0015g0231a0001c0001t0015g0233a0001c0001t0015g0234others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.671+6087C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446457 | ||||||
| chr12:19446467
|
C | T | 1 | a0001c0002t0045g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.671+6097C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446467 | ||||||
| chr12:19446516
|
T | C | 1 | a0001c0001t0022g0128 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.671+6146T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446516 | ||||||
| chr12:19446546
|
G | A | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+6176G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446546 | ||||||
| chr12:19446556
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02896.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.671+6186C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446556 | ||||||
| chr12:19446599
|
G | A | 37 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(34): Show | 37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.671+6229G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446599 | ||||||
| chr12:19446600
|
C | G | 37 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(34): Show | 37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.671+6230C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446600 | ||||||
| chr12:19446601
|
G | A | 10 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(7): Show | 10 | HG02735.hp2 HG03942.hp1 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.671+6231G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446601 | ||||||
| chr12:19446605
|
A | C | 2 | a0001c0001t0015g0231a0001c0001t0024g0232 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.671+6235A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446605 | ||||||
| chr12:19446621
|
A | G | 3 | a0001c0001t0015g0233a0001c0001t0015g0234a0001c0001t0015g0235 | 3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.671+6251A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446621 | ||||||
| chr12:19446671
|
G | A | 136 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(133): Show | 136 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.671+6301G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446671 | ||||||
| chr12:19446718
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0001g0116 | 2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.671+6348C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446718 | ||||||
| chr12:19446732
|
C | CAAA | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+6379_671+6381d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19446732 | |||||
| chr12:19446732
|
CA | C | 44 | a0001c0001t0001g0045a0001c0001t0001g0055a0001c0001t0001g0117others(41): Show | 44 | HG00323.hp2 HG00609.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.671+6381delA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19446732 | |||||
| chr12:19446732
|
CAA | C | 270 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0061others(267): Show | 271 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.671+6380_671+6381d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19446732 | |||||
| chr12:19446794
|
T | G | 325 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(322): Show | 326 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.671+6424T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446794 | ||||||
| chr12:19446837
|
G | A | 1 | a0001c0001t0003g0313 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.671+6467G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446837 | ||||||
| chr12:19446872
|
A | G | 1 | a0001c0001t0011g0299 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.671+6502A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446872 | ||||||
| chr12:19446912
|
A | G | 1 | a0001c0001t0031g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.671+6542A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446912 | ||||||
| chr12:19446967
|
T | G | 1 | a0001c0001t0006g0009 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.671+6597T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446967 | ||||||
| chr12:19447097
|
A | G | 1 | a0001c0001t0004g0298 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.671+6727A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447097 | ||||||
| chr12:19447247
|
T | G | 382 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(379): Show | 386 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(383): Show |
intron_variant | MODIFIER | c.671+6877T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447247 | ||||||
| chr12:19447298
|
T | C | 101 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(98): Show | 102 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.671+6928T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447298 | ||||||
| chr12:19447325
|
C | T | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.671+6955C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447325 | ||||||
| chr12:19447326
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.671+6956G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447326 | ||||||
| chr12:19447489
|
A | G | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+7119A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447489 | ||||||
| chr12:19447536
|
A | G | 1 | a0001c0001t0003g0313 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.671+7166A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447536 | ||||||
| chr12:19447618
|
A | G | 1 | a0001c0001t0004g0297 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.671+7248A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447618 | ||||||
| chr12:19447687
|
TTA | T | 324 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(321): Show | 325 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.671+7323_671+7324d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19447687 | |||||
| chr12:19447744
|
G | A | 1 | a0001c0001t0034g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.671+7374G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447744 | ||||||
| chr12:19447985
|
G | A | 8 | a0001c0001t0004g0396a0001c0001t0007g0003a0001c0001t0007g0315others(5): Show | 9 | HG02559.hp1 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+7615G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447985 | ||||||
| chr12:19448203
|
T | G | 110 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(107): Show | 111 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.671+7833T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448203 | ||||||
| chr12:19448258
|
A | G | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.671+7888A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448258 | ||||||
| chr12:19448310
|
G | A | 1 | a0001c0001t0004g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.671+7940G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448310 | ||||||
| chr12:19448422
|
T | A | 96 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(93): Show | 97 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.671+8052T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448422 | ||||||
| chr12:19448447
|
T | G | 1 | a0001c0002t0002g0057 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.671+8077T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448447 | ||||||
| chr12:19448498
|
A | G | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+8128A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448498 | ||||||
| chr12:19448500
|
T | G | 140 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(137): Show | 140 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.671+8130T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448500 | ||||||
| chr12:19448572
|
A | G | 1 | a0001c0001t0031g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.671+8202A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448572 | ||||||
| chr12:19448607
|
A | T | 84 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(81): Show | 84 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.671+8237A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448607 | ||||||
| chr12:19448640
|
A | G | 11 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(8): Show | 11 | HG01934.hp2 HG02735.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.671+8270A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448640 | ||||||
| chr12:19448666
|
A | G | 2 | a0001c0001t0020g0263a0001c0001t0020g0264 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.671+8296A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448666 | ||||||
| chr12:19448744
|
G | A | 41 | a0001c0001t0004g0004a0001c0001t0004g0265a0001c0001t0004g0266others(38): Show | 41 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.671+8374G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448744 | ||||||
| chr12:19448790
|
C | A | 1 | a0001c0001t0034g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.671+8420C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448790 | ||||||
| chr12:19448832
|
A | G | 2 | a0001c0001t0004g0266a0001c0001t0004g0267 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.671+8462A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448832 | ||||||
| chr12:19448846
|
C | A | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.671+8476C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448846 | ||||||
| chr12:19448895
|
G | A | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.671+8525G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448895 | ||||||
| chr12:19448977
|
G | A | 4 | a0001c0002t0001g0124a0001c0002t0001g0125a0001c0002t0001g0126others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+8607G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448977 | ||||||
| chr12:19449034
|
T | C | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.671+8664T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449034 | ||||||
| chr12:19449265
|
C | A | 1 | a0001c0002t0001g0054 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.671+8895C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449265 | ||||||
| chr12:19449478
|
T | C | 1 | a0001c0001t0031g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.671+9108T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449478 | ||||||
| chr12:19449505
|
G | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.671+9135G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449505 | ||||||
| chr12:19449516
|
A | G | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.671+9146A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449516 | ||||||
| chr12:19449553
|
T | C | 140 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(137): Show | 140 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.671+9183T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449553 | ||||||
| chr12:19449681
|
A | G | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.671+9311A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449681 | ||||||
| chr12:19449754
|
T | C | 1 | a0001c0001t0002g0166 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.671+9384T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449754 | ||||||
| chr12:19449825
|
T | C | 4 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170others(1): Show | 4 | HG00140.hp1 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+9455T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449825 | ||||||
| chr12:19449921
|
G | A | 328 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(325): Show | 329 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(326): Show |
intron_variant | MODIFIER | c.671+9551G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449921 | ||||||
| chr12:19450016
|
G | C | 328 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(325): Show | 329 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(326): Show |
intron_variant | MODIFIER | c.671+9646G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450016 | ||||||
| chr12:19450130
|
C | A | 76 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(73): Show | 76 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.671+9760C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450130 | ||||||
| chr12:19450160
|
A | AAGACCAG others(49): Show |
1 | a0001c0001t0002g0171 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.671+9792_671+9847d others(58): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19450160 | |||||
| chr12:19450192
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.671+9822C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450192 | ||||||
| chr12:19450318
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.671+9948C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450318 | ||||||
| chr12:19450322
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.671+9952C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450322 | ||||||
| chr12:19450349
|
A | T | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.671+9979A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450349 | ||||||
| chr12:19450355
|
A | T | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+9985A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450355 | ||||||
| chr12:19450458
|
T | C | 140 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(137): Show | 140 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.671+10088T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450458 | ||||||
| chr12:19450469
|
A | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0260a0001c0001t0001g0261others(1): Show | 4 | HG00735.hp2 HG01074.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+10099A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450469 | ||||||
| chr12:19450474
|
G | C | 1 | a0001c0002t0001g0058 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.671+10104G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450474 | ||||||
| chr12:19450567
|
T | C | 2 | a0001c0001t0014g0030a0001c0001t0014g0031 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.671+10197T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450567 | ||||||
| chr12:19450574
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.671+10204A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450574 | ||||||
| chr12:19450655
|
T | G | 140 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(137): Show | 140 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.671+10285T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450655 | ||||||
| chr12:19450667
|
C | CA | 135 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(132): Show | 136 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.671+10311dupA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19450667 | |||||
| chr12:19450668
|
AAAAAAAA others(7): Show |
A | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+10309_671+1032 others(18): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19450668 | |||||
| chr12:19450685
|
A | T | 37 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(34): Show | 37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.671+10315A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450685 | ||||||
| chr12:19450709
|
G | T | 1 | a0001c0001t0005g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.671+10339G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450709 | ||||||
| chr12:19450800
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.671+10430C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450800 | ||||||
| chr12:19450818
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.671+10448A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450818 | ||||||
| chr12:19450842
|
C | CA | 118 | a0001c0001t0001g0045a0001c0001t0001g0055a0001c0001t0001g0239others(115): Show | 119 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.671+10483dupA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19450842 | |||||
| chr12:19450859
|
A | AT | 19 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(16): Show | 19 | HG00438.hp2 HG01081.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.671+10500dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19450859 | |||||
| chr12:19450859
|
A | T | 1 | a0001c0001t0010g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.671+10489A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450859 | ||||||
| chr12:19450987
|
GT | G | 326 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(323): Show | 327 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(324): Show |
intron_variant | MODIFIER | c.671+10627delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19450987 | |||||
| chr12:19451147
|
C | G | 4 | a0001c0001t0006g0026a0001c0001t0006g0028a0001c0001t0014g0025others(1): Show | 4 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+10777C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451147 | ||||||
| chr12:19451199
|
C | T | 1 | a0001c0001t0003g0314 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.671+10829C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451199 | ||||||
| chr12:19451259
|
G | A | 41 | a0001c0001t0004g0004a0001c0001t0004g0265a0001c0001t0004g0266others(38): Show | 41 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.671+10889G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451259 | ||||||
| chr12:19451432
|
G | C | 398 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(395): Show | 402 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(399): Show |
intron_variant | MODIFIER | c.671+11062G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451432 | ||||||
| chr12:19451489
|
G | A | 328 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(325): Show | 329 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(326): Show |
intron_variant | MODIFIER | c.672-11021G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451489 | ||||||
| chr12:19451520
|
A | G | 2 | a0001c0001t0002g0205a0001c0001t0037g0203 | 2 | HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.672-10990A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451520 | ||||||
| chr12:19451558
|
G | A | 1 | a0001c0001t0018g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.672-10952G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451558 | ||||||
| chr12:19451573
|
G | T | 1 | a0001c0002t0001g0054 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.672-10937G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451573 | ||||||
| chr12:19451660
|
G | A | 2 | a0001c0001t0021g0269a0001c0001t0021g0270 | 2 | NA18948.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.672-10850G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451660 | ||||||
| chr12:19451686
|
A | AT | 137 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0055others(134): Show | 137 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.672-10808dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19451686 | |||||
| chr12:19451686
|
AT | A | 45 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(42): Show | 45 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.672-10808delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19451686 | |||||
| chr12:19451686
|
ATT | A | 100 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(97): Show | 101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.672-10809_672-1080 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19451686 | |||||
| chr12:19451753
|
G | A | 108 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(105): Show | 109 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.672-10757G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451753 | ||||||
| chr12:19451983
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.672-10527C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451983 | ||||||
| chr12:19451993
|
C | T | 1 | a0001c0001t0010g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.672-10517C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451993 | ||||||
| chr12:19452081
|
G | C | 1 | a0001c0001t0003g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.672-10429G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19452081 | ||||||
| chr12:19452162
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.672-10348A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19452162 | ||||||
| chr12:19452327
|
A | AC | 47 | a0001c0001t0004g0004a0001c0001t0004g0265a0001c0001t0004g0266others(44): Show | 47 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.672-10182dupC | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19452327 | |||||
| chr12:19452512
|
T | G | 11 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(8): Show | 11 | HG01934.hp2 HG02735.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.672-9998T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19452512 | ||||||
| chr12:19452515
|
G | T | 1 | a0001c0001t0002g0171 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.672-9995G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19452515 | ||||||
| chr12:19452516
|
T | G | 1 | a0001c0001t0002g0171 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.672-9994T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19452516 | ||||||
| chr12:19452672
|
G | C | 1 | a0001c0001t0003g0322 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.672-9838G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19452672 | ||||||
| chr12:19452961
|
C | CT | 145 | a0001c0001t0001g0055a0001c0001t0001g0108a0001c0001t0001g0114others(142): Show | 146 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.672-9527dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19452961 | |||||
| chr12:19452961
|
C | CTT | 13 | a0001c0001t0003g0311a0001c0001t0003g0321a0001c0001t0003g0376others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.672-9528_672-9527d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19452961 | |||||
| chr12:19452961
|
CT | C | 7 | a0001c0001t0001g0061a0001c0001t0001g0240a0001c0001t0002g0172others(4): Show | 7 | HG00639.hp2 HG01256.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.672-9527delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19452961 | |||||
| chr12:19452961
|
CTTTTT | C | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.672-9531_672-9527d others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19452961 | |||||
| chr12:19452961
|
CTTTTTTT others(4): Show |
C | 47 | a0001c0001t0004g0004a0001c0001t0004g0265a0001c0001t0004g0266others(44): Show | 47 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.672-9537_672-9527d others(13): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19452961 | |||||
| chr12:19452988
|
C | T | 1 | a0001c0001t0005g0149 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.672-9522C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19452988 | ||||||
| chr12:19453004
|
C | T | 101 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(98): Show | 102 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.672-9506C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453004 | ||||||
| chr12:19453037
|
C | T | 1 | a0001c0001t0003g0375 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.672-9473C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453037 | ||||||
| chr12:19453114
|
A | G | 328 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(325): Show | 329 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(326): Show |
intron_variant | MODIFIER | c.672-9396A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453114 | ||||||
| chr12:19453131
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02896.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.672-9379G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453131 | ||||||
| chr12:19453169
|
C | T | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-9341C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453169 | ||||||
| chr12:19453228
|
C | A | 1 | a0001c0001t0002g0171 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.672-9282C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453228 | ||||||
| chr12:19453230
|
A | G | 1 | a0001c0001t0002g0171 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.672-9280A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453230 | ||||||
| chr12:19453232
|
G | A | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.672-9278G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453232 | ||||||
| chr12:19453259
|
G | A | 1 | a0001c0002t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.672-9251G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453259 | ||||||
| chr12:19453279
|
A | T | 111 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(108): Show | 112 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.672-9231A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453279 | ||||||
| chr12:19453323
|
G | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02896.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.672-9187G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453323 | ||||||
| chr12:19453335
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02896.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.672-9175C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453335 | ||||||
| chr12:19453424
|
C | CT | 48 | a0001c0001t0004g0004a0001c0001t0004g0265a0001c0001t0004g0266others(45): Show | 48 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.672-9083dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19453424 | |||||
| chr12:19453424
|
C | CTT | 96 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(93): Show | 97 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.672-9084_672-9083d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19453424 | |||||
| chr12:19453424
|
C | CTTT | 3 | a0001c0001t0003g0375a0001c0001t0003g0381a0001c0001t0004g0282 | 3 | HG04184.hp2 HG04199.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.672-9085_672-9083d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19453424 | |||||
| chr12:19453428
|
C | T | 299 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(296): Show | 300 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.672-9082C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453428 | ||||||
| chr12:19453506
|
C | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0104a0001c0001t0001g0105others(2): Show | 5 | NA18944.hp1 NA18973.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-9004C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453506 | ||||||
| chr12:19453554
|
G | C | 1 | a0001c0001t0009g0167 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.672-8956G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453554 | ||||||
| chr12:19453578
|
C | T | 4 | a0001c0001t0006g0026a0001c0001t0006g0028a0001c0001t0014g0025others(1): Show | 4 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-8932C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453578 | ||||||
| chr12:19453815
|
A | G | 1 | a0001c0002t0001g0058 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.672-8695A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453815 | ||||||
| chr12:19454036
|
T | A | 3 | a0001c0001t0015g0233a0001c0001t0015g0234a0001c0001t0015g0235 | 3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.672-8474T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454036 | ||||||
| chr12:19454039
|
C | T | 45 | a0001c0001t0003g0310a0001c0001t0003g0374a0001c0001t0004g0004others(42): Show | 45 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.672-8471C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454039 | ||||||
| chr12:19454201
|
A | G | 1 | a0001c0001t0005g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.672-8309A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454201 | ||||||
| chr12:19454265
|
C | G | 1 | a0001c0001t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.672-8245C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454265 | ||||||
| chr12:19454359
|
CCA | C | 3 | a0001c0001t0002g0171a0001c0002t0001g0102a0001c0002t0038g0059 | 3 | NA18952.hp2 NA18957.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.672-8139_672-8138d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19454359 | |||||
| chr12:19454360
|
C | T | 31 | a0001c0001t0003g0321a0001c0001t0003g0373a0001c0001t0003g0379others(28): Show | 31 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-8150C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454360 | ||||||
| chr12:19454370
|
C | A | 1 | a0001c0001t0005g0132 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.672-8140C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454370 | ||||||
| chr12:19454454
|
C | T | 1 | a0001c0001t0006g0009 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.672-8056C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454454 | ||||||
| chr12:19454534
|
G | A | 2 | a0001c0002t0002g0057a0001c0002t0002g0122 | 2 | NA18991.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.672-7976G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454534 | ||||||
| chr12:19454548
|
C | T | 2 | a0001c0001t0004g0266a0001c0001t0004g0267 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.672-7962C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454548 | ||||||
| chr12:19454632
|
A | G | 2 | a0001c0001t0013g0160a0001c0001t0035g0159 | 2 | HG02145.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.672-7878A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454632 | ||||||
| chr12:19454702
|
C | T | 2 | a0001c0001t0017g0042a0001c0001t0017g0044 | 2 | HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.672-7808C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454702 | ||||||
| chr12:19454764
|
C | G | 34 | a0001c0001t0003g0313a0001c0001t0003g0321a0001c0001t0003g0371others(31): Show | 34 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.672-7746C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454764 | ||||||
| chr12:19454783
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0114 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.672-7727G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454783 | ||||||
| chr12:19454858
|
C | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-7652C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454858 | ||||||
| chr12:19454858
|
C | T | 1 | a0001c0001t0005g0131 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.672-7652C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454858 | ||||||
| chr12:19454942
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0008g0327 | 3 | HG02896.hp2 HG02897.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.672-7568G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454942 | ||||||
| chr12:19454946
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-7564A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454946 | ||||||
| chr12:19455002
|
G | T | 1 | a0001c0002t0010g0062 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.672-7508G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455002 | ||||||
| chr12:19455003
|
A | ATTT | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-7495_672-7493d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19455003 | |||||
| chr12:19455044
|
C | T | 2 | a0001c0001t0002g0205a0001c0001t0037g0203 | 2 | HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.672-7466C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455044 | ||||||
| chr12:19455067
|
A | G | 1 | a0001c0001t0007g0391 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.672-7443A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455067 | ||||||
| chr12:19455096
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-7414A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455096 | ||||||
| chr12:19455105
|
C | T | 54 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(51): Show | 54 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.672-7405C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455105 | ||||||
| chr12:19455160
|
A | AT | 31 | a0001c0001t0003g0313a0001c0001t0003g0321a0001c0001t0003g0373others(28): Show | 31 | HG00323.hp2 HG00639.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.672-7336dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19455160 | |||||
| chr12:19455160
|
AT | A | 8 | a0001c0001t0003g0328a0001c0001t0003g0329a0001c0001t0005g0153others(5): Show | 8 | HG01934.hp2 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-7336delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19455160 | |||||
| chr12:19455185
|
G | T | 8 | a0001c0001t0004g0396a0001c0001t0007g0003a0001c0001t0007g0315others(5): Show | 9 | HG02559.hp1 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.672-7325G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455185 | ||||||
| chr12:19455267
|
G | T | 1 | a0001c0002t0001g0089 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.672-7243G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455267 | ||||||
| chr12:19455270
|
G | A | 37 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(34): Show | 37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.672-7240G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455270 | ||||||
| chr12:19455272
|
C | T | 13 | a0001c0001t0015g0231a0001c0001t0015g0233a0001c0001t0015g0234others(10): Show | 13 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.672-7238C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455272 | ||||||
| chr12:19455460
|
A | C | 38 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(35): Show | 38 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.672-7050A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455460 | ||||||
| chr12:19455504
|
C | G | 24 | a0001c0002t0001g0056a0001c0002t0001g0072a0001c0002t0001g0073others(21): Show | 24 | HG01358.hp1 HG01928.hp2 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.672-7006C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455504 | ||||||
| chr12:19455570
|
G | A | 2 | a0001c0001t0002g0206a0001c0001t0004g0272 | 2 | HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.672-6940G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455570 | ||||||
| chr12:19455684
|
A | G | 4 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170others(1): Show | 4 | HG00140.hp1 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-6826A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455684 | ||||||
| chr12:19455695
|
C | T | 1 | a0001c0001t0028g0308 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.672-6815C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455695 | ||||||
| chr12:19455730
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-6780A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455730 | ||||||
| chr12:19455944
|
C | CT | 39 | a0001c0001t0002g0171a0001c0001t0003g0313a0001c0001t0003g0321others(36): Show | 39 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.672-6555dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19455944 | |||||
| chr12:19455955
|
T | C | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.672-6555T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455955 | ||||||
| chr12:19455955
|
T | TC | 109 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(106): Show | 109 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.672-6553dupC | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19455955 | |||||
| chr12:19456080
|
C | G | 4 | a0001c0001t0004g0317a0001c0001t0004g0318a0001c0001t0004g0320others(1): Show | 4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-6430C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456080 | ||||||
| chr12:19456082
|
A | T | 43 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(40): Show | 43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.672-6428A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456082 | ||||||
| chr12:19456162
|
A | G | 1 | a0001c0002t0001g0071 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.672-6348A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456162 | ||||||
| chr12:19456175
|
A | G | 1 | a0001c0001t0002g0199 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.672-6335A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456175 | ||||||
| chr12:19456227
|
A | G | 1 | a0001c0006t0033g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.672-6283A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456227 | ||||||
| chr12:19456330
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-6180A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456330 | ||||||
| chr12:19456526
|
A | G | 1 | a0001c0001t0020g0264 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.672-5984A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456526 | ||||||
| chr12:19456569
|
A | G | 149 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(146): Show | 150 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.672-5941A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456569 | ||||||
| chr12:19456619
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-5891C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456619 | ||||||
| chr12:19456713
|
A | G | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-5797A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456713 | ||||||
| chr12:19456778
|
T | C | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-5732T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456778 | ||||||
| chr12:19456791
|
A | T | 112 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(109): Show | 112 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(109): Show |
intron_variant | MODIFIER | c.672-5719A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456791 | ||||||
| chr12:19456819
|
A | G | 43 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(40): Show | 43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.672-5691A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456819 | ||||||
| chr12:19456945
|
C | A | 32 | a0001c0001t0003g0321a0001c0001t0003g0373a0001c0001t0003g0379others(29): Show | 32 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.672-5565C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456945 | ||||||
| chr12:19456995
|
G | A | 331 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(328): Show | 332 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(329): Show |
intron_variant | MODIFIER | c.672-5515G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456995 | ||||||
| chr12:19457018
|
A | G | 334 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(331): Show | 335 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.672-5492A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457018 | ||||||
| chr12:19457019
|
A | C | 334 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(331): Show | 335 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.672-5491A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457019 | ||||||
| chr12:19457093
|
A | G | 1 | a0001c0001t0006g0022 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.672-5417A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457093 | ||||||
| chr12:19457097
|
T | C | 86 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(83): Show | 86 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.672-5413T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457097 | ||||||
| chr12:19457279
|
C | T | 149 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(146): Show | 149 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.672-5231C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457279 | ||||||
| chr12:19457319
|
T | G | 1 | a0001c0001t0003g0330 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.672-5191T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457319 | ||||||
| chr12:19457324
|
G | A | 2 | a0001c0001t0015g0231a0001c0001t0024g0232 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.672-5186G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457324 | ||||||
| chr12:19457358
|
G | T | 1 | a0001c0002t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.672-5152G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457358 | ||||||
| chr12:19457803
|
C | G | 43 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(40): Show | 43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.672-4707C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457803 | ||||||
| chr12:19458032
|
A | C | 4 | a0001c0001t0002g0163a0001c0001t0002g0198a0001c0001t0002g0219others(1): Show | 4 | NA18940.hp2 NA18967.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-4478A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458032 | ||||||
| chr12:19458507
|
T | C | 334 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(331): Show | 335 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.672-4003T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458507 | ||||||
| chr12:19458585
|
C | G | 1 | a0001c0001t0007g0391 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.672-3925C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458585 | ||||||
| chr12:19458593
|
A | G | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-3917A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458593 | ||||||
| chr12:19458765
|
T | G | 5 | a0001c0001t0015g0231a0001c0001t0015g0233a0001c0001t0015g0234others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-3745T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458765 | ||||||
| chr12:19458835
|
G | A | 1 | a0001c0001t0004g0298 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.672-3675G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458835 | ||||||
| chr12:19458885
|
G | A | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-3625G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458885 | ||||||
| chr12:19458961
|
G | T | 334 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(331): Show | 335 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.672-3549G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458961 | ||||||
| chr12:19459028
|
T | A | 4 | a0001c0001t0006g0026a0001c0001t0006g0028a0001c0001t0014g0025others(1): Show | 4 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-3482T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459028 | ||||||
| chr12:19459076
|
T | C | 5 | a0001c0001t0015g0231a0001c0001t0015g0233a0001c0001t0015g0234others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-3434T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459076 | ||||||
| chr12:19459131
|
G | A | 1 | a0001c0002t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.672-3379G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459131 | ||||||
| chr12:19459164
|
T | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-3346T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459164 | ||||||
| chr12:19459384
|
A | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-3126A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459384 | ||||||
| chr12:19459539
|
C | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-2971C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459539 | ||||||
| chr12:19459560
|
A | G | 38 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(35): Show | 38 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.672-2950A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459560 | ||||||
| chr12:19459561
|
T | C | 6 | a0001c0001t0003g0313a0001c0001t0003g0321a0001c0001t0003g0373others(3): Show | 6 | HG01261.hp1 HG01515.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.672-2949T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459561 | ||||||
| chr12:19459567
|
A | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-2943A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459567 | ||||||
| chr12:19459755
|
T | C | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-2755T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459755 | ||||||
| chr12:19460050
|
T | C | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-2460T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460050 | ||||||
| chr12:19460093
|
C | T | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.672-2417C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460093 | ||||||
| chr12:19460094
|
G | A | 2 | a0001c0001t0015g0231a0001c0001t0024g0232 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.672-2416G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460094 | ||||||
| chr12:19460114
|
T | G | 38 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(35): Show | 38 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.672-2396T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460114 | ||||||
| chr12:19460135
|
G | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02896.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.672-2375G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460135 | ||||||
| chr12:19460391
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.672-2119G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460391 | ||||||
| chr12:19460443
|
C | T | 1 | a0001c0001t0024g0232 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.672-2067C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460443 | ||||||
| chr12:19460459
|
A | G | 1 | a0001c0001t0018g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.672-2051A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460459 | ||||||
| chr12:19460477
|
C | T | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-2033C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460477 | ||||||
| chr12:19460478
|
C | G | 1 | a0001c0001t0003g0397 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.672-2032C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460478 | ||||||
| chr12:19460542
|
T | C | 302 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(299): Show | 303 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.672-1968T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460542 | ||||||
| chr12:19460657
|
G | GT | 11 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0253others(8): Show | 11 | HG02074.hp2 HG02615.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.672-1838dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19460657 | |||||
| chr12:19460678
|
A | G | 334 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(331): Show | 335 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.672-1832A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460678 | ||||||
| chr12:19460780
|
G | A | 1 | a0001c0001t0008g0331 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.672-1730G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460780 | ||||||
| chr12:19460886
|
T | C | 152 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(149): Show | 153 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.672-1624T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460886 | ||||||
| chr12:19460915
|
A | G | 38 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(35): Show | 38 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.672-1595A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460915 | ||||||
| chr12:19460937
|
C | T | 90 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(87): Show | 91 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.672-1573C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460937 | ||||||
| chr12:19461114
|
A | G | 3 | a0001c0002t0001g0087a0001c0002t0001g0238a0001c0002t0010g0110 | 3 | HG01358.hp1 HG01928.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.672-1396A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461114 | ||||||
| chr12:19461180
|
G | A | 1 | a0001c0001t0004g0273 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.672-1330G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461180 | ||||||
| chr12:19461226
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-1284A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461226 | ||||||
| chr12:19461254
|
T | G | 38 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(35): Show | 38 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.672-1256T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461254 | ||||||
| chr12:19461270
|
T | G | 5 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044others(2): Show | 5 | HG01934.hp2 HG02055.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-1240T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461270 | ||||||
| chr12:19461338
|
C | G | 1 | a0001c0001t0004g0294 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.672-1172C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461338 | ||||||
| chr12:19461338
|
C | T | 28 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(25): Show | 28 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.672-1172C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461338 | ||||||
| chr12:19461460
|
T | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-1050T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461460 | ||||||
| chr12:19461489
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-1021G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461489 | ||||||
| chr12:19461590
|
A | G | 1 | a0001c0001t0004g0396 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.672-920A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461590 | ||||||
| chr12:19461704
|
T | A | 96 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(93): Show | 97 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.672-806T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461704 | ||||||
| chr12:19461728
|
T | C | 334 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(331): Show | 335 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.672-782T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461728 | ||||||
| chr12:19461848
|
T | G | 1 | a0001c0006t0033g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.672-662T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461848 | ||||||
| chr12:19461861
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-649C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461861 | ||||||
| chr12:19461940
|
A | G | 2 | a0001c0001t0006g0011a0001c0001t0006g0021 | 2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.672-570A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461940 | ||||||
| chr12:19462140
|
C | T | 5 | a0001c0001t0001g0248a0001c0001t0041g0251a0001c0003t0001g0250others(2): Show | 5 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-370C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19462140 | ||||||
| chr12:19462180
|
A | G | 334 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(331): Show | 335 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.672-330A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19462180 | ||||||
| chr12:19462307
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-203C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19462307 | ||||||
| chr12:19463019
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.879+302G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463019 | ||||||
| chr12:19463087
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02896.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.879+370G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463087 | ||||||
| chr12:19463100
|
G | T | 109 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(106): Show | 109 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.879+383G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463100 | ||||||
| chr12:19463150
|
A | G | 1 | a0001c0001t0006g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.879+433A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463150 | ||||||
| chr12:19463167
|
G | C | 43 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(40): Show | 43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.879+450G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463167 | ||||||
| chr12:19463228
|
G | A | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049 | 3 | HG01109.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.879+511G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463228 | ||||||
| chr12:19463317
|
T | C | 43 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(40): Show | 43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.879+600T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463317 | ||||||
| chr12:19463351
|
A | G | 3 | a0001c0002t0001g0087a0001c0002t0001g0238a0001c0002t0010g0110 | 3 | HG01358.hp1 HG01928.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.879+634A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463351 | ||||||
| chr12:19463621
|
A | G | 1 | a0001c0001t0034g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.879+904A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463621 | ||||||
| chr12:19463624
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+907G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463624 | ||||||
| chr12:19463640
|
C | T | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.879+923C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463640 | ||||||
| chr12:19463667
|
A | AT | 68 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(65): Show | 69 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.879+974dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19463667 | |||||
| chr12:19463667
|
A | ATT | 70 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(67): Show | 70 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.879+973_879+974dup others(2): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19463667 | |||||
| chr12:19463667
|
A | ATTT | 16 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(13): Show | 16 | HG01361.hp2 HG02027.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.879+972_879+974dup others(3): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19463667 | |||||
| chr12:19463667
|
AT | A | 88 | a0001c0001t0001g0099a0001c0001t0001g0106a0001c0001t0005g0133others(85): Show | 88 | HG00323.hp2 HG00558.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.879+974delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19463667 | |||||
| chr12:19463667
|
ATT | A | 48 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(45): Show | 48 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.879+973_879+974del others(2): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19463667 | |||||
| chr12:19463667
|
ATTTT | A | 7 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(4): Show | 7 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+971_879+974del others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19463667 | |||||
| chr12:19463890
|
T | G | 1 | a0001c0001t0012g0333 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.879+1173T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463890 | ||||||
| chr12:19463942
|
A | T | 37 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(34): Show | 37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.879+1225A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463942 | ||||||
| chr12:19464102
|
G | A | 2 | a0001c0001t0006g0012a0001c0001t0006g0013 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.879+1385G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464102 | ||||||
| chr12:19464107
|
C | T | 4 | a0001c0001t0003g0321a0001c0001t0003g0379a0001c0001t0003g0381others(1): Show | 4 | HG01261.hp1 HG04115.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+1390C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464107 | ||||||
| chr12:19464145
|
C | T | 1 | a0001c0001t0031g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.879+1428C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464145 | ||||||
| chr12:19464248
|
T | G | 1 | a0001c0002t0001g0047 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.879+1531T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464248 | ||||||
| chr12:19464354
|
G | T | 1 | a0001c0001t0008g0384 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.879+1637G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464354 | ||||||
| chr12:19464355
|
C | T | 1 | a0001c0001t0008g0384 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.879+1638C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464355 | ||||||
| chr12:19464403
|
T | C | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.879+1686T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464403 | ||||||
| chr12:19464423
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.879+1706C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464423 | ||||||
| chr12:19464437
|
G | A | 2 | a0001c0001t0014g0030a0001c0001t0014g0031 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.879+1720G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464437 | ||||||
| chr12:19464458
|
C | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+1741C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464458 | ||||||
| chr12:19464521
|
A | G | 1 | a0001c0002t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.879+1804A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464521 | ||||||
| chr12:19464551
|
GATTTTTA others(4): Show |
G | 1 | a0001c0001t0004g0281 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.879+1846_879+1856d others(13): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19464551 | |||||
| chr12:19464592
|
A | AT | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.879+1886dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19464592 | |||||
| chr12:19464667
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.879+1950A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464667 | ||||||
| chr12:19464679
|
C | T | 1 | a0001c0001t0014g0027 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.879+1962C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464679 | ||||||
| chr12:19464770
|
G | A | 1 | a0001c0001t0012g0335 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.879+2053G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464770 | ||||||
| chr12:19464885
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.879+2168C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464885 | ||||||
| chr12:19464916
|
A | G | 2 | a0001c0001t0003g0383a0001c0001t0008g0360 | 2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.879+2199A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464916 | ||||||
| chr12:19464953
|
A | G | 5 | a0001c0001t0015g0231a0001c0001t0015g0233a0001c0001t0015g0234others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+2236A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464953 | ||||||
| chr12:19465103
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+2386G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465103 | ||||||
| chr12:19465221
|
C | T | 1 | a0001c0001t0004g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.879+2504C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465221 | ||||||
| chr12:19465309
|
G | A | 4 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170others(1): Show | 4 | HG00140.hp1 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+2592G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465309 | ||||||
| chr12:19465404
|
TAAATA | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+2696_879+2700d others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19465404 | |||||
| chr12:19465421
|
G | A | 1 | a0001c0001t0022g0128 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.879+2704G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465421 | ||||||
| chr12:19465441
|
G | C | 48 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(45): Show | 48 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.879+2724G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465441 | ||||||
| chr12:19465564
|
T | G | 100 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(97): Show | 101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.879+2847T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465564 | ||||||
| chr12:19465614
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+2897A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465614 | ||||||
| chr12:19465621
|
G | A | 1 | a0001c0001t0003g0376 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.879+2904G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465621 | ||||||
| chr12:19465781
|
A | G | 1 | a0001c0001t0003g0314 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.879+3064A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465781 | ||||||
| chr12:19465791
|
CT | C | 266 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0055others(263): Show | 267 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.879+3092delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19465791 | |||||
| chr12:19465791
|
CTT | C | 10 | a0001c0001t0001g0051a0001c0001t0001g0248a0001c0001t0002g0220others(7): Show | 10 | HG01081.hp2 HG01257.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.879+3091_879+3092d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19465791 | |||||
| chr12:19465794
|
T | TTC | 7 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0039others(4): Show | 7 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+3078_879+3079i others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19465794 | |||||
| chr12:19465796
|
T | C | 1 | a0001c0001t0031g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.879+3079T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465796 | ||||||
| chr12:19465813
|
A | T | 3 | a0001c0001t0015g0233a0001c0001t0015g0234a0001c0001t0015g0235 | 3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.879+3096A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465813 | ||||||
| chr12:19465844
|
T | C | 1 | a0001c0001t0006g0022 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.879+3127T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465844 | ||||||
| chr12:19465858
|
C | T | 1 | a0001c0001t0011g0301 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.879+3141C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465858 | ||||||
| chr12:19465869
|
A | G | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.879+3152A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465869 | ||||||
| chr12:19465878
|
G | A | 2 | a0001c0001t0020g0263a0001c0001t0020g0264 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.879+3161G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465878 | ||||||
| chr12:19465934
|
A | G | 37 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0063others(34): Show | 37 | HG00558.hp2 HG01358.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.879+3217A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465934 | ||||||
| chr12:19465967
|
T | C | 1 | a0001c0001t0004g0317 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.879+3250T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465967 | ||||||
| chr12:19466028
|
G | T | 2 | a0001c0001t0015g0233a0001c0001t0015g0234 | 2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.879+3311G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466028 | ||||||
| chr12:19466122
|
T | C | 1 | a0001c0001t0002g0226 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.879+3405T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466122 | ||||||
| chr12:19466202
|
C | G | 1 | a0001c0001t0011g0293 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.879+3485C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466202 | ||||||
| chr12:19466426
|
G | A | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 4 | HG00597.hp2 HG02056.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+3709G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466426 | ||||||
| chr12:19466450
|
C | CA | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+3741dupA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19466450 | |||||
| chr12:19466533
|
C | G | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.879+3816C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466533 | ||||||
| chr12:19466537
|
G | A | 1 | a0001c0001t0011g0301 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.879+3820G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466537 | ||||||
| chr12:19466593
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+3876C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466593 | ||||||
| chr12:19466607
|
T | C | 333 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(330): Show | 334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.879+3890T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466607 | ||||||
| chr12:19466608
|
T | C | 333 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(330): Show | 334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.879+3891T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466608 | ||||||
| chr12:19466792
|
G | A | 1 | a0001c0005t0023g0033 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.879+4075G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466792 | ||||||
| chr12:19466968
|
C | T | 2 | a0001c0001t0002g0215a0001c0001t0002g0216 | 2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.879+4251C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466968 | ||||||
| chr12:19466982
|
T | C | 140 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(137): Show | 141 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.879+4265T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466982 | ||||||
| chr12:19467091
|
A | G | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.879+4374A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467091 | ||||||
| chr12:19467144
|
G | A | 2 | a0001c0001t0014g0030a0001c0001t0014g0031 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.879+4427G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467144 | ||||||
| chr12:19467214
|
C | CT | 76 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(73): Show | 76 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.879+4506dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19467214 | |||||
| chr12:19467358
|
A | G | 1 | a0001c0001t0004g0268 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.879+4641A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467358 | ||||||
| chr12:19467384
|
C | T | 1 | a0001c0001t0005g0132 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.879+4667C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467384 | ||||||
| chr12:19467507
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+4790T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467507 | ||||||
| chr12:19467513
|
C | T | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.879+4796C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467513 | ||||||
| chr12:19467515
|
A | T | 1 | a0001c0002t0001g0086 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.879+4798A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467515 | ||||||
| chr12:19467575
|
T | G | 1 | a0001c0001t0001g0112 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.879+4858T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467575 | ||||||
| chr12:19467653
|
A | G | 1 | a0001c0001t0004g0271 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.879+4936A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467653 | ||||||
| chr12:19467665
|
A | G | 11 | a0001c0001t0005g0134a0001c0001t0005g0135a0001c0001t0005g0136others(8): Show | 11 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+4948A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467665 | ||||||
| chr12:19467672
|
G | C | 1 | a0001c0001t0020g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.879+4955G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467672 | ||||||
| chr12:19467677
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.879+4960C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467677 | ||||||
| chr12:19467764
|
C | T | 1 | a0001c0001t0036g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.879+5047C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467764 | ||||||
| chr12:19468126
|
T | TGTGTGTG others(8): Show |
1 | a0001c0001t0008g0332 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.880-5122_880-5121i others(17): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468126 | ||||||
| chr12:19468126
|
T | TGTGTGTG others(10): Show |
1 | a0001c0001t0046g0032 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.880-5122_880-5121i others(19): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468126 | ||||||
| chr12:19468126
|
T | TTG | 3 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0037g0203 | 3 | HG01261.hp2 HG02622.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.880-5092_880-5091d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | |||||
| chr12:19468126
|
T | TTGTG | 19 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(16): Show | 19 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.880-5094_880-5091d others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | |||||
| chr12:19468126
|
T | TTGTGTGT others(1): Show |
36 | a0001c0001t0003g0338a0001c0001t0003g0339a0001c0001t0003g0340others(33): Show | 36 | HG00140.hp2 HG00609.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.880-5098_880-5091d others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | |||||
| chr12:19468126
|
T | TTGTGTGT others(3): Show |
16 | a0001c0001t0003g0312a0001c0001t0003g0328a0001c0001t0003g0341others(13): Show | 16 | HG01106.hp2 HG01891.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.880-5100_880-5091d others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | |||||
| chr12:19468126
|
T | TTGTGTGT others(5): Show |
40 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(37): Show | 41 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.880-5102_880-5091d others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | |||||
| chr12:19468126
|
T | TTGTGTGT others(7): Show |
67 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(64): Show | 67 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.880-5104_880-5091d others(16): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | |||||
| chr12:19468126
|
T | TTGTGTGT others(9): Show |
43 | a0001c0001t0003g0329a0001c0001t0003g0353a0001c0001t0003g0354others(40): Show | 43 | HG00558.hp1 HG01074.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.880-5106_880-5091d others(18): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | |||||
| chr12:19468126
|
T | TTGTGTGT others(11): Show |
7 | a0001c0001t0004g0292a0001c0001t0014g0020a0001c0001t0016g0035others(4): Show | 7 | HG00639.hp1 HG02572.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-5108_880-5091d others(20): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | |||||
| chr12:19468126
|
T | TTGTGTGT others(13): Show |
9 | a0001c0001t0003g0322a0001c0001t0003g0330a0001c0001t0003g0336others(6): Show | 9 | HG00408.hp1 NA18944.hp2 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-5110_880-5091d others(22): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | |||||
| chr12:19468126
|
T | TTGTGTGT others(19): Show |
1 | a0001c0001t0003g0378 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.880-5116_880-5091d others(28): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | |||||
| chr12:19468126
|
TTG | T | 3 | a0001c0001t0002g0225a0001c0001t0010g0060a0001c0006t0033g0041 | 3 | HG01934.hp2 NA18960.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.880-5092_880-5091d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | |||||
| chr12:19468126
|
TTGTGTGT others(5): Show |
T | 52 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(49): Show | 52 | HG00558.hp2 HG01109.hp1 HG01358.hp1 others(49): Show |
intron_variant | MODIFIER | c.880-5102_880-5091d others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | |||||
| chr12:19468260
|
T | G | 6 | a0001c0001t0013g0156a0001c0001t0013g0157a0001c0001t0013g0158others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-4988T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468260 | ||||||
| chr12:19468293
|
C | G | 151 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(148): Show | 152 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.880-4955C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468293 | ||||||
| chr12:19468316
|
G | A | 43 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(40): Show | 43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.880-4932G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468316 | ||||||
| chr12:19468464
|
T | C | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.880-4784T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468464 | ||||||
| chr12:19468553
|
A | T | 1 | a0001c0003t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.880-4695A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468553 | ||||||
| chr12:19468750
|
T | G | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.880-4498T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468750 | ||||||
| chr12:19468786
|
A | G | 399 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(396): Show | 403 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(400): Show |
intron_variant | MODIFIER | c.880-4462A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468786 | ||||||
| chr12:19469045
|
C | T | 49 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(46): Show | 49 | HG00558.hp2 HG01109.hp1 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.880-4203C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469045 | ||||||
| chr12:19469060
|
G | C | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.880-4188G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469060 | ||||||
| chr12:19469135
|
A | T | 7 | a0001c0001t0002g0001a0001c0001t0002g0195a0001c0001t0002g0197others(4): Show | 9 | NA18955.hp1 NA18963.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-4113A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469135 | ||||||
| chr12:19469169
|
A | G | 8 | a0001c0002t0001g0063a0001c0002t0001g0068a0001c0002t0001g0069others(5): Show | 8 | HG00558.hp2 HG02040.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-4079A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469169 | ||||||
| chr12:19469180
|
C | G | 37 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(34): Show | 37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.880-4068C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469180 | ||||||
| chr12:19469262
|
T | A | 57 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(54): Show | 57 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.880-3986T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469262 | ||||||
| chr12:19469284
|
G | A | 43 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(40): Show | 43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.880-3964G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469284 | ||||||
| chr12:19469411
|
C | A | 77 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.880-3837C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469411 | ||||||
| chr12:19469451
|
A | G | 37 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(34): Show | 37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.880-3797A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469451 | ||||||
| chr12:19469547
|
T | G | 2 | a0001c0001t0015g0231a0001c0001t0024g0232 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.880-3701T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469547 | ||||||
| chr12:19469557
|
C | G | 1 | a0001c0001t0003g0310 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.880-3691C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469557 | ||||||
| chr12:19469608
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-3640C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469608 | ||||||
| chr12:19469680
|
C | A | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.880-3568C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469680 | ||||||
| chr12:19469751
|
G | T | 2 | a0001c0001t0002g0206a0001c0001t0004g0272 | 2 | HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.880-3497G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469751 | ||||||
| chr12:19469768
|
T | G | 1 | a0001c0001t0017g0043 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.880-3480T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469768 | ||||||
| chr12:19470024
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.880-3224C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470024 | ||||||
| chr12:19470120
|
T | C | 1 | a0001c0001t0002g0174 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.880-3128T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470120 | ||||||
| chr12:19470151
|
A | C | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.880-3097A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470151 | ||||||
| chr12:19470164
|
C | CT | 111 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(108): Show | 111 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(108): Show |
intron_variant | MODIFIER | c.880-3072dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19470164 | |||||
| chr12:19470214
|
A | G | 5 | a0001c0002t0001g0109a0001c0002t0001g0124a0001c0002t0001g0125others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-3034A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470214 | ||||||
| chr12:19470244
|
C | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-3004C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470244 | ||||||
| chr12:19470294
|
G | A | 2 | a0001c0002t0001g0102a0001c0002t0038g0059 | 2 | NA18952.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.880-2954G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470294 | ||||||
| chr12:19470327
|
T | A | 99 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(96): Show | 100 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.880-2921T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470327 | ||||||
| chr12:19470390
|
G | A | 1 | a0001c0001t0005g0137 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.880-2858G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470390 | ||||||
| chr12:19470405
|
C | T | 10 | a0001c0001t0005g0134a0001c0001t0005g0135a0001c0001t0005g0136others(7): Show | 10 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-2843C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470405 | ||||||
| chr12:19470474
|
C | A | 333 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(330): Show | 334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.880-2774C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470474 | ||||||
| chr12:19470481
|
C | T | 2 | a0001c0001t0004g0266a0001c0001t0004g0267 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.880-2767C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470481 | ||||||
| chr12:19470599
|
C | T | 112 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(109): Show | 113 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.880-2649C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470599 | ||||||
| chr12:19470624
|
A | G | 5 | a0001c0001t0015g0231a0001c0001t0015g0233a0001c0001t0015g0234others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-2624A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470624 | ||||||
| chr12:19470631
|
A | G | 1 | a0001c0001t0003g0341 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.880-2617A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470631 | ||||||
| chr12:19470743
|
A | C | 3 | a0001c0001t0018g0228a0001c0001t0018g0229a0001c0001t0018g0230 | 3 | HG02922.hp1 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.880-2505A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470743 | ||||||
| chr12:19470807
|
T | G | 114 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(111): Show | 114 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.880-2441T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470807 | ||||||
| chr12:19470859
|
T | C | 1 | a0001c0002t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.880-2389T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470859 | ||||||
| chr12:19470934
|
C | G | 1 | a0001c0001t0002g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.880-2314C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470934 | ||||||
| chr12:19470999
|
C | T | 1 | a0001c0001t0034g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.880-2249C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470999 | ||||||
| chr12:19471053
|
C | A | 1 | a0001c0002t0001g0071 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.880-2195C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471053 | ||||||
| chr12:19471064
|
T | TCCTCCTC others(115): Show |
2 | a0001c0001t0003g0313a0001c0005t0023g0033 | 2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.880-2063_880-2062i others(124): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19471064 | |||||
| chr12:19471090
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-2158G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471090 | ||||||
| chr12:19471161
|
G | C | 4 | a0001c0001t0004g0317a0001c0001t0004g0318a0001c0001t0004g0320others(1): Show | 4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-2087G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471161 | ||||||
| chr12:19471194
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-2054T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471194 | ||||||
| chr12:19471300
|
G | A | 1 | a0001c0001t0003g0314 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.880-1948G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471300 | ||||||
| chr12:19471300
|
G | C | 5 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(2): Show | 5 | NA18982.hp1 NA18998.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-1948G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471300 | ||||||
| chr12:19471302
|
A | G | 1 | a0001c0002t0002g0144 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.880-1946A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471302 | ||||||
| chr12:19471377
|
A | C | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.880-1871A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471377 | ||||||
| chr12:19471505
|
A | T | 6 | a0001c0001t0013g0156a0001c0001t0013g0157a0001c0001t0013g0158others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-1743A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471505 | ||||||
| chr12:19471507
|
G | GT | 28 | a0001c0001t0002g0193a0001c0001t0006g0005a0001c0001t0006g0006others(25): Show | 28 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.880-1730dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19471507 | |||||
| chr12:19471657
|
C | G | 1 | a0001c0001t0047g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.880-1591C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471657 | ||||||
| chr12:19471666
|
C | T | 30 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(27): Show | 30 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.880-1582C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471666 | ||||||
| chr12:19471680
|
A | C | 2 | a0001c0001t0015g0231a0001c0001t0024g0232 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.880-1568A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471680 | ||||||
| chr12:19471868
|
C | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-1380C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471868 | ||||||
| chr12:19472055
|
A | G | 1 | a0001c0001t0004g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.880-1193A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472055 | ||||||
| chr12:19472115
|
G | T | 1 | a0001c0001t0002g0192 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.880-1133G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472115 | ||||||
| chr12:19472328
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-920T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472328 | ||||||
| chr12:19472359
|
A | T | 334 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(331): Show | 335 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.880-889A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472359 | ||||||
| chr12:19472482
|
C | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-766C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472482 | ||||||
| chr12:19472581
|
G | A | 1 | a0001c0002t0001g0072 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.880-667G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472581 | ||||||
| chr12:19472587
|
T | A | 3 | a0001c0001t0006g0022a0001c0001t0014g0020a0001c0001t0031g0029 | 3 | HG00639.hp1 HG01106.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-661T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472587 | ||||||
| chr12:19472634
|
T | C | 3 | a0001c0001t0003g0338a0001c0001t0003g0339a0001c0001t0012g0337 | 3 | HG00140.hp2 HG00738.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.880-614T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472634 | ||||||
| chr12:19472661
|
A | G | 3 | a0001c0001t0002g0174a0001c0001t0002g0190a0001c0001t0002g0191 | 3 | HG00597.hp1 NA18747.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.880-587A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472661 | ||||||
| chr12:19472758
|
C | T | 3 | a0001c0001t0015g0233a0001c0001t0015g0234a0001c0001t0015g0235 | 3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.880-490C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472758 | ||||||
| chr12:19472780
|
A | G | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.880-468A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472780 | ||||||
| chr12:19473137
|
A | G | 1 | a0001c0002t0001g0071 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.880-111A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19473137 | ||||||
| chr12:19473195
|
A | T | 1 | a0001c0001t0002g0189 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.880-53A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19473195 | ||||||
| chr12:19473375
|
A | AAATT | 119 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(116): Show | 119 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.987+21_987+24dupAA others(2): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473375 | |||||
| chr12:19473375
|
A | AAATTAAT others(1): Show |
4 | a0001c0001t0001g0061a0001c0001t0001g0097a0001c0001t0001g0106others(1): Show | 4 | HG01074.hp2 NA18944.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+24_987+25insAA others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473375 | |||||
| chr12:19473376
|
A | AATTAATT others(1): Show |
6 | a0001c0001t0001g0246a0001c0001t0001g0248a0001c0001t0001g0255others(3): Show | 6 | HG01081.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+24_987+25insAA others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | |||||
| chr12:19473376
|
A | AATTT | 7 | a0001c0001t0001g0247a0001c0001t0002g0174a0001c0001t0002g0184others(4): Show | 7 | HG00621.hp2 HG01168.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.987+64_987+67dupTT others(2): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | |||||
| chr12:19473376
|
A | AATTTATT others(1): Show |
9 | a0001c0001t0002g0166a0001c0001t0002g0187a0001c0001t0009g0186others(6): Show | 9 | HG01884.hp1 NA18942.hp1 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.987+60_987+67dupTT others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | |||||
| chr12:19473376
|
A | AATTTATT others(5): Show |
5 | a0001c0001t0002g0188a0001c0001t0002g0205a0001c0001t0016g0035others(2): Show | 5 | HG01192.hp1 HG02083.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+56_987+67dupTT others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | |||||
| chr12:19473376
|
A | AATTTATT others(9): Show |
1 | a0001c0001t0037g0203 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.987+52_987+67dupTT others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | |||||
| chr12:19473376
|
AATTT | A | 143 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(140): Show | 144 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+64_987+67delTT others(2): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | |||||
| chr12:19473376
|
AATTTATT others(1): Show |
A | 12 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0304others(9): Show | 12 | HG01109.hp1 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.987+60_987+67delTT others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | |||||
| chr12:19473376
|
AATTTATT others(5): Show |
A | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.987+56_987+67delTT others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | |||||
| chr12:19473380
|
T | A | 116 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(113): Show | 116 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.987+25T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473380 | ||||||
| chr12:19473384
|
T | A | 245 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(242): Show | 246 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.987+29T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473384 | ||||||
| chr12:19473388
|
T | A | 242 | a0001c0001t0001g0045a0001c0001t0001g0092a0001c0001t0001g0095others(239): Show | 243 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.987+33T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473388 | ||||||
| chr12:19473392
|
T | A | 242 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0108others(239): Show | 243 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.987+37T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473392 | ||||||
| chr12:19473396
|
T | A | 156 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0108others(153): Show | 157 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.987+41T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473396 | ||||||
| chr12:19473400
|
T | A | 112 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0117others(109): Show | 113 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.987+45T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473400 | ||||||
| chr12:19473404
|
T | A | 57 | a0001c0001t0001g0117a0001c0001t0004g0265a0001c0001t0004g0280others(54): Show | 57 | HG00735.hp1 HG01071.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.987+49T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473404 | ||||||
| chr12:19473408
|
T | A | 8 | a0001c0001t0013g0156a0001c0001t0013g0157a0001c0001t0013g0158others(5): Show | 8 | HG01891.hp1 HG01934.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+53T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473408 | ||||||
| chr12:19473412
|
T | A | 1 | a0001c0001t0034g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.987+57T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473412 | ||||||
| chr12:19473416
|
T | A | 1 | a0001c0001t0034g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.987+61T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473416 | ||||||
| chr12:19473440
|
C | T | 2 | a0001c0001t0004g0266a0001c0001t0004g0267 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.987+85C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473440 | ||||||
| chr12:19473525
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+170T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473525 | ||||||
| chr12:19473628
|
A | T | 60 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(57): Show | 60 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.987+273A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473628 | ||||||
| chr12:19473662
|
A | G | 1 | a0001c0001t0004g0265 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.987+307A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473662 | ||||||
| chr12:19473759
|
TAA | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+407_987+408del others(2): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473759 | |||||
| chr12:19473762
|
A | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+407A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473762 | ||||||
| chr12:19473763
|
A | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+408A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473763 | ||||||
| chr12:19473766
|
T | G | 4 | a0001c0002t0001g0124a0001c0002t0001g0125a0001c0002t0001g0126others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.987+411T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473766 | ||||||
| chr12:19473877
|
G | A | 1 | a0001c0001t0005g0137 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.987+522G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473877 | ||||||
| chr12:19473881
|
A | G | 140 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(137): Show | 141 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.987+526A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473881 | ||||||
| chr12:19473906
|
G | A | 1 | a0001c0001t0003g0323 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.987+551G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473906 | ||||||
| chr12:19473907
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+552G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473907 | ||||||
| chr12:19473924
|
T | C | 1 | a0001c0001t0020g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.987+569T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473924 | ||||||
| chr12:19474030
|
T | C | 45 | a0001c0001t0002g0206a0001c0001t0003g0363a0001c0001t0003g0378others(42): Show | 45 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.987+675T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474030 | ||||||
| chr12:19474109
|
T | G | 1 | a0001c0001t0004g0396 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.987+754T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474109 | ||||||
| chr12:19474331
|
A | G | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049 | 3 | HG01109.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.987+976A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474331 | ||||||
| chr12:19474441
|
G | A | 12 | a0001c0001t0003g0374a0001c0001t0016g0035a0001c0001t0016g0036others(9): Show | 12 | HG02055.hp1 HG02572.hp2 NA18953.hp2 others(9): Show |
intron_variant | MODIFIER | c.987+1086G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474441 | ||||||
| chr12:19474539
|
T | C | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.987+1184T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474539 | ||||||
| chr12:19474548
|
T | G | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.987+1193T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474548 | ||||||
| chr12:19474625
|
A | G | 43 | a0001c0001t0002g0206a0001c0001t0003g0363a0001c0001t0003g0378others(40): Show | 43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.987+1270A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474625 | ||||||
| chr12:19474726
|
A | C | 4 | a0001c0001t0004g0317a0001c0001t0004g0318a0001c0001t0004g0320others(1): Show | 4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+1371A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474726 | ||||||
| chr12:19474793
|
G | GT | 289 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(286): Show | 290 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.987+1447dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19474793 | |||||
| chr12:19474818
|
A | T | 2 | a0001c0001t0003g0383a0001c0001t0008g0360 | 2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.987+1463A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474818 | ||||||
| chr12:19474941
|
C | T | 9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | NA18953.hp2 NA18957.hp1 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.987+1586C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474941 | ||||||
| chr12:19475019
|
T | C | 3 | a0001c0001t0002g0174a0001c0001t0002g0190a0001c0001t0002g0191 | 3 | HG00597.hp1 NA18747.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.987+1664T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475019 | ||||||
| chr12:19475027
|
G | A | 2 | a0001c0001t0015g0231a0001c0001t0024g0232 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.987+1672G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475027 | ||||||
| chr12:19475052
|
A | T | 1 | a0001c0001t0003g0314 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.987+1697A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475052 | ||||||
| chr12:19475179
|
GTGTACAC | G | 399 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(396): Show | 403 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(400): Show |
intron_variant | MODIFIER | c.987+1837_987+1843d others(9): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19475179 | |||||
| chr12:19475191
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+1836C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475191 | ||||||
| chr12:19475204
|
G | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+1849G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475204 | ||||||
| chr12:19475295
|
CTAATTA | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+1944_987+1949d others(8): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19475295 | |||||
| chr12:19475326
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+1971A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475326 | ||||||
| chr12:19475356
|
A | G | 18 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(15): Show | 18 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.987+2001A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475356 | ||||||
| chr12:19475433
|
G | GGTATGTA others(1): Show |
8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+2089_987+2096d others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19475433 | |||||
| chr12:19475464
|
G | GTGTATAT others(3): Show |
8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+2110_987+2111i others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19475464 | |||||
| chr12:19475541
|
A | G | 1 | a0001c0001t0007g0391 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.987+2186A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475541 | ||||||
| chr12:19475583
|
T | C | 6 | a0001c0001t0013g0156a0001c0001t0013g0157a0001c0001t0013g0158others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+2228T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475583 | ||||||
| chr12:19475626
|
C | G | 1 | a0001c0001t0048g0377 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.987+2271C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475626 | ||||||
| chr12:19475646
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+2291A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475646 | ||||||
| chr12:19475678
|
T | C | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.987+2323T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475678 | ||||||
| chr12:19475683
|
A | C | 145 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(142): Show | 146 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.987+2328A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475683 | ||||||
| chr12:19475789
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+2434T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475789 | ||||||
| chr12:19475983
|
T | C | 30 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(27): Show | 30 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.987+2628T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475983 | ||||||
| chr12:19476021
|
A | G | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.987+2666A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476021 | ||||||
| chr12:19476045
|
G | C | 1 | a0001c0002t0045g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.987+2690G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476045 | ||||||
| chr12:19476046
|
T | C | 39 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(36): Show | 39 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.987+2691T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476046 | ||||||
| chr12:19476187
|
T | G | 6 | a0001c0001t0013g0156a0001c0001t0013g0157a0001c0001t0013g0158others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+2832T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476187 | ||||||
| chr12:19476257
|
A | T | 2 | a0001c0004t0002g0224a0001c0004t0009g0223 | 2 | NA18966.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.987+2902A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476257 | ||||||
| chr12:19476338
|
G | A | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0163others(46): Show | 52 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.987+2983G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476338 | ||||||
| chr12:19476373
|
G | A | 2 | a0001c0001t0004g0289a0001c0001t0004g0291 | 2 | NA18992.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.987+3018G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476373 | ||||||
| chr12:19476434
|
C | T | 2 | a0001c0001t0007g0394a0001c0001t0007g0395 | 2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.987+3079C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476434 | ||||||
| chr12:19476435
|
G | A | 1 | a0001c0001t0012g0337 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.987+3080G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476435 | ||||||
| chr12:19476521
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.987+3166T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476521 | ||||||
| chr12:19476530
|
CAG | C | 77 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.987+3178_987+3179d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19476530 | |||||
| chr12:19476585
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+3230G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476585 | ||||||
| chr12:19476621
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+3266C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476621 | ||||||
| chr12:19476622
|
G | A | 1 | a0001c0001t0002g0212 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.987+3267G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476622 | ||||||
| chr12:19476681
|
G | A | 330 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(327): Show | 331 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(328): Show |
intron_variant | MODIFIER | c.987+3326G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476681 | ||||||
| chr12:19476762
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+3407C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476762 | ||||||
| chr12:19476844
|
G | A | 109 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(106): Show | 109 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.987+3489G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476844 | ||||||
| chr12:19476850
|
A | G | 1 | a0001c0001t0004g0298 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.987+3495A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476850 | ||||||
| chr12:19476877
|
G | A | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0108others(2): Show | 5 | HG02486.hp1 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+3522G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476877 | ||||||
| chr12:19477027
|
A | T | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.987+3672A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477027 | ||||||
| chr12:19477090
|
A | G | 1 | a0001c0002t0001g0063 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.987+3735A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477090 | ||||||
| chr12:19477149
|
C | T | 2 | a0001c0001t0004g0266a0001c0001t0004g0267 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.987+3794C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477149 | ||||||
| chr12:19477263
|
T | C | 333 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(330): Show | 334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.987+3908T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477263 | ||||||
| chr12:19477264
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.987+3909A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477264 | ||||||
| chr12:19477273
|
T | C | 143 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(140): Show | 144 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+3918T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477273 | ||||||
| chr12:19477416
|
C | G | 3 | a0001c0001t0004g0274a0001c0001t0004g0279a0001c0001t0004g0280 | 3 | HG01099.hp2 HG01106.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.987+4061C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477416 | ||||||
| chr12:19477445
|
T | C | 2 | a0001c0001t0002g0175a0001c0001t0002g0199 | 2 | HG01978.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.987+4090T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477445 | ||||||
| chr12:19477741
|
T | A | 50 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(47): Show | 50 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.987+4386T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477741 | ||||||
| chr12:19477741
|
T | C | 3 | a0001c0001t0005g0153a0001c0001t0005g0154a0001c0001t0005g0155 | 3 | HG02647.hp1 HG02717.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.987+4386T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477741 | ||||||
| chr12:19477766
|
A | T | 2 | a0001c0001t0003g0363a0001c0001t0003g0378 | 2 | HG02300.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.987+4411A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477766 | ||||||
| chr12:19477803
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+4448C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477803 | ||||||
| chr12:19477818
|
C | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+4463C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477818 | ||||||
| chr12:19477828
|
G | C | 1 | a0001c0001t0002g0189 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.987+4473G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477828 | ||||||
| chr12:19478054
|
G | A | 13 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(10): Show | 13 | HG01934.hp2 HG02055.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.987+4699G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478054 | ||||||
| chr12:19478101
|
G | A | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.987+4746G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478101 | ||||||
| chr12:19478319
|
A | G | 334 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(331): Show | 335 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.987+4964A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478319 | ||||||
| chr12:19478465
|
T | A | 1 | a0001c0001t0001g0097 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.987+5110T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478465 | ||||||
| chr12:19478539
|
C | T | 1 | a0001c0001t0034g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.987+5184C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478539 | ||||||
| chr12:19478570
|
G | A | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.987+5215G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478570 | ||||||
| chr12:19478633
|
C | T | 1 | a0001c0001t0003g0350 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.987+5278C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478633 | ||||||
| chr12:19478842
|
A | G | 95 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(92): Show | 96 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.987+5487A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478842 | ||||||
| chr12:19478883
|
C | T | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.987+5528C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478883 | ||||||
| chr12:19478889
|
A | G | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.987+5534A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478889 | ||||||
| chr12:19478959
|
C | T | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.987+5604C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478959 | ||||||
| chr12:19479086
|
G | C | 6 | a0001c0001t0013g0156a0001c0001t0013g0157a0001c0001t0013g0158others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+5731G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479086 | ||||||
| chr12:19479140
|
C | G | 99 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(96): Show | 100 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.987+5785C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479140 | ||||||
| chr12:19479218
|
G | A | 2 | a0001c0001t0015g0231a0001c0001t0024g0232 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.987+5863G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479218 | ||||||
| chr12:19479258
|
TTGTTACA others(3): Show |
T | 1 | a0001c0001t0011g0301 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.987+5907_987+5916d others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479258 | |||||
| chr12:19479526
|
T | C | 1 | a0001c0001t0017g0043 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.987+6171T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479526 | ||||||
| chr12:19479553
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+6198A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479553 | ||||||
| chr12:19479584
|
G | C | 2 | a0001c0001t0020g0263a0001c0001t0020g0264 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.987+6229G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479584 | ||||||
| chr12:19479609
|
A | AATTATTT others(34): Show |
8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+6258_987+6298d others(43): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479609 | |||||
| chr12:19479640
|
G | T | 99 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(96): Show | 100 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.987+6285G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479640 | ||||||
| chr12:19479650
|
T | A | 77 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.987+6295T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479650 | ||||||
| chr12:19479705
|
A | C | 331 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(328): Show | 332 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(329): Show |
intron_variant | MODIFIER | c.987+6350A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479705 | ||||||
| chr12:19479717
|
G | GT | 31 | a0001c0001t0002g0002a0001c0001t0002g0163a0001c0001t0002g0166others(28): Show | 32 | HG00140.hp2 HG00738.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.987+6393dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
G | GTT | 41 | a0001c0001t0002g0183a0001c0001t0002g0185a0001c0001t0002g0213others(38): Show | 41 | HG00408.hp1 HG00621.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.987+6392_987+6393d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
G | GTTT | 28 | a0001c0001t0003g0310a0001c0001t0003g0311a0001c0001t0003g0314others(25): Show | 28 | HG00323.hp1 HG00609.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.987+6391_987+6393d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
G | GTTTT | 16 | a0001c0001t0003g0307a0001c0001t0003g0312a0001c0001t0003g0328others(13): Show | 17 | HG00438.hp1 HG01257.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.987+6390_987+6393d others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
G | GTTTTT | 6 | a0001c0001t0007g0395a0001c0001t0008g0367a0001c0001t0008g0384others(3): Show | 6 | HG02074.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+6389_987+6393d others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
G | GTTTTTTT | 9 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0010others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.987+6387_987+6393d others(9): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
G | GTTTTTTT others(1): Show |
15 | a0001c0001t0006g0005a0001c0001t0006g0012a0001c0001t0006g0013others(12): Show | 15 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.987+6386_987+6393d others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
GT | G | 6 | a0001c0001t0002g0219a0001c0001t0005g0132a0001c0001t0011g0319others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+6393delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
GTT | G | 24 | a0001c0001t0005g0133a0001c0001t0005g0135a0001c0001t0005g0137others(21): Show | 24 | HG00609.hp2 HG00735.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.987+6392_987+6393d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
GTTT | G | 12 | a0001c0001t0005g0130a0001c0001t0005g0131a0001c0001t0005g0134others(9): Show | 12 | HG01071.hp2 HG01167.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.987+6391_987+6393d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
GTTTTTT | G | 25 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0101others(22): Show | 25 | HG00558.hp2 HG01109.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.987+6388_987+6393d others(8): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
GTTTTTTT | G | 80 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(77): Show | 80 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(77): Show |
intron_variant | MODIFIER | c.987+6387_987+6393d others(9): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
GTTTTTTT others(4): Show |
G | 40 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(37): Show | 40 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.987+6383_987+6393d others(13): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
GTTTTTTT others(5): Show |
G | 2 | a0001c0001t0005g0148a0001c0001t0015g0234 | 2 | HG02818.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.987+6382_987+6393d others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0015g0233a0001c0001t0015g0235 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.987+6381_987+6393d others(15): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479717
|
GTTTTTTT others(12): Show |
G | 1 | a0001c0001t0006g0009 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.987+6375_987+6393d others(21): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | |||||
| chr12:19479723
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+6368T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479723 | ||||||
| chr12:19479830
|
A | G | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.987+6475A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479830 | ||||||
| chr12:19479839
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.987+6484C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479839 | ||||||
| chr12:19479918
|
A | G | 99 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(96): Show | 100 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.987+6563A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479918 | ||||||
| chr12:19479944
|
C | G | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.987+6589C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479944 | ||||||
| chr12:19480002
|
C | G | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.987+6647C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480002 | ||||||
| chr12:19480137
|
C | G | 1 | a0001c0001t0001g0247 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.987+6782C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480137 | ||||||
| chr12:19480178
|
C | T | 1 | a0001c0001t0016g0039 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.987+6823C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480178 | ||||||
| chr12:19480305
|
A | T | 1 | a0001c0002t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.987+6950A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480305 | ||||||
| chr12:19480312
|
C | G | 2 | a0001c0001t0015g0231a0001c0001t0024g0232 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.987+6957C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480312 | ||||||
| chr12:19480356
|
C | T | 1 | a0001c0001t0007g0394 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.987+7001C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480356 | ||||||
| chr12:19480357
|
G | A | 3 | a0001c0001t0020g0227a0001c0001t0020g0263a0001c0001t0020g0264 | 3 | HG02258.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.987+7002G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480357 | ||||||
| chr12:19480411
|
G | A | 4 | a0001c0001t0004g0317a0001c0001t0004g0318a0001c0001t0004g0320others(1): Show | 4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+7056G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480411 | ||||||
| chr12:19480431
|
G | T | 1 | a0001c0001t0001g0098 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.987+7076G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480431 | ||||||
| chr12:19480433
|
G | T | 1 | a0001c0001t0001g0098 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.987+7078G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480433 | ||||||
| chr12:19480435
|
T | G | 1 | a0001c0001t0001g0098 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.987+7080T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480435 | ||||||
| chr12:19480473
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.987+7118G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480473 | ||||||
| chr12:19480507
|
C | G | 2 | a0001c0001t0015g0231a0001c0001t0024g0232 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.987+7152C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480507 | ||||||
| chr12:19480508
|
C | T | 1 | a0001c0001t0003g0345 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.987+7153C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480508 | ||||||
| chr12:19480532
|
C | G | 1 | a0001c0001t0003g0358 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.987+7177C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480532 | ||||||
| chr12:19480557
|
T | C | 1 | a0001c0001t0002g0170 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.987+7202T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480557 | ||||||
| chr12:19480571
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+7216T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480571 | ||||||
| chr12:19480587
|
A | ATT | 11 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(8): Show | 11 | HG02055.hp1 HG02572.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.987+7233_987+7234d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19480587 | |||||
| chr12:19480844
|
C | A | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.987+7489C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480844 | ||||||
| chr12:19480939
|
G | T | 53 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(50): Show | 53 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.987+7584G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480939 | ||||||
| chr12:19480978
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+7623A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480978 | ||||||
| chr12:19480987
|
T | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+7632T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480987 | ||||||
| chr12:19480998
|
T | G | 1 | a0001c0001t0002g0219 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.987+7643T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480998 | ||||||
| chr12:19481075
|
A | G | 9 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0177others(6): Show | 10 | HG00639.hp2 HG00738.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.987+7720A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481075 | ||||||
| chr12:19481082
|
G | C | 330 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(327): Show | 331 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(328): Show |
intron_variant | MODIFIER | c.987+7727G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481082 | ||||||
| chr12:19481086
|
T | A | 1 | a0001c0001t0002g0201 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.987+7731T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481086 | ||||||
| chr12:19481092
|
C | CT | 96 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0101others(93): Show | 99 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.987+7763dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | |||||
| chr12:19481092
|
C | CTT | 34 | a0001c0001t0002g0170a0001c0001t0002g0179a0001c0001t0002g0202others(31): Show | 34 | HG00323.hp2 HG00621.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.987+7762_987+7763d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | |||||
| chr12:19481092
|
C | CTTT | 6 | a0001c0001t0004g0267a0001c0001t0005g0133a0001c0001t0005g0139others(3): Show | 6 | HG00639.hp1 HG01106.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.987+7761_987+7763d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | |||||
| chr12:19481092
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0005g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.987+7750_987+7763d others(16): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | |||||
| chr12:19481092
|
C | CTTTTTTT others(8): Show |
3 | a0001c0001t0005g0141a0001c0001t0005g0257a0001c0001t0022g0237 | 3 | HG02559.hp2 HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.987+7749_987+7763d others(17): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | |||||
| chr12:19481092
|
C | CTTTTTTT others(15): Show |
2 | a0001c0001t0005g0150a0001c0001t0005g0236 | 2 | HG01243.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.987+7742_987+7763d others(24): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | |||||
| chr12:19481092
|
CT | C | 7 | a0001c0001t0001g0051a0001c0001t0001g0239a0001c0001t0001g0240others(4): Show | 7 | HG01167.hp1 HG01257.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+7763delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | |||||
| chr12:19481092
|
CTT | C | 7 | a0001c0001t0012g0335a0001c0001t0013g0156a0001c0001t0013g0157others(4): Show | 7 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.987+7762_987+7763d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | |||||
| chr12:19481092
|
CTTT | C | 9 | a0001c0001t0003g0355a0001c0001t0003g0364a0001c0001t0003g0370others(6): Show | 9 | HG01358.hp2 HG02630.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.987+7761_987+7763d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | |||||
| chr12:19481092
|
CTTTT | C | 83 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(80): Show | 84 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+7760_987+7763d others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | |||||
| chr12:19481092
|
CTTTTT | C | 9 | a0001c0001t0003g0347a0001c0001t0003g0373a0001c0001t0005g0153others(6): Show | 9 | HG01346.hp1 HG01515.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.987+7759_987+7763d others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | |||||
| chr12:19481092
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0024g0232 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.987+7754_987+7763d others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | |||||
| chr12:19481113
|
T | C | 2 | a0001c0001t0003g0343a0001c0001t0003g0345 | 2 | NA18945.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.987+7758T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481113 | ||||||
| chr12:19481155
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+7800T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481155 | ||||||
| chr12:19481160
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+7805A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481160 | ||||||
| chr12:19481165
|
A | G | 1 | a0001c0001t0003g0336 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.987+7810A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481165 | ||||||
| chr12:19481202
|
G | A | 2 | a0001c0001t0002g0174a0001c0001t0002g0190 | 2 | HG00597.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.987+7847G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481202 | ||||||
| chr12:19481258
|
A | G | 11 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(8): Show | 11 | HG02055.hp1 HG02572.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.987+7903A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481258 | ||||||
| chr12:19481422
|
C | T | 2 | a0001c0001t0006g0015a0001c0001t0006g0024 | 2 | HG03017.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.987+8067C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481422 | ||||||
| chr12:19481503
|
G | A | 1 | a0001c0001t0017g0042 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.987+8148G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481503 | ||||||
| chr12:19481563
|
T | C | 150 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(147): Show | 151 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.987+8208T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481563 | ||||||
| chr12:19481646
|
A | T | 150 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(147): Show | 151 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.987+8291A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481646 | ||||||
| chr12:19481679
|
G | A | 2 | a0001c0001t0003g0313a0001c0001t0003g0381 | 2 | HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.987+8324G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481679 | ||||||
| chr12:19481766
|
A | G | 37 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(34): Show | 37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.987+8411A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481766 | ||||||
| chr12:19481861
|
G | A | 1 | a0001c0001t0004g0281 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.987+8506G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481861 | ||||||
| chr12:19481925
|
C | G | 136 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(133): Show | 136 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.987+8570C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481925 | ||||||
| chr12:19482061
|
C | A | 109 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(106): Show | 109 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.987+8706C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482061 | ||||||
| chr12:19482081
|
C | T | 109 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(106): Show | 109 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.987+8726C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482081 | ||||||
| chr12:19482344
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+8989C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482344 | ||||||
| chr12:19482382
|
A | G | 94 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(91): Show | 95 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.987+9027A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482382 | ||||||
| chr12:19482404
|
T | C | 1 | a0001c0001t0007g0391 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.987+9049T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482404 | ||||||
| chr12:19482455
|
G | A | 1 | a0001c0001t0004g0272 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.987+9100G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482455 | ||||||
| chr12:19482476
|
C | T | 6 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0108others(3): Show | 6 | HG02486.hp1 HG02723.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.987+9121C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482476 | ||||||
| chr12:19482529
|
G | C | 60 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(57): Show | 60 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.987+9174G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482529 | ||||||
| chr12:19482529
|
G | T | 53 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(50): Show | 53 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.987+9174G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482529 | ||||||
| chr12:19482589
|
G | A | 1 | a0001c0001t0031g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.987+9234G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482589 | ||||||
| chr12:19482642
|
G | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0108others(1): Show | 4 | HG02723.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+9287G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482642 | ||||||
| chr12:19482805
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.987+9450G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482805 | ||||||
| chr12:19482873
|
G | T | 1 | a0001c0001t0005g0132 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.987+9518G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482873 | ||||||
| chr12:19482912
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+9557T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482912 | ||||||
| chr12:19482946
|
T | G | 39 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(36): Show | 39 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.987+9591T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482946 | ||||||
| chr12:19483013
|
G | A | 1 | a0001c0001t0007g0391 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.987+9658G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483013 | ||||||
| chr12:19483070
|
G | T | 1 | a0001c0006t0033g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.987+9715G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483070 | ||||||
| chr12:19483171
|
G | C | 1 | a0001c0001t0007g0395 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.987+9816G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483171 | ||||||
| chr12:19483202
|
T | C | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.987+9847T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483202 | ||||||
| chr12:19483207
|
G | A | 1 | a0001c0001t0004g0302 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.987+9852G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483207 | ||||||
| chr12:19483220
|
C | T | 1 | a0001c0001t0016g0039 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.987+9865C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483220 | ||||||
| chr12:19483408
|
T | C | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.987+10053T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483408 | ||||||
| chr12:19483681
|
A | T | 2 | a0001c0001t0005g0141a0001c0001t0005g0150 | 2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.988-10119A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483681 | ||||||
| chr12:19483932
|
TGTC | T | 109 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(106): Show | 109 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.988-9865_988-9863d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19483932 | |||||
| chr12:19483933
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.988-9867G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483933 | ||||||
| chr12:19483935
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.988-9865C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483935 | ||||||
| chr12:19483936
|
G | A | 1 | a0001c0001t0004g0317 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.988-9864G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483936 | ||||||
| chr12:19483955
|
G | A | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-9845G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483955 | ||||||
| chr12:19484042
|
C | T | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.988-9758C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484042 | ||||||
| chr12:19484250
|
AT | A | 81 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(78): Show | 84 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.988-9525delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19484250 | |||||
| chr12:19484250
|
ATT | A | 246 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0090others(243): Show | 247 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.988-9526_988-9525d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19484250 | |||||
| chr12:19484250
|
ATTT | A | 44 | a0001c0001t0001g0051a0001c0001t0001g0061a0001c0001t0001g0240others(41): Show | 44 | HG00558.hp2 HG00735.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.988-9527_988-9525d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19484250 | |||||
| chr12:19484317
|
C | T | 1 | a0001c0001t0003g0339 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.988-9483C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484317 | ||||||
| chr12:19484340
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-9460C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484340 | ||||||
| chr12:19484500
|
G | A | 1 | a0001c0001t0003g0330 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.988-9300G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484500 | ||||||
| chr12:19484615
|
C | T | 1 | a0001c0001t0004g0272 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.988-9185C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484615 | ||||||
| chr12:19484633
|
A | G | 141 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(138): Show | 142 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.988-9167A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484633 | ||||||
| chr12:19484663
|
G | A | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.988-9137G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484663 | ||||||
| chr12:19484664
|
C | T | 139 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(136): Show | 139 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.988-9136C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484664 | ||||||
| chr12:19484807
|
G | T | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-8993G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484807 | ||||||
| chr12:19484815
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-8985T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484815 | ||||||
| chr12:19484947
|
C | T | 1 | a0001c0001t0023g0309 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.988-8853C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484947 | ||||||
| chr12:19484949
|
G | A | 5 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0016others(2): Show | 5 | HG01934.hp1 HG03017.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-8851G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484949 | ||||||
| chr12:19485032
|
C | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-8768C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485032 | ||||||
| chr12:19485117
|
G | T | 5 | a0001c0001t0015g0231a0001c0001t0015g0233a0001c0001t0015g0234others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-8683G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485117 | ||||||
| chr12:19485123
|
A | G | 2 | a0001c0001t0004g0385a0001c0001t0007g0386 | 2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.988-8677A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485123 | ||||||
| chr12:19485201
|
G | A | 5 | a0001c0001t0015g0231a0001c0001t0015g0233a0001c0001t0015g0234others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-8599G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485201 | ||||||
| chr12:19485241
|
C | G | 47 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0163others(44): Show | 50 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.988-8559C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485241 | ||||||
| chr12:19485485
|
T | C | 2 | a0001c0002t0001g0070a0001c0002t0010g0062 | 2 | HG02040.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.988-8315T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485485 | ||||||
| chr12:19485708
|
C | CA | 79 | a0001c0001t0001g0055a0001c0001t0002g0206a0001c0001t0004g0004others(76): Show | 79 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.988-8076dupA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19485708 | |||||
| chr12:19485708
|
C | CAA | 204 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0061others(201): Show | 205 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.988-8077_988-8076d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19485708 | |||||
| chr12:19485708
|
C | CAAA | 10 | a0001c0001t0001g0045a0001c0001t0001g0101a0001c0001t0001g0256others(7): Show | 10 | HG01358.hp2 HG01515.hp1 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.988-8078_988-8076d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19485708 | |||||
| chr12:19485740
|
A | G | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.988-8060A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485740 | ||||||
| chr12:19485948
|
C | CT | 63 | a0001c0001t0001g0098a0001c0001t0001g0101a0001c0001t0001g0118others(60): Show | 64 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.988-7832dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19485948 | |||||
| chr12:19485948
|
CT | C | 41 | a0001c0001t0001g0095a0001c0001t0001g0104a0001c0001t0002g0204others(38): Show | 41 | HG00639.hp1 HG01106.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.988-7832delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19485948 | |||||
| chr12:19485948
|
CTT | C | 35 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(32): Show | 35 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.988-7833_988-7832d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19485948 | |||||
| chr12:19485952
|
T | C | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.988-7848T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485952 | ||||||
| chr12:19485965
|
TTTTC | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-7834_988-7831d others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485965 | ||||||
| chr12:19486082
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-7718A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486082 | ||||||
| chr12:19486101
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-7699C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486101 | ||||||
| chr12:19486203
|
G | A | 1 | a0001c0001t0023g0309 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.988-7597G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486203 | ||||||
| chr12:19486262
|
T | C | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-7538T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486262 | ||||||
| chr12:19486277
|
C | T | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0163others(46): Show | 52 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.988-7523C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486277 | ||||||
| chr12:19486304
|
A | G | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.988-7496A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486304 | ||||||
| chr12:19486388
|
A | G | 1 | a0001c0001t0002g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.988-7412A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486388 | ||||||
| chr12:19486529
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.988-7271T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486529 | ||||||
| chr12:19486572
|
A | G | 43 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(40): Show | 43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.988-7228A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486572 | ||||||
| chr12:19486584
|
C | T | 1 | a0001c0001t0004g0281 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.988-7216C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486584 | ||||||
| chr12:19486742
|
A | G | 1 | a0001c0002t0002g0080 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.988-7058A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486742 | ||||||
| chr12:19486798
|
C | G | 2 | a0001c0001t0003g0313a0001c0005t0023g0033 | 2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.988-7002C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486798 | ||||||
| chr12:19486808
|
C | CT | 40 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(37): Show | 40 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.988-6982dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19486808 | |||||
| chr12:19486813
|
T | C | 2 | a0001c0001t0017g0043a0001c0001t0017g0044 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.988-6987T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486813 | ||||||
| chr12:19486909
|
C | T | 113 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(110): Show | 113 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.988-6891C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486909 | ||||||
| chr12:19487007
|
T | C | 1 | a0001c0001t0004g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.988-6793T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487007 | ||||||
| chr12:19487102
|
A | G | 1 | a0001c0001t0035g0159 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.988-6698A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487102 | ||||||
| chr12:19487166
|
A | G | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-6634A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487166 | ||||||
| chr12:19487271
|
G | A | 41 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(38): Show | 41 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.988-6529G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487271 | ||||||
| chr12:19487478
|
G | T | 1 | a0001c0001t0004g0265 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.988-6322G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487478 | ||||||
| chr12:19487544
|
C | T | 2 | a0001c0001t0014g0030a0001c0001t0014g0031 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.988-6256C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487544 | ||||||
| chr12:19487576
|
A | C | 31 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(28): Show | 31 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.988-6224A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487576 | ||||||
| chr12:19487601
|
T | C | 2 | a0001c0001t0004g0388a0001c0001t0007g0387 | 2 | HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.988-6199T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487601 | ||||||
| chr12:19487713
|
C | T | 1 | a0001c0001t0024g0232 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.988-6087C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487713 | ||||||
| chr12:19487758
|
T | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-6042T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487758 | ||||||
| chr12:19487798
|
A | G | 1 | a0001c0006t0033g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.988-6002A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487798 | ||||||
| chr12:19487881
|
A | C | 39 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(36): Show | 39 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.988-5919A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487881 | ||||||
| chr12:19487965
|
T | C | 1 | a0001c0002t0001g0070 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.988-5835T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487965 | ||||||
| chr12:19488126
|
A | AT | 148 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(145): Show | 149 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.988-5659dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19488126 | |||||
| chr12:19488147
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-5653G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488147 | ||||||
| chr12:19488204
|
A | G | 1 | a0001c0001t0003g0340 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.988-5596A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488204 | ||||||
| chr12:19488217
|
G | A | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-5583G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488217 | ||||||
| chr12:19488235
|
C | T | 8 | a0001c0001t0004g0396a0001c0001t0007g0003a0001c0001t0007g0315others(5): Show | 9 | HG02559.hp1 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-5565C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488235 | ||||||
| chr12:19488290
|
A | AT | 47 | a0001c0001t0001g0101a0001c0001t0001g0121a0001c0001t0002g0202others(44): Show | 47 | HG00323.hp2 HG00609.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.988-5492dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19488290 | |||||
| chr12:19488290
|
AT | A | 9 | a0001c0001t0001g0051a0001c0001t0016g0035a0001c0001t0016g0036others(6): Show | 9 | HG01257.hp1 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-5492delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19488290 | |||||
| chr12:19488319
|
G | A | 3 | a0001c0002t0001g0054a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG03139.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.988-5481G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488319 | ||||||
| chr12:19488345
|
C | T | 3 | a0001c0003t0001g0250a0001c0003t0001g0252a0001c0003t0044g0249 | 3 | HG01081.hp2 HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.988-5455C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488345 | ||||||
| chr12:19488367
|
A | G | 1 | a0001c0001t0003g0378 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.988-5433A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488367 | ||||||
| chr12:19488453
|
G | A | 21 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(18): Show | 21 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.988-5347G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488453 | ||||||
| chr12:19488482
|
A | G | 2 | a0001c0001t0003g0340a0001c0001t0003g0370 | 2 | NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.988-5318A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488482 | ||||||
| chr12:19488483
|
G | A | 2 | a0001c0001t0003g0340a0001c0001t0003g0370 | 2 | NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.988-5317G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488483 | ||||||
| chr12:19488543
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-5257A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488543 | ||||||
| chr12:19488551
|
T | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-5249T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488551 | ||||||
| chr12:19488553
|
T | C | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0108others(2): Show | 5 | HG02486.hp1 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-5247T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488553 | ||||||
| chr12:19488590
|
T | C | 11 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(8): Show | 11 | HG02055.hp1 HG02572.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.988-5210T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488590 | ||||||
| chr12:19488651
|
T | G | 30 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(27): Show | 30 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.988-5149T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488651 | ||||||
| chr12:19488829
|
C | T | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-4971C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488829 | ||||||
| chr12:19488910
|
C | T | 1 | a0001c0001t0003g0354 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.988-4890C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488910 | ||||||
| chr12:19488912
|
C | T | 1 | a0001c0001t0007g0400 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.988-4888C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488912 | ||||||
| chr12:19489331
|
GCAGGGGA others(6): Show |
G | 1 | a0001c0001t0004g0297 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.988-4466_988-4454d others(15): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489331 | |||||
| chr12:19489352
|
A | G | 1 | a0001c0002t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.988-4448A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19489352 | ||||||
| chr12:19489407
|
A | G | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.988-4393A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19489407 | ||||||
| chr12:19489611
|
G | A | 1 | a0001c0001t0003g0370 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.988-4189G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19489611 | ||||||
| chr12:19489731
|
CTG | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-4065_988-4064d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489731 | |||||
| chr12:19489870
|
G | GT | 58 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(55): Show | 59 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.988-3921dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489870 | |||||
| chr12:19489942
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-3858A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19489942 | ||||||
| chr12:19489990
|
C | CT | 130 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0055others(127): Show | 130 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.988-3785dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489990 | |||||
| chr12:19489990
|
C | CTT | 40 | a0001c0001t0001g0094a0001c0001t0001g0108a0001c0001t0001g0121others(37): Show | 40 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.988-3786_988-3785d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489990 | |||||
| chr12:19489990
|
C | CTTT | 13 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0099others(10): Show | 13 | HG02071.hp2 HG02280.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.988-3787_988-3785d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489990 | |||||
| chr12:19489990
|
CTTTTTT | C | 9 | a0001c0001t0002g0185a0001c0001t0005g0138a0001c0001t0005g0142others(6): Show | 9 | HG00621.hp2 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.988-3790_988-3785d others(8): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489990 | |||||
| chr12:19489990
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0034g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.988-3795_988-3785d others(13): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489990 | |||||
| chr12:19489990
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.988-3798_988-3785d others(16): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489990 | |||||
| chr12:19490045
|
C | T | 58 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(55): Show | 58 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.988-3755C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490045 | ||||||
| chr12:19490138
|
A | G | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 4 | HG00597.hp2 HG02056.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-3662A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490138 | ||||||
| chr12:19490150
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-3650T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490150 | ||||||
| chr12:19490166
|
C | G | 1 | a0001c0001t0006g0022 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.988-3634C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490166 | ||||||
| chr12:19490215
|
T | C | 1 | a0001c0001t0004g0284 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.988-3585T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490215 | ||||||
| chr12:19490270
|
A | C | 11 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(8): Show | 11 | HG02055.hp1 HG02572.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.988-3530A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490270 | ||||||
| chr12:19490339
|
T | G | 1 | a0001c0001t0003g0307 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.988-3461T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490339 | ||||||
| chr12:19490416
|
C | T | 2 | a0001c0001t0004g0268a0001c0001t0004g0283 | 2 | HG00438.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.988-3384C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490416 | ||||||
| chr12:19490456
|
A | ACTG | 38 | a0001c0001t0003g0310a0001c0001t0003g0312a0001c0001t0003g0322others(35): Show | 38 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.988-3341_988-3339d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19490456 | |||||
| chr12:19490537
|
C | T | 1 | a0001c0001t0015g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.988-3263C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490537 | ||||||
| chr12:19490707
|
C | T | 1 | a0001c0001t0008g0372 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.988-3093C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490707 | ||||||
| chr12:19490724
|
C | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-3076C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490724 | ||||||
| chr12:19490995
|
T | A | 5 | a0001c0002t0001g0109a0001c0002t0001g0124a0001c0002t0001g0125others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-2805T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490995 | ||||||
| chr12:19491069
|
T | C | 1 | a0001c0001t0006g0022 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.988-2731T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491069 | ||||||
| chr12:19491099
|
G | C | 1 | a0001c0001t0005g0147 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.988-2701G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491099 | ||||||
| chr12:19491133
|
C | T | 113 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(110): Show | 113 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.988-2667C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491133 | ||||||
| chr12:19491281
|
A | T | 34 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(31): Show | 34 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.988-2519A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491281 | ||||||
| chr12:19491290
|
A | C | 1 | a0001c0001t0005g0147 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.988-2510A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491290 | ||||||
| chr12:19491317
|
T | G | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.988-2483T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491317 | ||||||
| chr12:19491455
|
G | A | 1 | a0001c0002t0001g0111 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.988-2345G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491455 | ||||||
| chr12:19491507
|
C | A | 147 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(144): Show | 149 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.988-2293C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491507 | ||||||
| chr12:19491592
|
G | A | 333 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(330): Show | 334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.988-2208G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491592 | ||||||
| chr12:19491716
|
A | AT | 37 | a0001c0001t0003g0375a0001c0001t0004g0277a0001c0001t0004g0278others(34): Show | 37 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.988-2073dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19491716 | |||||
| chr12:19491849
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.988-1951G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491849 | ||||||
| chr12:19491855
|
T | TGA | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-1944_988-1943d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19491855 | |||||
| chr12:19491858
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-1942C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491858 | ||||||
| chr12:19491866
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-1934T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491866 | ||||||
| chr12:19491989
|
C | CACA | 8 | a0001c0001t0004g0396a0001c0001t0007g0003a0001c0001t0007g0315others(5): Show | 9 | HG02559.hp1 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-1810_988-1809i others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19491989 | |||||
| chr12:19491991
|
G | T | 8 | a0001c0001t0004g0396a0001c0001t0007g0003a0001c0001t0007g0315others(5): Show | 9 | HG02559.hp1 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-1809G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491991 | ||||||
| chr12:19491992
|
C | T | 8 | a0001c0001t0004g0396a0001c0001t0007g0003a0001c0001t0007g0315others(5): Show | 9 | HG02559.hp1 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-1808C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491992 | ||||||
| chr12:19491998
|
A | G | 6 | a0001c0001t0003g0313a0001c0001t0003g0321a0001c0001t0003g0373others(3): Show | 6 | HG01261.hp1 HG01515.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.988-1802A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491998 | ||||||
| chr12:19492038
|
A | G | 1 | a0001c0001t0006g0006 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.988-1762A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492038 | ||||||
| chr12:19492040
|
G | A | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-1760G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492040 | ||||||
| chr12:19492088
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-1712C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492088 | ||||||
| chr12:19492262
|
G | A | 2 | a0001c0001t0004g0266a0001c0001t0004g0267 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.988-1538G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492262 | ||||||
| chr12:19492313
|
A | G | 53 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(50): Show | 53 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.988-1487A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492313 | ||||||
| chr12:19492574
|
T | C | 1 | a0001c0001t0002g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.988-1226T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492574 | ||||||
| chr12:19492585
|
A | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0114 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.988-1215A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492585 | ||||||
| chr12:19492604
|
A | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-1196A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492604 | ||||||
| chr12:19492740
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-1060A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492740 | ||||||
| chr12:19492859
|
A | C | 93 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(90): Show | 94 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.988-941A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492859 | ||||||
| chr12:19492859
|
A | T | 1 | a0001c0001t0003g0336 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.988-941A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492859 | ||||||
| chr12:19492927
|
G | T | 3 | a0001c0001t0003g0338a0001c0001t0003g0339a0001c0001t0012g0337 | 3 | HG00140.hp2 HG00738.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.988-873G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492927 | ||||||
| chr12:19492998
|
C | G | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0108others(1): Show | 4 | HG02723.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-802C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492998 | ||||||
| chr12:19493382
|
T | C | 334 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(331): Show | 335 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.988-418T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493382 | ||||||
| chr12:19493423
|
A | C | 1 | a0001c0002t0001g0053 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.988-377A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493423 | ||||||
| chr12:19493475
|
C | A | 1 | a0001c0001t0003g0322 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.988-325C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493475 | ||||||
| chr12:19493595
|
T | C | 11 | a0001c0001t0002g0164a0001c0001t0002g0207a0001c0001t0002g0208others(8): Show | 11 | HG01081.hp1 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.988-205T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493595 | ||||||
| chr12:19493598
|
A | C | 114 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(111): Show | 114 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.988-202A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493598 | ||||||
| chr12:19493632
|
A | G | 41 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(38): Show | 41 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.988-168A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493632 | ||||||
| chr12:19493640
|
C | T | 32 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(29): Show | 32 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.988-160C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493640 | ||||||
| chr12:19493641
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-159G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493641 | ||||||
| chr12:19493663
|
C | T | 36 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0108others(33): Show | 36 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.988-137C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493663 | ||||||
| chr12:19493755
|
C | T | 1 | a0001c0001t0034g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.988-45C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493755 | ||||||
| chr12:19494009
|
CTGGTGTA others(5): Show |
C | 139 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(136): Show | 140 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1174+28_1174+39del others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19494009 | |||||
| chr12:19494259
|
G | A | 1 | a0001c0001t0012g0335 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1174+273G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494259 | ||||||
| chr12:19494320
|
AAGTAATC others(3): Show |
A | 1 | a0001c0001t0001g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1174+335_1174+344d others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494320 | ||||||
| chr12:19494329
|
A | G | 2 | a0001c0001t0003g0383a0001c0001t0008g0360 | 2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1174+343A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494329 | ||||||
| chr12:19494399
|
A | G | 2 | a0001c0001t0002g0206a0001c0001t0004g0272 | 2 | HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1174+413A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494399 | ||||||
| chr12:19494498
|
C | CT | 77 | a0001c0001t0001g0045a0001c0001t0001g0055a0001c0001t0001g0092others(74): Show | 77 | HG00408.hp1 HG00597.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1174+533dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19494498 | |||||
| chr12:19494498
|
CT | C | 9 | a0001c0001t0002g0216a0001c0001t0003g0357a0001c0001t0004g0266others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174+533delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19494498 | |||||
| chr12:19494498
|
CTTTT | C | 7 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(4): Show | 7 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1174+530_1174+533d others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19494498 | |||||
| chr12:19494521
|
A | C | 1 | a0001c0001t0003g0354 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1174+535A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494521 | ||||||
| chr12:19494542
|
G | C | 147 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(144): Show | 148 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1174+556G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494542 | ||||||
| chr12:19494590
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+604G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494590 | ||||||
| chr12:19494627
|
G | A | 1 | a0001c0001t0006g0022 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1174+641G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494627 | ||||||
| chr12:19494662
|
G | T | 1 | a0001c0001t0031g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1174+676G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494662 | ||||||
| chr12:19494679
|
C | G | 1 | a0001c0001t0004g0281 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1174+693C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494679 | ||||||
| chr12:19494694
|
T | A | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1174+708T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494694 | ||||||
| chr12:19494741
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+755T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494741 | ||||||
| chr12:19494798
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+812G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494798 | ||||||
| chr12:19494851
|
G | C | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1174+865G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494851 | ||||||
| chr12:19494932
|
G | A | 398 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(395): Show | 402 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(399): Show |
intron_variant | MODIFIER | c.1174+946G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494932 | ||||||
| chr12:19494978
|
C | T | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1174+992C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494978 | ||||||
| chr12:19495052
|
C | T | 1 | a0001c0001t0007g0315 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1174+1066C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495052 | ||||||
| chr12:19495077
|
T | C | 1 | a0001c0001t0005g0133 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1174+1091T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495077 | ||||||
| chr12:19495125
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+1139G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495125 | ||||||
| chr12:19495173
|
G | A | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1174+1187G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495173 | ||||||
| chr12:19495211
|
A | G | 145 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(142): Show | 146 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1174+1225A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495211 | ||||||
| chr12:19495257
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+1271A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495257 | ||||||
| chr12:19495481
|
A | AT | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+1503dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495481 | |||||
| chr12:19495481
|
A | C | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174+1495A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495481 | ||||||
| chr12:19495540
|
A | G | 2 | a0001c0001t0003g0310a0001c0001t0003g0374 | 2 | HG00609.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1174+1554A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495540 | ||||||
| chr12:19495547
|
C | CT | 33 | a0001c0001t0001g0117a0001c0001t0004g0396a0001c0001t0006g0005others(30): Show | 34 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1174+1575dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495547 | |||||
| chr12:19495547
|
C | CTTTTTTT others(3): Show |
1 | a0001c0006t0033g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1174+1566_1174+157 others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495547 | |||||
| chr12:19495547
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0034g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1174+1565_1174+157 others(15): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495547 | |||||
| chr12:19495547
|
C | CTTTTTTT others(5): Show |
9 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(6): Show | 9 | HG02055.hp1 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174+1564_1174+157 others(16): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495547 | |||||
| chr12:19495547
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0016g0039a0001c0001t0017g0042 | 2 | HG02572.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1174+1563_1174+157 others(17): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495547 | |||||
| chr12:19495547
|
CT | C | 30 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(27): Show | 30 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1174+1575delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495547 | |||||
| chr12:19495547
|
CTT | C | 6 | a0001c0001t0013g0156a0001c0001t0013g0157a0001c0001t0013g0158others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174+1574_1174+157 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495547 | |||||
| chr12:19495567
|
A | G | 2 | a0001c0001t0004g0266a0001c0001t0004g0267 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1174+1581A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495567 | ||||||
| chr12:19495885
|
C | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+1899C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495885 | ||||||
| chr12:19495889
|
G | A | 139 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(136): Show | 140 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1174+1903G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495889 | ||||||
| chr12:19496086
|
G | A | 1 | a0001c0001t0022g0128 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1174+2100G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496086 | ||||||
| chr12:19496132
|
C | G | 2 | a0001c0001t0003g0312a0001c0001t0003g0328 | 2 | NA18940.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1174+2146C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496132 | ||||||
| chr12:19496160
|
CTT | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+2176_1174+217 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19496160 | |||||
| chr12:19496162
|
T | C | 97 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(94): Show | 98 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1174+2176T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496162 | ||||||
| chr12:19496255
|
C | T | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1174+2269C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496255 | ||||||
| chr12:19496299
|
G | A | 2 | a0001c0001t0004g0266a0001c0001t0004g0267 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1174+2313G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496299 | ||||||
| chr12:19496374
|
G | T | 1 | a0001c0001t0004g0291 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1174+2388G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496374 | ||||||
| chr12:19496664
|
C | CTTTTTTT | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+2685_1174+269 others(11): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19496664 | |||||
| chr12:19496725
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1174+2739A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496725 | ||||||
| chr12:19496939
|
G | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+2953G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496939 | ||||||
| chr12:19496961
|
C | T | 1 | a0001c0002t0001g0109 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1174+2975C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496961 | ||||||
| chr12:19497032
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+3046T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497032 | ||||||
| chr12:19497070
|
G | A | 138 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(135): Show | 139 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1175-3027G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497070 | ||||||
| chr12:19497144
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-2953T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497144 | ||||||
| chr12:19497148
|
C | G | 1 | a0001c0002t0002g0066 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1175-2949C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497148 | ||||||
| chr12:19497184
|
T | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-2913T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497184 | ||||||
| chr12:19497326
|
G | GT | 4 | a0001c0001t0004g0396a0001c0001t0007g0003a0001c0001t0007g0392others(1): Show | 5 | HG03041.hp2 HG03471.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175-2770dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497326 | |||||
| chr12:19497326
|
GTGTTT | G | 7 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(4): Show | 7 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1175-2769_1175-276 others(9): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497326 | |||||
| chr12:19497328
|
G | GT | 127 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0163others(124): Show | 130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1175-2745dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497328 | |||||
| chr12:19497328
|
G | GTT | 38 | a0001c0001t0002g0165a0001c0001t0002g0170a0001c0001t0002g0175others(35): Show | 38 | HG00438.hp1 HG00639.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1175-2746_1175-274 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497328 | |||||
| chr12:19497328
|
G | GTTT | 27 | a0001c0001t0001g0118a0001c0001t0002g0184a0001c0001t0002g0192others(24): Show | 27 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1175-2747_1175-274 others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497328 | |||||
| chr12:19497328
|
G | GTTTT | 98 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0055others(95): Show | 98 | HG00558.hp2 HG00597.hp2 HG01074.hp2 others(95): Show |
intron_variant | MODIFIER | c.1175-2748_1175-274 others(8): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497328 | |||||
| chr12:19497328
|
G | GTTTTT | 52 | a0001c0001t0001g0045a0001c0001t0001g0091a0001c0001t0001g0094others(49): Show | 52 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1175-2749_1175-274 others(9): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497328 | |||||
| chr12:19497328
|
G | GTTTTTT | 19 | a0001c0001t0001g0095a0001c0001t0001g0121a0001c0001t0001g0241others(16): Show | 19 | HG00609.hp2 HG01243.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1175-2750_1175-274 others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497328 | |||||
| chr12:19497328
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0004g0283 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1175-2754_1175-274 others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497328 | |||||
| chr12:19497328
|
G | T | 5 | a0001c0001t0004g0396a0001c0001t0007g0003a0001c0001t0007g0392others(2): Show | 6 | HG02559.hp1 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1175-2769G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497328 | ||||||
| chr12:19497378
|
C | T | 1 | a0001c0001t0016g0036 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1175-2719C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497378 | ||||||
| chr12:19497494
|
A | C | 1 | a0001c0002t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1175-2603A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497494 | ||||||
| chr12:19497497
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-2600A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497497 | ||||||
| chr12:19497570
|
G | A | 1 | a0001c0001t0008g0384 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1175-2527G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497570 | ||||||
| chr12:19497628
|
A | G | 2 | a0001c0001t0002g0171a0001c0001t0002g0183 | 2 | NA18950.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1175-2469A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497628 | ||||||
| chr12:19497684
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-2413C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497684 | ||||||
| chr12:19497702
|
T | C | 13 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(10): Show | 13 | HG01934.hp2 HG02055.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1175-2395T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497702 | ||||||
| chr12:19497713
|
C | G | 4 | a0001c0001t0006g0026a0001c0001t0006g0028a0001c0001t0014g0025others(1): Show | 4 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-2384C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497713 | ||||||
| chr12:19497834
|
C | T | 2 | a0001c0001t0004g0266a0001c0001t0004g0267 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1175-2263C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497834 | ||||||
| chr12:19497895
|
A | C | 1 | a0001c0001t0002g0205 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1175-2202A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497895 | ||||||
| chr12:19498075
|
C | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1175-2022C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19498075 | ||||||
| chr12:19498203
|
A | G | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1175-1894A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19498203 | ||||||
| chr12:19498305
|
G | C | 334 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(331): Show | 335 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.1175-1792G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19498305 | ||||||
| chr12:19498402
|
T | C | 43 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(40): Show | 43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1175-1695T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19498402 | ||||||
| chr12:19498555
|
A | G | 1 | a0001c0002t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1175-1542A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19498555 | ||||||
| chr12:19498601
|
C | T | 41 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(38): Show | 41 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1175-1496C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19498601 | ||||||
| chr12:19498894
|
C | T | 6 | a0001c0001t0002g0175a0001c0001t0002g0180a0001c0001t0002g0192others(3): Show | 6 | HG01069.hp1 HG01168.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1175-1203C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19498894 | ||||||
| chr12:19499041
|
A | G | 5 | a0001c0001t0003g0307a0001c0001t0003g0355a0001c0001t0003g0398others(2): Show | 5 | HG01123.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175-1056A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499041 | ||||||
| chr12:19499058
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-1039C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499058 | ||||||
| chr12:19499171
|
T | C | 2 | a0001c0001t0004g0266a0001c0001t0004g0267 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1175-926T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499171 | ||||||
| chr12:19499332
|
G | A | 40 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(37): Show | 40 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1175-765G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499332 | ||||||
| chr12:19499353
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1175-744C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499353 | ||||||
| chr12:19499378
|
C | T | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1175-719C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499378 | ||||||
| chr12:19499468
|
G | T | 3 | a0001c0001t0015g0233a0001c0001t0015g0234a0001c0001t0015g0235 | 3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1175-629G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499468 | ||||||
| chr12:19499613
|
CT | C | 7 | a0001c0001t0005g0135a0001c0001t0016g0038a0001c0001t0016g0039others(4): Show | 7 | HG01952.hp1 NA18953.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.1175-482delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19499613 | |||||
| chr12:19499614
|
T | TA | 74 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(71): Show | 74 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.1175-483_1175-482i others(3): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499614 | ||||||
| chr12:19499614
|
T | TAA | 55 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(52): Show | 55 | HG00735.hp2 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1175-483_1175-482i others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499614 | ||||||
| chr12:19499614
|
T | TAAA | 7 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0244others(4): Show | 7 | HG00597.hp2 HG01884.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175-483_1175-482i others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499614 | ||||||
| chr12:19499615
|
T | A | 327 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(324): Show | 328 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.1175-482T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499615 | ||||||
| chr12:19499632
|
A | G | 1 | a0001c0001t0004g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1175-465A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499632 | ||||||
| chr12:19499660
|
G | T | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1175-437G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499660 | ||||||
| chr12:19499746
|
G | GAT | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-345_1175-344d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19499746 | |||||
| chr12:19499786
|
T | G | 4 | a0001c0001t0004g0317a0001c0001t0004g0318a0001c0001t0004g0320others(1): Show | 4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-311T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499786 | ||||||
| chr12:19499835
|
G | T | 3 | a0001c0002t0001g0087a0001c0002t0001g0238a0001c0002t0010g0110 | 3 | HG01358.hp1 HG01928.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1175-262G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499835 | ||||||
| chr12:19499940
|
A | G | 40 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(37): Show | 40 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1175-157A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499940 | ||||||
| chr12:19499954
|
C | G | 1 | a0001c0001t0002g0206 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1175-143C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499954 | ||||||
| chr12:19500478
|
A | G | 1 | a0001c0001t0004g0194 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1299+257A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19500478 | ||||||
| chr12:19500633
|
C | G | 1 | a0001c0001t0008g0327 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1299+412C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19500633 | ||||||
| chr12:19500767
|
A | G | 172 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(169): Show | 173 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1299+546A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19500767 | ||||||
| chr12:19500818
|
A | G | 51 | a0001c0001t0002g0202a0001c0002t0001g0047a0001c0002t0001g0048others(48): Show | 51 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1299+597A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19500818 | ||||||
| chr12:19500991
|
C | G | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1299+770C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19500991 | ||||||
| chr12:19501073
|
T | TAACTCTA others(5): Show |
1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+854_1299+855i others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501073 | |||||
| chr12:19501077
|
C | A | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+856C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501077 | ||||||
| chr12:19501079
|
C | A | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+858C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501079 | ||||||
| chr12:19501084
|
T | A | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+863T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501084 | ||||||
| chr12:19501090
|
G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+869G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501090 | ||||||
| chr12:19501091
|
A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+870A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501091 | ||||||
| chr12:19501097
|
A | G | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+876A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501097 | ||||||
| chr12:19501100
|
C | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+879C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501100 | ||||||
| chr12:19501105
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1299+884G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501105 | ||||||
| chr12:19501107
|
A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+886A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501107 | ||||||
| chr12:19501110
|
A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+889A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501110 | ||||||
| chr12:19501113
|
T | A | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+892T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501113 | ||||||
| chr12:19501114
|
G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+893G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501114 | ||||||
| chr12:19501115
|
A | C | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+894A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501115 | ||||||
| chr12:19501116
|
G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+895G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501116 | ||||||
| chr12:19501117
|
G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+896G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501117 | ||||||
| chr12:19501120
|
A | G | 3 | a0001c0001t0004g0388a0001c0001t0007g0387a0001c0001t0007g0389 | 3 | HG03834.hp2 NA20805.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1299+899A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501120 | ||||||
| chr12:19501121
|
G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+900G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501121 | ||||||
| chr12:19501122
|
G | C | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+901G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501122 | ||||||
| chr12:19501134
|
A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+913A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501134 | ||||||
| chr12:19501135
|
G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+914G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501135 | ||||||
| chr12:19501139
|
G | A | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+918G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501139 | ||||||
| chr12:19501140
|
G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+919G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501140 | ||||||
| chr12:19501149
|
G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+928G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501149 | ||||||
| chr12:19501151
|
A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+930A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501151 | ||||||
| chr12:19501152
|
A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+931A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501152 | ||||||
| chr12:19501153
|
A | C | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+932A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501153 | ||||||
| chr12:19501154
|
A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+933A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501154 | ||||||
| chr12:19501157
|
C | A | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+936C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501157 | ||||||
| chr12:19501165
|
A | C | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+944A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501165 | ||||||
| chr12:19501168
|
A | C | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+947A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501168 | ||||||
| chr12:19501171
|
AATACAAA others(4): Show |
A | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+951_1299+961d others(13): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501171 | ||||||
| chr12:19501184
|
A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+963A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501184 | ||||||
| chr12:19501279
|
C | T | 120 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(117): Show | 120 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(117): Show |
intron_variant | MODIFIER | c.1299+1058C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501279 | ||||||
| chr12:19501288
|
A | G | 13 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(10): Show | 13 | HG01934.hp2 HG02055.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1299+1067A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501288 | ||||||
| chr12:19501331
|
C | CA | 12 | a0001c0001t0002g0221a0001c0001t0002g0226a0001c0001t0004g0273others(9): Show | 12 | HG01361.hp1 HG01934.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.1299+1128dupA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501331 | |||||
| chr12:19501331
|
C | CAAA | 7 | a0001c0001t0016g0036a0001c0001t0016g0038a0001c0001t0016g0039others(4): Show | 7 | HG02055.hp1 NA18953.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1299+1126_1299+112 others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501331 | |||||
| chr12:19501331
|
CA | C | 7 | a0001c0001t0008g0382a0001c0001t0014g0027a0001c0001t0015g0231others(4): Show | 7 | HG00323.hp2 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1299+1128delA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501331 | |||||
| chr12:19501343
|
A | G | 2 | a0001c0001t0015g0233a0001c0001t0015g0234 | 2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1299+1122A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501343 | ||||||
| chr12:19501562
|
A | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+1341A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501562 | ||||||
| chr12:19501647
|
AATT | A | 72 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(69): Show | 72 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1299+1429_1299+143 others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501647 | |||||
| chr12:19501648
|
ATT | A | 93 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(90): Show | 94 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1299+1428_1299+142 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501648 | ||||||
| chr12:19501658
|
C | T | 3 | a0001c0002t0001g0065a0001c0002t0002g0066a0001c0002t0043g0064 | 3 | HG02071.hp1 HG02129.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1299+1437C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501658 | ||||||
| chr12:19501767
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1299+1546A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501767 | ||||||
| chr12:19501776
|
G | A | 1 | a0001c0001t0015g0235 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1299+1555G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501776 | ||||||
| chr12:19501797
|
G | GT | 8 | a0001c0001t0001g0095a0001c0001t0001g0117a0001c0001t0001g0118others(5): Show | 8 | HG00408.hp2 HG00609.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+1596dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | |||||
| chr12:19501797
|
G | GTTTGT | 21 | a0001c0001t0002g0206a0001c0001t0004g0265a0001c0001t0004g0272others(18): Show | 21 | HG00438.hp2 HG00621.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.1299+1579_1299+158 others(9): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | |||||
| chr12:19501797
|
G | GTTTGTT | 18 | a0001c0001t0004g0004a0001c0001t0004g0268a0001c0001t0004g0271others(15): Show | 18 | HG00558.hp1 HG01106.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.1299+1579_1299+158 others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | |||||
| chr12:19501797
|
G | GTTTTT | 67 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0312others(64): Show | 68 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1299+1592_1299+159 others(9): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | |||||
| chr12:19501797
|
G | GTTTTTT | 39 | a0001c0001t0003g0311a0001c0001t0003g0321a0001c0001t0003g0323others(36): Show | 39 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1299+1591_1299+159 others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | |||||
| chr12:19501797
|
G | GTTTTTTG others(1): Show |
7 | a0001c0001t0016g0036a0001c0001t0016g0038a0001c0001t0016g0039others(4): Show | 7 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1299+1582_1299+158 others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | |||||
| chr12:19501797
|
G | GTTTTTTT | 13 | a0001c0001t0003g0353a0001c0001t0003g0363a0001c0001t0004g0320others(10): Show | 13 | HG01106.hp1 HG01934.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.1299+1590_1299+159 others(11): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | |||||
| chr12:19501797
|
G | T | 2 | a0001c0001t0004g0266a0001c0001t0004g0267 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1299+1576G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501797 | ||||||
| chr12:19501797
|
GT | G | 130 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(127): Show | 133 | HG00140.hp1 HG00558.hp2 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.1299+1596delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | |||||
| chr12:19501797
|
GTT | G | 15 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0242others(12): Show | 15 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1299+1595_1299+159 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | |||||
| chr12:19501798
|
T | TTTG | 6 | a0001c0001t0005g0137a0001c0001t0005g0150a0001c0001t0005g0155others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1299+1579_1299+158 others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501798 | |||||
| chr12:19501799
|
T | TTG | 30 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(27): Show | 30 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1299+1579_1299+158 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501799 | |||||
| chr12:19501802
|
T | G | 1 | a0001c0001t0002g0212 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1299+1581T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501802 | ||||||
| chr12:19501839
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+1618C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501839 | ||||||
| chr12:19501840
|
G | A | 1 | a0001c0001t0004g0287 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1299+1619G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501840 | ||||||
| chr12:19501852
|
C | T | 8 | a0001c0001t0001g0055a0001c0001t0001g0091a0001c0001t0001g0104others(5): Show | 8 | NA18944.hp1 NA18960.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.1299+1631C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501852 | ||||||
| chr12:19501866
|
G | T | 4 | a0001c0001t0004g0317a0001c0001t0004g0318a0001c0001t0004g0320others(1): Show | 4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+1645G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501866 | ||||||
| chr12:19501951
|
G | A | 2 | a0001c0001t0015g0231a0001c0001t0024g0232 | 2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1299+1730G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501951 | ||||||
| chr12:19502101
|
C | T | 30 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(27): Show | 30 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1299+1880C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502101 | ||||||
| chr12:19502113
|
A | G | 1 | a0001c0001t0002g0163 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1299+1892A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502113 | ||||||
| chr12:19502128
|
A | G | 6 | a0001c0001t0013g0156a0001c0001t0013g0157a0001c0001t0013g0158others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1299+1907A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502128 | ||||||
| chr12:19502237
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+2016C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502237 | ||||||
| chr12:19502258
|
C | T | 2 | a0001c0001t0003g0361a0001c0001t0008g0332 | 2 | NA19005.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1299+2037C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502258 | ||||||
| chr12:19502268
|
G | A | 1 | a0001c0001t0004g0294 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1299+2047G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502268 | ||||||
| chr12:19502302
|
T | G | 1 | a0001c0001t0034g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1299+2081T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502302 | ||||||
| chr12:19502397
|
G | A | 3 | a0001c0001t0015g0233a0001c0001t0015g0234a0001c0001t0015g0235 | 3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1299+2176G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502397 | ||||||
| chr12:19502429
|
C | T | 1 | a0001c0001t0020g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1299+2208C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502429 | ||||||
| chr12:19502439
|
T | C | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1299+2218T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502439 | ||||||
| chr12:19502569
|
A | G | 1 | a0001c0001t0002g0211 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1299+2348A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502569 | ||||||
| chr12:19502584
|
A | G | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1299+2363A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502584 | ||||||
| chr12:19502652
|
C | CT | 42 | a0001c0001t0002g0166a0001c0001t0002g0206a0001c0001t0004g0004others(39): Show | 42 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1299+2444dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19502652 | |||||
| chr12:19502652
|
CT | C | 9 | a0001c0001t0002g0163a0001c0001t0016g0035a0001c0001t0016g0036others(6): Show | 9 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.1299+2444delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19502652 | |||||
| chr12:19502705
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+2484A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502705 | ||||||
| chr12:19502732
|
T | C | 1 | a0001c0003t0044g0249 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1299+2511T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502732 | ||||||
| chr12:19502849
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1299+2628C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502849 | ||||||
| chr12:19502851
|
T | C | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1299+2630T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502851 | ||||||
| chr12:19502930
|
C | T | 1 | a0001c0001t0009g0162 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1299+2709C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502930 | ||||||
| chr12:19502969
|
A | G | 1 | a0001c0001t0008g0325 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1299+2748A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502969 | ||||||
| chr12:19503017
|
G | A | 1 | a0001c0001t0009g0162 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1299+2796G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503017 | ||||||
| chr12:19503139
|
G | C | 5 | a0001c0002t0001g0109a0001c0002t0001g0124a0001c0002t0001g0125others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+2918G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503139 | ||||||
| chr12:19503180
|
G | A | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1299+2959G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503180 | ||||||
| chr12:19503328
|
G | GGT | 9 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0108others(6): Show | 9 | HG02083.hp1 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1299+3124_1299+312 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19503328 | |||||
| chr12:19503329
|
G | GTA | 40 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(37): Show | 40 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.1299+3109_1299+311 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19503329 | |||||
| chr12:19503347
|
A | ATG | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+3140_1299+314 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19503347 | |||||
| chr12:19503373
|
G | A | 1 | a0001c0001t0004g0278 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1299+3152G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503373 | ||||||
| chr12:19503398
|
C | T | 3 | a0001c0002t0001g0054a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG03139.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1299+3177C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503398 | ||||||
| chr12:19503416
|
G | C | 4 | a0001c0001t0004g0317a0001c0001t0004g0318a0001c0001t0004g0320others(1): Show | 4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+3195G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503416 | ||||||
| chr12:19503430
|
A | C | 5 | a0001c0001t0015g0231a0001c0001t0015g0233a0001c0001t0015g0234others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+3209A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503430 | ||||||
| chr12:19503542
|
T | C | 3 | a0001c0001t0004g0274a0001c0001t0004g0279a0001c0001t0004g0280 | 3 | HG01099.hp2 HG01106.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1299+3321T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503542 | ||||||
| chr12:19503564
|
C | A | 111 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(108): Show | 111 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.1299+3343C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503564 | ||||||
| chr12:19503626
|
A | G | 1 | a0001c0001t0004g0297 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1299+3405A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503626 | ||||||
| chr12:19503707
|
A | G | 1 | a0001c0001t0007g0389 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1299+3486A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503707 | ||||||
| chr12:19503872
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+3651T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503872 | ||||||
| chr12:19503983
|
T | C | 2 | a0001c0001t0002g0205a0001c0001t0037g0203 | 2 | HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1299+3762T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503983 | ||||||
| chr12:19504020
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1299+3799G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504020 | ||||||
| chr12:19504079
|
C | T | 92 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(89): Show | 93 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1299+3858C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504079 | ||||||
| chr12:19504080
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+3859G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504080 | ||||||
| chr12:19504213
|
C | G | 1 | a0001c0002t0001g0058 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1299+3992C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504213 | ||||||
| chr12:19504269
|
C | G | 1 | a0002c0007t0002g0200 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1299+4048C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504269 | ||||||
| chr12:19504280
|
G | A | 113 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(110): Show | 113 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.1299+4059G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504280 | ||||||
| chr12:19504296
|
G | A | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1299+4075G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504296 | ||||||
| chr12:19504297
|
C | T | 1 | a0001c0001t0003g0376 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1299+4076C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504297 | ||||||
| chr12:19504308
|
C | T | 1 | a0001c0001t0004g0273 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1299+4087C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504308 | ||||||
| chr12:19504320
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1299+4099C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504320 | ||||||
| chr12:19504380
|
G | GC | 54 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0055others(51): Show | 54 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.1299+4167dupC | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19504380 | |||||
| chr12:19504380
|
GC | G | 138 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(135): Show | 139 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1299+4167delC | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19504380 | |||||
| chr12:19504388
|
C | T | 3 | a0001c0002t0001g0054a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG03139.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1299+4167C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504388 | ||||||
| chr12:19504403
|
AT | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+4189delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19504403 | |||||
| chr12:19504405
|
T | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+4184T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504405 | ||||||
| chr12:19504411
|
G | A | 113 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(110): Show | 113 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.1299+4190G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504411 | ||||||
| chr12:19504461
|
C | T | 113 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(110): Show | 113 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.1299+4240C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504461 | ||||||
| chr12:19504478
|
G | A | 5 | a0001c0001t0003g0307a0001c0001t0003g0355a0001c0001t0003g0398others(2): Show | 5 | HG01123.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+4257G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504478 | ||||||
| chr12:19504483
|
A | G | 1 | a0001c0001t0002g0163 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1299+4262A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504483 | ||||||
| chr12:19504572
|
A | G | 1 | a0001c0002t0002g0144 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1299+4351A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504572 | ||||||
| chr12:19504606
|
A | G | 3 | a0001c0001t0006g0022a0001c0001t0014g0020a0001c0001t0031g0029 | 3 | HG00639.hp1 HG01106.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1299+4385A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504606 | ||||||
| chr12:19504645
|
A | G | 174 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(171): Show | 175 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.1299+4424A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504645 | ||||||
| chr12:19504735
|
T | C | 2 | a0001c0001t0012g0324a0001c0001t0012g0362 | 2 | HG02027.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1299+4514T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504735 | ||||||
| chr12:19504795
|
A | G | 139 | a0001c0001t0002g0206a0001c0001t0003g0307a0001c0001t0003g0310others(136): Show | 140 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1299+4574A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504795 | ||||||
| chr12:19504871
|
T | C | 1 | a0001c0001t0005g0134 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1299+4650T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504871 | ||||||
| chr12:19504872
|
A | G | 4 | a0001c0001t0003g0347a0001c0001t0003g0354a0001c0001t0007g0348others(1): Show | 4 | HG02040.hp2 HG02132.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+4651A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504872 | ||||||
| chr12:19504873
|
G | T | 2 | a0001c0001t0004g0287a0001c0001t0025g0288 | 2 | HG01243.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1299+4652G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504873 | ||||||
| chr12:19505124
|
C | G | 7 | a0001c0001t0002g0001a0001c0001t0002g0195a0001c0001t0002g0197others(4): Show | 9 | NA18955.hp1 NA18963.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+4903C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505124 | ||||||
| chr12:19505169
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+4948G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505169 | ||||||
| chr12:19505223
|
A | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+5002A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505223 | ||||||
| chr12:19505337
|
TTAAGGTG others(7): Show |
T | 1 | a0001c0001t0002g0163 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1299+5117_1299+513 others(18): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505337 | ||||||
| chr12:19505397
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+5176G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505397 | ||||||
| chr12:19505445
|
G | A | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1299+5224G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505445 | ||||||
| chr12:19505527
|
A | C | 1 | a0001c0002t0010g0067 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1299+5306A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505527 | ||||||
| chr12:19505533
|
A | T | 1 | a0001c0001t0007g0400 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1299+5312A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505533 | ||||||
| chr12:19505605
|
C | G | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1299+5384C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505605 | ||||||
| chr12:19505761
|
T | TTTTG | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+5560_1299+556 others(8): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19505761 | |||||
| chr12:19505889
|
C | G | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1299+5668C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505889 | ||||||
| chr12:19505926
|
C | A | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1299+5705C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505926 | ||||||
| chr12:19505930
|
G | C | 304 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(301): Show | 305 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.1299+5709G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505930 | ||||||
| chr12:19505969
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+5748C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505969 | ||||||
| chr12:19505979
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+5758T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505979 | ||||||
| chr12:19506040
|
C | T | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1299+5819C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19506040 | ||||||
| chr12:19506144
|
C | T | 5 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(2): Show | 5 | HG00597.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+5923C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19506144 | ||||||
| chr12:19506167
|
G | A | 1 | a0001c0001t0003g0375 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1299+5946G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19506167 | ||||||
| chr12:19506204
|
C | G | 39 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(36): Show | 39 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1299+5983C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19506204 | ||||||
| chr12:19506222
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+6001T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19506222 | ||||||
| chr12:19507013
|
G | T | 1 | a0001c0001t0008g0325 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1300-5385G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507013 | ||||||
| chr12:19507151
|
A | C | 1 | a0001c0001t0009g0181 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1300-5247A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507151 | ||||||
| chr12:19507220
|
A | G | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099 | 3 | HG02056.hp1 HG02071.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1300-5178A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507220 | ||||||
| chr12:19507508
|
A | G | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1300-4890A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507508 | ||||||
| chr12:19507509
|
A | C | 1 | a0001c0001t0001g0093 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1300-4889A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507509 | ||||||
| chr12:19507577
|
A | T | 179 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(176): Show | 179 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(176): Show |
intron_variant | MODIFIER | c.1300-4821A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507577 | ||||||
| chr12:19507632
|
C | CAGTT | 3 | a0001c0001t0015g0233a0001c0001t0015g0234a0001c0001t0015g0235 | 3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1300-4765_1300-476 others(8): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19507632 | |||||
| chr12:19507636
|
A | C | 3 | a0001c0001t0015g0233a0001c0001t0015g0234a0001c0001t0015g0235 | 3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1300-4762A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507636 | ||||||
| chr12:19507638
|
G | GT | 3 | a0001c0001t0015g0233a0001c0001t0015g0234a0001c0001t0015g0235 | 3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1300-4760_1300-475 others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507638 | ||||||
| chr12:19507640
|
T | A | 3 | a0001c0001t0015g0233a0001c0001t0015g0234a0001c0001t0015g0235 | 3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1300-4758T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507640 | ||||||
| chr12:19507726
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-4672G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507726 | ||||||
| chr12:19507772
|
A | G | 1 | a0001c0002t0002g0078 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1300-4626A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507772 | ||||||
| chr12:19507905
|
T | A | 1 | a0001c0001t0032g0178 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1300-4493T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507905 | ||||||
| chr12:19507906
|
A | T | 1 | a0001c0001t0032g0178 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1300-4492A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507906 | ||||||
| chr12:19507924
|
A | G | 1 | a0001c0002t0001g0083 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1300-4474A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507924 | ||||||
| chr12:19508046
|
A | C | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1300-4352A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508046 | ||||||
| chr12:19508063
|
TGCTTGGT others(2): Show |
T | 7 | a0001c0001t0001g0055a0001c0001t0001g0091a0001c0001t0001g0104others(4): Show | 7 | NA18944.hp1 NA18960.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.1300-4329_1300-432 others(13): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19508063 | |||||
| chr12:19508104
|
T | C | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-4294T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508104 | ||||||
| chr12:19508123
|
C | T | 1 | a0001c0001t0013g0157 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1300-4275C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508123 | ||||||
| chr12:19508139
|
T | C | 54 | a0001c0001t0002g0202a0001c0002t0001g0047a0001c0002t0001g0048others(51): Show | 54 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1300-4259T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508139 | ||||||
| chr12:19508202
|
T | C | 1 | a0001c0001t0006g0008 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1300-4196T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508202 | ||||||
| chr12:19508223
|
A | G | 4 | a0001c0001t0005g0140a0001c0001t0005g0236a0001c0001t0005g0257others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-4175A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508223 | ||||||
| chr12:19508326
|
G | A | 111 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(108): Show | 111 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.1300-4072G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508326 | ||||||
| chr12:19508353
|
G | A | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 4 | HG00597.hp2 HG02056.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-4045G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508353 | ||||||
| chr12:19508363
|
A | G | 1 | a0001c0002t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1300-4035A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508363 | ||||||
| chr12:19508438
|
T | A | 1 | a0001c0002t0001g0083 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1300-3960T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508438 | ||||||
| chr12:19508503
|
C | T | 398 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(395): Show | 402 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(399): Show |
intron_variant | MODIFIER | c.1300-3895C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508503 | ||||||
| chr12:19508632
|
T | C | 1 | a0001c0001t0005g0130 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1300-3766T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508632 | ||||||
| chr12:19508644
|
T | C | 1 | a0001c0001t0034g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1300-3754T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508644 | ||||||
| chr12:19508772
|
AACAAAT | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-3625_1300-362 others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508772 | ||||||
| chr12:19508840
|
C | A | 1 | a0001c0001t0039g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1300-3558C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508840 | ||||||
| chr12:19508872
|
C | G | 1 | a0001c0001t0003g0359 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1300-3526C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508872 | ||||||
| chr12:19508923
|
A | G | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1300-3475A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508923 | ||||||
| chr12:19509121
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-3277A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19509121 | ||||||
| chr12:19509253
|
G | A | 331 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(328): Show | 332 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(329): Show |
intron_variant | MODIFIER | c.1300-3145G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19509253 | ||||||
| chr12:19509404
|
T | G | 1 | a0001c0001t0005g0137 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1300-2994T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19509404 | ||||||
| chr12:19509520
|
C | T | 93 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(90): Show | 94 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1300-2878C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19509520 | ||||||
| chr12:19509570
|
A | C | 1 | a0001c0001t0032g0178 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1300-2828A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19509570 | ||||||
| chr12:19509793
|
C | T | 1 | a0001c0001t0011g0301 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1300-2605C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19509793 | ||||||
| chr12:19509816
|
CTTTCTTT others(8): Show |
C | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1300-2578_1300-256 others(19): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19509816 | |||||
| chr12:19509820
|
C | CT | 43 | a0001c0001t0001g0244a0001c0001t0002g0176a0001c0001t0002g0198others(40): Show | 43 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.1300-2552dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19509820 | |||||
| chr12:19509820
|
C | CTT | 6 | a0001c0001t0005g0132a0001c0001t0005g0153a0001c0001t0005g0154others(3): Show | 6 | HG02148.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1300-2553_1300-255 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19509820 | |||||
| chr12:19509820
|
CT | C | 128 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(125): Show | 128 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.1300-2552delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19509820 | |||||
| chr12:19509820
|
CTT | C | 83 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0312others(80): Show | 84 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1300-2553_1300-255 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19509820 | |||||
| chr12:19509820
|
CTTT | C | 53 | a0001c0001t0002g0206a0001c0001t0003g0311a0001c0001t0003g0330others(50): Show | 53 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1300-2554_1300-255 others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19509820 | |||||
| chr12:19509820
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0248 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1300-2562_1300-255 others(15): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19509820 | |||||
| chr12:19509977
|
C | T | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1300-2421C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19509977 | ||||||
| chr12:19510126
|
T | A | 1 | a0001c0001t0002g0210 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1300-2272T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510126 | ||||||
| chr12:19510285
|
A | C | 32 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(29): Show | 32 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1300-2113A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510285 | ||||||
| chr12:19510288
|
C | G | 1 | a0001c0001t0002g0166 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1300-2110C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510288 | ||||||
| chr12:19510508
|
C | T | 1 | a0001c0002t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1300-1890C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510508 | ||||||
| chr12:19510564
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-1834G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510564 | ||||||
| chr12:19510568
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-1830G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510568 | ||||||
| chr12:19510653
|
A | G | 5 | a0001c0002t0001g0109a0001c0002t0001g0124a0001c0002t0001g0125others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-1745A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510653 | ||||||
| chr12:19510800
|
A | G | 32 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(29): Show | 32 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1300-1598A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510800 | ||||||
| chr12:19510865
|
C | CT | 62 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0164others(59): Show | 65 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1300-1516dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19510865 | |||||
| chr12:19510865
|
C | CTTTTTTT | 18 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0245others(15): Show | 18 | HG02055.hp2 HG02257.hp1 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.1300-1522_1300-151 others(11): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19510865 | |||||
| chr12:19510865
|
C | CTTTTTTT others(1): Show |
144 | a0001c0001t0001g0051a0001c0001t0001g0108a0001c0001t0001g0113others(141): Show | 145 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1300-1523_1300-151 others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19510865 | |||||
| chr12:19510865
|
C | CTTTTTTT others(2): Show |
108 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0055others(105): Show | 108 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.1300-1524_1300-151 others(13): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19510865 | |||||
| chr12:19510865
|
C | CTTTTTTT others(3): Show |
45 | a0001c0001t0001g0095a0001c0001t0001g0244a0001c0001t0001g0248others(42): Show | 45 | HG00609.hp2 HG01081.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.1300-1525_1300-151 others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19510865 | |||||
| chr12:19510865
|
C | CTTTTTTT others(4): Show |
13 | a0001c0001t0005g0132a0001c0001t0005g0134a0001c0001t0005g0135others(10): Show | 13 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1300-1526_1300-151 others(15): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19510865 | |||||
| chr12:19510865
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0005g0146 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1300-1527_1300-151 others(16): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19510865 | |||||
| chr12:19511117
|
G | A | 108 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(105): Show | 108 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1300-1281G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511117 | ||||||
| chr12:19511175
|
T | C | 142 | a0001c0001t0001g0108a0001c0001t0001g0114a0001c0001t0002g0206others(139): Show | 143 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1300-1223T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511175 | ||||||
| chr12:19511176
|
C | T | 1 | a0001c0001t0004g0281 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1300-1222C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511176 | ||||||
| chr12:19511271
|
G | A | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1300-1127G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511271 | ||||||
| chr12:19511328
|
T | G | 1 | a0001c0001t0002g0215 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1300-1070T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511328 | ||||||
| chr12:19511358
|
T | G | 2 | a0001c0001t0007g0315a0001c0001t0007g0316 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1300-1040T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511358 | ||||||
| chr12:19511388
|
T | A | 1 | a0001c0001t0005g0137 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1300-1010T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511388 | ||||||
| chr12:19511419
|
G | GA | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1300-975dupA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19511419 | |||||
| chr12:19511923
|
T | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0104a0001c0001t0001g0105others(2): Show | 5 | NA18944.hp1 NA18973.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1300-475T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511923 | ||||||
| chr12:19511984
|
C | G | 6 | a0001c0001t0013g0156a0001c0001t0013g0157a0001c0001t0013g0158others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1300-414C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511984 | ||||||
| chr12:19512193
|
T | G | 1 | a0001c0001t0032g0178 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1300-205T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19512193 | ||||||
| chr12:19512479
|
A | G | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1367+14A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19512479 | ||||||
| chr12:19512602
|
A | G | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1367+137A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19512602 | ||||||
| chr12:19512651
|
A | T | 1 | a0001c0001t0017g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1367+186A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19512651 | ||||||
| chr12:19512669
|
CTT | C | 35 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(32): Show | 35 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1367+214_1367+215d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19512669 | |||||
| chr12:19512738
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1367+273G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19512738 | ||||||
| chr12:19512818
|
C | T | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1367+353C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19512818 | ||||||
| chr12:19513206
|
T | C | 332 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(329): Show | 333 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(330): Show |
intron_variant | MODIFIER | c.1367+741T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513206 | ||||||
| chr12:19513322
|
A | AT | 184 | a0001c0001t0001g0108a0001c0001t0001g0114a0001c0001t0002g0206others(181): Show | 185 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1367+864dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19513322 | |||||
| chr12:19513329
|
T | TTA | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1367+864_1367+865i others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513329 | ||||||
| chr12:19513481
|
G | T | 1 | a0001c0001t0032g0178 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1367+1016G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513481 | ||||||
| chr12:19513711
|
C | T | 4 | a0001c0002t0001g0124a0001c0002t0001g0125a0001c0002t0001g0126others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-960C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513711 | ||||||
| chr12:19513719
|
T | G | 37 | a0001c0001t0002g0180a0001c0001t0005g0129a0001c0001t0005g0130others(34): Show | 37 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.1368-952T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513719 | ||||||
| chr12:19513788
|
A | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1368-883A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513788 | ||||||
| chr12:19513794
|
A | G | 27 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1368-877A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513794 | ||||||
| chr12:19513886
|
G | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0010g0100 | 3 | NA18952.hp1 NA18978.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1368-785G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513886 | ||||||
| chr12:19513892
|
A | AT | 12 | a0001c0001t0002g0001a0001c0001t0002g0195a0001c0001t0002g0197others(9): Show | 14 | HG00621.hp1 HG02055.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1368-762dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19513892 | |||||
| chr12:19513892
|
AT | A | 88 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(85): Show | 88 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.1368-762delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19513892 | |||||
| chr12:19513892
|
ATT | A | 71 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(68): Show | 71 | HG00609.hp2 HG01081.hp2 HG01109.hp1 others(68): Show |
intron_variant | MODIFIER | c.1368-763_1368-762d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19513892 | |||||
| chr12:19513945
|
C | CT | 11 | a0001c0001t0003g0354a0001c0001t0003g0363a0001c0001t0004g0277others(8): Show | 11 | HG02486.hp2 HG02738.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.1368-712dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19513945 | |||||
| chr12:19513945
|
CT | C | 18 | a0001c0001t0001g0118a0001c0001t0001g0245a0001c0001t0003g0361others(15): Show | 19 | HG00558.hp1 HG01167.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.1368-712delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19513945 | |||||
| chr12:19513973
|
T | C | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1368-698T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513973 | ||||||
| chr12:19513989
|
T | C | 1 | a0001c0001t0004g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1368-682T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513989 | ||||||
| chr12:19513999
|
G | GT | 5 | a0001c0001t0002g0163a0001c0001t0003g0312a0001c0001t0003g0390others(2): Show | 5 | HG01433.hp1 NA18940.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1368-665dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19513999 | |||||
| chr12:19514000
|
T | G | 1 | a0001c0001t0004g0285 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1368-671T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514000 | ||||||
| chr12:19514008
|
G | GT | 7 | a0001c0001t0003g0336a0001c0001t0004g0279a0001c0001t0004g0285others(4): Show | 7 | HG01192.hp2 HG03516.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.1368-655dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19514008 | |||||
| chr12:19514008
|
G | T | 1 | a0001c0001t0002g0197 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1368-663G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514008 | ||||||
| chr12:19514031
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1368-640A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514031 | ||||||
| chr12:19514117
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1368-554G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514117 | ||||||
| chr12:19514191
|
G | GGGTTTCA others(3): Show |
1 | a0001c0001t0032g0178 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1368-479_1368-478i others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19514191 | |||||
| chr12:19514278
|
G | C | 1 | a0001c0001t0004g0285 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1368-393G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514278 | ||||||
| chr12:19514280
|
A | C | 1 | a0001c0001t0004g0285 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1368-391A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514280 | ||||||
| chr12:19514285
|
C | A | 1 | a0001c0001t0004g0285 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1368-386C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514285 | ||||||
| chr12:19514289
|
C | T | 6 | a0001c0001t0004g0273a0001c0001t0004g0276a0001c0001t0004g0281others(3): Show | 6 | HG00621.hp1 HG02015.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.1368-382C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514289 | ||||||
| chr12:19514455
|
C | T | 1 | a0001c0001t0012g0335 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1368-216C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514455 | ||||||
| chr12:19514602
|
T | G | 4 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0016others(1): Show | 4 | HG01934.hp1 HG03017.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1368-69T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514602 | ||||||
| chr12:19514640
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1368-31C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514640 | ||||||
| chr12:19514903
|
A | T | 1 | a0001c0001t0002g0197 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1481+119A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19514903 | ||||||
| chr12:19514912
|
CT | C | 29 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(26): Show | 29 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1481+140delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 19514912 | |||||
| chr12:19514995
|
T | C | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049 | 3 | HG01109.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1481+211T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19514995 | ||||||
| chr12:19515152
|
A | AT | 111 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(108): Show | 111 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(108): Show |
intron_variant | MODIFIER | c.1481+376dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 19515152 | |||||
| chr12:19515184
|
C | A | 1 | a0001c0001t0007g0392 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1481+400C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515184 | ||||||
| chr12:19515207
|
T | C | 2 | a0001c0001t0004g0266a0001c0001t0004g0267 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1481+423T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515207 | ||||||
| chr12:19515333
|
T | C | 2 | a0001c0001t0003g0313a0001c0005t0023g0033 | 2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1481+549T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515333 | ||||||
| chr12:19515558
|
T | C | 41 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(38): Show | 41 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1481+774T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515558 | ||||||
| chr12:19515592
|
C | CT | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1481+814dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 19515592 | |||||
| chr12:19515756
|
C | T | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1481+972C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515756 | ||||||
| chr12:19515769
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1481+985A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515769 | ||||||
| chr12:19515829
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1481+1045G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515829 | ||||||
| chr12:19515953
|
C | T | 1 | a0001c0001t0003g0378 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1481+1169C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515953 | ||||||
| chr12:19515964
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1481+1180G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515964 | ||||||
| chr12:19515996
|
G | T | 1 | a0001c0001t0020g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1481+1212G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515996 | ||||||
| chr12:19516018
|
G | A | 31 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(28): Show | 31 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1481+1234G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516018 | ||||||
| chr12:19516131
|
T | C | 2 | a0001c0001t0034g0046a0001c0006t0033g0041 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1481+1347T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516131 | ||||||
| chr12:19516396
|
A | G | 96 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(93): Show | 97 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1481+1612A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516396 | ||||||
| chr12:19516397
|
G | T | 96 | a0001c0001t0003g0307a0001c0001t0003g0310a0001c0001t0003g0311others(93): Show | 97 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1481+1613G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516397 | ||||||
| chr12:19516434
|
C | G | 1 | a0001c0001t0007g0389 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1481+1650C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516434 | ||||||
| chr12:19516517
|
T | C | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0163others(46): Show | 52 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1482-1570T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516517 | ||||||
| chr12:19516521
|
A | G | 99 | a0001c0001t0001g0108a0001c0001t0001g0114a0001c0001t0003g0307others(96): Show | 100 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1482-1566A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516521 | ||||||
| chr12:19516566
|
A | G | 55 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(52): Show | 55 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.1482-1521A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516566 | ||||||
| chr12:19516623
|
A | G | 3 | a0001c0001t0017g0042a0001c0001t0017g0043a0001c0001t0017g0044 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1482-1464A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516623 | ||||||
| chr12:19516699
|
C | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1482-1388C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516699 | ||||||
| chr12:19516710
|
T | G | 42 | a0001c0001t0002g0206a0001c0001t0004g0004a0001c0001t0004g0265others(39): Show | 42 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1482-1377T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516710 | ||||||
| chr12:19517162
|
T | C | 1 | a0001c0001t0017g0042 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1482-925T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517162 | ||||||
| chr12:19517241
|
T | G | 36 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0131others(33): Show | 36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1482-846T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517241 | ||||||
| chr12:19517261
|
C | T | 1 | a0001c0001t0009g0209 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1482-826C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517261 | ||||||
| chr12:19517289
|
A | G | 3 | a0001c0001t0015g0233a0001c0001t0015g0234a0001c0001t0015g0235 | 3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1482-798A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517289 | ||||||
| chr12:19517439
|
A | G | 2 | a0001c0001t0003g0383a0001c0001t0008g0360 | 2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1482-648A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517439 | ||||||
| chr12:19517468
|
A | G | 1 | a0001c0001t0011g0319 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1482-619A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517468 | ||||||
| chr12:19517574
|
G | A | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1482-513G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517574 | ||||||
| chr12:19517686
|
T | C | 1 | a0001c0001t0004g0298 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1482-401T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517686 | ||||||
| chr12:19517693
|
C | T | 1 | a0001c0006t0033g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1482-394C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517693 | ||||||
| chr12:19517914
|
A | G | 8 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1482-173A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517914 | ||||||
| chr12:19518010
|
T | C | 30 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007others(27): Show | 30 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1482-77T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19518010 |