Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 11016 |
|---|---|
| ensemblid | ENSG00000170653.19 |
| hgncid | 792 |
| symbol | ATF7 |
| name | activating transcription factor 7 |
| refseq_nuc | NM_006856.3 |
| refseq_prot | NP_006847.1 |
| ensembl_nuc | ENST00000420353.7 |
| ensembl_prot | ENSP00000399465.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 53512054 |
| end | 53626382 |
| strand | - |
| ver | v1.2 |
| region | chr12:53512054-53626382 |
| region5000 | chr12:53507054-53631382 |
| regionname0 | ATF7_chr12_53512054_53626382 |
| regionname5000 | ATF7_chr12_53507054_53631382 |
| 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 | 483 | 329 | 83 | 66 | 124 | 12 | 42 | 94 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0002 | 0/0 | 483 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| 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 | 1452 | 310 | 77 | 61 | 119 | 10 | 41 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| c0002 | 0/0 | 1452 | 11 | 0 | 5 | 4 | 2 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| c0003 | 0/0 | 1452 | 6 | 6 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| c0004 | 0/0 | 1452 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| c0005 | 0/0 | 1452 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| c0006 | 0/0 | 1452 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 5209 | 219 | 68 | 46 | 71 | 8 | 24 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0002 | 0/0 | 5209 | 36 | 0 | 4 | 22 | 1 | 9 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0003 | 0/0 | 5209 | 15 | 7 | 1 | 5 | 0 | 2 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0004 | 0/0 | 5209 | 10 | 0 | 0 | 10 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0005 | 0/0 | 5209 | 6 | 0 | 4 | 0 | 2 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0006 | 0/0 | 5209 | 5 | 0 | 0 | 5 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0007 | 0/0 | 5209 | 5 | 0 | 4 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0008 | 0/0 | 5209 | 4 | 4 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0009 | 0/0 | 5209 | 4 | 0 | 3 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0010 | 0/0 | 5209 | 3 | 1 | 2 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0011 | 0/0 | 5209 | 2 | 0 | 0 | 0 | 1 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0012 | 0/0 | 5209 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0013 | 0/0 | 5209 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0014 | 0/0 | 5209 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0015 | 0/0 | 5209 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0016 | 0/0 | 5209 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0017 | 0/0 | 5209 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0018 | 0/0 | 5209 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0019 | 0/0 | 5209 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0020 | 0/0 | 5209 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0021 | 0/0 | 5209 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0022 | 0/0 | 5209 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0023 | 0/0 | 5209 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0024 | 0/0 | 5209 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0025 | 0/0 | 5209 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0026 | 0/0 | 5209 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0027 | 0/0 | 5209 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0028 | 0/0 | 5209 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0029 | 0/0 | 5209 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| t0030 | 0/0 | 5209 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| 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 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0266 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| 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 | 1452 | 310 | 77 | 61 | 119 | 10 | 41 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0002 | 0/0 | 1452 | 11 | 0 | 5 | 4 | 2 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0003 | 0/0 | 1452 | 6 | 6 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0005 | 0/0 | 1452 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0006 | 0/0 | 1452 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0002c0004 | 0/0 | 1452 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6660 | 211 | 66 | 46 | 66 | 8 | 23 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0002 | 0/0 | 6660 | 36 | 0 | 4 | 22 | 1 | 9 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0003 | 0/0 | 6660 | 14 | 7 | 0 | 5 | 0 | 2 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0004 | 0/0 | 6660 | 10 | 0 | 0 | 10 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0006 | 0/0 | 6660 | 5 | 0 | 0 | 5 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0007 | 0/0 | 6660 | 5 | 0 | 4 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0009 | 0/0 | 6660 | 4 | 0 | 3 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0010 | 0/0 | 6660 | 3 | 1 | 2 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0011 | 0/0 | 6660 | 2 | 0 | 0 | 0 | 1 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0012 | 0/0 | 6660 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0013 | 0/0 | 6660 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0014 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0015 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0016 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0017 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0018 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0019 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0020 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0021 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0022 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0023 | 0/0 | 6660 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0024 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0025 | 0/0 | 6660 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0026 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0027 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0028 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0001t0029 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0002t0001 | 0/0 | 6660 | 4 | 0 | 0 | 4 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0002t0003 | 0/0 | 6660 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0002t0005 | 0/0 | 6660 | 6 | 0 | 4 | 0 | 2 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0003t0001 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0003t0008 | 0/0 | 6660 | 4 | 4 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0003t0030 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0005t0001 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0001c0006t0001 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| a0002c0004t0001 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | copy fasta | chr12 | 53507054 | 53631382 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0266 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0007g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0009g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0009g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0009g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0010g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0010g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0011g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0011g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0012g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0012g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0013g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0013g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0014g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0016g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0017g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0018g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0019g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0020g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0021g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0022g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0023g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0024g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0025g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0026g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0027g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0028g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0029g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0005g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0003t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0003t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0003t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0003t0008g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0003t0030g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0005t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0006t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0002c0004t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | GBR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | GBR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0297 | EUR | GBR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00140 | hp2 | a0001 | c0001 | t0011 | g0081 | EUR | GBR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | FIN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00280 | hp2 | a0001 | c0002 | t0005 | g0159 | EUR | FIN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00621 | hp2 | a0001 | c0001 | t0007 | g0130 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00673 | hp2 | a0001 | c0001 | t0027 | g0194 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00733 | hp2 | a0001 | c0002 | t0005 | g0166 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01070 | hp2 | a0001 | c0001 | t0025 | g0315 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01074 | hp2 | a0001 | c0001 | t0010 | g0071 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01081 | hp2 | a0001 | c0001 | t0010 | g0070 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01168 | hp2 | a0001 | c0002 | t0005 | g0171 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01169 | hp1 | a0001 | c0002 | t0005 | g0172 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01175 | hp1 | a0001 | c0002 | t0003 | g0189 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0136 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01261 | hp2 | a0001 | c0001 | t0009 | g0099 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0041 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01496 | hp2 | a0001 | c0002 | t0005 | g0181 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | IBS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0235 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01934 | hp2 | a0001 | c0001 | t0023 | g0302 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01943 | hp2 | a0001 | c0001 | t0007 | g0113 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01993 | hp2 | a0001 | c0001 | t0007 | g0114 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02080 | hp1 | a0001 | c0006 | t0001 | g0082 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02135 | hp2 | a0001 | c0001 | t0013 | g0021 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0138 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | CDX | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CDX | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0323 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02293 | hp2 | a0001 | c0001 | t0009 | g0079 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02647 | hp2 | a0001 | c0001 | t0016 | g0308 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0322 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02735 | hp1 | a0001 | c0001 | t0024 | g0239 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03130 | hp2 | a0001 | c0003 | t0008 | g0228 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03195 | hp2 | a0001 | c0003 | t0030 | g0330 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0221 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03540 | hp2 | a0001 | c0003 | t0008 | g0230 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03688 | hp1 | a0001 | c0001 | t0021 | g0103 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03710 | hp1 | a0001 | c0001 | t0019 | g0290 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03831 | hp1 | a0001 | c0001 | t0014 | g0030 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04184 | hp1 | a0001 | c0001 | t0029 | g0236 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04199 | hp2 | a0001 | c0005 | t0001 | g0068 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04228 | hp2 | a0001 | c0001 | t0011 | g0083 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18943 | hp2 | a0001 | c0001 | t0018 | g0273 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18947 | hp1 | a0001 | c0001 | t0006 | g0143 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18948 | hp1 | a0001 | c0001 | t0012 | g0254 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18962 | hp2 | a0001 | c0001 | t0012 | g0284 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0145 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18999 | hp1 | a0001 | c0001 | t0017 | g0173 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19002 | hp2 | a0001 | c0001 | t0022 | g0169 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19010 | hp2 | a0001 | c0001 | t0020 | g0316 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19043 | hp2 | a0001 | c0001 | t0015 | g0032 | AFR | LWK | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19062 | hp1 | a0001 | c0001 | t0026 | g0298 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19080 | hp1 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19087 | hp1 | a0001 | c0001 | t0013 | g0020 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19088 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19240 | hp2 | a0001 | c0003 | t0008 | g0227 | AFR | YRI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | TSI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20805 | hp1 | a0001 | c0002 | t0005 | g0182 | EUR | TSI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | GIH | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20905 | hp2 | a0001 | c0001 | t0009 | g0077 | SAS | GIH | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02486 | hp1 | a0001 | c0001 | t0028 | g0224 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02559 | hp2 | a0001 | c0003 | t0008 | g0225 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | USA | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | USA | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20300 | hp2 | a0001 | c0001 | t0010 | g0072 | AFR | USA | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA21309 | hp1 | a0002 | c0004 | t0001 | g0208 | AFR | LWK | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0266 | REF | REF | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0039 | REF | REF | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53537486
|
G | T | 1 | a0002 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.331C>A | p.Pro111Thr | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/12 | 456/6660 | 331/1452 | 111/483 | chr12 | 53537486 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53524654
|
T | C | 1 | a0001c0003 | 6 | HG01891.hp2 HG02559.hp2 HG03130.hp2 others(3): Show |
synonymous_variant | LOW | c.1035A>G | p.Ala345Ala | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 10/12 | 1160/6660 | 1035/1452 | 345/483 | chr12 | 53524654 | ||
| chr12:53531789
|
C | T | 1 | a0001c0005 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.882G>A | p.Gln294Gln | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/12 | 1007/6660 | 882/1452 | 294/483 | chr12 | 53531789 | ||
| chr12:53537538
|
G | A | 1 | a0001c0006 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.279C>T | p.Pro93Pro | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/12 | 404/6660 | 279/1452 | 93/483 | chr12 | 53537538 | ||
| chr12:53552626
|
G | A | 1 | a0001c0002 | 11 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(8): Show |
synonymous_variant | LOW | c.60C>T | p.Asn20Asn | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/12 | 185/6660 | 60/1452 | 20/483 | chr12 | 53552626 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53512063
|
C | T | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5074G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 5074 | chr12 | 53512063 | |||||
| chr12:53512635
|
T | C | 1 | a0001c0001t0009 | 4 | HG01261.hp2 HG01433.hp2 HG02293.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4502A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 4502 | chr12 | 53512635 | |||||
| chr12:53512648
|
A | G | 1 | a0001c0001t0009 | 4 | HG01261.hp2 HG01433.hp2 HG02293.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4489T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 4489 | chr12 | 53512648 | |||||
| chr12:53512839
|
A | C | 1 | a0001c0003t0008 | 4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4298T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 4298 | chr12 | 53512839 | |||||
| chr12:53513226
|
C | T | 1 | a0001c0001t0010 | 3 | HG01074.hp2 HG01081.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3911G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3911 | chr12 | 53513226 | |||||
| chr12:53513283
|
C | T | 6 | a0001c0001t0003a0001c0001t0004a0001c0001t0017others(3): Show | 33 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3854G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3854 | chr12 | 53513283 | |||||
| chr12:53513493
|
G | A | 3 | a0001c0001t0002a0001c0001t0007a0001c0001t0013 | 43 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3644C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3644 | chr12 | 53513493 | |||||
| chr12:53513624
|
A | G | 1 | a0001c0001t0021 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3513T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3513 | chr12 | 53513624 | |||||
| chr12:53513707
|
T | C | 1 | a0001c0001t0019 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3430A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3430 | chr12 | 53513707 | |||||
| chr12:53513822
|
C | T | 1 | a0001c0001t0019 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3315G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3315 | chr12 | 53513822 | |||||
| chr12:53514041
|
G | C | 2 | a0001c0001t0011a0001c0001t0021 | 3 | HG00140.hp2 HG03688.hp1 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3096C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3096 | chr12 | 53514041 | |||||
| chr12:53514130
|
A | G | 1 | a0001c0001t0018 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3007T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3007 | chr12 | 53514130 | |||||
| chr12:53514215
|
C | T | 1 | a0001c0001t0017 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2922G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 2922 | chr12 | 53514215 | |||||
| chr12:53514890
|
T | C | 1 | a0001c0001t0022 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2247A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 2247 | chr12 | 53514890 | |||||
| chr12:53514968
|
G | A | 1 | a0001c0001t0023 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2169C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 2169 | chr12 | 53514968 | |||||
| chr12:53515005
|
G | A | 1 | a0001c0001t0006 | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2132C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 2132 | chr12 | 53515005 | |||||
| chr12:53515055
|
C | T | 1 | a0001c0002t0005 | 6 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2082G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 2082 | chr12 | 53515055 | |||||
| chr12:53515301
|
A | G | 1 | a0001c0001t0007 | 5 | HG00621.hp2 HG01261.hp1 HG01943.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1836T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 1836 | chr12 | 53515301 | |||||
| chr12:53515473
|
C | T | 1 | a0001c0001t0006 | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1664G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 1664 | chr12 | 53515473 | |||||
| chr12:53515507
|
A | G | 1 | a0001c0001t0016 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1630T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 1630 | chr12 | 53515507 | |||||
| chr12:53515635
|
T | A | 1 | a0001c0001t0024 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1502A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 1502 | chr12 | 53515635 | |||||
| chr12:53515810
|
C | T | 1 | a0001c0001t0015 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1327G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 1327 | chr12 | 53515810 | |||||
| chr12:53515981
|
G | C | 1 | a0001c0001t0004 | 10 | HG02074.hp1 NA18946.hp2 NA18948.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1156C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 1156 | chr12 | 53515981 | |||||
| chr12:53516175
|
G | A | 1 | a0001c0001t0025 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*962C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 962 | chr12 | 53516175 | |||||
| chr12:53516227
|
G | A | 1 | a0001c0001t0026 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*910C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 910 | chr12 | 53516227 | |||||
| chr12:53516625
|
A | C | 1 | a0001c0001t0014 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 512 | chr12 | 53516625 | |||||
| chr12:53516657
|
G | C | 1 | a0001c0001t0012 | 2 | NA18948.hp1 NA18962.hp2 |
3_prime_UTR_variant | MODIFIER | c.*480C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 480 | chr12 | 53516657 | |||||
| chr12:53516759
|
G | A | 1 | a0001c0001t0027 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*378C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 378 | chr12 | 53516759 | |||||
| chr12:53516935
|
G | A | 1 | a0001c0001t0013 | 2 | HG02135.hp2 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*202C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 202 | chr12 | 53516935 | |||||
| chr12:53516976
|
C | A | 1 | a0001c0001t0028 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*161G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 161 | chr12 | 53516976 | |||||
| chr12:53517097
|
G | A | 1 | a0001c0001t0029 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*40C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 40 | chr12 | 53517097 | |||||
| chr12:53626333
|
T | C | 1 | a0001c0003t0030 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/12 | 25333 | chr12 | 53626333 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53517480
|
T | G | 1 | a0001c0001t0001g0329 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1235-126A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53517480 | ||||||
| chr12:53517524
|
C | T | 2 | a0001c0001t0002g0131a0001c0001t0002g0135 | 2 | HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1235-170G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53517524 | ||||||
| chr12:53517761
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1235-407G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53517761 | ||||||
| chr12:53517875
|
T | A | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1235-521A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53517875 | ||||||
| chr12:53517974
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0200 | 3 | HG01358.hp1 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1235-620G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53517974 | ||||||
| chr12:53518028
|
C | A | 1 | a0001c0001t0001g0215 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1235-674G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53518028 | ||||||
| chr12:53518450
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1235-1096T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53518450 | ||||||
| chr12:53518452
|
T | C | 6 | a0001c0003t0001g0235a0001c0003t0008g0225a0001c0003t0008g0227others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1235-1098A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53518452 | ||||||
| chr12:53518499
|
C | G | 4 | a0001c0003t0008g0225a0001c0003t0008g0227a0001c0003t0008g0228others(1): Show | 4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-1145G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53518499 | ||||||
| chr12:53518815
|
C | G | 251 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(248): Show | 251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1235-1461G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53518815 | ||||||
| chr12:53518882
|
C | CA | 14 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0088others(11): Show | 14 | HG00597.hp1 HG00621.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.1235-1529dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53518882 | ||||||
| chr12:53518958
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1235-1604C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53518958 | ||||||
| chr12:53519033
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1235-1679T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519033 | ||||||
| chr12:53519053
|
C | CA | 8 | a0001c0001t0001g0063a0001c0001t0001g0150a0001c0001t0001g0151others(5): Show | 8 | HG02145.hp1 HG03225.hp2 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.1235-1700dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519053 | ||||||
| chr12:53519053
|
CA | C | 19 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(16): Show | 19 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1235-1700delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519053 | ||||||
| chr12:53519177
|
G | T | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1235-1823C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519177 | ||||||
| chr12:53519246
|
G | C | 1 | a0001c0001t0001g0253 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1235-1892C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519246 | ||||||
| chr12:53519443
|
T | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0096 | 3 | HG00738.hp2 HG01243.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1235-2089A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519443 | ||||||
| chr12:53519501
|
A | G | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1235-2147T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519501 | ||||||
| chr12:53519563
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1235-2209C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519563 | ||||||
| chr12:53519642
|
T | G | 40 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(37): Show | 40 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.1235-2288A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519642 | ||||||
| chr12:53519648
|
T | C | 6 | a0001c0001t0001g0101a0001c0001t0006g0141a0001c0001t0006g0142others(3): Show | 6 | HG01884.hp1 NA18947.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1235-2294A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519648 | ||||||
| chr12:53519950
|
G | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0158 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1235-2596C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519950 | ||||||
| chr12:53520161
|
G | T | 1 | a0001c0001t0001g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1235-2807C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520161 | ||||||
| chr12:53520369
|
G | A | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1234+2907C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520369 | ||||||
| chr12:53520527
|
C | CA | 25 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0198others(22): Show | 25 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.1234+2748dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520527 | ||||||
| chr12:53520627
|
A | T | 4 | a0001c0003t0008g0225a0001c0003t0008g0227a0001c0003t0008g0228others(1): Show | 4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234+2649T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520627 | ||||||
| chr12:53520681
|
T | C | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234+2595A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520681 | ||||||
| chr12:53520705
|
T | G | 1 | a0001c0001t0022g0169 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1234+2571A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520705 | ||||||
| chr12:53520765
|
T | C | 1 | a0001c0001t0003g0185 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1234+2511A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520765 | ||||||
| chr12:53520896
|
C | T | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1234+2380G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520896 | ||||||
| chr12:53520993
|
A | AT | 54 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(51): Show | 54 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.1234+2282dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520993 | ||||||
| chr12:53520993
|
AT | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234+2282delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520993 | ||||||
| chr12:53521045
|
C | T | 250 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(247): Show | 250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1234+2231G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521045 | ||||||
| chr12:53521137
|
C | T | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234+2139G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521137 | ||||||
| chr12:53521233
|
A | C | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(252): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1234+2043T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521233 | ||||||
| chr12:53521234
|
C | T | 2 | a0001c0003t0001g0235a0001c0003t0030g0330 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1234+2042G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521234 | ||||||
| chr12:53521401
|
G | A | 1 | a0001c0006t0001g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1234+1875C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521401 | ||||||
| chr12:53521458
|
G | A | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1234+1818C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521458 | ||||||
| chr12:53521681
|
T | C | 1 | a0001c0001t0028g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1234+1595A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521681 | ||||||
| chr12:53521738
|
C | G | 40 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1234+1538G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521738 | ||||||
| chr12:53522052
|
G | A | 24 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(21): Show | 24 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1234+1224C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522052 | ||||||
| chr12:53522170
|
G | A | 2 | a0001c0001t0012g0254a0001c0001t0012g0284 | 2 | NA18948.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1234+1106C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522170 | ||||||
| chr12:53522449
|
C | T | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1234+827G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522449 | ||||||
| chr12:53522503
|
A | G | 2 | a0001c0001t0002g0124a0001c0001t0002g0128 | 2 | HG00423.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1234+773T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522503 | ||||||
| chr12:53522506
|
C | A | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234+770G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522506 | ||||||
| chr12:53522507
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0282 | 2 | NA18954.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1234+769G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522507 | ||||||
| chr12:53522514
|
G | A | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234+762C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522514 | ||||||
| chr12:53522677
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234+599G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522677 | ||||||
| chr12:53522695
|
G | A | 22 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0065others(19): Show | 22 | HG00140.hp2 HG00738.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1234+581C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522695 | ||||||
| chr12:53522846
|
G | A | 1 | a0001c0001t0028g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1234+430C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522846 | ||||||
| chr12:53522931
|
T | C | 23 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(20): Show | 23 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1234+345A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522931 | ||||||
| chr12:53523019
|
T | G | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1234+257A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53523019 | ||||||
| chr12:53523100
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1234+176A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53523100 | ||||||
| chr12:53523103
|
C | T | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1234+173G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53523103 | ||||||
| chr12:53523164
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0158 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1234+112G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53523164 | ||||||
| chr12:53523765
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1126-381T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 10/11 | chr12 | 53523765 | ||||||
| chr12:53524068
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1125+496A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 10/11 | chr12 | 53524068 | ||||||
| chr12:53524162
|
A | C | 1 | a0001c0001t0001g0271 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1125+402T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 10/11 | chr12 | 53524162 | ||||||
| chr12:53524338
|
G | A | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1125+226C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 10/11 | chr12 | 53524338 | ||||||
| chr12:53524865
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-104G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53524865 | ||||||
| chr12:53525065
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.928-304C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53525065 | ||||||
| chr12:53525244
|
T | G | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928-483A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53525244 | ||||||
| chr12:53525310
|
G | GC | 3 | a0001c0001t0001g0038a0001c0001t0001g0149a0001c0001t0001g0158 | 3 | HG02723.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.928-550dupG | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53525310 | ||||||
| chr12:53525424
|
A | C | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-663T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53525424 | ||||||
| chr12:53525554
|
G | C | 1 | a0001c0001t0010g0072 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.928-793C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53525554 | ||||||
| chr12:53525852
|
A | C | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-1091T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53525852 | ||||||
| chr12:53525916
|
A | C | 52 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0040others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.928-1155T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53525916 | ||||||
| chr12:53526107
|
G | A | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-1346C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526107 | ||||||
| chr12:53526163
|
G | T | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928-1402C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526163 | ||||||
| chr12:53526174
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.928-1413G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526174 | ||||||
| chr12:53526203
|
G | A | 1 | a0001c0001t0002g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.928-1442C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526203 | ||||||
| chr12:53526208
|
C | CA | 59 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0031others(56): Show | 59 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.928-1448dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526208 | ||||||
| chr12:53526208
|
CA | C | 49 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0155others(46): Show | 49 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.928-1448delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526208 | ||||||
| chr12:53526249
|
C | T | 1 | a0001c0001t0001g0259 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.928-1488G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526249 | ||||||
| chr12:53526296
|
CT | C | 40 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.928-1536delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526296 | ||||||
| chr12:53526315
|
CCCTCCTC others(2): Show |
C | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-1563_928-1555d others(11): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526315 | ||||||
| chr12:53526416
|
CTCTT | C | 6 | a0001c0003t0001g0235a0001c0003t0008g0225a0001c0003t0008g0227others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-1659_928-1656d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526416 | ||||||
| chr12:53526424
|
TATG | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0095others(1): Show | 4 | HG01943.hp1 HG02683.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-1666_928-1664d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526424 | ||||||
| chr12:53526614
|
G | T | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG01891.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-1853C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526614 | ||||||
| chr12:53526632
|
C | T | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-1871G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526632 | ||||||
| chr12:53526680
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.928-1919C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526680 | ||||||
| chr12:53526741
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.928-1980G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526741 | ||||||
| chr12:53526966
|
C | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.928-2205G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526966 | ||||||
| chr12:53527107
|
C | T | 53 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0034others(50): Show | 53 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.928-2346G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53527107 | ||||||
| chr12:53527146
|
G | A | 19 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(16): Show | 19 | HG00408.hp2 HG01099.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.928-2385C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53527146 | ||||||
| chr12:53527405
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.928-2644G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53527405 | ||||||
| chr12:53527587
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.928-2826A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53527587 | ||||||
| chr12:53527986
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.928-3225G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53527986 | ||||||
| chr12:53528032
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.928-3271T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528032 | ||||||
| chr12:53528042
|
C | T | 6 | a0001c0001t0001g0303a0001c0001t0006g0141a0001c0001t0006g0142others(3): Show | 6 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-3281G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528042 | ||||||
| chr12:53528064
|
A | G | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | NA18971.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.928-3303T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528064 | ||||||
| chr12:53528071
|
A | G | 257 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.928-3310T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528071 | ||||||
| chr12:53528076
|
T | C | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-3315A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528076 | ||||||
| chr12:53528092
|
C | T | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-3331G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528092 | ||||||
| chr12:53528399
|
G | A | 52 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0040others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.927+3345C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528399 | ||||||
| chr12:53528501
|
G | T | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.927+3243C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528501 | ||||||
| chr12:53528529
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.927+3215C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528529 | ||||||
| chr12:53528559
|
T | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.927+3185A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528559 | ||||||
| chr12:53528619
|
T | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.927+3125A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528619 | ||||||
| chr12:53528749
|
C | T | 1 | a0001c0001t0028g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.927+2995G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528749 | ||||||
| chr12:53528803
|
A | T | 1 | a0001c0001t0001g0276 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.927+2941T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528803 | ||||||
| chr12:53529060
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.927+2684G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529060 | ||||||
| chr12:53529095
|
A | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0012 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.927+2649T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529095 | ||||||
| chr12:53529279
|
A | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.927+2465T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529279 | ||||||
| chr12:53529302
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.927+2442G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529302 | ||||||
| chr12:53529313
|
C | A | 2 | a0001c0003t0001g0235a0001c0003t0030g0330 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.927+2431G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529313 | ||||||
| chr12:53529619
|
C | T | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+2125G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529619 | ||||||
| chr12:53529654
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.927+2090A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529654 | ||||||
| chr12:53529664
|
CAT | C | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+2078_927+2079d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529664 | ||||||
| chr12:53529664
|
CATATATA others(13): Show |
C | 4 | a0001c0003t0008g0225a0001c0003t0008g0227a0001c0003t0008g0228others(1): Show | 4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+2060_927+2079d others(22): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529664 | ||||||
| chr12:53529694
|
C | T | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+2050G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529694 | ||||||
| chr12:53529694
|
CAT | C | 13 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(10): Show | 13 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.927+2048_927+2049d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529694 | ||||||
| chr12:53529700
|
T | TACAC | 4 | a0001c0001t0006g0141a0001c0001t0006g0143a0001c0001t0006g0144others(1): Show | 4 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+2043_927+2044i others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529700 | ||||||
| chr12:53529700
|
T | TACACATA others(11): Show |
1 | a0001c0001t0006g0142 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.927+2043_927+2044i others(20): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529700 | ||||||
| chr12:53529702
|
T | C | 1 | a0001c0001t0006g0142 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.927+2042A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529702 | ||||||
| chr12:53529702
|
T | TACAC | 5 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+2041_927+2042i others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529702 | ||||||
| chr12:53529704
|
T | C | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+2040A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529704 | ||||||
| chr12:53529704
|
T | TATACACA others(11): Show |
1 | a0001c0001t0001g0203 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.927+2039_927+2040i others(20): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529704 | ||||||
| chr12:53529710
|
T | C | 13 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(10): Show | 13 | HG01243.hp2 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.927+2034A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | ||||||
| chr12:53529710
|
T | TAC | 7 | a0001c0001t0010g0070a0001c0001t0010g0071a0001c0001t0010g0072others(4): Show | 7 | HG01074.hp2 HG01081.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+2032_927+2033d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | ||||||
| chr12:53529710
|
T | TACACACA others(3): Show |
16 | a0001c0001t0001g0242a0001c0001t0001g0251a0001c0001t0001g0252others(13): Show | 16 | HG00140.hp1 HG00738.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.927+2024_927+2033d others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | ||||||
| chr12:53529710
|
T | TACACACA others(5): Show |
43 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0167others(40): Show | 43 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.927+2022_927+2033d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | ||||||
| chr12:53529710
|
T | TACACACA others(7): Show |
63 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0056others(60): Show | 63 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.927+2020_927+2033d others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | ||||||
| chr12:53529710
|
T | TACACACA others(9): Show |
49 | a0001c0001t0001g0149a0001c0001t0001g0158a0001c0001t0001g0197others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.927+2018_927+2033d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | ||||||
| chr12:53529710
|
T | TACACACA others(11): Show |
9 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(6): Show | 9 | HG00639.hp1 HG01934.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+2016_927+2033d others(20): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | ||||||
| chr12:53529710
|
T | TACACACA others(13): Show |
2 | a0001c0003t0001g0235a0001c0003t0030g0330 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.927+2014_927+2033d others(22): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | ||||||
| chr12:53529710
|
T | TACACACA others(15): Show |
1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.927+2012_927+2033d others(24): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | ||||||
| chr12:53529710
|
T | TATACACA others(5): Show |
1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+2033_927+2034i others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | ||||||
| chr12:53529710
|
T | TATACACA others(7): Show |
6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+2033_927+2034i others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | ||||||
| chr12:53529710
|
T | TATACACA others(9): Show |
20 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0023others(17): Show | 20 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.927+2033_927+2034i others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | ||||||
| chr12:53529710
|
T | TATACACA others(11): Show |
13 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0121others(10): Show | 13 | HG00423.hp2 HG00609.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.927+2033_927+2034i others(20): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | ||||||
| chr12:53529710
|
T | TATACACA others(13): Show |
2 | a0001c0001t0002g0122a0001c0001t0002g0153 | 2 | HG03942.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.927+2033_927+2034i others(22): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | ||||||
| chr12:53529734
|
C | CACACACA others(25): Show |
1 | a0001c0001t0001g0042 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.927+2009_927+2010i others(34): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | ||||||
| chr12:53529734
|
C | CACACACA others(23): Show |
1 | a0001c0001t0001g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.927+2009_927+2010i others(32): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | ||||||
| chr12:53529734
|
C | CACACACA others(19): Show |
1 | a0001c0001t0001g0097 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.927+2009_927+2010i others(28): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | ||||||
| chr12:53529734
|
C | CACACACA others(21): Show |
5 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0052others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+2009_927+2010i others(30): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | ||||||
| chr12:53529734
|
C | CACACACA others(19): Show |
5 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+2009_927+2010i others(28): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | ||||||
| chr12:53529734
|
C | CACACACA others(15): Show |
1 | a0001c0001t0001g0198 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.927+2009_927+2010i others(24): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | ||||||
| chr12:53529734
|
C | CACACACA others(13): Show |
1 | a0001c0001t0001g0211 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.927+2009_927+2010i others(22): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | ||||||
| chr12:53529734
|
C | CACACACA others(11): Show |
2 | a0001c0001t0001g0046a0001c0001t0014g0030 | 2 | HG02647.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.927+2009_927+2010i others(20): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | ||||||
| chr12:53529734
|
C | CACACACA others(7): Show |
3 | a0001c0001t0006g0141a0001c0001t0006g0143a0001c0001t0006g0144 | 3 | NA18947.hp1 NA18984.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.927+2009_927+2010i others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | ||||||
| chr12:53529734
|
C | CACACACA others(9): Show |
3 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0055 | 3 | HG02257.hp2 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.927+2009_927+2010i others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | ||||||
| chr12:53529734
|
C | CACACACA others(5): Show |
1 | a0001c0001t0006g0145 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.927+2009_927+2010i others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | ||||||
| chr12:53529736
|
T | C | 103 | a0001c0001t0001g0038a0001c0001t0001g0056a0001c0001t0001g0167others(100): Show | 103 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.927+2008A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529736 | ||||||
| chr12:53529738
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0018g0273 | 2 | HG02723.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.927+2006A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529738 | ||||||
| chr12:53529857
|
C | T | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.927+1887G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529857 | ||||||
| chr12:53529912
|
T | A | 172 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(169): Show | 172 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.927+1832A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529912 | ||||||
| chr12:53529982
|
T | C | 1 | a0001c0001t0029g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.927+1762A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529982 | ||||||
| chr12:53530383
|
T | G | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.927+1361A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53530383 | ||||||
| chr12:53530404
|
G | A | 1 | a0001c0001t0007g0113 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.927+1340C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53530404 | ||||||
| chr12:53530426
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.927+1318A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53530426 | ||||||
| chr12:53530509
|
T | C | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(252): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.927+1235A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53530509 | ||||||
| chr12:53530567
|
T | C | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.927+1177A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53530567 | ||||||
| chr12:53530568
|
A | AT | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+1175dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53530568 | ||||||
| chr12:53530575
|
T | A | 39 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(36): Show | 39 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.927+1169A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53530575 | ||||||
| chr12:53531079
|
G | C | 40 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.927+665C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531079 | ||||||
| chr12:53531156
|
C | T | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+588G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531156 | ||||||
| chr12:53531157
|
A | G | 69 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0034others(66): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.927+587T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531157 | ||||||
| chr12:53531175
|
T | C | 69 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0034others(66): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.927+569A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531175 | ||||||
| chr12:53531208
|
G | C | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.927+536C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531208 | ||||||
| chr12:53531422
|
C | CA | 17 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0150others(14): Show | 17 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.927+321dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531422 | ||||||
| chr12:53531447
|
C | T | 1 | a0001c0001t0001g0311 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.927+297G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531447 | ||||||
| chr12:53531461
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.927+283A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531461 | ||||||
| chr12:53531574
|
A | G | 44 | a0001c0001t0001g0155a0001c0001t0002g0001a0001c0001t0002g0022others(41): Show | 44 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.927+170T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531574 | ||||||
| chr12:53531587
|
G | A | 40 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.927+157C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531587 | ||||||
| chr12:53531973
|
A | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.775-77T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 8/11 | chr12 | 53531973 | ||||||
| chr12:53532124
|
G | C | 19 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(16): Show | 19 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.775-228C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 8/11 | chr12 | 53532124 | ||||||
| chr12:53532468
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.774+42A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 8/11 | chr12 | 53532468 | ||||||
| chr12:53532478
|
G | A | 86 | a0001c0001t0001g0056a0001c0001t0001g0183a0001c0001t0001g0237others(83): Show | 86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.774+32C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 8/11 | chr12 | 53532478 | ||||||
| chr12:53532639
|
GA | G | 76 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0033others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.661-17delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 7/11 | chr12 | 53532639 | ||||||
| chr12:53532705
|
G | A | 19 | a0001c0001t0001g0195a0001c0001t0001g0199a0001c0001t0001g0200others(16): Show | 19 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.661-82C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 7/11 | chr12 | 53532705 | ||||||
| chr12:53532842
|
G | T | 1 | a0001c0001t0002g0110 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.661-219C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 7/11 | chr12 | 53532842 | ||||||
| chr12:53532872
|
T | A | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(252): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.661-249A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 7/11 | chr12 | 53532872 | ||||||
| chr12:53532990
|
T | C | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0157 | 3 | HG02145.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.660+170A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 7/11 | chr12 | 53532990 | ||||||
| chr12:53533066
|
T | C | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+94A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 7/11 | chr12 | 53533066 | ||||||
| chr12:53533105
|
G | A | 40 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.660+55C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 7/11 | chr12 | 53533105 | ||||||
| chr12:53533419
|
A | T | 1 | a0001c0001t0001g0277 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.561-160T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53533419 | ||||||
| chr12:53533770
|
C | A | 52 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0040others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.561-511G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53533770 | ||||||
| chr12:53533896
|
C | T | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.560+606G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53533896 | ||||||
| chr12:53533922
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.560+580T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53533922 | ||||||
| chr12:53533977
|
T | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0180a0001c0001t0003g0165 | 3 | NA18954.hp1 NA18970.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.560+525A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53533977 | ||||||
| chr12:53533999
|
T | C | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(252): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.560+503A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53533999 | ||||||
| chr12:53534080
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.560+422C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53534080 | ||||||
| chr12:53534342
|
TAAA | T | 15 | a0001c0001t0001g0242a0001c0001t0001g0251a0001c0001t0001g0262others(12): Show | 15 | HG00140.hp1 HG00738.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.560+157_560+159del others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53534342 | ||||||
| chr12:53534360
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.560+142A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53534360 | ||||||
| chr12:53535008
|
C | G | 1 | a0001c0001t0001g0307 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.403-349G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535008 | ||||||
| chr12:53535149
|
T | C | 4 | a0001c0003t0008g0225a0001c0003t0008g0227a0001c0003t0008g0228others(1): Show | 4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-490A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535149 | ||||||
| chr12:53535328
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0097a0001c0001t0014g0030 | 2 | HG01099.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.403-679_403-670dup others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | ||||||
| chr12:53535328
|
C | CAAAAAAA others(4): Show |
15 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0045others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.403-680_403-670dup others(11): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | ||||||
| chr12:53535328
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.403-681_403-670dup others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | ||||||
| chr12:53535328
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0015g0032 | 3 | HG02572.hp2 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.403-684_403-670dup others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | ||||||
| chr12:53535328
|
C | CAAAAAAA others(9): Show |
6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(3): Show | 6 | HG02145.hp2 HG02523.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.403-685_403-670dup others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | ||||||
| chr12:53535328
|
C | CAAAAAAA others(10): Show |
19 | a0001c0001t0002g0001a0001c0001t0002g0110a0001c0001t0002g0119others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.403-686_403-670dup others(17): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | ||||||
| chr12:53535328
|
C | CAAAAAAA others(11): Show |
10 | a0001c0001t0002g0116a0001c0001t0002g0118a0001c0001t0002g0120others(7): Show | 10 | HG02056.hp2 HG02300.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.403-670_403-669ins others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | ||||||
| chr12:53535328
|
C | CAAAAAAA others(12): Show |
10 | a0001c0001t0002g0024a0001c0001t0002g0112a0001c0001t0002g0115others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.403-670_403-669ins others(19): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | ||||||
| chr12:53535328
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0002g0026 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.403-670_403-669ins others(20): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | ||||||
| chr12:53535328
|
C | CAAAAAAA others(14): Show |
2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | NA18941.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.403-670_403-669ins others(21): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | ||||||
| chr12:53535328
|
C | CAAAAAAA others(16): Show |
4 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(1): Show | 4 | NA18947.hp1 NA18984.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-670_403-669ins others(23): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | ||||||
| chr12:53535328
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0006g0145 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.403-670_403-669ins others(24): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | ||||||
| chr12:53535533
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.403-874A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535533 | ||||||
| chr12:53535576
|
G | A | 1 | a0001c0001t0003g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.403-917C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535576 | ||||||
| chr12:53535599
|
G | T | 70 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0034others(67): Show | 70 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.403-940C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535599 | ||||||
| chr12:53535652
|
G | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | NA18944.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.403-993C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535652 | ||||||
| chr12:53535684
|
C | G | 1 | a0001c0001t0002g0154 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.403-1025G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535684 | ||||||
| chr12:53535758
|
C | T | 19 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(16): Show | 19 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.403-1099G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535758 | ||||||
| chr12:53535881
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.403-1222G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535881 | ||||||
| chr12:53535882
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0240 | 2 | NA19068.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.403-1223C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535882 | ||||||
| chr12:53535888
|
C | G | 6 | a0001c0001t0001g0066a0001c0001t0001g0091a0001c0001t0009g0041others(3): Show | 6 | HG01261.hp2 HG01433.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-1229G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535888 | ||||||
| chr12:53536033
|
A | C | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(252): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.403-1374T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536033 | ||||||
| chr12:53536226
|
T | C | 6 | a0001c0003t0001g0235a0001c0003t0008g0225a0001c0003t0008g0227others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+1189A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536226 | ||||||
| chr12:53536299
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.402+1116G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536299 | ||||||
| chr12:53536315
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.402+1100G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536315 | ||||||
| chr12:53536316
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.402+1099C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536316 | ||||||
| chr12:53536615
|
C | T | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.402+800G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536615 | ||||||
| chr12:53536616
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.402+799C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536616 | ||||||
| chr12:53536758
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.402+657G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536758 | ||||||
| chr12:53537161
|
T | C | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(252): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.402+254A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53537161 | ||||||
| chr12:53537223
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.402+192G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53537223 | ||||||
| chr12:53537263
|
TTCTCCAT others(1): Show |
T | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.402+144_402+151del others(8): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53537263 | ||||||
| chr12:53537274
|
GCCC | G | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.402+138_402+140del others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53537274 | ||||||
| chr12:53537725
|
A | G | 1 | a0001c0001t0004g0186 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.265-173T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53537725 | ||||||
| chr12:53537844
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.265-292G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53537844 | ||||||
| chr12:53537991
|
A | C | 70 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0034others(67): Show | 70 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.265-439T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53537991 | ||||||
| chr12:53538149
|
A | G | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.265-597T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53538149 | ||||||
| chr12:53538241
|
G | A | 19 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(16): Show | 19 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.265-689C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53538241 | ||||||
| chr12:53538535
|
T | C | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.265-983A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53538535 | ||||||
| chr12:53538912
|
T | C | 14 | a0001c0001t0001g0197a0001c0001t0001g0201a0001c0001t0001g0202others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.265-1360A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53538912 | ||||||
| chr12:53538972
|
C | A | 5 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0153others(2): Show | 5 | HG02698.hp2 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-1420G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53538972 | ||||||
| chr12:53539050
|
A | G | 56 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(53): Show | 56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.265-1498T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539050 | ||||||
| chr12:53539229
|
G | T | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | NA18971.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.265-1677C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539229 | ||||||
| chr12:53539282
|
A | G | 1 | a0001c0001t0003g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.265-1730T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539282 | ||||||
| chr12:53539561
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-2009G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539561 | ||||||
| chr12:53539686
|
C | CAATG | 11 | a0001c0001t0001g0036a0001c0001t0001g0060a0001c0001t0001g0061others(8): Show | 11 | HG01433.hp1 HG02135.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.265-2138_265-2135d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539686 | ||||||
| chr12:53539686
|
CAATG | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.265-2138_265-2135d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539686 | ||||||
| chr12:53539686
|
CAATGAAT others(5): Show |
C | 20 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(17): Show | 20 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.265-2146_265-2135d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539686 | ||||||
| chr12:53539686
|
CAATGAAT others(9): Show |
C | 178 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(175): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.265-2150_265-2135d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539686 | ||||||
| chr12:53539686
|
CAATGAAT others(17): Show |
C | 1 | a0001c0001t0001g0256 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.265-2158_265-2135d others(26): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539686 | ||||||
| chr12:53539792
|
G | C | 1 | a0001c0001t0001g0305 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.265-2240C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539792 | ||||||
| chr12:53539969
|
C | G | 1 | a0001c0001t0003g0185 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.265-2417G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539969 | ||||||
| chr12:53539976
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.265-2424C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539976 | ||||||
| chr12:53540014
|
C | A | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-2462G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53540014 | ||||||
| chr12:53540291
|
C | T | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.265-2739G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53540291 | ||||||
| chr12:53540348
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.265-2796C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53540348 | ||||||
| chr12:53540352
|
C | CA | 58 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(55): Show | 58 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.265-2801dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53540352 | ||||||
| chr12:53540352
|
CA | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0170others(5): Show | 8 | HG01099.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.265-2801delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53540352 | ||||||
| chr12:53540590
|
G | A | 1 | a0001c0001t0028g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.264+2740C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53540590 | ||||||
| chr12:53540775
|
G | C | 3 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024 | 3 | NA18941.hp1 NA18973.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.264+2555C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53540775 | ||||||
| chr12:53541156
|
A | C | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.264+2174T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541156 | ||||||
| chr12:53541257
|
G | A | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+2073C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541257 | ||||||
| chr12:53541311
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.264+2019A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541311 | ||||||
| chr12:53541516
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.264+1814G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541516 | ||||||
| chr12:53541537
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.264+1793C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541537 | ||||||
| chr12:53541730
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.264+1600G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541730 | ||||||
| chr12:53541744
|
G | T | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.264+1586C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541744 | ||||||
| chr12:53541859
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.264+1471A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541859 | ||||||
| chr12:53542019
|
G | A | 195 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.264+1311C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542019 | ||||||
| chr12:53542107
|
G | GT | 7 | a0001c0001t0001g0067a0001c0001t0001g0075a0001c0001t0001g0089others(4): Show | 7 | HG00741.hp2 HG01361.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+1222dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | ||||||
| chr12:53542107
|
G | GTTTTTTT others(1): Show |
13 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0045others(10): Show | 13 | HG01099.hp1 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.264+1215_264+1222d others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | ||||||
| chr12:53542107
|
G | GTTTTTTT others(2): Show |
6 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0048others(3): Show | 6 | HG01109.hp2 HG02055.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.264+1214_264+1222d others(11): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | ||||||
| chr12:53542107
|
G | GTTTTTTT others(3): Show |
5 | a0001c0001t0001g0203a0001c0003t0008g0227a0001c0003t0008g0228others(2): Show | 5 | HG01243.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+1213_264+1222d others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | ||||||
| chr12:53542107
|
G | GTTTTTTT others(4): Show |
95 | a0001c0001t0001g0149a0001c0001t0001g0158a0001c0001t0001g0193others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.264+1212_264+1222d others(13): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | ||||||
| chr12:53542107
|
G | GTTTTTTT others(5): Show |
29 | a0001c0001t0001g0038a0001c0001t0001g0183a0001c0001t0001g0195others(26): Show | 29 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.264+1211_264+1222d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | ||||||
| chr12:53542107
|
G | GTTTTTTT others(6): Show |
5 | a0001c0001t0001g0251a0001c0001t0001g0265a0001c0001t0001g0266others(2): Show | 5 | HG01192.hp1 HG01358.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+1210_264+1222d others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | ||||||
| chr12:53542107
|
G | GTTTTTTT others(7): Show |
1 | a0001c0001t0001g0056 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.264+1209_264+1222d others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | ||||||
| chr12:53542107
|
G | GTTTTTTT others(8): Show |
3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.264+1208_264+1222d others(17): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | ||||||
| chr12:53542107
|
G | GTTTTTTT others(9): Show |
1 | a0001c0001t0001g0232 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.264+1207_264+1222d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | ||||||
| chr12:53542107
|
G | GTTTTTTT others(10): Show |
2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.264+1206_264+1222d others(19): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | ||||||
| chr12:53542151
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0211 | 2 | NA18998.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.264+1179G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542151 | ||||||
| chr12:53542319
|
C | T | 24 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(21): Show | 24 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.264+1011G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542319 | ||||||
| chr12:53542342
|
G | A | 48 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0040others(45): Show | 48 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.264+988C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542342 | ||||||
| chr12:53542391
|
C | T | 247 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.264+939G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542391 | ||||||
| chr12:53542427
|
C | CA | 12 | a0001c0001t0001g0249a0001c0001t0001g0295a0001c0001t0001g0297others(9): Show | 12 | HG00140.hp1 HG00621.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.264+902dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542427 | ||||||
| chr12:53542461
|
C | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.264+869G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542461 | ||||||
| chr12:53542495
|
T | C | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.264+835A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542495 | ||||||
| chr12:53542754
|
A | G | 10 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0240others(7): Show | 10 | HG00423.hp1 HG02135.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.264+576T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542754 | ||||||
| chr12:53543050
|
T | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.264+280A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53543050 | ||||||
| chr12:53543055
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.264+275T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53543055 | ||||||
| chr12:53543084
|
T | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0095others(1): Show | 4 | HG01943.hp1 HG02683.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+246A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53543084 | ||||||
| chr12:53543094
|
G | T | 40 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(37): Show | 40 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.264+236C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53543094 | ||||||
| chr12:53543261
|
C | A | 1 | a0001c0001t0001g0249 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.264+69G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53543261 | ||||||
| chr12:53543323
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA18968.hp1 | splice_region_variant&intron_variant | LOW | c.264+7A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53543323 | ||||||
| chr12:53543668
|
C | T | 259 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(256): Show | 259 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.146-220G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53543668 | ||||||
| chr12:53543835
|
T | C | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.146-387A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53543835 | ||||||
| chr12:53544106
|
C | T | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.146-658G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53544106 | ||||||
| chr12:53544163
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.146-715G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53544163 | ||||||
| chr12:53544692
|
A | G | 311 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.146-1244T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53544692 | ||||||
| chr12:53544694
|
G | A | 87 | a0001c0001t0001g0056a0001c0001t0001g0237a0001c0001t0001g0238others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.146-1246C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53544694 | ||||||
| chr12:53544771
|
A | C | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.146-1323T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53544771 | ||||||
| chr12:53544906
|
CA | C | 256 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(253): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.146-1459delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53544906 | ||||||
| chr12:53544979
|
A | G | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.146-1531T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53544979 | ||||||
| chr12:53545024
|
T | C | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.146-1576A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545024 | ||||||
| chr12:53545048
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.146-1600A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545048 | ||||||
| chr12:53545129
|
G | A | 256 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(253): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.146-1681C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545129 | ||||||
| chr12:53545235
|
G | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0180a0001c0001t0003g0165 | 3 | NA18954.hp1 NA18970.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.146-1787C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545235 | ||||||
| chr12:53545329
|
T | A | 1 | a0001c0001t0002g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.146-1881A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545329 | ||||||
| chr12:53545432
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.146-1984C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545432 | ||||||
| chr12:53545481
|
C | T | 1 | a0001c0001t0003g0177 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.146-2033G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545481 | ||||||
| chr12:53545485
|
C | T | 39 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.146-2037G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545485 | ||||||
| chr12:53545499
|
G | A | 6 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0086others(3): Show | 6 | HG00735.hp1 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-2051C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545499 | ||||||
| chr12:53545505
|
T | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0180a0001c0001t0003g0165 | 3 | NA18954.hp1 NA18970.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.146-2057A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545505 | ||||||
| chr12:53545673
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.146-2225A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545673 | ||||||
| chr12:53545754
|
G | A | 4 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0153others(1): Show | 4 | HG03491.hp2 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-2306C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545754 | ||||||
| chr12:53545829
|
C | T | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.146-2381G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545829 | ||||||
| chr12:53545920
|
C | T | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.146-2472G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545920 | ||||||
| chr12:53546060
|
C | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0084a0001c0001t0001g0089 | 3 | HG03704.hp1 HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.146-2612G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546060 | ||||||
| chr12:53546065
|
G | A | 175 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.146-2617C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546065 | ||||||
| chr12:53546101
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.146-2653G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546101 | ||||||
| chr12:53546196
|
A | AAAAC | 4 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0055others(1): Show | 4 | HG00609.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-2752_146-2749d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546196 | ||||||
| chr12:53546196
|
A | AAAACAAA others(1): Show |
16 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(13): Show | 16 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.146-2756_146-2749d others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546196 | ||||||
| chr12:53546196
|
A | C | 3 | a0001c0001t0001g0198a0001c0001t0003g0027a0001c0001t0003g0028 | 3 | HG02922.hp2 HG03130.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.146-2748T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546196 | ||||||
| chr12:53546262
|
T | C | 256 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(253): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.146-2814A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546262 | ||||||
| chr12:53546313
|
T | C | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.146-2865A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546313 | ||||||
| chr12:53546375
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0004g0188 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.146-2928_146-2927i others(17): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546375 | ||||||
| chr12:53546375
|
A | AAAAAAAC others(7): Show |
194 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(191): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.146-2941_146-2928d others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546375 | ||||||
| chr12:53546383
|
A | AAAAAACA others(7): Show |
3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.146-2936_146-2935i others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546383 | ||||||
| chr12:53546456
|
CT | C | 6 | a0001c0001t0001g0062a0001c0001t0006g0141a0001c0001t0006g0142others(3): Show | 6 | HG01515.hp2 NA18947.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-3009delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546456 | ||||||
| chr12:53546460
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.146-3012A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546460 | ||||||
| chr12:53546463
|
T | C | 4 | a0001c0002t0001g0324a0001c0002t0001g0325a0001c0002t0001g0326others(1): Show | 4 | NA18962.hp1 NA18964.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-3015A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546463 | ||||||
| chr12:53546473
|
C | CAG | 256 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(253): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.146-3027_146-3026d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546473 | ||||||
| chr12:53546558
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.146-3110G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546558 | ||||||
| chr12:53546633
|
A | T | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.146-3185T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546633 | ||||||
| chr12:53546692
|
T | C | 314 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(311): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.146-3244A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546692 | ||||||
| chr12:53546694
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.146-3246G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546694 | ||||||
| chr12:53546732
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.146-3284C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546732 | ||||||
| chr12:53546747
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.146-3299C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546747 | ||||||
| chr12:53546820
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.146-3372G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546820 | ||||||
| chr12:53546872
|
C | G | 4 | a0001c0003t0008g0225a0001c0003t0008g0227a0001c0003t0008g0228others(1): Show | 4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-3424G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546872 | ||||||
| chr12:53546977
|
C | CT | 17 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0167others(14): Show | 17 | HG00738.hp2 HG01255.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.146-3530dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546977 | ||||||
| chr12:53546977
|
CTTTTTTT others(4): Show |
C | 19 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(16): Show | 19 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.146-3540_146-3530d others(13): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546977 | ||||||
| chr12:53546998
|
T | C | 12 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0063others(9): Show | 12 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.146-3550A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546998 | ||||||
| chr12:53547078
|
G | A | 16 | a0001c0001t0001g0242a0001c0001t0001g0251a0001c0001t0001g0262others(13): Show | 16 | HG00140.hp1 HG00639.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.146-3630C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547078 | ||||||
| chr12:53547132
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.146-3684G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547132 | ||||||
| chr12:53547133
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.146-3685G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547133 | ||||||
| chr12:53547283
|
C | CT | 135 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(132): Show | 135 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.146-3836dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547283 | ||||||
| chr12:53547283
|
C | CTT | 21 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0241others(18): Show | 21 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.146-3837_146-3836d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547283 | ||||||
| chr12:53547283
|
C | CTTT | 9 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(6): Show | 9 | HG02572.hp1 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.146-3838_146-3836d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547283 | ||||||
| chr12:53547283
|
C | CTTTT | 7 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(4): Show | 7 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-3839_146-3836d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547283 | ||||||
| chr12:53547283
|
CT | C | 49 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0040others(46): Show | 49 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.146-3836delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547283 | ||||||
| chr12:53547475
|
A | G | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.146-4027T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547475 | ||||||
| chr12:53547644
|
C | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.146-4196G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547644 | ||||||
| chr12:53547747
|
T | TTATG | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(15): Show | 18 | HG00621.hp2 HG01074.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.146-4303_146-4300d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547747 | ||||||
| chr12:53547747
|
TTATG | T | 67 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0078others(64): Show | 67 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.146-4303_146-4300d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547747 | ||||||
| chr12:53547747
|
TTATGTAT others(1): Show |
T | 24 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0043others(21): Show | 24 | HG01099.hp1 HG01109.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.146-4307_146-4300d others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547747 | ||||||
| chr12:53547747
|
TTATGTAT others(5): Show |
T | 128 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(125): Show | 128 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.146-4311_146-4300d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547747 | ||||||
| chr12:53547747
|
TTATGTAT others(9): Show |
T | 2 | a0001c0001t0001g0038a0001c0001t0001g0101 | 2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.146-4315_146-4300d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547747 | ||||||
| chr12:53547752
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.146-4304A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547752 | ||||||
| chr12:53547910
|
G | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.146-4462C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547910 | ||||||
| chr12:53548037
|
AT | A | 175 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.145+4503delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53548037 | ||||||
| chr12:53548191
|
G | A | 4 | a0001c0003t0008g0225a0001c0003t0008g0227a0001c0003t0008g0228others(1): Show | 4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+4350C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53548191 | ||||||
| chr12:53548535
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0053 | 3 | HG01109.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.145+4006C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53548535 | ||||||
| chr12:53548611
|
G | A | 199 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.145+3930C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53548611 | ||||||
| chr12:53548773
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.145+3768T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53548773 | ||||||
| chr12:53548878
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.145+3663C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53548878 | ||||||
| chr12:53549005
|
G | A | 40 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(37): Show | 40 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.145+3536C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549005 | ||||||
| chr12:53549008
|
C | T | 1 | a0001c0001t0021g0103 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.145+3533G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549008 | ||||||
| chr12:53549153
|
G | A | 3 | a0001c0001t0011g0081a0001c0001t0011g0083a0001c0001t0021g0103 | 3 | HG00140.hp2 HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.145+3388C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549153 | ||||||
| chr12:53549187
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.145+3354A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549187 | ||||||
| chr12:53549273
|
C | T | 59 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0040others(56): Show | 59 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.145+3268G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549273 | ||||||
| chr12:53549282
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.145+3259C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549282 | ||||||
| chr12:53549297
|
AAG | A | 190 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(187): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.145+3242_145+3243d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549297 | ||||||
| chr12:53549298
|
AG | A | 56 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(53): Show | 56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.145+3242delC | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549298 | ||||||
| chr12:53549490
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.145+3051C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549490 | ||||||
| chr12:53549575
|
G | C | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.145+2966C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549575 | ||||||
| chr12:53549723
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG02622.hp2 HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.145+2818G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549723 | ||||||
| chr12:53549879
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.145+2662G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549879 | ||||||
| chr12:53549880
|
G | A | 1 | a0001c0001t0006g0142 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.145+2661C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549880 | ||||||
| chr12:53549998
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.145+2543C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549998 | ||||||
| chr12:53550061
|
G | A | 19 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(16): Show | 19 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.145+2480C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550061 | ||||||
| chr12:53550076
|
A | G | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.145+2465T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550076 | ||||||
| chr12:53550093
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.145+2448G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550093 | ||||||
| chr12:53550094
|
A | G | 2 | a0001c0003t0001g0235a0001c0003t0030g0330 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.145+2447T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550094 | ||||||
| chr12:53550151
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0014g0030 | 2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.145+2390G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550151 | ||||||
| chr12:53550184
|
G | A | 1 | a0001c0001t0009g0079 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.145+2357C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550184 | ||||||
| chr12:53550244
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.145+2297T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550244 | ||||||
| chr12:53550323
|
C | CA | 9 | a0001c0001t0003g0175a0001c0001t0003g0178a0001c0002t0003g0189others(6): Show | 9 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.145+2217dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550323 | ||||||
| chr12:53550323
|
CAAAA | C | 70 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(67): Show | 70 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.145+2214_145+2217d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550323 | ||||||
| chr12:53550327
|
A | AAAAT | 31 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0057others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.145+2213_145+2214i others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550327 | ||||||
| chr12:53550327
|
A | AAAATAAA others(1): Show |
11 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0069others(8): Show | 11 | HG00639.hp2 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.145+2213_145+2214i others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550327 | ||||||
| chr12:53550327
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.145+2202_145+2213d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550327 | ||||||
| chr12:53550327
|
AAAAAAAA others(9): Show |
A | 2 | a0001c0003t0001g0235a0001c0003t0030g0330 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.145+2198_145+2213d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550327 | ||||||
| chr12:53550331
|
A | T | 65 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0034others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.145+2210T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550331 | ||||||
| chr12:53550331
|
AAAAT | A | 79 | a0001c0001t0001g0056a0001c0001t0001g0237a0001c0001t0001g0238others(76): Show | 79 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.145+2206_145+2209d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550331 | ||||||
| chr12:53550334
|
AT | A | 42 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.145+2206delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550334 | ||||||
| chr12:53550335
|
T | A | 42 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0105others(39): Show | 42 | HG00280.hp2 HG00408.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.145+2206A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550335 | ||||||
| chr12:53550337
|
A | T | 1 | a0001c0001t0003g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.145+2204T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550337 | ||||||
| chr12:53550339
|
T | A | 56 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0001t0001g0179others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.145+2202A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550339 | ||||||
| chr12:53550343
|
T | A | 18 | a0001c0001t0001g0170a0001c0001t0001g0183a0001c0001t0001g0191others(15): Show | 18 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.145+2198A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550343 | ||||||
| chr12:53550347
|
T | A | 3 | a0001c0001t0001g0214a0001c0001t0001g0219a0001c0001t0003g0176 | 3 | HG01993.hp1 HG02886.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.145+2194A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550347 | ||||||
| chr12:53550465
|
T | A | 4 | a0001c0003t0008g0225a0001c0003t0008g0227a0001c0003t0008g0228others(1): Show | 4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+2076A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550465 | ||||||
| chr12:53550569
|
G | C | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.145+1972C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550569 | ||||||
| chr12:53551646
|
A | C | 1 | a0001c0001t0001g0257 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.145+895T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53551646 | ||||||
| chr12:53551761
|
A | G | 181 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.145+780T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53551761 | ||||||
| chr12:53551969
|
C | A | 3 | a0001c0001t0002g0118a0001c0001t0002g0119a0001c0001t0002g0133 | 3 | HG00408.hp1 NA18955.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.145+572G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53551969 | ||||||
| chr12:53552020
|
C | T | 44 | a0001c0001t0001g0155a0001c0001t0002g0001a0001c0001t0002g0022others(41): Show | 44 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.145+521G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552020 | ||||||
| chr12:53552088
|
A | G | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0157 | 3 | HG02145.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.145+453T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552088 | ||||||
| chr12:53552107
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.145+434G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552107 | ||||||
| chr12:53552140
|
T | G | 1 | a0001c0001t0001g0247 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.145+401A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552140 | ||||||
| chr12:53552148
|
A | G | 1 | a0001c0006t0001g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.145+393T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552148 | ||||||
| chr12:53552262
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.145+279T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552262 | ||||||
| chr12:53552270
|
A | G | 43 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.145+271T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552270 | ||||||
| chr12:53552302
|
C | T | 1 | a0001c0001t0007g0113 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.145+239G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552302 | ||||||
| chr12:53552435
|
C | G | 51 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0040others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.145+106G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552435 | ||||||
| chr12:53552811
|
C | G | 179 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.49-174G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53552811 | ||||||
| chr12:53552992
|
A | G | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49-355T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53552992 | ||||||
| chr12:53553022
|
T | C | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.49-385A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53553022 | ||||||
| chr12:53553205
|
T | C | 1 | a0001c0003t0001g0235 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49-568A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53553205 | ||||||
| chr12:53553278
|
T | A | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49-641A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53553278 | ||||||
| chr12:53553388
|
G | T | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.49-751C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53553388 | ||||||
| chr12:53553456
|
T | G | 1 | a0001c0001t0002g0112 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.49-819A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53553456 | ||||||
| chr12:53553843
|
C | A | 1 | a0001c0001t0002g0115 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.49-1206G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53553843 | ||||||
| chr12:53554013
|
G | A | 1 | a0001c0001t0026g0298 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.49-1376C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554013 | ||||||
| chr12:53554127
|
TTTTA | T | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.49-1494_49-1491del others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554127 | ||||||
| chr12:53554331
|
A | T | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.49-1694T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554331 | ||||||
| chr12:53554384
|
G | A | 3 | a0001c0001t0001g0300a0001c0001t0001g0317a0001c0001t0020g0316 | 3 | HG00544.hp1 HG00673.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.49-1747C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554384 | ||||||
| chr12:53554634
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.49-1997C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554634 | ||||||
| chr12:53554660
|
C | T | 2 | a0001c0001t0002g0131a0001c0001t0002g0135 | 2 | HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.49-2023G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554660 | ||||||
| chr12:53554770
|
C | A | 23 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0199others(20): Show | 23 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.49-2133G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554770 | ||||||
| chr12:53554870
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0027g0194 | 2 | HG00673.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.49-2233C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554870 | ||||||
| chr12:53554870
|
G | GA | 18 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0034others(15): Show | 18 | HG00609.hp1 HG02145.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-2234dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554870 | ||||||
| chr12:53554870
|
G | GAA | 192 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(189): Show | 192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.49-2235_49-2234dup others(2): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554870 | ||||||
| chr12:53554870
|
G | GAAA | 21 | a0001c0001t0001g0052a0001c0001t0001g0101a0001c0001t0001g0149others(18): Show | 21 | HG00140.hp1 HG00544.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.49-2236_49-2234dup others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554870 | ||||||
| chr12:53554870
|
G | GAAAA | 17 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(14): Show | 17 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.49-2237_49-2234dup others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554870 | ||||||
| chr12:53555002
|
A | G | 16 | a0001c0001t0001g0242a0001c0001t0001g0251a0001c0001t0001g0262others(13): Show | 16 | HG00140.hp1 HG00639.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.49-2365T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555002 | ||||||
| chr12:53555078
|
G | A | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.49-2441C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555078 | ||||||
| chr12:53555101
|
C | T | 1 | a0001c0001t0003g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.49-2464G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555101 | ||||||
| chr12:53555176
|
G | A | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49-2539C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555176 | ||||||
| chr12:53555325
|
C | CA | 50 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(47): Show | 50 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.49-2689dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555325 | ||||||
| chr12:53555398
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0149a0001c0001t0001g0158 | 3 | HG02723.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.49-2761C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555398 | ||||||
| chr12:53555437
|
A | G | 6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-2800T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555437 | ||||||
| chr12:53555490
|
A | AT | 33 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(30): Show | 33 | HG00544.hp2 HG00621.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.49-2854dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | ||||||
| chr12:53555490
|
AT | A | 14 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0045others(11): Show | 14 | HG01109.hp2 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.49-2854delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | ||||||
| chr12:53555490
|
ATTT | A | 41 | a0001c0001t0001g0017a0001c0001t0001g0056a0001c0001t0001g0158others(38): Show | 41 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.49-2856_49-2854del others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | ||||||
| chr12:53555490
|
ATTTT | A | 111 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0038others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.49-2857_49-2854del others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | ||||||
| chr12:53555490
|
ATTTTT | A | 26 | a0001c0001t0001g0167a0001c0001t0001g0183a0001c0001t0001g0191others(23): Show | 26 | HG02165.hp1 HG02258.hp1 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.49-2858_49-2854del others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | ||||||
| chr12:53555490
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.49-2863_49-2854del others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | ||||||
| chr12:53555490
|
ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-2864_49-2854del others(11): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | ||||||
| chr12:53555490
|
ATTTTTTT others(5): Show |
A | 25 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0057others(22): Show | 25 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.49-2865_49-2854del others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | ||||||
| chr12:53555534
|
G | A | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.49-2897C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555534 | ||||||
| chr12:53555671
|
C | T | 179 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.49-3034G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555671 | ||||||
| chr12:53555737
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.49-3100G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555737 | ||||||
| chr12:53555753
|
G | A | 1 | a0001c0005t0001g0068 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.49-3116C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555753 | ||||||
| chr12:53556074
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0149a0001c0001t0001g0158 | 3 | HG02723.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.49-3437G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556074 | ||||||
| chr12:53556312
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.49-3675C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556312 | ||||||
| chr12:53556479
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.49-3842A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556479 | ||||||
| chr12:53556524
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.49-3887C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556524 | ||||||
| chr12:53556593
|
A | G | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.49-3956T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556593 | ||||||
| chr12:53556671
|
C | T | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.49-4034G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556671 | ||||||
| chr12:53556784
|
A | G | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.49-4147T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556784 | ||||||
| chr12:53556821
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0301 | 2 | HG02015.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.49-4184G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556821 | ||||||
| chr12:53556965
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.49-4328G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556965 | ||||||
| chr12:53557092
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.49-4455G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557092 | ||||||
| chr12:53557184
|
T | A | 40 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(37): Show | 40 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.49-4547A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557184 | ||||||
| chr12:53557265
|
G | T | 44 | a0001c0001t0001g0155a0001c0001t0002g0001a0001c0001t0002g0022others(41): Show | 44 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.49-4628C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557265 | ||||||
| chr12:53557462
|
C | A | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.49-4825G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557462 | ||||||
| chr12:53557541
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.49-4904G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557541 | ||||||
| chr12:53557632
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-4995G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557632 | ||||||
| chr12:53557663
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.49-5026G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557663 | ||||||
| chr12:53557977
|
T | C | 43 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-5340A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557977 | ||||||
| chr12:53558517
|
A | C | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.49-5880T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53558517 | ||||||
| chr12:53558629
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49-5992G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53558629 | ||||||
| chr12:53558757
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49-6120C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53558757 | ||||||
| chr12:53558940
|
T | C | 1 | a0001c0001t0003g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.49-6303A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53558940 | ||||||
| chr12:53558979
|
G | C | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.49-6342C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53558979 | ||||||
| chr12:53559101
|
G | A | 2 | a0001c0003t0001g0235a0001c0003t0030g0330 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.49-6464C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559101 | ||||||
| chr12:53559121
|
TA | T | 7 | a0001c0001t0001g0046a0001c0001t0001g0256a0001c0001t0001g0295others(4): Show | 7 | HG01168.hp2 HG02647.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-6485delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559121 | ||||||
| chr12:53559169
|
T | C | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-6532A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559169 | ||||||
| chr12:53559220
|
T | C | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-6583A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559220 | ||||||
| chr12:53559237
|
C | CT | 181 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.49-6601dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559237 | ||||||
| chr12:53559548
|
G | A | 2 | a0001c0001t0002g0131a0001c0001t0002g0135 | 2 | HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.49-6911C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559548 | ||||||
| chr12:53559556
|
G | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.49-6919C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559556 | ||||||
| chr12:53559590
|
A | C | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-6953T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559590 | ||||||
| chr12:53559656
|
G | C | 22 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0065others(19): Show | 22 | HG00140.hp2 HG00738.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.49-7019C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559656 | ||||||
| chr12:53559678
|
C | CA | 178 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(175): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.49-7042dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559678 | ||||||
| chr12:53559678
|
C | CAA | 30 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(27): Show | 30 | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.49-7043_49-7042dup others(2): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559678 | ||||||
| chr12:53559750
|
A | T | 200 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.49-7113T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559750 | ||||||
| chr12:53559963
|
C | T | 199 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.49-7326G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559963 | ||||||
| chr12:53560083
|
C | T | 6 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0086others(3): Show | 6 | HG00735.hp1 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-7446G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53560083 | ||||||
| chr12:53560220
|
C | A | 1 | a0001c0001t0001g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.49-7583G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53560220 | ||||||
| chr12:53560424
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.49-7787C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53560424 | ||||||
| chr12:53560424
|
G | GT | 6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-7788dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53560424 | ||||||
| chr12:53560948
|
CT | C | 50 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(47): Show | 50 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.49-8312delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53560948 | ||||||
| chr12:53560972
|
G | T | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.49-8335C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53560972 | ||||||
| chr12:53560992
|
C | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.49-8355G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53560992 | ||||||
| chr12:53561013
|
T | A | 199 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.49-8376A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561013 | ||||||
| chr12:53561092
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.49-8455G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561092 | ||||||
| chr12:53561231
|
C | T | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-8594G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561231 | ||||||
| chr12:53561282
|
C | T | 40 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(37): Show | 40 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.49-8645G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561282 | ||||||
| chr12:53561329
|
T | TA | 58 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0033others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.49-8693dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561329 | ||||||
| chr12:53561329
|
TA | T | 195 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.49-8693delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561329 | ||||||
| chr12:53561329
|
TAA | T | 6 | a0001c0001t0001g0101a0001c0001t0001g0248a0001c0001t0001g0251others(3): Show | 6 | HG01515.hp1 HG01884.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-8694_49-8693del others(2): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561329 | ||||||
| chr12:53561389
|
A | T | 87 | a0001c0001t0001g0056a0001c0001t0001g0237a0001c0001t0001g0238others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.49-8752T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561389 | ||||||
| chr12:53561701
|
A | C | 40 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(37): Show | 40 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.49-9064T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561701 | ||||||
| chr12:53561922
|
C | T | 43 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-9285G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561922 | ||||||
| chr12:53561958
|
TGAA | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-9324_49-9322del others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561958 | ||||||
| chr12:53562121
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.49-9484C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562121 | ||||||
| chr12:53562181
|
A | G | 87 | a0001c0001t0001g0056a0001c0001t0001g0237a0001c0001t0001g0238others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.49-9544T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562181 | ||||||
| chr12:53562250
|
G | A | 1 | a0001c0001t0009g0041 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.49-9613C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562250 | ||||||
| chr12:53562255
|
C | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0261 | 2 | NA18983.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.49-9618G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562255 | ||||||
| chr12:53562258
|
T | C | 1 | a0001c0001t0006g0142 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.49-9621A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562258 | ||||||
| chr12:53562306
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.49-9669G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562306 | ||||||
| chr12:53562321
|
C | A | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-9684G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562321 | ||||||
| chr12:53562635
|
C | CA | 19 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(16): Show | 19 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.49-9999dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562635 | ||||||
| chr12:53562635
|
CA | C | 12 | a0001c0001t0001g0073a0001c0001t0006g0141a0001c0001t0006g0142others(9): Show | 12 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.49-9999delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562635 | ||||||
| chr12:53562659
|
C | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0261 | 2 | NA18983.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.49-10022G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562659 | ||||||
| chr12:53562662
|
A | G | 199 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.49-10025T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562662 | ||||||
| chr12:53562730
|
C | A | 1 | a0001c0001t0001g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.49-10093G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562730 | ||||||
| chr12:53562797
|
C | A | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-10160G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562797 | ||||||
| chr12:53563026
|
T | C | 315 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.49-10389A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563026 | ||||||
| chr12:53563043
|
C | A | 6 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0086others(3): Show | 6 | HG00735.hp1 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-10406G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563043 | ||||||
| chr12:53563058
|
G | A | 199 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.49-10421C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563058 | ||||||
| chr12:53563177
|
T | C | 45 | a0001c0001t0001g0149a0001c0001t0001g0158a0001c0001t0001g0193others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.49-10540A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563177 | ||||||
| chr12:53563459
|
GA | G | 195 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.49-10823delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563459 | ||||||
| chr12:53563546
|
G | T | 28 | a0001c0001t0001g0168a0001c0001t0001g0180a0001c0001t0003g0165others(25): Show | 28 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.49-10909C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563546 | ||||||
| chr12:53563570
|
T | C | 43 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-10933A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563570 | ||||||
| chr12:53563702
|
T | A | 66 | a0001c0001t0001g0056a0001c0001t0001g0237a0001c0001t0001g0238others(63): Show | 66 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.49-11065A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563702 | ||||||
| chr12:53563744
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.49-11107C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563744 | ||||||
| chr12:53563798
|
G | A | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-11161C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563798 | ||||||
| chr12:53563802
|
T | C | 28 | a0001c0001t0001g0168a0001c0001t0001g0180a0001c0001t0003g0165others(25): Show | 28 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.49-11165A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563802 | ||||||
| chr12:53563843
|
G | C | 1 | a0001c0001t0002g0132 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.49-11206C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563843 | ||||||
| chr12:53563886
|
A | G | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.49-11249T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563886 | ||||||
| chr12:53563939
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.49-11302T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563939 | ||||||
| chr12:53564175
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.49-11538C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564175 | ||||||
| chr12:53564259
|
C | T | 43 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0023others(40): Show | 43 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-11622G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564259 | ||||||
| chr12:53564293
|
C | T | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(252): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.49-11656G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564293 | ||||||
| chr12:53564301
|
A | G | 199 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.49-11664T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564301 | ||||||
| chr12:53564386
|
C | G | 1 | a0001c0001t0003g0177 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.49-11749G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564386 | ||||||
| chr12:53564471
|
C | A | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49-11834G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564471 | ||||||
| chr12:53564475
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.49-11838A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564475 | ||||||
| chr12:53564680
|
A | G | 6 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0179others(3): Show | 6 | HG02258.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-12043T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564680 | ||||||
| chr12:53564689
|
G | T | 4 | a0001c0001t0004g0160a0001c0001t0004g0162a0001c0001t0004g0163others(1): Show | 4 | HG02074.hp1 NA18971.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-12052C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564689 | ||||||
| chr12:53564921
|
G | A | 178 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(175): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.49-12284C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564921 | ||||||
| chr12:53565035
|
C | T | 1 | a0001c0001t0006g0143 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.49-12398G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53565035 | ||||||
| chr12:53565302
|
GT | G | 20 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(17): Show | 20 | HG01099.hp1 HG01109.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.49-12666delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53565302 | ||||||
| chr12:53565493
|
C | CG | 26 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0085others(23): Show | 26 | HG00673.hp2 HG00735.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.49-12857dupC | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53565493 | ||||||
| chr12:53565493
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.49-12856G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53565493 | ||||||
| chr12:53565501
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.49-12864T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53565501 | ||||||
| chr12:53565602
|
C | T | 2 | a0001c0001t0001g0300a0001c0001t0020g0316 | 2 | HG00673.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.49-12965G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53565602 | ||||||
| chr12:53565905
|
A | G | 19 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(16): Show | 19 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.49-13268T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53565905 | ||||||
| chr12:53566142
|
A | G | 3 | a0001c0001t0003g0184a0001c0001t0017g0173a0001c0001t0022g0169 | 3 | NA18999.hp1 NA19002.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.49-13505T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566142 | ||||||
| chr12:53566405
|
A | G | 90 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.49-13768T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566405 | ||||||
| chr12:53566449
|
A | G | 1 | a0001c0002t0003g0189 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.49-13812T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566449 | ||||||
| chr12:53566700
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.49-14063C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566700 | ||||||
| chr12:53566740
|
G | GT | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-14104dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566740 | ||||||
| chr12:53566753
|
T | C | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-14116A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566753 | ||||||
| chr12:53566767
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0158 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.49-14130C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566767 | ||||||
| chr12:53566836
|
C | T | 1 | a0001c0001t0029g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.49-14199G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566836 | ||||||
| chr12:53566952
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.49-14315G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566952 | ||||||
| chr12:53566998
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49-14361G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566998 | ||||||
| chr12:53567103
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.49-14466G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567103 | ||||||
| chr12:53567159
|
G | A | 6 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0179others(3): Show | 6 | HG02258.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-14522C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567159 | ||||||
| chr12:53567178
|
A | G | 87 | a0001c0001t0001g0056a0001c0001t0001g0237a0001c0001t0001g0238others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.49-14541T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567178 | ||||||
| chr12:53567232
|
T | G | 1 | a0001c0001t0002g0022 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.49-14595A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567232 | ||||||
| chr12:53567509
|
C | A | 2 | a0001c0001t0003g0322a0001c0001t0003g0323 | 2 | HG02280.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.49-14872G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567509 | ||||||
| chr12:53567671
|
G | C | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-15034C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567671 | ||||||
| chr12:53567693
|
A | AATTGCTT others(3): Show |
1 | a0001c0001t0002g0022 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.49-15066_49-15057d others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567693 | ||||||
| chr12:53567709
|
G | T | 51 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0040others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.49-15072C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567709 | ||||||
| chr12:53568225
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.49-15588G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53568225 | ||||||
| chr12:53568392
|
G | GCA | 6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-15757_49-15756d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53568392 | ||||||
| chr12:53568644
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0015 | 2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.49-16007A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53568644 | ||||||
| chr12:53568789
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.49-16152T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53568789 | ||||||
| chr12:53568793
|
G | C | 1 | a0001c0006t0001g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.49-16156C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53568793 | ||||||
| chr12:53568827
|
G | T | 175 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.49-16190C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53568827 | ||||||
| chr12:53569129
|
G | A | 87 | a0001c0001t0001g0056a0001c0001t0001g0237a0001c0001t0001g0238others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.49-16492C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53569129 | ||||||
| chr12:53569518
|
G | A | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49-16881C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53569518 | ||||||
| chr12:53569670
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.49-17033T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53569670 | ||||||
| chr12:53569679
|
T | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0098 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.49-17042A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53569679 | ||||||
| chr12:53569681
|
A | AT | 98 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(95): Show | 98 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.49-17045dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53569681 | ||||||
| chr12:53569714
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49-17077C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53569714 | ||||||
| chr12:53569824
|
A | G | 56 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(53): Show | 56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.49-17187T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53569824 | ||||||
| chr12:53570030
|
G | T | 51 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0040others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.49-17393C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570030 | ||||||
| chr12:53570267
|
A | G | 4 | a0001c0001t0001g0196a0001c0001t0001g0217a0001c0001t0001g0218others(1): Show | 4 | HG00597.hp2 NA18959.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-17630T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570267 | ||||||
| chr12:53570268
|
T | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0329 | 2 | HG01943.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.49-17631A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570268 | ||||||
| chr12:53570349
|
G | T | 51 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0040others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.49-17712C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570349 | ||||||
| chr12:53570729
|
CTGTGTGC others(1): Show |
C | 6 | a0001c0001t0002g0001a0001c0001t0002g0116a0001c0001t0002g0122others(3): Show | 6 | HG00741.hp2 HG02135.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-18100_49-18093d others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570729 | ||||||
| chr12:53570729
|
CTGTGTGC others(5): Show |
C | 1 | a0001c0001t0002g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.49-18104_49-18093d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570729 | ||||||
| chr12:53570729
|
CTGTGTGC others(13): Show |
C | 4 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0136others(1): Show | 4 | HG01261.hp1 HG01943.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-18112_49-18093d others(22): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570729 | ||||||
| chr12:53570730
|
TGTGTGC | T | 12 | a0001c0001t0002g0026a0001c0001t0002g0110a0001c0001t0002g0112others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.49-18099_49-18094d others(8): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570730 | ||||||
| chr12:53570732
|
TGTGC | T | 13 | a0001c0001t0002g0022a0001c0001t0002g0109a0001c0001t0002g0115others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.49-18099_49-18096d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570732 | ||||||
| chr12:53570734
|
TGC | T | 7 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0117others(4): Show | 7 | HG02698.hp2 NA18941.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-18099_49-18098d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570734 | ||||||
| chr12:53570736
|
C | CGT | 5 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0150others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-18101_49-18100d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570736 | ||||||
| chr12:53570736
|
CGT | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(71): Show | 74 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.49-18101_49-18100d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570736 | ||||||
| chr12:53570736
|
CGTGT | C | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0075others(5): Show | 8 | HG01361.hp1 HG02630.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.49-18103_49-18100d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570736 | ||||||
| chr12:53570736
|
CGTGTGT | C | 54 | a0001c0001t0001g0038a0001c0001t0001g0149a0001c0001t0001g0158others(51): Show | 54 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.49-18105_49-18100d others(8): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570736 | ||||||
| chr12:53570736
|
CGTGTGTG others(1): Show |
C | 121 | a0001c0001t0001g0018a0001c0001t0001g0056a0001c0001t0001g0168others(118): Show | 121 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.49-18107_49-18100d others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570736 | ||||||
| chr12:53570736
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0003g0177 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.49-18109_49-18100d others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570736 | ||||||
| chr12:53570736
|
CGTGTGTG others(5): Show |
C | 1 | a0001c0001t0001g0272 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.49-18111_49-18100d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570736 | ||||||
| chr12:53570777
|
A | G | 43 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0023others(40): Show | 43 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-18140T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570777 | ||||||
| chr12:53570850
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.49-18213T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570850 | ||||||
| chr12:53571078
|
G | A | 4 | a0001c0003t0008g0225a0001c0003t0008g0227a0001c0003t0008g0228others(1): Show | 4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-18441C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571078 | ||||||
| chr12:53571084
|
C | A | 56 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(53): Show | 56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.49-18447G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571084 | ||||||
| chr12:53571411
|
T | C | 4 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0309others(1): Show | 4 | HG00735.hp2 HG01934.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-18774A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571411 | ||||||
| chr12:53571552
|
A | G | 3 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0003g0178 | 3 | HG02622.hp1 HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.49-18915T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571552 | ||||||
| chr12:53571638
|
TA | T | 7 | a0001c0001t0001g0058a0001c0001t0001g0074a0001c0001t0001g0217others(4): Show | 7 | HG00639.hp2 HG01167.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-19002delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571638 | ||||||
| chr12:53571639
|
A | T | 229 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(226): Show | 229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.49-19002T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571639 | ||||||
| chr12:53571640
|
A | T | 4 | a0001c0001t0001g0217a0001c0001t0001g0232a0001c0001t0001g0295others(1): Show | 4 | HG01167.hp1 HG02698.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-19003T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571640 | ||||||
| chr12:53571770
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.49-19133A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571770 | ||||||
| chr12:53571935
|
C | T | 175 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.49-19298G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571935 | ||||||
| chr12:53572071
|
A | C | 1 | a0001c0001t0001g0240 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.49-19434T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572071 | ||||||
| chr12:53572264
|
A | C | 2 | a0001c0003t0001g0235a0001c0003t0030g0330 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.49-19627T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572264 | ||||||
| chr12:53572273
|
C | A | 1 | a0001c0001t0003g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.49-19636G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572273 | ||||||
| chr12:53572562
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0297 | 2 | HG00140.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.49-19925C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572562 | ||||||
| chr12:53572669
|
G | C | 1 | a0001c0001t0001g0180 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.49-20032C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572669 | ||||||
| chr12:53572699
|
C | T | 1 | a0001c0001t0028g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.49-20062G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572699 | ||||||
| chr12:53572787
|
A | T | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-20150T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572787 | ||||||
| chr12:53572803
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.49-20166A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572803 | ||||||
| chr12:53572853
|
T | G | 87 | a0001c0001t0001g0056a0001c0001t0001g0237a0001c0001t0001g0238others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.49-20216A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572853 | ||||||
| chr12:53573084
|
C | CA | 22 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(19): Show | 22 | HG01099.hp1 HG01109.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.49-20448dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573084 | ||||||
| chr12:53573282
|
C | T | 87 | a0001c0001t0001g0056a0001c0001t0001g0237a0001c0001t0001g0238others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.49-20645G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573282 | ||||||
| chr12:53573374
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.49-20737A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573374 | ||||||
| chr12:53573599
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.49-20962G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573599 | ||||||
| chr12:53573616
|
T | C | 1 | a0001c0001t0003g0174 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.49-20979A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573616 | ||||||
| chr12:53573644
|
T | G | 44 | a0001c0001t0001g0155a0001c0001t0002g0001a0001c0001t0002g0022others(41): Show | 44 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.49-21007A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573644 | ||||||
| chr12:53573658
|
T | A | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.49-21021A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573658 | ||||||
| chr12:53573777
|
C | T | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-21140G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573777 | ||||||
| chr12:53573811
|
G | T | 44 | a0001c0001t0001g0155a0001c0001t0002g0001a0001c0001t0002g0022others(41): Show | 44 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.49-21174C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573811 | ||||||
| chr12:53573944
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0055 | 2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.49-21307G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573944 | ||||||
| chr12:53574487
|
C | T | 6 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0086others(3): Show | 6 | HG00735.hp1 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-21850G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574487 | ||||||
| chr12:53574718
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.49-22081C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574718 | ||||||
| chr12:53574800
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.49-22163C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574800 | ||||||
| chr12:53574915
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.49-22278C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574915 | ||||||
| chr12:53574932
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.49-22295A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574932 | ||||||
| chr12:53574953
|
C | CA | 93 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(90): Show | 93 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.49-22317dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574953 | ||||||
| chr12:53574953
|
CA | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0034others(6): Show | 9 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.49-22317delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574953 | ||||||
| chr12:53574974
|
G | A | 4 | a0001c0001t0001g0251a0001c0001t0001g0278a0001c0001t0001g0283others(1): Show | 4 | HG01192.hp1 HG01515.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-22337C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574974 | ||||||
| chr12:53575174
|
G | A | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-22537C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575174 | ||||||
| chr12:53575179
|
A | G | 1 | a0001c0001t0011g0083 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22542T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575179 | ||||||
| chr12:53575182
|
C | T | 1 | a0001c0001t0011g0083 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22545G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575182 | ||||||
| chr12:53575187
|
C | A | 1 | a0001c0001t0011g0083 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22550G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575187 | ||||||
| chr12:53575197
|
T | C | 1 | a0001c0001t0011g0083 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22560A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575197 | ||||||
| chr12:53575198
|
G | A | 1 | a0001c0001t0011g0083 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22561C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575198 | ||||||
| chr12:53575199
|
A | G | 1 | a0001c0001t0011g0083 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22562T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575199 | ||||||
| chr12:53575206
|
G | A | 1 | a0001c0001t0011g0083 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22569C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575206 | ||||||
| chr12:53575208
|
G | C | 1 | a0001c0001t0011g0083 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22571C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575208 | ||||||
| chr12:53575407
|
T | TA | 56 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0054others(53): Show | 56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.49-22771dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575407 | ||||||
| chr12:53575407
|
TA | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(10): Show | 13 | HG00099.hp1 HG01074.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.49-22771delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575407 | ||||||
| chr12:53575574
|
C | CA | 7 | a0001c0001t0001g0056a0001c0001t0001g0086a0001c0001t0001g0233others(4): Show | 7 | HG00597.hp1 HG01169.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-22938dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575574 | ||||||
| chr12:53575574
|
C | CAAAAAAA others(3): Show |
50 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(47): Show | 50 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.49-22947_49-22938d others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575574 | ||||||
| chr12:53575574
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0002g0122a0001c0001t0002g0128a0001c0001t0002g0131 | 3 | HG00423.hp2 HG01433.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.49-22948_49-22938d others(13): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575574 | ||||||
| chr12:53575682
|
T | C | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-23045A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575682 | ||||||
| chr12:53575988
|
A | G | 1 | a0001c0001t0025g0315 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.49-23351T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575988 | ||||||
| chr12:53576102
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0158 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.49-23465T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53576102 | ||||||
| chr12:53576140
|
T | G | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.49-23503A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53576140 | ||||||
| chr12:53576377
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.49-23740A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53576377 | ||||||
| chr12:53576409
|
T | A | 1 | a0001c0001t0006g0145 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.49-23772A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53576409 | ||||||
| chr12:53576701
|
AAAAC | A | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-24068_49-24065d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53576701 | ||||||
| chr12:53577023
|
T | C | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+23930A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577023 | ||||||
| chr12:53577212
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.48+23741G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577212 | ||||||
| chr12:53577411
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0158 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.48+23542A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577411 | ||||||
| chr12:53577413
|
G | A | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+23540C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577413 | ||||||
| chr12:53577426
|
AAC | A | 56 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(53): Show | 56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.48+23525_48+23526d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577426 | ||||||
| chr12:53577444
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0014g0030 | 2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.48+23509G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577444 | ||||||
| chr12:53577471
|
C | T | 180 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(177): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.48+23482G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577471 | ||||||
| chr12:53577513
|
G | T | 1 | a0001c0001t0001g0306 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.48+23440C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577513 | ||||||
| chr12:53577542
|
C | T | 87 | a0001c0001t0001g0056a0001c0001t0001g0237a0001c0001t0001g0238others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.48+23411G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577542 | ||||||
| chr12:53577702
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.48+23251G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577702 | ||||||
| chr12:53577717
|
G | GA | 45 | a0001c0001t0001g0218a0001c0001t0002g0001a0001c0001t0002g0022others(42): Show | 45 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.48+23235dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577717 | ||||||
| chr12:53577728
|
A | AAAAG | 52 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(49): Show | 52 | HG00280.hp2 HG00733.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.48+23221_48+23224d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577728 | ||||||
| chr12:53577728
|
A | G | 1 | a0001c0001t0004g0186 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.48+23225T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577728 | ||||||
| chr12:53577730
|
AAG | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+23221_48+23222d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577730 | ||||||
| chr12:53577732
|
G | A | 49 | a0001c0001t0001g0155a0001c0001t0002g0001a0001c0001t0002g0022others(46): Show | 49 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.48+23221C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577732 | ||||||
| chr12:53577736
|
G | A | 51 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.48+23217C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577736 | ||||||
| chr12:53577771
|
G | C | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+23182C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577771 | ||||||
| chr12:53578048
|
G | A | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+22905C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578048 | ||||||
| chr12:53578124
|
G | A | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+22829C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578124 | ||||||
| chr12:53578367
|
C | CA | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(56): Show | 59 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.48+22585dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578367 | ||||||
| chr12:53578367
|
CA | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01258.hp2 HG01433.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+22585delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578367 | ||||||
| chr12:53578367
|
CAA | C | 211 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.48+22584_48+22585d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578367 | ||||||
| chr12:53578367
|
CAAA | C | 11 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(8): Show | 11 | HG02257.hp1 HG02486.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+22583_48+22585d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578367 | ||||||
| chr12:53578783
|
C | CA | 7 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0151others(4): Show | 7 | HG02145.hp1 HG03688.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+22169dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578783 | ||||||
| chr12:53578783
|
CA | C | 133 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0033others(130): Show | 133 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.48+22169delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578783 | ||||||
| chr12:53579344
|
CCAAAATA others(12): Show |
C | 1 | a0001c0001t0001g0007 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.48+21590_48+21608d others(21): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53579344 | ||||||
| chr12:53579444
|
C | T | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.48+21509G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53579444 | ||||||
| chr12:53579551
|
C | CA | 22 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0034others(19): Show | 22 | HG00597.hp2 HG00738.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+21401dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53579551 | ||||||
| chr12:53579842
|
C | CCT | 44 | a0001c0001t0001g0155a0001c0001t0002g0001a0001c0001t0002g0022others(41): Show | 44 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.48+21109_48+21110d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53579842 | ||||||
| chr12:53579843
|
C | T | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+21110G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53579843 | ||||||
| chr12:53579958
|
C | T | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+20995G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53579958 | ||||||
| chr12:53579990
|
G | C | 180 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(177): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.48+20963C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53579990 | ||||||
| chr12:53580075
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.48+20878G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580075 | ||||||
| chr12:53580210
|
C | T | 40 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(37): Show | 40 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.48+20743G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580210 | ||||||
| chr12:53580235
|
A | T | 1 | a0001c0001t0001g0274 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.48+20718T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580235 | ||||||
| chr12:53580267
|
CA | C | 19 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(16): Show | 19 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.48+20685delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580267 | ||||||
| chr12:53580332
|
G | T | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | NA18971.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.48+20621C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580332 | ||||||
| chr12:53580387
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.48+20566C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580387 | ||||||
| chr12:53580559
|
A | G | 56 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(53): Show | 56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.48+20394T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580559 | ||||||
| chr12:53580621
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.48+20332C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580621 | ||||||
| chr12:53580663
|
C | CA | 10 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0200others(7): Show | 10 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+20289dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580663 | ||||||
| chr12:53580663
|
CA | C | 52 | a0001c0001t0001g0067a0001c0001t0001g0076a0001c0001t0001g0149others(49): Show | 52 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.48+20289delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580663 | ||||||
| chr12:53580845
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.48+20108G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580845 | ||||||
| chr12:53581021
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0012 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.48+19932T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581021 | ||||||
| chr12:53581022
|
G | C | 1 | a0001c0001t0003g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48+19931C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581022 | ||||||
| chr12:53581029
|
T | G | 1 | a0001c0001t0001g0076 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.48+19924A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581029 | ||||||
| chr12:53581111
|
CA | C | 56 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(53): Show | 56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.48+19841delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581111 | ||||||
| chr12:53581119
|
A | T | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.48+19834T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581119 | ||||||
| chr12:53581223
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.48+19730A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581223 | ||||||
| chr12:53581541
|
C | G | 1 | a0001c0001t0001g0005 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.48+19412G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581541 | ||||||
| chr12:53581604
|
G | T | 4 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0291others(1): Show | 4 | HG02135.hp1 HG02523.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+19349C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581604 | ||||||
| chr12:53581704
|
T | C | 1 | a0001c0001t0002g0024 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.48+19249A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581704 | ||||||
| chr12:53581774
|
C | T | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+19179G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581774 | ||||||
| chr12:53581874
|
G | A | 1 | a0001c0001t0014g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.48+19079C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581874 | ||||||
| chr12:53581930
|
C | T | 70 | a0001c0001t0001g0056a0001c0001t0001g0237a0001c0001t0001g0238others(67): Show | 70 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.48+19023G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581930 | ||||||
| chr12:53581967
|
A | T | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG01891.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+18986T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581967 | ||||||
| chr12:53582122
|
A | T | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+18831T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582122 | ||||||
| chr12:53582197
|
C | T | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+18756G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582197 | ||||||
| chr12:53582198
|
G | A | 2 | a0001c0001t0002g0131a0001c0001t0002g0135 | 2 | HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.48+18755C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582198 | ||||||
| chr12:53582199
|
C | T | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.48+18754G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582199 | ||||||
| chr12:53582200
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0197 | 2 | HG00099.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.48+18753C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582200 | ||||||
| chr12:53582212
|
C | T | 1 | a0001c0001t0028g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.48+18741G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582212 | ||||||
| chr12:53582306
|
C | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG02145.hp1 HG02723.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+18647G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582306 | ||||||
| chr12:53582326
|
T | TA | 8 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0214others(5): Show | 8 | HG00423.hp1 HG01169.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+18626dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582326 | ||||||
| chr12:53582483
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.48+18470G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582483 | ||||||
| chr12:53582494
|
GA | G | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+18458delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582494 | ||||||
| chr12:53582563
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.48+18390T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582563 | ||||||
| chr12:53582664
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.48+18289G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582664 | ||||||
| chr12:53583041
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.48+17912T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583041 | ||||||
| chr12:53583066
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.48+17887A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583066 | ||||||
| chr12:53583244
|
C | G | 1 | a0001c0001t0001g0269 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.48+17709G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583244 | ||||||
| chr12:53583460
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.48+17493A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583460 | ||||||
| chr12:53583533
|
T | G | 229 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(226): Show | 229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.48+17420A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583533 | ||||||
| chr12:53583640
|
C | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0158 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.48+17313G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583640 | ||||||
| chr12:53583641
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.48+17312C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583641 | ||||||
| chr12:53583705
|
G | T | 11 | a0001c0001t0001g0155a0001c0001t0002g0147a0001c0001t0002g0148others(8): Show | 11 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.48+17248C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583705 | ||||||
| chr12:53583926
|
C | CAAATAAG others(9): Show |
1 | a0001c0001t0001g0012 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.48+17011_48+17026d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583926 | ||||||
| chr12:53584197
|
T | G | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+16756A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53584197 | ||||||
| chr12:53584229
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.48+16724C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53584229 | ||||||
| chr12:53584312
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+16641G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53584312 | ||||||
| chr12:53584365
|
T | C | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+16588A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53584365 | ||||||
| chr12:53584504
|
C | T | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+16449G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53584504 | ||||||
| chr12:53584517
|
T | C | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+16436A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53584517 | ||||||
| chr12:53584931
|
A | G | 241 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(238): Show | 241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.48+16022T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53584931 | ||||||
| chr12:53585048
|
C | T | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+15905G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585048 | ||||||
| chr12:53585131
|
C | A | 4 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(1): Show | 4 | NA18941.hp1 NA18973.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+15822G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585131 | ||||||
| chr12:53585465
|
C | A | 38 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0023others(35): Show | 38 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.48+15488G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585465 | ||||||
| chr12:53585465
|
C | T | 1 | a0001c0001t0003g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.48+15488G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585465 | ||||||
| chr12:53585552
|
A | T | 1 | a0001c0001t0002g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.48+15401T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585552 | ||||||
| chr12:53585632
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+15321T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585632 | ||||||
| chr12:53585721
|
A | C | 240 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(237): Show | 240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.48+15232T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585721 | ||||||
| chr12:53585721
|
ACACTGAT others(5): Show |
A | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+15220_48+15231d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585721 | ||||||
| chr12:53586002
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.48+14951G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586002 | ||||||
| chr12:53586148
|
C | T | 1 | a0001c0001t0009g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.48+14805G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586148 | ||||||
| chr12:53586307
|
C | T | 213 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(210): Show | 213 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.48+14646G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586307 | ||||||
| chr12:53586410
|
TA | T | 195 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.48+14542delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586410 | ||||||
| chr12:53586650
|
A | G | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+14303T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586650 | ||||||
| chr12:53586783
|
T | A | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+14170A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586783 | ||||||
| chr12:53586801
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+14152T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586801 | ||||||
| chr12:53586810
|
C | G | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+14143G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586810 | ||||||
| chr12:53586832
|
C | T | 11 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+14121G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586832 | ||||||
| chr12:53587037
|
C | T | 218 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(215): Show | 218 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.48+13916G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587037 | ||||||
| chr12:53587093
|
A | G | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+13860T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587093 | ||||||
| chr12:53587104
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.48+13849G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587104 | ||||||
| chr12:53587204
|
T | C | 1 | a0001c0001t0028g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.48+13749A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587204 | ||||||
| chr12:53587275
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0097 | 2 | HG01099.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.48+13678C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587275 | ||||||
| chr12:53587353
|
C | T | 7 | a0001c0001t0002g0109a0001c0001t0002g0118a0001c0001t0002g0119others(4): Show | 7 | HG00408.hp1 HG02056.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+13600G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587353 | ||||||
| chr12:53587366
|
C | CAA | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+13585_48+13586d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(5): Show |
63 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0180others(60): Show | 63 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.48+13575_48+13586d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(6): Show |
37 | a0001c0001t0001g0168a0001c0001t0001g0179a0001c0001t0001g0265others(34): Show | 37 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.48+13574_48+13586d others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(7): Show |
5 | a0001c0001t0001g0197a0001c0001t0001g0245a0001c0001t0001g0294others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+13573_48+13586d others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0003g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.48+13572_48+13586d others(17): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0280 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.48+13571_48+13586d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(16): Show |
9 | a0001c0001t0001g0243a0001c0001t0001g0248a0001c0001t0001g0252others(6): Show | 9 | HG01256.hp2 HG03195.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+13586_48+13587i others(25): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(17): Show |
30 | a0001c0001t0001g0201a0001c0001t0001g0205a0001c0001t0001g0212others(27): Show | 30 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.48+13586_48+13587i others(26): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(18): Show |
34 | a0001c0001t0001g0056a0001c0001t0001g0193a0001c0001t0001g0195others(31): Show | 34 | HG00597.hp1 HG01081.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.48+13586_48+13587i others(27): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(19): Show |
11 | a0001c0001t0001g0210a0001c0001t0001g0216a0001c0001t0001g0277others(8): Show | 11 | HG00408.hp2 HG00735.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+13586_48+13587i others(28): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(20): Show |
5 | a0001c0001t0001g0238a0001c0001t0001g0257a0001c0001t0001g0258others(2): Show | 5 | HG00423.hp1 HG00621.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+13586_48+13587i others(29): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(21): Show |
3 | a0001c0001t0001g0203a0001c0001t0001g0215a0001c0001t0001g0261 | 3 | HG01243.hp2 HG02015.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.48+13586_48+13587i others(30): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(22): Show |
7 | a0001c0001t0001g0204a0001c0001t0001g0209a0001c0001t0001g0219others(4): Show | 7 | HG00099.hp2 HG00609.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+13586_48+13587i others(31): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(23): Show |
1 | a0001c0001t0001g0202 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.48+13586_48+13587i others(32): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0300 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.48+13586_48+13587i others(33): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0237 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.48+13586_48+13587i others(34): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(28): Show |
1 | a0001c0001t0001g0321 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.48+13586_48+13587i others(37): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587366
|
C | CAAAAAAA others(29): Show |
3 | a0001c0001t0001g0244a0001c0001t0001g0246a0001c0001t0027g0194 | 3 | HG00673.hp2 NA18994.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.48+13586_48+13587i others(38): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | ||||||
| chr12:53587568
|
G | A | 39 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0023others(36): Show | 39 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.48+13385C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587568 | ||||||
| chr12:53587589
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.48+13364G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587589 | ||||||
| chr12:53587642
|
G | C | 240 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(237): Show | 240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.48+13311C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587642 | ||||||
| chr12:53587671
|
CA | C | 14 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.48+13281delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587671 | ||||||
| chr12:53587820
|
C | CATATATA others(1): Show |
4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0090others(1): Show | 4 | HG00639.hp2 HG01099.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+13125_48+13132d others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | ||||||
| chr12:53587820
|
C | CATATATA others(3): Show |
2 | a0001c0001t0001g0073a0001c0001t0001g0245 | 2 | HG01070.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.48+13123_48+13132d others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | ||||||
| chr12:53587820
|
C | CATATATA others(5): Show |
3 | a0001c0001t0001g0247a0001c0001t0001g0319a0001c0001t0010g0072 | 3 | HG00639.hp1 NA18941.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.48+13121_48+13132d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | ||||||
| chr12:53587820
|
C | CATATATA others(7): Show |
3 | a0001c0001t0001g0040a0001c0001t0001g0255a0001c0001t0025g0315 | 3 | HG01070.hp2 HG03017.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.48+13119_48+13132d others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | ||||||
| chr12:53587820
|
C | CATATATA others(9): Show |
1 | a0001c0001t0029g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.48+13117_48+13132d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | ||||||
| chr12:53587820
|
C | CATATATA others(13): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0091a0001c0006t0001g0082 | 3 | HG02080.hp1 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.48+13113_48+13132d others(22): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | ||||||
| chr12:53587820
|
C | CATATATA others(17): Show |
1 | a0001c0001t0001g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.48+13109_48+13132d others(26): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | ||||||
| chr12:53587820
|
C | CATATATA others(19): Show |
1 | a0001c0001t0001g0251 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.48+13132_48+13133i others(28): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | ||||||
| chr12:53587820
|
C | CATATATA others(13): Show |
2 | a0001c0003t0001g0235a0001c0003t0030g0330 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.48+13132_48+13133i others(22): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | ||||||
| chr12:53587824
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.48+13129A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587824 | ||||||
| chr12:53587839
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.48+13114T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587839 | ||||||
| chr12:53587839
|
ATATATT | A | 35 | a0001c0001t0001g0149a0001c0001t0001g0195a0001c0001t0001g0196others(32): Show | 35 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.48+13108_48+13113d others(8): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587839 | ||||||
| chr12:53587840
|
TATA | T | 21 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0023others(18): Show | 21 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.48+13110_48+13112d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587840 | ||||||
| chr12:53587841
|
A | AT | 3 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143 | 3 | NA18947.hp1 NA18984.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.48+13111dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587841 | ||||||
| chr12:53587841
|
ATAT | A | 14 | a0001c0001t0001g0170a0001c0001t0001g0183a0001c0001t0001g0190others(11): Show | 14 | HG02056.hp2 HG02165.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.48+13109_48+13111d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587841 | ||||||
| chr12:53587843
|
A | AT | 6 | a0001c0001t0001g0037a0001c0001t0001g0105a0001c0001t0001g0106others(3): Show | 6 | HG01891.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+13109dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0264a0001c0001t0001g0297 | 2 | HG00140.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0038a0001c0001t0001g0234 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(23): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(16): Show |
3 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0002t0005g0171 | 3 | HG01168.hp1 HG01168.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(25): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0009g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(34): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0055 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(30): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0093 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(32): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(19): Show |
4 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0085others(1): Show | 4 | HG00735.hp1 HG01261.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+13109_48+13110i others(28): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0011g0081 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(29): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(21): Show |
5 | a0001c0001t0001g0031a0001c0001t0001g0065a0001c0001t0001g0084others(2): Show | 5 | HG01943.hp1 HG02148.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+13109_48+13110i others(30): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0329 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(26): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0094a0001c0001t0009g0079 | 2 | HG01243.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(28): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0080 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.48+13109_48+13110i others(30): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0066a0001c0001t0001g0100 | 2 | NA18943.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(24): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0089 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(25): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0047a0001c0001t0001g0078 | 2 | HG02257.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(26): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0150 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(29): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(14): Show |
4 | a0001c0001t0001g0097a0001c0001t0001g0232a0001c0001t0001g0233others(1): Show | 4 | HG01099.hp1 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+13109_48+13110i others(23): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0151a0001c0001t0001g0157 | 2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(25): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0146a0001c0001t0009g0041 | 2 | HG01433.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(26): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0087 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(28): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(25): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0060a0001c0005t0001g0068 | 2 | HG02559.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0102 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.48+13109_48+13110i others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0313 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.48+13109_48+13110i others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(3): Show |
3 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0057 | 3 | HG00099.hp1 HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.48+13109_48+13110i others(13): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0076 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.48+13109_48+13110i others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(1): Show |
6 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 6 | HG01074.hp2 HG01081.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+13109_48+13110i others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATATAT others(3): Show |
8 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 8 | HG01109.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.48+13109_48+13110i others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | ATATTTTT others(6): Show |
1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+13109_48+13110i others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
A | T | 7 | a0001c0001t0001g0012a0001c0001t0002g0115a0001c0001t0006g0141others(4): Show | 7 | HG02897.hp1 HG03195.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+13110T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
AT | A | 17 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(14): Show | 17 | HG00423.hp2 HG00544.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.48+13109delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587843
|
ATTT | A | 13 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0179others(10): Show | 13 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.48+13107_48+13109d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | ||||||
| chr12:53587844
|
T | TA | 14 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0033others(11): Show | 14 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | ||||||
| chr12:53587844
|
T | TATA | 3 | a0001c0001t0001g0018a0001c0001t0001g0036a0001c0001t0014g0030 | 3 | HG02257.hp1 HG03831.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.48+13108_48+13109i others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | ||||||
| chr12:53587844
|
T | TATATATA others(2): Show |
12 | a0001c0001t0001g0237a0001c0001t0001g0241a0001c0001t0001g0250others(9): Show | 12 | HG00408.hp2 HG00423.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(11): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | ||||||
| chr12:53587844
|
T | TATATATA others(4): Show |
14 | a0001c0001t0001g0244a0001c0001t0001g0246a0001c0001t0001g0259others(11): Show | 14 | HG02135.hp1 HG02293.hp1 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(13): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | ||||||
| chr12:53587844
|
T | TATATATA others(6): Show |
16 | a0001c0001t0001g0238a0001c0001t0001g0242a0001c0001t0001g0257others(13): Show | 16 | HG01192.hp1 HG01361.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | ||||||
| chr12:53587844
|
T | TATATATA others(8): Show |
8 | a0001c0001t0001g0056a0001c0001t0001g0253a0001c0001t0001g0256others(5): Show | 8 | HG00597.hp1 HG00735.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(17): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | ||||||
| chr12:53587844
|
T | TATATATA others(10): Show |
4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0292others(1): Show | 4 | HG03654.hp2 HG03710.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(19): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | ||||||
| chr12:53587844
|
T | TATATATA others(12): Show |
8 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0265others(5): Show | 8 | HG01255.hp2 HG01358.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(21): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | ||||||
| chr12:53587844
|
T | TATATATA others(14): Show |
4 | a0001c0001t0001g0280a0001c0001t0001g0320a0001c0001t0001g0321others(1): Show | 4 | HG04228.hp2 NA18971.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(23): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | ||||||
| chr12:53587844
|
T | TATATATA others(20): Show |
3 | a0001c0001t0001g0061a0001c0001t0001g0301a0001c0001t0001g0304 | 3 | HG02683.hp1 NA18970.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.48+13108_48+13109i others(29): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | ||||||
| chr12:53587844
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0019 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.48+13108_48+13109i others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | ||||||
| chr12:53587845
|
T | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0245a0001c0001t0001g0247others(6): Show | 9 | HG00639.hp1 HG01070.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+13108A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587845 | ||||||
| chr12:53587846
|
T | A | 67 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0240others(64): Show | 67 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.48+13107A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587846 | ||||||
| chr12:53587847
|
T | A | 7 | a0001c0001t0001g0245a0001c0001t0001g0247a0001c0001t0001g0319others(4): Show | 7 | HG00639.hp1 HG01070.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+13106A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587847 | ||||||
| chr12:53587848
|
T | A | 40 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0240others(37): Show | 40 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.48+13105A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587848 | ||||||
| chr12:53587849
|
T | A | 2 | a0001c0001t0001g0245a0001c0001t0012g0254 | 2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.48+13104A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587849 | ||||||
| chr12:53587850
|
T | A | 14 | a0001c0001t0001g0253a0001c0001t0001g0280a0001c0001t0001g0281others(11): Show | 14 | HG00673.hp1 HG00735.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.48+13103A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587850 | ||||||
| chr12:53587851
|
T | A | 1 | a0001c0001t0012g0254 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.48+13102A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587851 | ||||||
| chr12:53587852
|
T | A | 9 | a0001c0001t0001g0253a0001c0001t0001g0280a0001c0001t0001g0281others(6): Show | 9 | HG00735.hp2 HG01934.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+13101A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587852 | ||||||
| chr12:53587854
|
T | A | 1 | a0001c0001t0004g0162 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.48+13099A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587854 | ||||||
| chr12:53587866
|
ACACGAAG others(7): Show |
A | 1 | a0001c0001t0001g0255 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.48+13073_48+13086d others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587866 | ||||||
| chr12:53588747
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.48+12206G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53588747 | ||||||
| chr12:53588850
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0069a0001c0001t0001g0076others(2): Show | 5 | HG00733.hp1 HG01256.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+12103T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53588850 | ||||||
| chr12:53588903
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.48+12050C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53588903 | ||||||
| chr12:53589756
|
C | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0329 | 2 | HG01943.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.48+11197G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53589756 | ||||||
| chr12:53590106
|
G | T | 1 | a0001c0001t0001g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.48+10847C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53590106 | ||||||
| chr12:53590130
|
C | G | 1 | a0001c0001t0001g0251 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.48+10823G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53590130 | ||||||
| chr12:53590367
|
G | A | 10 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 10 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.48+10586C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53590367 | ||||||
| chr12:53590724
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.48+10229A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53590724 | ||||||
| chr12:53590750
|
A | G | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.48+10203T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53590750 | ||||||
| chr12:53590959
|
T | C | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+9994A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53590959 | ||||||
| chr12:53591124
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.48+9829A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53591124 | ||||||
| chr12:53591249
|
CACGGCTA others(3): Show |
C | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.48+9694_48+9703del others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53591249 | ||||||
| chr12:53591633
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.48+9320A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53591633 | ||||||
| chr12:53591789
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+9164A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53591789 | ||||||
| chr12:53592002
|
G | C | 1 | a0001c0001t0001g0278 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.48+8951C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53592002 | ||||||
| chr12:53592267
|
A | G | 5 | a0001c0001t0002g0109a0001c0001t0002g0118a0001c0001t0002g0119others(2): Show | 5 | HG00408.hp1 HG02056.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+8686T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53592267 | ||||||
| chr12:53592570
|
A | AATAGATT others(5): Show |
1 | a0001c0001t0001g0255 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.48+8371_48+8382dup others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53592570 | ||||||
| chr12:53592619
|
G | A | 1 | a0001c0001t0003g0185 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.48+8334C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53592619 | ||||||
| chr12:53592984
|
C | T | 11 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+7969G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53592984 | ||||||
| chr12:53593140
|
A | G | 44 | a0001c0001t0001g0042a0001c0001t0001g0193a0001c0001t0001g0195others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.48+7813T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53593140 | ||||||
| chr12:53593231
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.48+7722G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53593231 | ||||||
| chr12:53594045
|
G | A | 315 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.48+6908C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594045 | ||||||
| chr12:53594242
|
A | C | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+6711T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594242 | ||||||
| chr12:53594568
|
G | A | 1 | a0001c0001t0004g0160 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.48+6385C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594568 | ||||||
| chr12:53594625
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.48+6328G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594625 | ||||||
| chr12:53594807
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.48+6146C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594807 | ||||||
| chr12:53594825
|
T | C | 6 | a0001c0001t0001g0155a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+6128A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594825 | ||||||
| chr12:53594874
|
C | A | 1 | a0001c0001t0007g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.48+6079G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594874 | ||||||
| chr12:53594880
|
C | T | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.48+6073G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594880 | ||||||
| chr12:53594887
|
C | CA | 18 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(15): Show | 18 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.48+6065dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594887 | ||||||
| chr12:53594887
|
CA | C | 6 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0179others(3): Show | 6 | HG02258.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+6065delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594887 | ||||||
| chr12:53594901
|
G | A | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+6052C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594901 | ||||||
| chr12:53594901
|
GA | G | 10 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0240others(7): Show | 10 | HG00423.hp1 HG02135.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+6051delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594901 | ||||||
| chr12:53594902
|
A | G | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+6051T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594902 | ||||||
| chr12:53595000
|
T | C | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+5953A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53595000 | ||||||
| chr12:53595054
|
G | T | 1 | a0001c0001t0003g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48+5899C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53595054 | ||||||
| chr12:53595159
|
T | C | 11 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+5794A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53595159 | ||||||
| chr12:53595720
|
T | C | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+5233A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53595720 | ||||||
| chr12:53596019
|
C | T | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+4934G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596019 | ||||||
| chr12:53596087
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.48+4866A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596087 | ||||||
| chr12:53596110
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.48+4843A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596110 | ||||||
| chr12:53596129
|
C | G | 1 | a0001c0001t0024g0239 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.48+4824G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596129 | ||||||
| chr12:53596157
|
G | A | 1 | a0001c0001t0007g0130 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.48+4796C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596157 | ||||||
| chr12:53596396
|
TGAG | T | 43 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.48+4554_48+4556del others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596396 | ||||||
| chr12:53596422
|
C | T | 6 | a0001c0001t0001g0066a0001c0001t0001g0091a0001c0001t0009g0041others(3): Show | 6 | HG01261.hp2 HG01433.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+4531G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596422 | ||||||
| chr12:53596540
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.48+4413G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596540 | ||||||
| chr12:53596565
|
C | A | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+4388G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596565 | ||||||
| chr12:53596847
|
T | C | 43 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.48+4106A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596847 | ||||||
| chr12:53596866
|
T | C | 90 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.48+4087A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596866 | ||||||
| chr12:53596872
|
C | T | 92 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(89): Show | 92 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.48+4081G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596872 | ||||||
| chr12:53597020
|
A | C | 11 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+3933T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597020 | ||||||
| chr12:53597035
|
G | C | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+3918C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597035 | ||||||
| chr12:53597111
|
T | C | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.48+3842A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597111 | ||||||
| chr12:53597186
|
G | GT | 10 | a0001c0001t0001g0149a0001c0001t0001g0158a0001c0001t0001g0202others(7): Show | 10 | HG01167.hp2 HG02970.hp2 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+3766dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597186 | ||||||
| chr12:53597380
|
C | T | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+3573G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597380 | ||||||
| chr12:53597385
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.48+3568A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597385 | ||||||
| chr12:53597537
|
C | T | 51 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0040others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.48+3416G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597537 | ||||||
| chr12:53597678
|
G | A | 17 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0044others(14): Show | 17 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.48+3275C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597678 | ||||||
| chr12:53597737
|
A | G | 1 | a0001c0001t0002g0026 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.48+3216T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597737 | ||||||
| chr12:53597782
|
T | C | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+3171A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597782 | ||||||
| chr12:53597787
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.48+3166G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597787 | ||||||
| chr12:53597788
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.48+3165C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597788 | ||||||
| chr12:53597808
|
C | CA | 44 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.48+3144dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597808 | ||||||
| chr12:53597808
|
C | CAA | 6 | a0001c0001t0001g0108a0001c0001t0001g0195a0001c0002t0001g0324others(3): Show | 6 | HG01934.hp1 HG02896.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+3143_48+3144dup others(2): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597808 | ||||||
| chr12:53597808
|
C | CAAA | 10 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 10 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.48+3142_48+3144dup others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597808 | ||||||
| chr12:53598725
|
T | C | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+2228A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53598725 | ||||||
| chr12:53598794
|
T | C | 6 | a0001c0001t0001g0155a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+2159A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53598794 | ||||||
| chr12:53598867
|
A | G | 43 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.48+2086T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53598867 | ||||||
| chr12:53599053
|
A | ACAGTGTC others(12): Show |
1 | a0001c0001t0022g0169 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.48+1881_48+1899dup others(19): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599053 | ||||||
| chr12:53599123
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.48+1830G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599123 | ||||||
| chr12:53599138
|
A | G | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG00423.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.48+1815T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599138 | ||||||
| chr12:53599339
|
G | C | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.48+1614C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599339 | ||||||
| chr12:53599457
|
G | GAT | 87 | a0001c0001t0001g0056a0001c0001t0001g0237a0001c0001t0001g0238others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.48+1494_48+1495dup others(2): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599457 | ||||||
| chr12:53599471
|
C | CTA | 16 | a0001c0001t0001g0042a0001c0001t0001g0105a0001c0001t0001g0106others(13): Show | 16 | HG01891.hp1 HG02486.hp1 HG02698.hp2 others(13): Show |
intron_variant | MODIFIER | c.48+1480_48+1481dup others(2): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599471 | ||||||
| chr12:53599471
|
C | CTATA | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+1478_48+1481dup others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599471 | ||||||
| chr12:53599471
|
C | CTATATA | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+1476_48+1481dup others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599471 | ||||||
| chr12:53599779
|
C | A | 90 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.48+1174G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599779 | ||||||
| chr12:53599874
|
G | A | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+1079C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599874 | ||||||
| chr12:53600226
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.48+727T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53600226 | ||||||
| chr12:53600584
|
G | A | 1 | a0001c0001t0002g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.48+369C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53600584 | ||||||
| chr12:53600627
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.48+326G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53600627 | ||||||
| chr12:53600633
|
G | A | 11 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+320C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53600633 | ||||||
| chr12:53600867
|
C | G | 90 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.48+86G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53600867 | ||||||
| chr12:53600901
|
G | A | 1 | a0001c0001t0009g0099 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.48+52C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53600901 | ||||||
| chr12:53601052
|
T | C | 6 | a0001c0001t0001g0155a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-31A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53601052 | ||||||
| chr12:53601069
|
C | CA | 33 | a0001c0001t0001g0078a0001c0001t0001g0084a0001c0001t0001g0089others(30): Show | 33 | HG00544.hp1 HG00673.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.-21-49dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53601069 | ||||||
| chr12:53601293
|
T | C | 78 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(75): Show | 78 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-21-272A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53601293 | ||||||
| chr12:53601412
|
T | C | 1 | a0001c0006t0001g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-21-391A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53601412 | ||||||
| chr12:53601707
|
A | G | 92 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(89): Show | 92 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-21-686T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53601707 | ||||||
| chr12:53601754
|
C | T | 78 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(75): Show | 78 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-21-733G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53601754 | ||||||
| chr12:53602147
|
C | A | 1 | a0001c0001t0001g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21-1126G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602147 | ||||||
| chr12:53602222
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0282 | 2 | NA18954.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-21-1201C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602222 | ||||||
| chr12:53602235
|
A | G | 1 | a0001c0001t0003g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-21-1214T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602235 | ||||||
| chr12:53602274
|
A | C | 1 | a0001c0002t0001g0326 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-21-1253T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602274 | ||||||
| chr12:53602495
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-21-1474G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602495 | ||||||
| chr12:53602793
|
G | T | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-1772C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602793 | ||||||
| chr12:53602797
|
T | G | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-21-1776A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602797 | ||||||
| chr12:53602859
|
A | G | 92 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(89): Show | 92 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-21-1838T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602859 | ||||||
| chr12:53602860
|
C | A | 4 | a0001c0003t0008g0225a0001c0003t0008g0227a0001c0003t0008g0228others(1): Show | 4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-1839G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602860 | ||||||
| chr12:53603039
|
C | T | 78 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(75): Show | 78 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-21-2018G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53603039 | ||||||
| chr12:53603063
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-21-2042G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53603063 | ||||||
| chr12:53603388
|
A | C | 2 | a0001c0001t0001g0220a0001c0001t0003g0221 | 2 | HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-21-2367T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53603388 | ||||||
| chr12:53603796
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-21-2775G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53603796 | ||||||
| chr12:53603867
|
T | C | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-21-2846A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53603867 | ||||||
| chr12:53604073
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-21-3052T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53604073 | ||||||
| chr12:53604214
|
C | A | 43 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.-21-3193G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53604214 | ||||||
| chr12:53604297
|
C | G | 10 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 10 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21-3276G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53604297 | ||||||
| chr12:53604892
|
G | A | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-3871C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53604892 | ||||||
| chr12:53605272
|
C | G | 1 | a0001c0001t0001g0243 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-21-4251G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605272 | ||||||
| chr12:53605295
|
A | G | 2 | a0001c0003t0001g0235a0001c0003t0030g0330 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-21-4274T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605295 | ||||||
| chr12:53605337
|
T | C | 240 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(237): Show | 240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.-21-4316A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605337 | ||||||
| chr12:53605356
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-21-4335A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605356 | ||||||
| chr12:53605375
|
G | A | 2 | a0001c0001t0012g0254a0001c0001t0012g0284 | 2 | NA18948.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-21-4354C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605375 | ||||||
| chr12:53605389
|
C | CA | 164 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(161): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.-21-4369dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605389 | ||||||
| chr12:53605389
|
C | CAA | 17 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(14): Show | 17 | HG00423.hp2 HG00733.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-4370_-21-4369d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605389 | ||||||
| chr12:53605389
|
CA | C | 11 | a0001c0001t0001g0155a0001c0001t0002g0147a0001c0001t0002g0148others(8): Show | 11 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21-4369delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605389 | ||||||
| chr12:53605474
|
G | T | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-4453C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605474 | ||||||
| chr12:53605575
|
T | C | 315 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-21-4554A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605575 | ||||||
| chr12:53605844
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-21-4823A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605844 | ||||||
| chr12:53606035
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-21-5014T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606035 | ||||||
| chr12:53606050
|
C | T | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-5029G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606050 | ||||||
| chr12:53606090
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-21-5069A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606090 | ||||||
| chr12:53606128
|
G | A | 175 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 175 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.-21-5107C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606128 | ||||||
| chr12:53606139
|
A | G | 175 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 175 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.-21-5118T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606139 | ||||||
| chr12:53606247
|
G | A | 218 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(215): Show | 218 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.-21-5226C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606247 | ||||||
| chr12:53606318
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-21-5297C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606318 | ||||||
| chr12:53606352
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-21-5331C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606352 | ||||||
| chr12:53606406
|
G | A | 3 | a0001c0001t0002g0118a0001c0001t0002g0119a0001c0001t0002g0133 | 3 | HG00408.hp1 NA18955.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-21-5385C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606406 | ||||||
| chr12:53606498
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-21-5477A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606498 | ||||||
| chr12:53606546
|
C | A | 11 | a0001c0001t0001g0155a0001c0001t0002g0147a0001c0001t0002g0148others(8): Show | 11 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21-5525G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606546 | ||||||
| chr12:53606554
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-21-5533C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606554 | ||||||
| chr12:53606564
|
A | T | 1 | a0001c0001t0002g0120 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-21-5543T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606564 | ||||||
| chr12:53606809
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-21-5788G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606809 | ||||||
| chr12:53606842
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-21-5821G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606842 | ||||||
| chr12:53607012
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-21-5991C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607012 | ||||||
| chr12:53607065
|
T | C | 1 | a0001c0001t0001g0328 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-21-6044A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607065 | ||||||
| chr12:53607093
|
G | T | 1 | a0001c0001t0001g0256 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-21-6072C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607093 | ||||||
| chr12:53607271
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-21-6250C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607271 | ||||||
| chr12:53607352
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-21-6331G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607352 | ||||||
| chr12:53607437
|
A | C | 78 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(75): Show | 78 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-21-6416T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607437 | ||||||
| chr12:53607453
|
G | A | 175 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 175 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.-21-6432C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607453 | ||||||
| chr12:53607481
|
T | C | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-6460A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607481 | ||||||
| chr12:53607660
|
A | C | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-6639T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607660 | ||||||
| chr12:53607668
|
T | C | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-6647A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607668 | ||||||
| chr12:53607679
|
A | G | 1 | a0001c0001t0002g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-21-6658T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607679 | ||||||
| chr12:53607763
|
A | G | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-21-6742T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607763 | ||||||
| chr12:53607886
|
A | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0055 | 3 | HG02257.hp2 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-21-6865T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607886 | ||||||
| chr12:53607986
|
G | A | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-6965C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607986 | ||||||
| chr12:53608015
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-21-6994G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608015 | ||||||
| chr12:53608200
|
T | C | 11 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21-7179A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608200 | ||||||
| chr12:53608218
|
C | CA | 20 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(17): Show | 20 | HG01109.hp2 HG02055.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.-21-7198dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608218 | ||||||
| chr12:53608218
|
CA | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-21-7198delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608218 | ||||||
| chr12:53608218
|
CAA | C | 32 | a0001c0001t0001g0017a0001c0001t0001g0033a0001c0001t0001g0034others(29): Show | 32 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.-21-7199_-21-7198d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608218 | ||||||
| chr12:53608316
|
A | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0158 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-21-7295T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608316 | ||||||
| chr12:53608550
|
C | T | 310 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-21-7529G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608550 | ||||||
| chr12:53608815
|
C | T | 90 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-21-7794G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608815 | ||||||
| chr12:53609157
|
C | CT | 86 | a0001c0001t0001g0056a0001c0001t0001g0237a0001c0001t0001g0238others(83): Show | 86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-21-8137dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609157 | ||||||
| chr12:53609157
|
C | CTTTT | 15 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0037others(12): Show | 15 | HG01891.hp1 HG02486.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.-21-8140_-21-8137d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609157 | ||||||
| chr12:53609381
|
C | T | 13 | a0001c0001t0001g0197a0001c0001t0001g0201a0001c0001t0001g0202others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.-21-8360G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609381 | ||||||
| chr12:53609424
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-21-8403C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609424 | ||||||
| chr12:53609470
|
TA | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.-21-8450delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609470 | ||||||
| chr12:53609470
|
TAA | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0058others(12): Show | 15 | HG00735.hp1 HG01515.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.-21-8451_-21-8450d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609470 | ||||||
| chr12:53609641
|
TA | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0034others(34): Show | 37 | HG01167.hp1 HG01168.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.-21-8621delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609641 | ||||||
| chr12:53609742
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-21-8721C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609742 | ||||||
| chr12:53609821
|
C | CTTTGTTT others(4): Show |
1 | a0001c0001t0014g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-21-8801_-21-8800i others(13): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609821 | ||||||
| chr12:53609821
|
C | CTTTTTTT others(3): Show |
141 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0029others(138): Show | 141 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-21-8810_-21-8801d others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609821 | ||||||
| chr12:53609821
|
C | CTTTTTTT others(4): Show |
103 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0037others(100): Show | 103 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-21-8811_-21-8801d others(13): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609821 | ||||||
| chr12:53609821
|
C | CTTTTTTT others(5): Show |
11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0246others(8): Show | 11 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21-8812_-21-8801d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609821 | ||||||
| chr12:53609822
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-21-8801A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609822 | ||||||
| chr12:53609915
|
C | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-21-8894G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609915 | ||||||
| chr12:53609964
|
G | A | 22 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0065others(19): Show | 22 | HG00140.hp2 HG00738.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-8943C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609964 | ||||||
| chr12:53609973
|
C | T | 6 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0086others(3): Show | 6 | HG00735.hp1 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-8952G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609973 | ||||||
| chr12:53610005
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-21-8984G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610005 | ||||||
| chr12:53610037
|
G | A | 4 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-9016C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610037 | ||||||
| chr12:53610052
|
A | T | 11 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21-9031T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610052 | ||||||
| chr12:53610220
|
G | A | 1 | a0001c0001t0003g0323 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-21-9199C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610220 | ||||||
| chr12:53610325
|
G | C | 51 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0040others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.-21-9304C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610325 | ||||||
| chr12:53610327
|
C | T | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-21-9306G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610327 | ||||||
| chr12:53610441
|
T | A | 22 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0065others(19): Show | 22 | HG00140.hp2 HG00738.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-9420A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610441 | ||||||
| chr12:53610497
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-21-9476C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610497 | ||||||
| chr12:53610564
|
C | CA | 37 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(34): Show | 37 | HG00408.hp1 HG01099.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-21-9544dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610564 | ||||||
| chr12:53610564
|
CA | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0155others(11): Show | 14 | HG00621.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21-9544delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610564 | ||||||
| chr12:53610614
|
A | C | 1 | a0001c0001t0001g0247 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-21-9593T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610614 | ||||||
| chr12:53610671
|
G | A | 11 | a0001c0001t0001g0155a0001c0001t0002g0147a0001c0001t0002g0148others(8): Show | 11 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21-9650C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610671 | ||||||
| chr12:53610687
|
T | C | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-21-9666A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610687 | ||||||
| chr12:53610902
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0158 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-21-9881T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610902 | ||||||
| chr12:53610993
|
A | AT | 10 | a0001c0001t0001g0029a0001c0001t0001g0155a0001c0001t0001g0195others(7): Show | 10 | HG00140.hp1 HG00733.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21-9973dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610993 | ||||||
| chr12:53611091
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-21-10070C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611091 | ||||||
| chr12:53611220
|
C | T | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-10199G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611220 | ||||||
| chr12:53611229
|
G | C | 1 | a0001c0001t0021g0103 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-21-10208C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611229 | ||||||
| chr12:53611314
|
C | G | 69 | a0001c0001t0001g0105a0001c0001t0001g0167a0001c0001t0001g0168others(66): Show | 69 | HG00280.hp2 HG00408.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.-21-10293G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611314 | ||||||
| chr12:53611328
|
G | A | 6 | a0001c0001t0001g0155a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-10307C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611328 | ||||||
| chr12:53611452
|
A | AAAAC | 91 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(88): Show | 91 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-21-10435_-21-1043 others(8): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611452 | ||||||
| chr12:53611558
|
A | G | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-21-10537T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611558 | ||||||
| chr12:53611711
|
C | A | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | NA18959.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-21-10690G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611711 | ||||||
| chr12:53611945
|
GAT | G | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-10926_-21-1092 others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611945 | ||||||
| chr12:53611949
|
T | C | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-10928A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611949 | ||||||
| chr12:53612100
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-21-11079G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612100 | ||||||
| chr12:53612116
|
C | T | 1 | a0001c0001t0002g0112 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-21-11095G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612116 | ||||||
| chr12:53612385
|
C | G | 10 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 10 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21-11364G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612385 | ||||||
| chr12:53612392
|
T | C | 6 | a0001c0001t0001g0155a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-11371A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612392 | ||||||
| chr12:53612518
|
C | T | 5 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0306others(2): Show | 5 | HG00544.hp1 HG00673.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-11497G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612518 | ||||||
| chr12:53612741
|
C | T | 51 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0040others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.-21-11720G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612741 | ||||||
| chr12:53612786
|
C | T | 1 | a0001c0001t0003g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-21-11765G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612786 | ||||||
| chr12:53612872
|
C | T | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-11851G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612872 | ||||||
| chr12:53612880
|
T | G | 1 | a0001c0001t0002g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-21-11859A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612880 | ||||||
| chr12:53612918
|
C | T | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02145.hp1 HG02970.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-11897G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612918 | ||||||
| chr12:53613005
|
A | C | 1 | a0001c0001t0021g0103 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-21-11984T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53613005 | ||||||
| chr12:53613040
|
T | A | 87 | a0001c0001t0001g0056a0001c0001t0001g0237a0001c0001t0001g0238others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-21-12019A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53613040 | ||||||
| chr12:53613196
|
T | C | 1 | a0001c0001t0001g0296 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-21-12175A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53613196 | ||||||
| chr12:53613255
|
T | TAAAAC | 257 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(254): Show | 257 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.-21-12235_-21-1223 others(9): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53613255 | ||||||
| chr12:53613339
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-21-12318G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53613339 | ||||||
| chr12:53614432
|
G | A | 90 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-22+11847C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53614432 | ||||||
| chr12:53614574
|
G | A | 11 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-22+11705C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53614574 | ||||||
| chr12:53614593
|
A | T | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+11686T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53614593 | ||||||
| chr12:53614843
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-22+11436C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53614843 | ||||||
| chr12:53614955
|
C | T | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02145.hp1 HG02970.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+11324G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53614955 | ||||||
| chr12:53615046
|
C | T | 4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG01175.hp2 HG01515.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+11233G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615046 | ||||||
| chr12:53615064
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-22+11215C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615064 | ||||||
| chr12:53615154
|
C | A | 6 | a0001c0001t0001g0155a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+11125G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615154 | ||||||
| chr12:53615154
|
C | T | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+11125G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615154 | ||||||
| chr12:53615310
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22+10969C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615310 | ||||||
| chr12:53615315
|
C | T | 90 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-22+10964G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615315 | ||||||
| chr12:53615611
|
C | T | 78 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(75): Show | 78 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-22+10668G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615611 | ||||||
| chr12:53615777
|
G | A | 3 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145 | 3 | NA18947.hp1 NA18965.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-22+10502C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615777 | ||||||
| chr12:53616087
|
C | T | 2 | a0001c0001t0002g0131a0001c0001t0002g0135 | 2 | HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-22+10192G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616087 | ||||||
| chr12:53616193
|
T | A | 78 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(75): Show | 78 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-22+10086A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616193 | ||||||
| chr12:53616337
|
G | C | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-22+9942C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616337 | ||||||
| chr12:53616415
|
G | T | 6 | a0001c0001t0001g0155a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+9864C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616415 | ||||||
| chr12:53616572
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-22+9707T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616572 | ||||||
| chr12:53616761
|
A | T | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG01891.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+9518T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616761 | ||||||
| chr12:53616763
|
T | C | 2 | a0001c0001t0001g0220a0001c0001t0003g0221 | 2 | HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-22+9516A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616763 | ||||||
| chr12:53616783
|
G | A | 28 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(25): Show | 28 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.-22+9496C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616783 | ||||||
| chr12:53616894
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-22+9385C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616894 | ||||||
| chr12:53616914
|
C | T | 1 | a0001c0002t0001g0324 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-22+9365G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616914 | ||||||
| chr12:53616945
|
C | CA | 57 | a0001c0001t0001g0015a0001c0001t0001g0085a0001c0001t0001g0086others(54): Show | 57 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.-22+9333dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616945 | ||||||
| chr12:53617082
|
C | G | 1 | a0001c0001t0001g0042 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-22+9197G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617082 | ||||||
| chr12:53617124
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-22+9155C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617124 | ||||||
| chr12:53617143
|
C | T | 1 | a0001c0001t0003g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-22+9136G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617143 | ||||||
| chr12:53617252
|
G | C | 43 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.-22+9027C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617252 | ||||||
| chr12:53617414
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-22+8865C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617414 | ||||||
| chr12:53617636
|
A | T | 1 | a0001c0001t0001g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-22+8643T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617636 | ||||||
| chr12:53617703
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0297 | 3 | HG00140.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-22+8576G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617703 | ||||||
| chr12:53617804
|
G | T | 90 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-22+8475C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617804 | ||||||
| chr12:53617889
|
C | CA | 98 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(95): Show | 98 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-22+8389dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617889 | ||||||
| chr12:53617889
|
CA | C | 18 | a0001c0001t0001g0061a0001c0001t0001g0149a0001c0001t0001g0150others(15): Show | 18 | HG02145.hp1 HG02683.hp1 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.-22+8389delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617889 | ||||||
| chr12:53617889
|
CAAAA | C | 43 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.-22+8386_-22+8389d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617889 | ||||||
| chr12:53617945
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-22+8334T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617945 | ||||||
| chr12:53618221
|
A | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG02559.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-22+8058T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618221 | ||||||
| chr12:53618380
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-22+7899A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618380 | ||||||
| chr12:53618426
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-22+7853C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618426 | ||||||
| chr12:53618577
|
TAA | T | 10 | a0001c0001t0004g0025a0001c0001t0004g0160a0001c0001t0004g0161others(7): Show | 10 | HG02074.hp1 NA18946.hp2 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.-22+7700_-22+7701d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618577 | ||||||
| chr12:53618702
|
A | ATT | 88 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(85): Show | 88 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.-22+7575_-22+7576d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618702 | ||||||
| chr12:53618703
|
TTG | T | 18 | a0001c0001t0001g0101a0001c0001t0001g0149a0001c0001t0001g0150others(15): Show | 18 | HG01884.hp1 HG02145.hp1 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.-22+7574_-22+7575d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618703 | ||||||
| chr12:53618717
|
G | T | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-22+7562C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618717 | ||||||
| chr12:53618845
|
C | T | 10 | a0001c0001t0004g0025a0001c0001t0004g0160a0001c0001t0004g0161others(7): Show | 10 | HG02074.hp1 NA18946.hp2 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.-22+7434G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618845 | ||||||
| chr12:53618935
|
C | T | 4 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0153others(1): Show | 4 | HG03491.hp2 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+7344G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618935 | ||||||
| chr12:53619292
|
C | T | 2 | a0001c0001t0002g0110a0001c0001t0002g0137 | 2 | HG00741.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-22+6987G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619292 | ||||||
| chr12:53619359
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-22+6920C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619359 | ||||||
| chr12:53619419
|
A | C | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | NA18994.hp2 NA19002.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-22+6860T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619419 | ||||||
| chr12:53619480
|
C | A | 17 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(14): Show | 17 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+6799G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619480 | ||||||
| chr12:53619486
|
C | CA | 89 | a0001c0001t0001g0015a0001c0001t0001g0098a0001c0001t0001g0101others(86): Show | 89 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-22+6792dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619486 | ||||||
| chr12:53619486
|
C | CAA | 17 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(14): Show | 17 | HG01433.hp1 HG02074.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+6791_-22+6792d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619486 | ||||||
| chr12:53619570
|
T | G | 90 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-22+6709A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619570 | ||||||
| chr12:53619577
|
C | T | 17 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(14): Show | 17 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+6702G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619577 | ||||||
| chr12:53619594
|
C | A | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-22+6685G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619594 | ||||||
| chr12:53619668
|
T | C | 184 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(181): Show | 184 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.-22+6611A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619668 | ||||||
| chr12:53619673
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-22+6606T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619673 | ||||||
| chr12:53620347
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-22+5932G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620347 | ||||||
| chr12:53620377
|
C | A | 1 | a0001c0001t0016g0308 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-22+5902G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620377 | ||||||
| chr12:53620500
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-22+5779G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620500 | ||||||
| chr12:53620575
|
C | CA | 94 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(91): Show | 94 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.-22+5703dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620575 | ||||||
| chr12:53620575
|
C | CAA | 9 | a0001c0001t0001g0297a0001c0001t0002g0026a0001c0001t0002g0132others(6): Show | 9 | HG00140.hp1 HG01175.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22+5702_-22+5703d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620575 | ||||||
| chr12:53620575
|
CA | C | 68 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0038others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.-22+5703delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620575 | ||||||
| chr12:53620621
|
T | C | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22+5658A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620621 | ||||||
| chr12:53620735
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-22+5544G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620735 | ||||||
| chr12:53620813
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-22+5466G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620813 | ||||||
| chr12:53620863
|
G | GA | 103 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(100): Show | 103 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-22+5415dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620863 | ||||||
| chr12:53621055
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-22+5224T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621055 | ||||||
| chr12:53621313
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-22+4966G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621313 | ||||||
| chr12:53621452
|
A | G | 263 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(260): Show | 263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.-22+4827T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621452 | ||||||
| chr12:53621475
|
TA | T | 17 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(14): Show | 17 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+4803delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621475 | ||||||
| chr12:53621627
|
C | CA | 21 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(18): Show | 21 | HG01175.hp1 HG01891.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.-22+4651dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621627 | ||||||
| chr12:53621652
|
G | A | 1 | a0001c0001t0025g0315 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-22+4627C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621652 | ||||||
| chr12:53621707
|
T | C | 1 | a0001c0001t0026g0298 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-22+4572A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621707 | ||||||
| chr12:53621721
|
G | A | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+4558C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621721 | ||||||
| chr12:53621730
|
A | C | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+4549T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621730 | ||||||
| chr12:53621758
|
C | T | 44 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.-22+4521G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621758 | ||||||
| chr12:53621766
|
G | A | 1 | a0001c0001t0007g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-22+4513C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621766 | ||||||
| chr12:53621786
|
C | T | 1 | a0001c0001t0009g0041 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-22+4493G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621786 | ||||||
| chr12:53621788
|
C | CA | 34 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0098others(31): Show | 34 | HG00544.hp1 HG00673.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-22+4490dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621788 | ||||||
| chr12:53621788
|
CA | C | 61 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0034others(58): Show | 61 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.-22+4490delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621788 | ||||||
| chr12:53621788
|
CAA | C | 40 | a0001c0001t0001g0190a0001c0001t0002g0001a0001c0001t0002g0022others(37): Show | 40 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.-22+4489_-22+4490d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621788 | ||||||
| chr12:53621788
|
CAAA | C | 34 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(31): Show | 34 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.-22+4488_-22+4490d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621788 | ||||||
| chr12:53622226
|
C | T | 1 | a0001c0001t0029g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-22+4053G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622226 | ||||||
| chr12:53622304
|
AAAT | A | 297 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.-22+3972_-22+3974d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622304 | ||||||
| chr12:53622304
|
AAATAATA others(2): Show |
A | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22+3966_-22+3974d others(11): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622304 | ||||||
| chr12:53622529
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG01891.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+3750C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622529 | ||||||
| chr12:53622652
|
C | CA | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0101others(14): Show | 17 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+3626dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622652 | ||||||
| chr12:53622652
|
C | CAA | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+3625_-22+3626d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622652 | ||||||
| chr12:53622652
|
CA | C | 45 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.-22+3626delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622652 | ||||||
| chr12:53622652
|
CAAA | C | 16 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(13): Show | 16 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(13): Show |
intron_variant | MODIFIER | c.-22+3624_-22+3626d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622652 | ||||||
| chr12:53622663
|
A | G | 44 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.-22+3616T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622663 | ||||||
| chr12:53622669
|
AT | A | 77 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(74): Show | 77 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.-22+3609delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622669 | ||||||
| chr12:53622670
|
T | A | 1 | a0001c0001t0002g0140 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+3609A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622670 | ||||||
| chr12:53622784
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-22+3495C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622784 | ||||||
| chr12:53622809
|
C | CA | 5 | a0001c0001t0006g0141a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+3469dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622809 | ||||||
| chr12:53622948
|
C | T | 6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+3331G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622948 | ||||||
| chr12:53623000
|
T | C | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+3279A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623000 | ||||||
| chr12:53623032
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-22+3247C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623032 | ||||||
| chr12:53623077
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-22+3202G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623077 | ||||||
| chr12:53623099
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-22+3180G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623099 | ||||||
| chr12:53623276
|
A | C | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-22+3003T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623276 | ||||||
| chr12:53623537
|
T | G | 44 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.-22+2742A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623537 | ||||||
| chr12:53623781
|
C | G | 2 | a0001c0001t0001g0029a0001c0001t0014g0030 | 2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-22+2498G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623781 | ||||||
| chr12:53623827
|
G | A | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22+2452C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623827 | ||||||
| chr12:53623828
|
T | C | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22+2451A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623828 | ||||||
| chr12:53623863
|
G | A | 37 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(34): Show | 37 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.-22+2416C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623863 | ||||||
| chr12:53623891
|
G | A | 44 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.-22+2388C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623891 | ||||||
| chr12:53624095
|
A | T | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-22+2184T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53624095 | ||||||
| chr12:53624241
|
G | A | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | NA18971.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-22+2038C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53624241 | ||||||
| chr12:53624366
|
T | C | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+1913A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53624366 | ||||||
| chr12:53624864
|
C | T | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG02135.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-22+1415G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53624864 | ||||||
| chr12:53625022
|
C | A | 86 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0240others(83): Show | 86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-22+1257G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625022 | ||||||
| chr12:53625147
|
T | C | 2 | a0001c0001t0003g0322a0001c0001t0003g0323 | 2 | HG02280.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-22+1132A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625147 | ||||||
| chr12:53625161
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-22+1118G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625161 | ||||||
| chr12:53625172
|
A | G | 1 | a0001c0001t0004g0025 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-22+1107T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625172 | ||||||
| chr12:53625455
|
C | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(11): Show | 14 | HG01884.hp2 HG02622.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.-22+824G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625455 | ||||||
| chr12:53625458
|
T | C | 4 | a0001c0002t0001g0324a0001c0002t0001g0325a0001c0002t0001g0326others(1): Show | 4 | NA18962.hp1 NA18964.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+821A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625458 | ||||||
| chr12:53625691
|
A | G | 3 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024 | 3 | NA18941.hp1 NA18973.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.-22+588T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625691 | ||||||
| chr12:53625793
|
T | G | 1 | a0001c0001t0001g0328 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-22+486A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625793 | ||||||
| chr12:53625834
|
C | T | 2 | a0001c0001t0013g0020a0001c0001t0013g0021 | 2 | HG02135.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-22+445G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625834 | ||||||
| chr12:53625937
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-22+342G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625937 | ||||||
| chr12:53626056
|
C | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(14): Show | 17 | HG01884.hp2 HG02257.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.-22+223G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53626056 | ||||||
| chr12:53626130
|
C | G | 1 | a0001c0001t0002g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-22+149G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53626130 | ||||||
| chr12:53626142
|
G | C | 1 | a0001c0001t0001g0329 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-22+137C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53626142 |