Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55729 |
|---|---|
| ensemblid | ENSG00000171681.13 |
| hgncid | 20092 |
| symbol | ATF7IP |
| name | activating transcription factor 7 interacting protein |
| refseq_nuc | NM_018179.5 |
| refseq_prot | NP_060649.3 |
| ensembl_nuc | ENST00000261168.9 |
| ensembl_prot | ENSP00000261168.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 14365682 |
| end | 14502930 |
| strand | + |
| ver | v1.2 |
| region | chr12:14365682-14502930 |
| region5000 | chr12:14360682-14507930 |
| regionname0 | ATF7IP_chr12_14365682_14502930 |
| regionname5000 | ATF7IP_chr12_14360682_14507930 |
| 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 | 0/0 | 1270 | 135 | 25 | 23 | 63 | 4 | 20 | 53 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0002 | 0/1 | 1270 | 102 | 10 | 22 | 52 | 6 | 11 | 38 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003 | 1/0 | 1270 | 72 | 45 | 9 | 12 | 2 | 3 | 12 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0004 | 0/0 | 1270 | 9 | 2 | 6 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0005 | 0/0 | 1270 | 9 | 0 | 2 | 3 | 0 | 4 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0006 | 0/0 | 1270 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0007 | 0/0 | 1270 | 3 | 0 | 0 | 0 | 3 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0008 | 0/0 | 1270 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0009 | 0/0 | 1270 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0010 | 0/0 | 1270 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0011 | 0/0 | 1265 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0012 | 0/0 | 1270 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0013 | 0/0 | 1270 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0014 | 0/0 | 1270 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| 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 | 0/0 | 3813 | 134 | 24 | 23 | 63 | 4 | 20 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0002 | 0/1 | 3813 | 74 | 10 | 8 | 42 | 5 | 8 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0003 | 1/0 | 3813 | 57 | 33 | 8 | 10 | 2 | 3 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0004 | 0/0 | 3813 | 15 | 0 | 14 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0005 | 0/0 | 3813 | 13 | 12 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0006 | 0/0 | 3813 | 13 | 0 | 0 | 10 | 0 | 3 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0007 | 0/0 | 3813 | 9 | 0 | 2 | 3 | 0 | 4 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0008 | 0/0 | 3813 | 8 | 2 | 5 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0009 | 0/0 | 3813 | 6 | 6 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0010 | 0/0 | 3813 | 3 | 0 | 0 | 0 | 3 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0011 | 0/0 | 3813 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0012 | 0/0 | 3813 | 2 | 0 | 2 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0013 | 0/0 | 3813 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0014 | 0/0 | 3813 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0015 | 0/0 | 3813 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0016 | 0/0 | 3813 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0017 | 0/0 | 3813 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0018 | 0/0 | 3813 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0019 | 0/0 | 3798 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| c0020 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 5012 | 78 | 1 | 21 | 42 | 6 | 7 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0002 | 0/0 | 5006 | 60 | 4 | 6 | 32 | 4 | 14 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0003 | 0/0 | 5006 | 48 | 3 | 14 | 24 | 3 | 4 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0004 | 0/0 | 5012 | 19 | 5 | 2 | 10 | 0 | 2 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0005 | 0/0 | 5012 | 17 | 10 | 6 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0006 | 0/0 | 5007 | 11 | 11 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0007 | 0/0 | 5013 | 11 | 11 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0008 | 0/0 | 5013 | 11 | 0 | 0 | 8 | 0 | 3 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0009 | 0/0 | 5012 | 10 | 9 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0010 | 0/0 | 5012 | 9 | 0 | 2 | 3 | 0 | 4 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0011 | 0/0 | 5012 | 8 | 6 | 2 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0012 | 0/0 | 5012 | 7 | 7 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0013 | 0/0 | 5011 | 6 | 0 | 4 | 2 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0014 | 0/0 | 5011 | 5 | 5 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0015 | 0/0 | 5011 | 5 | 5 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0016 | 0/0 | 5007 | 3 | 3 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0017 | 0/0 | 5006 | 3 | 0 | 0 | 3 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0018 | 1/0 | 5011 | 3 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0019 | 0/0 | 5011 | 3 | 0 | 0 | 3 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0020 | 0/0 | 5006 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0021 | 0/0 | 5006 | 2 | 0 | 2 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0022 | 0/0 | 5006 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0023 | 0/0 | 5011 | 2 | 0 | 2 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0024 | 0/0 | 5012 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0025 | 0/0 | 5012 | 2 | 0 | 0 | 0 | 2 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0026 | 0/0 | 5012 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0027 | 0/0 | 5006 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0028 | 0/0 | 5012 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0029 | 0/0 | 5006 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0030 | 0/0 | 5006 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0031 | 0/0 | 5006 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0032 | 0/0 | 5006 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0033 | 0/0 | 5006 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0034 | 0/0 | 5011 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0035 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0036 | 0/0 | 5012 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0037 | 0/0 | 5012 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0038 | 0/0 | 5013 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0039 | 0/0 | 5012 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0040 | 0/0 | 5013 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| t0041 | 0/0 | 5013 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0299 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| 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 | 0/0 | 3813 | 134 | 24 | 23 | 63 | 4 | 20 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0020 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0002c0002 | 0/1 | 3813 | 74 | 10 | 8 | 42 | 5 | 8 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0002c0004 | 0/0 | 3813 | 15 | 0 | 14 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0002c0006 | 0/0 | 3813 | 13 | 0 | 0 | 10 | 0 | 3 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0003 | 1/0 | 3813 | 57 | 33 | 8 | 10 | 2 | 3 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0005 | 0/0 | 3813 | 13 | 12 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0014 | 0/0 | 3813 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0004c0008 | 0/0 | 3813 | 8 | 2 | 5 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0004c0018 | 0/0 | 3813 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0005c0007 | 0/0 | 3813 | 9 | 0 | 2 | 3 | 0 | 4 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0006c0009 | 0/0 | 3813 | 6 | 6 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0007c0010 | 0/0 | 3813 | 3 | 0 | 0 | 0 | 3 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0008c0011 | 0/0 | 3813 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0009c0012 | 0/0 | 3813 | 2 | 0 | 2 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0010c0013 | 0/0 | 3813 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0011c0019 | 0/0 | 3798 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0012c0017 | 0/0 | 3813 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0013c0016 | 0/0 | 3813 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0014c0015 | 0/0 | 3813 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 8818 | 57 | 4 | 6 | 32 | 1 | 14 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0003 | 0/0 | 8818 | 47 | 3 | 14 | 24 | 3 | 3 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0006 | 0/0 | 8819 | 11 | 11 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0014 | 0/0 | 8823 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0016 | 0/0 | 8819 | 3 | 3 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0017 | 0/0 | 8818 | 3 | 0 | 0 | 3 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0019 | 0/0 | 8823 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0021 | 0/0 | 8818 | 2 | 0 | 2 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0022 | 0/0 | 8818 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0027 | 0/0 | 8818 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0029 | 0/0 | 8818 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0030 | 0/0 | 8818 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0031 | 0/0 | 8818 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0032 | 0/0 | 8818 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0033 | 0/0 | 8818 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0001t0040 | 0/0 | 8825 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0001c0020t0036 | 0/0 | 8824 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0002c0002t0001 | 0/1 | 8824 | 61 | 1 | 7 | 40 | 5 | 7 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0002c0002t0009 | 0/0 | 8824 | 10 | 9 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0002c0002t0026 | 0/0 | 8824 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0002c0002t0037 | 0/0 | 8824 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0002c0004t0001 | 0/0 | 8824 | 15 | 0 | 14 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0002c0006t0008 | 0/0 | 8825 | 11 | 0 | 0 | 8 | 0 | 3 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0002c0006t0019 | 0/0 | 8823 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0003t0004 | 0/0 | 8824 | 19 | 5 | 2 | 10 | 0 | 2 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0003t0005 | 0/0 | 8824 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0003t0011 | 0/0 | 8824 | 6 | 6 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0003t0012 | 0/0 | 8824 | 7 | 7 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0003t0013 | 0/0 | 8823 | 4 | 0 | 4 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0003t0014 | 0/0 | 8823 | 4 | 4 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0003t0015 | 0/0 | 8823 | 5 | 5 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0003t0018 | 1/0 | 8823 | 3 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0003t0023 | 0/0 | 8823 | 2 | 0 | 2 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0003t0025 | 0/0 | 8824 | 2 | 0 | 0 | 0 | 2 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0003t0028 | 0/0 | 8824 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0003t0034 | 0/0 | 8823 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0003t0035 | 0/0 | 8823 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0005t0007 | 0/0 | 8825 | 11 | 11 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0005t0038 | 0/0 | 8825 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0005t0041 | 0/0 | 8825 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0003c0014t0013 | 0/0 | 8823 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0004c0008t0005 | 0/0 | 8824 | 8 | 2 | 5 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0004c0018t0005 | 0/0 | 8824 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0005c0007t0010 | 0/0 | 8824 | 9 | 0 | 2 | 3 | 0 | 4 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0006c0009t0005 | 0/0 | 8824 | 6 | 6 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0007c0010t0002 | 0/0 | 8818 | 3 | 0 | 0 | 0 | 3 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0008c0011t0024 | 0/0 | 8824 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0009c0012t0011 | 0/0 | 8824 | 2 | 0 | 2 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0010c0013t0020 | 0/0 | 8818 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0011c0019t0001 | 0/0 | 8809 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0012c0017t0001 | 0/0 | 8824 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0013c0016t0039 | 0/0 | 8824 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| a0014c0015t0003 | 0/0 | 8818 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | copy fasta | chr12 | 14360682 | 14507930 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0014g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0016g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0016g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0016g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0017g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0017g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0017g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0019g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0021g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0021g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0022g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0022g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0027g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0029g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0030g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0031g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0032g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0033g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0040g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0020t0036g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0299 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0026g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0026g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0037g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0019g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0019g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0011g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0011g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0011g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0011g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0012g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0012g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0012g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0012g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0012g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0013g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0013g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0013g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0013g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0014g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0014g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0014g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0014g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0015g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0015g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0015g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0015g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0015g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0018g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0018g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0018g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0023g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0023g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0025g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0025g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0028g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0034g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0035g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0038g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0041g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0014t0013g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0014t0013g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0018t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0006c0009t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0006c0009t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0006c0009t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0006c0009t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0006c0009t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0006c0009t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0007c0010t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0007c0010t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0007c0010t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0008c0011t0024g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0008c0011t0024g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0009c0012t0011g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0009c0012t0011g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0010c0013t0020g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0010c0013t0020g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0011c0019t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0012c0017t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0013c0016t0039g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0014c0015t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0025 | g0172 | EUR | GBR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0285 | EUR | GBR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0235 | EUR | GBR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0095 | EUR | GBR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00280 | hp1 | a0003 | c0003 | t0025 | g0171 | EUR | FIN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00280 | hp2 | a0004 | c0008 | t0005 | g0252 | EUR | FIN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00438 | hp2 | a0002 | c0006 | t0008 | g0227 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00609 | hp2 | a0005 | c0007 | t0010 | g0319 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00639 | hp1 | a0003 | c0003 | t0013 | g0159 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00639 | hp2 | a0002 | c0004 | t0001 | g0340 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00673 | hp1 | a0001 | c0001 | t0032 | g0103 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00673 | hp2 | a0002 | c0006 | t0008 | g0221 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0284 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00733 | hp2 | a0003 | c0003 | t0004 | g0196 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00741 | hp2 | a0003 | c0003 | t0013 | g0161 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01069 | hp2 | a0002 | c0004 | t0001 | g0291 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01071 | hp1 | a0002 | c0004 | t0001 | g0216 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01074 | hp2 | a0002 | c0004 | t0001 | g0233 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01081 | hp1 | a0004 | c0008 | t0005 | g0253 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01099 | hp1 | a0003 | c0003 | t0023 | g0151 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01106 | hp2 | a0002 | c0004 | t0001 | g0242 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01109 | hp2 | a0002 | c0002 | t0009 | g0005 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01167 | hp1 | a0009 | c0012 | t0011 | g0338 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0298 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01168 | hp1 | a0004 | c0008 | t0005 | g0280 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01169 | hp1 | a0004 | c0008 | t0005 | g0283 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01169 | hp2 | a0009 | c0012 | t0011 | g0339 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01175 | hp2 | a0002 | c0004 | t0001 | g0231 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01243 | hp1 | a0001 | c0001 | t0029 | g0060 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01243 | hp2 | a0002 | c0004 | t0001 | g0229 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0122 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01257 | hp1 | a0001 | c0001 | t0021 | g0033 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01258 | hp1 | a0001 | c0001 | t0021 | g0036 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0210 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01261 | hp1 | a0002 | c0004 | t0001 | g0238 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01261 | hp2 | a0003 | c0003 | t0013 | g0160 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01346 | hp1 | a0005 | c0007 | t0010 | g0318 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01358 | hp1 | a0002 | c0004 | t0001 | g0241 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01361 | hp2 | a0004 | c0008 | t0005 | g0293 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01496 | hp2 | a0004 | c0018 | t0005 | g0276 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0309 | EUR | IBS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01515 | hp2 | a0007 | c0010 | t0002 | g0049 | EUR | IBS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0100 | EUR | IBS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01516 | hp2 | a0007 | c0010 | t0002 | g0011 | EUR | IBS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01517 | hp1 | a0007 | c0010 | t0002 | g0022 | EUR | IBS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0308 | EUR | IBS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01884 | hp1 | a0001 | c0001 | t0016 | g0127 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01884 | hp2 | a0003 | c0003 | t0005 | g0316 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01891 | hp1 | a0008 | c0011 | t0024 | g0147 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01891 | hp2 | a0003 | c0003 | t0018 | g0155 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01934 | hp1 | a0003 | c0005 | t0041 | g0337 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01934 | hp2 | a0002 | c0004 | t0001 | g0240 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0306 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01993 | hp1 | a0002 | c0004 | t0001 | g0230 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02004 | hp1 | a0002 | c0004 | t0001 | g0232 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02004 | hp2 | a0003 | c0003 | t0013 | g0162 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02055 | hp1 | a0003 | c0003 | t0015 | g0166 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02055 | hp2 | a0001 | c0020 | t0036 | g0131 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02132 | hp2 | a0005 | c0007 | t0010 | g0320 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02135 | hp1 | a0002 | c0006 | t0019 | g0228 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02135 | hp2 | a0001 | c0001 | t0019 | g0062 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0132 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02145 | hp2 | a0003 | c0005 | t0007 | g0329 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02148 | hp1 | a0005 | c0007 | t0010 | g0317 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02148 | hp2 | a0002 | c0004 | t0001 | g0243 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | CDX | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CDX | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02165 | hp1 | a0001 | c0001 | t0040 | g0139 | EAS | CDX | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | CDX | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02257 | hp1 | a0003 | c0003 | t0004 | g0201 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02257 | hp2 | a0003 | c0003 | t0014 | g0156 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02273 | hp2 | a0002 | c0004 | t0001 | g0239 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02280 | hp1 | a0003 | c0003 | t0011 | g0314 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02280 | hp2 | a0003 | c0003 | t0015 | g0168 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02300 | hp1 | a0003 | c0003 | t0023 | g0152 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02451 | hp1 | a0003 | c0003 | t0011 | g0315 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02451 | hp2 | a0003 | c0005 | t0007 | g0325 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02572 | hp1 | a0002 | c0002 | t0009 | g0211 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02572 | hp2 | a0003 | c0005 | t0007 | g0330 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0307 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02615 | hp1 | a0002 | c0002 | t0009 | g0213 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0134 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02622 | hp1 | a0001 | c0001 | t0022 | g0082 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02622 | hp2 | a0002 | c0002 | t0009 | g0289 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02630 | hp1 | a0003 | c0003 | t0012 | g0001 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02630 | hp2 | a0003 | c0003 | t0014 | g0157 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0129 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02647 | hp2 | a0003 | c0005 | t0007 | g0336 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02683 | hp2 | a0013 | c0016 | t0039 | g0245 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02717 | hp1 | a0003 | c0003 | t0014 | g0170 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02717 | hp2 | a0001 | c0001 | t0014 | g0125 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02723 | hp1 | a0006 | c0009 | t0005 | g0176 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02723 | hp2 | a0010 | c0013 | t0020 | g0115 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02735 | hp2 | a0001 | c0001 | t0027 | g0023 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02738 | hp2 | a0003 | c0003 | t0034 | g0150 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02818 | hp2 | a0003 | c0005 | t0038 | g0331 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02895 | hp1 | a0003 | c0003 | t0018 | g0153 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0133 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02896 | hp1 | a0006 | c0009 | t0005 | g0178 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02897 | hp1 | a0006 | c0009 | t0005 | g0177 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0137 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02922 | hp1 | a0003 | c0003 | t0015 | g0167 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02922 | hp2 | a0003 | c0003 | t0012 | g0001 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02965 | hp1 | a0003 | c0005 | t0007 | g0326 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02965 | hp2 | a0003 | c0003 | t0012 | g0182 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02970 | hp1 | a0003 | c0003 | t0012 | g0179 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02970 | hp2 | a0003 | c0003 | t0004 | g0198 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02976 | hp1 | a0002 | c0002 | t0009 | g0287 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0076 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03041 | hp1 | a0002 | c0002 | t0009 | g0215 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03098 | hp1 | a0006 | c0009 | t0005 | g0173 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03098 | hp2 | a0003 | c0003 | t0015 | g0169 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03130 | hp1 | a0001 | c0001 | t0016 | g0075 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03130 | hp2 | a0003 | c0005 | t0007 | g0328 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03139 | hp1 | a0003 | c0005 | t0007 | g0335 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03139 | hp2 | a0006 | c0009 | t0005 | g0174 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03195 | hp1 | a0004 | c0008 | t0005 | g0003 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03195 | hp2 | a0003 | c0003 | t0012 | g0180 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03209 | hp2 | a0003 | c0005 | t0007 | g0332 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03225 | hp1 | a0003 | c0005 | t0007 | g0327 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0135 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0128 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03239 | hp2 | a0014 | c0015 | t0003 | g0094 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03453 | hp1 | a0003 | c0005 | t0007 | g0333 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03453 | hp2 | a0003 | c0003 | t0035 | g0343 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03486 | hp1 | a0003 | c0003 | t0011 | g0341 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03486 | hp2 | a0003 | c0003 | t0004 | g0200 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03490 | hp1 | a0001 | c0001 | t0033 | g0093 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03490 | hp2 | a0005 | c0007 | t0010 | g0002 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03491 | hp1 | a0003 | c0003 | t0004 | g0188 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03491 | hp2 | a0002 | c0006 | t0008 | g0220 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03492 | hp1 | a0005 | c0007 | t0010 | g0002 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03492 | hp2 | a0003 | c0003 | t0004 | g0190 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03516 | hp1 | a0006 | c0009 | t0005 | g0175 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03516 | hp2 | a0002 | c0002 | t0009 | g0288 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03540 | hp1 | a0002 | c0002 | t0009 | g0006 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03540 | hp2 | a0001 | c0001 | t0022 | g0081 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03579 | hp1 | a0003 | c0003 | t0004 | g0197 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03579 | hp2 | a0003 | c0003 | t0011 | g0184 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03704 | hp2 | a0002 | c0006 | t0008 | g0295 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03710 | hp1 | a0002 | c0006 | t0008 | g0208 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03831 | hp1 | a0002 | c0002 | t0037 | g0237 | SAS | BEB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | BEB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0246 | SAS | BEB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0112 | SAS | BEB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0271 | SAS | BEB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | BEB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04115 | hp2 | a0005 | c0007 | t0010 | g0323 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0206 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04204 | hp1 | a0001 | c0001 | t0030 | g0040 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0236 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04228 | hp2 | a0005 | c0007 | t0010 | g0321 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18522 | hp1 | a0002 | c0002 | t0009 | g0212 | AFR | YRI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18522 | hp2 | a0003 | c0003 | t0004 | g0199 | AFR | YRI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | CHB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | CHB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | CHB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18747 | hp2 | a0002 | c0006 | t0019 | g0222 | EAS | CHB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18906 | hp1 | a0003 | c0003 | t0005 | g0158 | AFR | YRI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18906 | hp2 | a0003 | c0003 | t0028 | g0183 | AFR | YRI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18939 | hp1 | a0003 | c0003 | t0004 | g0187 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18945 | hp2 | a0002 | c0002 | t0026 | g0273 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18946 | hp1 | a0001 | c0001 | t0017 | g0032 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18946 | hp2 | a0002 | c0006 | t0008 | g0217 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18947 | hp2 | a0001 | c0001 | t0017 | g0046 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18950 | hp2 | a0012 | c0017 | t0001 | g0266 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18967 | hp1 | a0001 | c0001 | t0031 | g0009 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18967 | hp2 | a0003 | c0003 | t0004 | g0186 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18968 | hp1 | a0003 | c0003 | t0004 | g0193 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18977 | hp2 | a0002 | c0006 | t0008 | g0223 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18981 | hp2 | a0002 | c0006 | t0008 | g0224 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18986 | hp1 | a0003 | c0003 | t0004 | g0202 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19002 | hp1 | a0011 | c0019 | t0001 | g0313 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19003 | hp2 | a0003 | c0014 | t0013 | g0163 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19007 | hp2 | a0003 | c0003 | t0004 | g0194 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19010 | hp2 | a0005 | c0007 | t0010 | g0322 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19030 | hp1 | a0003 | c0003 | t0012 | g0181 | AFR | LWK | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0136 | AFR | LWK | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19043 | hp1 | a0003 | c0003 | t0011 | g0324 | AFR | LWK | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19043 | hp2 | a0010 | c0013 | t0020 | g0117 | AFR | LWK | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19056 | hp1 | a0003 | c0003 | t0004 | g0203 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19057 | hp2 | a0002 | c0006 | t0008 | g0219 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19067 | hp1 | a0002 | c0006 | t0008 | g0226 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19072 | hp1 | a0003 | c0003 | t0004 | g0192 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19074 | hp2 | a0003 | c0014 | t0013 | g0164 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19079 | hp2 | a0002 | c0002 | t0026 | g0272 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19084 | hp2 | a0001 | c0001 | t0017 | g0048 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19088 | hp2 | a0002 | c0006 | t0008 | g0256 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19090 | hp1 | a0003 | c0003 | t0004 | g0189 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19091 | hp1 | a0003 | c0003 | t0004 | g0185 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19240 | hp1 | a0003 | c0003 | t0014 | g0149 | AFR | YRI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0138 | AFR | YRI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20129 | hp1 | a0003 | c0003 | t0015 | g0165 | AFR | ASW | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20129 | hp2 | a0004 | c0008 | t0005 | g0294 | AFR | ASW | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | TSI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0277 | EUR | TSI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20805 | hp1 | a0002 | c0004 | t0001 | g0247 | EUR | TSI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0146 | EUR | TSI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | GIH | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0244 | SAS | GIH | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01123 | hp1 | a0004 | c0008 | t0005 | g0279 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01123 | hp2 | a0003 | c0003 | t0004 | g0195 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02109 | hp1 | a0001 | c0001 | t0016 | g0126 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02109 | hp2 | a0002 | c0002 | t0009 | g0214 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02486 | hp1 | a0003 | c0005 | t0007 | g0334 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02486 | hp2 | a0003 | c0003 | t0011 | g0204 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02559 | hp1 | a0008 | c0011 | t0024 | g0148 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG06807 | hp1 | a0003 | c0003 | t0012 | g0001 | AFR | USA | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | USA | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18955 | hp2 | a0003 | c0003 | t0004 | g0191 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0234 | AFR | LWK | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0130 | AFR | LWK | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0299 | REF | REF | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0018 | g0154 | REF | REF | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14424423
|
GCCTCTGG others(8): Show |
G | 1 | a0011 | 1 | NA19002.hp1 | disruptive_inframe_deletion | MODERATE | c.522_536delAACCTCTG others(7): Show |
p.Thr175_Ala179del | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 675/8823 | 522/3813 | 174/1270 | INFO_REALIGN_3_PRIME | chr12 | 14424423 | |
| chr12:14424573
|
A | G | 1 | a0010 | 2 | HG02723.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.658A>G | p.Ile220Val | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 811/8823 | 658/3813 | 220/1270 | chr12 | 14424573 | ||
| chr12:14424747
|
G | A | 1 | a0005 | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
missense_variant | MODERATE | c.832G>A | p.Glu278Lys | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 985/8823 | 832/3813 | 278/1270 | chr12 | 14424747 | ||
| chr12:14424838
|
C | G | 1 | a0009 | 2 | HG01167.hp1 HG01169.hp2 |
missense_variant | MODERATE | c.923C>G | p.Pro308Arg | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 1076/8823 | 923/3813 | 308/1270 | chr12 | 14424838 | ||
| chr12:14424958
|
A | T | 5 | a0002a0004a0011others(2): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
missense_variant | MODERATE | c.1043A>T | p.Asn348Ile | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 1196/8823 | 1043/3813 | 348/1270 | chr12 | 14424958 | ||
| chr12:14425420
|
C | T | 1 | a0007 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.1505C>T | p.Ser502Leu | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 1658/8823 | 1505/3813 | 502/1270 | chr12 | 14425420 | ||
| chr12:14434367
|
A | G | 5 | a0001a0004a0007others(2): Show | 150 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(147): Show |
missense_variant | MODERATE | c.1589A>G | p.Lys530Arg | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/15 | 1742/8823 | 1589/3813 | 530/1270 | chr12 | 14434367 | ||
| chr12:14460537
|
G | A | 1 | a0006 | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
missense_variant | MODERATE | c.2201G>A | p.Ser734Asn | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/15 | 2354/8823 | 2201/3813 | 734/1270 | chr12 | 14460537 | ||
| chr12:14460845
|
T | C | 1 | a0008 | 2 | HG01891.hp1 HG02559.hp1 |
missense_variant | MODERATE | c.2509T>C | p.Ser837Pro | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/15 | 2662/8823 | 2509/3813 | 837/1270 | chr12 | 14460845 | ||
| chr12:14481110
|
G | A | 1 | a0013 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.3205G>A | p.Ala1069Thr | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/15 | 3358/8823 | 3205/3813 | 1069/1270 | chr12 | 14481110 | ||
| chr12:14481185
|
A | G | 1 | a0014 | 1 | HG03239.hp2 | missense_variant&splice_region_variant | MODERATE | c.3280A>G | p.Ser1094Gly | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/15 | 3433/8823 | 3280/3813 | 1094/1270 | chr12 | 14481185 | ||
| chr12:14497663
|
C | T | 1 | a0012 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.3403C>T | p.Arg1135Cys | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 3556/8823 | 3403/3813 | 1135/1270 | chr12 | 14497663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14424338
|
C | T | 1 | a0003c0014 | 2 | NA19003.hp2 NA19074.hp2 |
synonymous_variant | LOW | c.423C>T | p.Ala141Ala | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 576/8823 | 423/3813 | 141/1270 | chr12 | 14424338 | ||
| chr12:14424360
|
C | T | 1 | a0001c0020 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.445C>T | p.Leu149Leu | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 598/8823 | 445/3813 | 149/1270 | chr12 | 14424360 | ||
| chr12:14424917
|
A | T | 1 | a0008c0011 | 2 | HG01891.hp1 HG02559.hp1 |
synonymous_variant | LOW | c.1002A>T | p.Ser334Ser | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 1155/8823 | 1002/3813 | 334/1270 | chr12 | 14424917 | ||
| chr12:14460697
|
A | G | 1 | a0004c0018 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.2361A>G | p.Val787Val | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/15 | 2514/8823 | 2361/3813 | 787/1270 | chr12 | 14460697 | ||
| chr12:14460766
|
A | G | 1 | a0002c0006 | 13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
synonymous_variant | LOW | c.2430A>G | p.Pro810Pro | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/15 | 2583/8823 | 2430/3813 | 810/1270 | chr12 | 14460766 | ||
| chr12:14478405
|
G | A | 1 | a0003c0005 | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
synonymous_variant | LOW | c.3030G>A | p.Pro1010Pro | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/15 | 3183/8823 | 3030/3813 | 1010/1270 | chr12 | 14478405 | ||
| chr12:14496262
|
A | G | 1 | a0002c0004 | 15 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(12): Show |
synonymous_variant | LOW | c.3312A>G | p.Thr1104Thr | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/15 | 3465/8823 | 3312/3813 | 1104/1270 | chr12 | 14496262 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14365687
|
T | C | 1 | a0001c0001t0027 | 1 | HG02735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-148T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/15 | 58229 | chr12 | 14365687 | |||||
| chr12:14498115
|
T | G | 1 | a0003c0003t0028 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 42 | chr12 | 14498115 | |||||
| chr12:14498214
|
A | G | 1 | a0002c0002t0026 | 2 | NA18945.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*141A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 141 | chr12 | 14498214 | |||||
| chr12:14498482
|
A | G | 1 | a0003c0005t0041 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*409A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 409 | chr12 | 14498482 | |||||
| chr12:14498533
|
GAAAT | G | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(13): Show | 137 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*468_*471delTAAA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 468 | INFO_REALIGN_3_PRIME | chr12 | 14498533 | ||||
| chr12:14498654
|
C | T | 1 | a0001c0001t0017 | 3 | NA18946.hp1 NA18947.hp2 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*581C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 581 | chr12 | 14498654 | |||||
| chr12:14498658
|
A | G | 2 | a0003c0003t0012a0005c0007t0010 | 16 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*585A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 585 | chr12 | 14498658 | |||||
| chr12:14498814
|
C | T | 2 | a0003c0003t0012a0005c0007t0010 | 16 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*741C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 741 | chr12 | 14498814 | |||||
| chr12:14498851
|
A | AT | 24 | a0001c0020t0036a0002c0002t0001a0002c0002t0009others(21): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*790dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 791 | INFO_REALIGN_3_PRIME | chr12 | 14498851 | ||||
| chr12:14498851
|
A | ATT | 2 | a0001c0001t0040a0002c0006t0008 | 12 | HG00438.hp2 HG00673.hp2 HG02165.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*789_*790dupTT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 791 | INFO_REALIGN_3_PRIME | chr12 | 14498851 | ||||
| chr12:14498864
|
A | T | 28 | a0001c0001t0019a0001c0001t0040a0001c0020t0036others(25): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*791A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 791 | chr12 | 14498864 | |||||
| chr12:14499037
|
G | A | 5 | a0001c0020t0036a0003c0003t0004a0003c0003t0011others(2): Show | 29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*964G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 964 | chr12 | 14499037 | |||||
| chr12:14499121
|
C | T | 6 | a0001c0001t0003a0001c0001t0022a0001c0001t0027others(3): Show | 53 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1048C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1048 | chr12 | 14499121 | |||||
| chr12:14499147
|
A | G | 1 | a0003c0003t0015 | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1074A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1074 | chr12 | 14499147 | |||||
| chr12:14499238
|
G | A | 2 | a0003c0003t0013a0003c0014t0013 | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1165G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1165 | chr12 | 14499238 | |||||
| chr12:14499547
|
G | C | 1 | a0002c0002t0037 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1474G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1474 | chr12 | 14499547 | |||||
| chr12:14499576
|
T | C | 1 | a0010c0013t0020 | 2 | HG02723.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1503T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1503 | chr12 | 14499576 | |||||
| chr12:14499738
|
C | T | 3 | a0001c0001t0019a0002c0006t0008a0002c0006t0019 | 14 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1665C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1665 | chr12 | 14499738 | |||||
| chr12:14499824
|
C | CA | 3 | a0003c0005t0007a0003c0005t0038a0003c0005t0041 | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1761dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1762 | INFO_REALIGN_3_PRIME | chr12 | 14499824 | ||||
| chr12:14499898
|
T | G | 1 | a0001c0001t0022 | 2 | HG02622.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1825T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1825 | chr12 | 14499898 | |||||
| chr12:14500090
|
C | G | 4 | a0003c0003t0025a0003c0005t0007a0003c0005t0038others(1): Show | 15 | HG00099.hp1 HG00280.hp1 HG01934.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2017C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2017 | chr12 | 14500090 | |||||
| chr12:14500137
|
C | G | 1 | a0001c0001t0006 | 11 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2064C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2064 | chr12 | 14500137 | |||||
| chr12:14500449
|
T | C | 2 | a0003c0003t0023a0003c0003t0034 | 3 | HG01099.hp1 HG02300.hp1 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2376T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2376 | chr12 | 14500449 | |||||
| chr12:14500657
|
G | A | 1 | a0001c0001t0021 | 2 | HG01257.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2584G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2584 | chr12 | 14500657 | |||||
| chr12:14500666
|
A | G | 1 | a0001c0001t0033 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2593A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2593 | chr12 | 14500666 | |||||
| chr12:14500733
|
T | A | 36 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(33): Show | 222 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*2660T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2660 | chr12 | 14500733 | |||||
| chr12:14500922
|
C | T | 1 | a0003c0003t0012 | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2849C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2849 | chr12 | 14500922 | |||||
| chr12:14500933
|
C | T | 7 | a0002c0002t0001a0002c0002t0026a0002c0002t0037others(4): Show | 82 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2860C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2860 | chr12 | 14500933 | |||||
| chr12:14501142
|
G | C | 1 | a0003c0003t0035 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3069G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 3069 | chr12 | 14501142 | |||||
| chr12:14501196
|
G | A | 1 | a0003c0003t0004 | 19 | HG00733.hp2 HG01123.hp2 HG02257.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3123G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 3123 | chr12 | 14501196 | |||||
| chr12:14501481
|
T | C | 1 | a0001c0001t0029 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3408T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 3408 | chr12 | 14501481 | |||||
| chr12:14501575
|
G | T | 1 | a0001c0001t0040 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3502G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 3502 | chr12 | 14501575 | |||||
| chr12:14501675
|
C | T | 1 | a0008c0011t0024 | 2 | HG01891.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3602C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 3602 | chr12 | 14501675 | |||||
| chr12:14501848
|
C | T | 1 | a0001c0001t0030 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3775C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 3775 | chr12 | 14501848 | |||||
| chr12:14502422
|
CA | C | 14 | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(11): Show | 123 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*4352delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 4352 | INFO_REALIGN_3_PRIME | chr12 | 14502422 | ||||
| chr12:14502700
|
A | T | 1 | a0003c0003t0023 | 2 | HG01099.hp1 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4627A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 4627 | chr12 | 14502700 | |||||
| chr12:14502809
|
T | C | 1 | a0013c0016t0039 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4736T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 4736 | chr12 | 14502809 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14365929
|
C | T | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8+102C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14365929 | ||||||
| chr12:14365961
|
C | T | 1 | a0001c0001t0002g0342 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-8+134C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14365961 | ||||||
| chr12:14366282
|
A | G | 1 | a0003c0003t0011g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+455A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14366282 | ||||||
| chr12:14366615
|
C | T | 1 | a0002c0004t0001g0340 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-8+788C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14366615 | ||||||
| chr12:14366622
|
A | G | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-8+795A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14366622 | ||||||
| chr12:14366802
|
T | G | 1 | a0004c0008t0005g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-8+975T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14366802 | ||||||
| chr12:14366833
|
TAAAAA | T | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8+1010_-8+1014del others(5): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14366833 | |||||
| chr12:14366843
|
C | A | 1 | a0002c0002t0001g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-8+1016C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14366843 | ||||||
| chr12:14366865
|
G | A | 2 | a0002c0002t0009g0005a0002c0002t0009g0006 | 2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-8+1038G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14366865 | ||||||
| chr12:14366909
|
A | T | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8+1082A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14366909 | ||||||
| chr12:14367192
|
T | C | 1 | a0001c0001t0002g0007 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-8+1365T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367192 | ||||||
| chr12:14367307
|
T | C | 141 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(138): Show | 141 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-8+1480T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367307 | ||||||
| chr12:14367497
|
G | T | 1 | a0001c0001t0003g0146 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-8+1670G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367497 | ||||||
| chr12:14367571
|
A | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-8+1744A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367571 | ||||||
| chr12:14367646
|
T | C | 1 | a0001c0001t0003g0008 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-8+1819T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367646 | ||||||
| chr12:14367767
|
A | G | 142 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(139): Show | 142 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.-8+1940A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367767 | ||||||
| chr12:14367836
|
T | C | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-8+2009T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367836 | ||||||
| chr12:14367867
|
A | G | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+2040A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367867 | ||||||
| chr12:14368014
|
A | C | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+2187A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368014 | ||||||
| chr12:14368125
|
T | G | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-8+2298T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368125 | ||||||
| chr12:14368243
|
A | C | 1 | a0001c0001t0002g0143 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-8+2416A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368243 | ||||||
| chr12:14368248
|
T | C | 141 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(138): Show | 141 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-8+2421T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368248 | ||||||
| chr12:14368285
|
C | G | 2 | a0003c0003t0011g0314a0003c0003t0011g0315 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-8+2458C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368285 | ||||||
| chr12:14368442
|
G | T | 179 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(176): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-8+2615G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368442 | ||||||
| chr12:14368490
|
C | T | 114 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.-8+2663C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368490 | ||||||
| chr12:14368653
|
A | G | 29 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(26): Show | 29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.-8+2826A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368653 | ||||||
| chr12:14368870
|
G | C | 1 | a0001c0001t0031g0009 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3043G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368870 | ||||||
| chr12:14368875
|
T | C | 1 | a0001c0001t0031g0009 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3048T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368875 | ||||||
| chr12:14368876
|
T | G | 1 | a0001c0001t0031g0009 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3049T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368876 | ||||||
| chr12:14368877
|
T | C | 1 | a0001c0001t0031g0009 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3050T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368877 | ||||||
| chr12:14368878
|
A | G | 1 | a0001c0001t0031g0009 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3051A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368878 | ||||||
| chr12:14368879
|
A | T | 1 | a0001c0001t0031g0009 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3052A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368879 | ||||||
| chr12:14368880
|
A | G | 1 | a0001c0001t0031g0009 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3053A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368880 | ||||||
| chr12:14368881
|
A | T | 1 | a0001c0001t0031g0009 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3054A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368881 | ||||||
| chr12:14368891
|
A | G | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+3064A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368891 | ||||||
| chr12:14369118
|
CT | C | 173 | a0001c0001t0002g0010a0001c0001t0003g0012a0002c0002t0001g0004others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-8+3307delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14369118 | |||||
| chr12:14369125
|
T | C | 2 | a0002c0002t0001g0205a0002c0002t0001g0206 | 2 | HG00621.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-8+3298T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369125 | ||||||
| chr12:14369175
|
A | G | 17 | a0002c0002t0001g0296a0002c0002t0001g0297a0002c0002t0001g0298others(14): Show | 17 | HG00597.hp2 HG01167.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8+3348A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369175 | ||||||
| chr12:14369199
|
C | T | 1 | a0002c0006t0008g0295 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-8+3372C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369199 | ||||||
| chr12:14369383
|
C | T | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+3556C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369383 | ||||||
| chr12:14369432
|
G | T | 7 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(4): Show | 9 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+3605G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369432 | ||||||
| chr12:14369549
|
G | C | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-8+3722G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369549 | ||||||
| chr12:14369587
|
C | G | 1 | a0002c0002t0001g0310 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-8+3760C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369587 | ||||||
| chr12:14369707
|
T | C | 65 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(62): Show | 65 | HG01175.hp1 HG01243.hp1 HG01257.hp1 others(62): Show |
intron_variant | MODIFIER | c.-8+3880T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369707 | ||||||
| chr12:14369761
|
GCTAGTTT others(18): Show |
G | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+3946_-8+3970del others(25): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14369761 | |||||
| chr12:14369783
|
A | G | 1 | a0003c0003t0005g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-8+3956A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369783 | ||||||
| chr12:14369939
|
A | AT | 8 | a0001c0001t0002g0069a0002c0002t0001g0312a0003c0003t0012g0001others(5): Show | 10 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+4127dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14369939 | |||||
| chr12:14369967
|
C | T | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+4140C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369967 | ||||||
| chr12:14369968
|
G | A | 1 | a0001c0001t0006g0070 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-8+4141G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369968 | ||||||
| chr12:14370001
|
G | A | 1 | a0002c0002t0001g0207 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-8+4174G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370001 | ||||||
| chr12:14370135
|
C | T | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+4308C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370135 | ||||||
| chr12:14370197
|
A | G | 2 | a0004c0008t0005g0293a0004c0008t0005g0294 | 2 | HG01361.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-8+4370A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370197 | ||||||
| chr12:14370213
|
A | G | 186 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.-8+4386A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370213 | ||||||
| chr12:14370302
|
T | C | 2 | a0002c0006t0008g0208a0002c0006t0008g0295 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-8+4475T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370302 | ||||||
| chr12:14370315
|
G | A | 1 | a0002c0002t0001g0312 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-8+4488G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370315 | ||||||
| chr12:14370384
|
C | T | 1 | a0001c0001t0003g0142 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-8+4557C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370384 | ||||||
| chr12:14370474
|
G | A | 185 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(182): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-8+4647G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370474 | ||||||
| chr12:14370540
|
A | C | 1 | a0001c0001t0002g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-8+4713A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370540 | ||||||
| chr12:14370633
|
A | G | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-8+4806A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370633 | ||||||
| chr12:14370740
|
A | G | 42 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(39): Show | 42 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.-8+4913A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370740 | ||||||
| chr12:14370796
|
A | C | 1 | a0001c0001t0003g0141 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8+4969A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370796 | ||||||
| chr12:14370811
|
C | A | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-8+4984C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370811 | ||||||
| chr12:14370899
|
A | G | 1 | a0003c0003t0004g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8+5072A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370899 | ||||||
| chr12:14370957
|
C | A | 2 | a0003c0003t0011g0184a0003c0003t0028g0183 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-8+5130C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370957 | ||||||
| chr12:14371004
|
G | A | 2 | a0001c0001t0002g0013a0001c0001t0002g0014 | 2 | NA18953.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-8+5177G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371004 | ||||||
| chr12:14371038
|
G | T | 180 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(177): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-8+5211G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371038 | ||||||
| chr12:14371136
|
A | G | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-8+5309A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371136 | ||||||
| chr12:14371507
|
T | C | 2 | a0002c0002t0001g0209a0002c0002t0001g0210 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-8+5680T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371507 | ||||||
| chr12:14371564
|
A | G | 186 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.-8+5737A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371564 | ||||||
| chr12:14371565
|
A | C | 186 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.-8+5738A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371565 | ||||||
| chr12:14371613
|
A | G | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-8+5786A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371613 | ||||||
| chr12:14371987
|
A | G | 186 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.-8+6160A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371987 | ||||||
| chr12:14372164
|
C | T | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+6337C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14372164 | ||||||
| chr12:14372215
|
C | T | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+6388C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14372215 | ||||||
| chr12:14372232
|
T | A | 1 | a0003c0003t0014g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-8+6405T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14372232 | ||||||
| chr12:14372360
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-8+6533C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14372360 | ||||||
| chr12:14372460
|
C | CA | 146 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0015others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.-8+6649dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14372460 | |||||
| chr12:14372460
|
C | CAA | 14 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(11): Show | 16 | HG01071.hp1 HG01109.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8+6648_-8+6649dup others(2): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14372460 | |||||
| chr12:14372993
|
G | A | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+7166G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14372993 | ||||||
| chr12:14373092
|
C | T | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+7265C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373092 | ||||||
| chr12:14373255
|
C | T | 1 | a0001c0001t0002g0342 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-8+7428C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373255 | ||||||
| chr12:14373305
|
CAT | C | 141 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(138): Show | 141 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-8+7479_-8+7480del others(2): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373305 | ||||||
| chr12:14373386
|
C | A | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+7559C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373386 | ||||||
| chr12:14373446
|
A | G | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-8+7619A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373446 | ||||||
| chr12:14373450
|
G | C | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-8+7623G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373450 | ||||||
| chr12:14373516
|
A | C | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+7689A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373516 | ||||||
| chr12:14373535
|
T | A | 1 | a0002c0006t0008g0217 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-8+7708T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373535 | ||||||
| chr12:14373595
|
G | C | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+7768G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373595 | ||||||
| chr12:14373674
|
A | G | 2 | a0003c0003t0011g0314a0003c0003t0011g0315 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-8+7847A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373674 | ||||||
| chr12:14373789
|
T | C | 2 | a0003c0003t0011g0184a0003c0003t0028g0183 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-8+7962T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373789 | ||||||
| chr12:14373816
|
C | T | 1 | a0003c0003t0025g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-8+7989C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373816 | ||||||
| chr12:14373926
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-8+8099G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373926 | ||||||
| chr12:14373946
|
A | G | 2 | a0003c0014t0013g0163a0003c0014t0013g0164 | 2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-8+8119A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373946 | ||||||
| chr12:14373969
|
A | C | 65 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(62): Show | 65 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.-8+8142A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373969 | ||||||
| chr12:14374033
|
A | AT | 142 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(139): Show | 142 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.-8+8215dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14374033 | |||||
| chr12:14374036
|
T | A | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8+8209T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374036 | ||||||
| chr12:14374076
|
T | C | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+8249T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374076 | ||||||
| chr12:14374096
|
A | AC | 3 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0311 | 3 | NA18947.hp1 NA18979.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-8+8270dupC | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14374096 | |||||
| chr12:14374107
|
T | C | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+8280T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374107 | ||||||
| chr12:14374154
|
G | C | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+8327G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374154 | ||||||
| chr12:14374272
|
A | AT | 40 | a0001c0001t0002g0019a0001c0001t0002g0064a0001c0001t0002g0065others(37): Show | 40 | HG00280.hp2 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-8+8466dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14374272 | |||||
| chr12:14374272
|
A | ATT | 86 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-8+8465_-8+8466dup others(2): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14374272 | |||||
| chr12:14374272
|
AT | A | 10 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0014t0013g0163others(7): Show | 11 | HG00609.hp2 HG00639.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+8466delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14374272 | |||||
| chr12:14374378
|
T | C | 5 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0023g0151others(2): Show | 5 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+8551T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374378 | ||||||
| chr12:14374460
|
T | C | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+8633T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374460 | ||||||
| chr12:14374578
|
A | C | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+8751A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374578 | ||||||
| chr12:14374711
|
G | A | 2 | a0002c0006t0008g0208a0002c0006t0008g0295 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-8+8884G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374711 | ||||||
| chr12:14374727
|
C | G | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+8900C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374727 | ||||||
| chr12:14374805
|
A | G | 1 | a0001c0001t0040g0139 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-8+8978A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374805 | ||||||
| chr12:14374819
|
T | C | 1 | a0001c0001t0003g0074 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-8+8992T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374819 | ||||||
| chr12:14374835
|
A | G | 114 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.-8+9008A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374835 | ||||||
| chr12:14374988
|
T | TTTTTTTT others(2060): Show |
1 | a0001c0001t0002g0069 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-8+9161_-8+9162ins others(2067): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374988 | ||||||
| chr12:14374988
|
T | TTTTTTTT others(2063): Show |
1 | a0001c0001t0002g0061 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-8+9161_-8+9162ins others(2070): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374988 | ||||||
| chr12:14374988
|
T | TTTTTTTT others(2060): Show |
1 | a0001c0001t0019g0062 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-8+9161_-8+9162ins others(2067): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374988 | ||||||
| chr12:14374988
|
T | TTTTTTTT others(2059): Show |
1 | a0001c0001t0002g0063 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-8+9161_-8+9162ins others(2066): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374988 | ||||||
| chr12:14374989
|
A | C | 4 | a0001c0001t0002g0061a0001c0001t0002g0063a0001c0001t0002g0069others(1): Show | 4 | HG02135.hp2 NA18977.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+9162A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374989 | ||||||
| chr12:14374990
|
A | G | 4 | a0001c0001t0002g0061a0001c0001t0002g0063a0001c0001t0002g0069others(1): Show | 4 | HG02135.hp2 NA18977.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+9163A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374990 | ||||||
| chr12:14374993
|
C | CG | 4 | a0001c0001t0002g0061a0001c0001t0002g0063a0001c0001t0002g0069others(1): Show | 4 | HG02135.hp2 NA18977.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+9166_-8+9167ins others(1): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374993 | ||||||
| chr12:14375222
|
T | A | 3 | a0003c0003t0004g0198a0003c0003t0004g0199a0003c0003t0004g0200 | 3 | HG02970.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-8+9395T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375222 | ||||||
| chr12:14375271
|
G | C | 2 | a0001c0001t0006g0076a0001c0001t0016g0075 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-8+9444G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375271 | ||||||
| chr12:14375319
|
G | A | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+9492G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375319 | ||||||
| chr12:14375526
|
G | A | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-8+9699G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375526 | ||||||
| chr12:14375587
|
A | T | 2 | a0002c0002t0001g0206a0002c0002t0001g0286 | 2 | HG00438.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-8+9760A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375587 | ||||||
| chr12:14375768
|
C | T | 1 | a0002c0002t0001g0285 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-8+9941C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375768 | ||||||
| chr12:14375860
|
G | A | 185 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(182): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-8+10033G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375860 | ||||||
| chr12:14375905
|
G | A | 1 | a0001c0001t0003g0077 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-8+10078G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375905 | ||||||
| chr12:14376121
|
T | C | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+10294T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376121 | ||||||
| chr12:14376336
|
C | T | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+10509C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376336 | ||||||
| chr12:14376386
|
C | T | 1 | a0002c0002t0001g0296 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-8+10559C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376386 | ||||||
| chr12:14376638
|
A | G | 2 | a0006c0009t0005g0177a0006c0009t0005g0178 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-8+10811A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376638 | ||||||
| chr12:14376692
|
G | T | 1 | a0005c0007t0010g0322 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-8+10865G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376692 | ||||||
| chr12:14376713
|
T | C | 12 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(9): Show | 12 | HG03491.hp1 HG03492.hp2 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8+10886T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376713 | ||||||
| chr12:14376791
|
T | C | 2 | a0003c0003t0011g0184a0003c0003t0028g0183 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-8+10964T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376791 | ||||||
| chr12:14376979
|
A | C | 1 | a0002c0004t0001g0247 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-8+11152A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376979 | ||||||
| chr12:14376992
|
T | G | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+11165T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376992 | ||||||
| chr12:14377126
|
C | T | 2 | a0002c0006t0008g0227a0002c0006t0019g0228 | 2 | HG00438.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-8+11299C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377126 | ||||||
| chr12:14377135
|
C | A | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8+11308C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377135 | ||||||
| chr12:14377192
|
A | G | 1 | a0003c0005t0041g0337 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-8+11365A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377192 | ||||||
| chr12:14377271
|
A | G | 19 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(16): Show | 19 | HG00733.hp2 HG01123.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8+11444A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377271 | ||||||
| chr12:14377334
|
C | T | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+11507C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377334 | ||||||
| chr12:14377357
|
A | AT | 11 | a0001c0001t0002g0342a0001c0001t0003g0072a0001c0001t0003g0077others(8): Show | 13 | HG01243.hp1 HG02080.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+11546dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14377357 | |||||
| chr12:14377379
|
G | T | 10 | a0001c0001t0006g0070a0001c0001t0006g0076a0001c0001t0006g0132others(7): Show | 10 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+11552G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377379 | ||||||
| chr12:14377516
|
C | T | 11 | a0001c0001t0006g0070a0001c0001t0006g0076a0001c0001t0006g0129others(8): Show | 11 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+11689C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377516 | ||||||
| chr12:14377644
|
C | T | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+11817C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377644 | ||||||
| chr12:14377674
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-8+11847C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377674 | ||||||
| chr12:14377675
|
G | A | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+11848G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377675 | ||||||
| chr12:14377814
|
A | G | 5 | a0001c0001t0002g0058a0001c0001t0002g0061a0001c0001t0002g0063others(2): Show | 5 | HG02135.hp2 NA18977.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+11987A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377814 | ||||||
| chr12:14377931
|
C | T | 1 | a0003c0003t0011g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+12104C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377931 | ||||||
| chr12:14377948
|
T | C | 2 | a0001c0001t0003g0078a0001c0001t0003g0079 | 2 | NA18955.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-8+12121T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377948 | ||||||
| chr12:14378100
|
C | CT | 143 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(140): Show | 146 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-8+12288dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14378100 | |||||
| chr12:14378100
|
C | CTT | 25 | a0002c0002t0001g0225a0002c0002t0001g0249a0002c0002t0001g0284others(22): Show | 25 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8+12287_-8+12288d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14378100 | |||||
| chr12:14378105
|
T | TC | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+12278_-8+12279i others(3): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378105 | ||||||
| chr12:14378137
|
G | A | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-8+12310G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378137 | ||||||
| chr12:14378178
|
A | G | 18 | a0003c0003t0011g0204a0003c0003t0011g0314a0003c0003t0011g0315others(15): Show | 18 | HG01934.hp1 HG02145.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8+12351A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378178 | ||||||
| chr12:14378277
|
A | T | 186 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.-8+12450A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378277 | ||||||
| chr12:14378377
|
C | T | 2 | a0003c0014t0013g0163a0003c0014t0013g0164 | 2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-8+12550C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378377 | ||||||
| chr12:14378403
|
T | C | 1 | a0001c0001t0003g0080 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-8+12576T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378403 | ||||||
| chr12:14378562
|
A | G | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+12735A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378562 | ||||||
| chr12:14378611
|
G | A | 185 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(182): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-8+12784G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378611 | ||||||
| chr12:14378630
|
T | C | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+12803T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378630 | ||||||
| chr12:14378857
|
T | C | 1 | a0003c0003t0011g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+13030T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378857 | ||||||
| chr12:14379102
|
C | G | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+13275C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14379102 | ||||||
| chr12:14379250
|
T | G | 2 | a0003c0003t0012g0001a0003c0003t0012g0179 | 4 | HG02630.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+13423T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14379250 | ||||||
| chr12:14379331
|
C | T | 1 | a0003c0014t0013g0164 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-8+13504C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14379331 | ||||||
| chr12:14379391
|
A | C | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+13564A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14379391 | ||||||
| chr12:14379767
|
C | T | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+13940C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14379767 | ||||||
| chr12:14380242
|
A | G | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8+14415A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380242 | ||||||
| chr12:14380287
|
GTC | G | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+14464_-8+14465d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14380287 | |||||
| chr12:14380474
|
A | T | 1 | a0001c0001t0002g0057 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-8+14647A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380474 | ||||||
| chr12:14380556
|
G | A | 179 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(176): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-8+14729G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380556 | ||||||
| chr12:14380612
|
T | G | 5 | a0001c0001t0002g0084a0001c0001t0003g0083a0001c0001t0022g0081others(2): Show | 5 | HG02622.hp1 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+14785T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380612 | ||||||
| chr12:14380631
|
T | C | 1 | a0001c0001t0003g0085 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-8+14804T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380631 | ||||||
| chr12:14380839
|
C | T | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+15012C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380839 | ||||||
| chr12:14380867
|
C | G | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-8+15040C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380867 | ||||||
| chr12:14380916
|
G | A | 1 | a0003c0003t0011g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-8+15089G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380916 | ||||||
| chr12:14381258
|
G | T | 5 | a0001c0001t0003g0074a0001c0001t0003g0078a0001c0001t0003g0079others(2): Show | 5 | HG02165.hp1 HG03239.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+15431G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14381258 | ||||||
| chr12:14381264
|
T | C | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-8+15437T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14381264 | ||||||
| chr12:14381492
|
G | A | 179 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(176): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-8+15665G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14381492 | ||||||
| chr12:14381526
|
C | T | 8 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0013g0159others(5): Show | 10 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+15699C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14381526 | ||||||
| chr12:14381590
|
GT | G | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+15770delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14381590 | |||||
| chr12:14381867
|
G | GT | 335 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(332): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-8+16051dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14381867 | |||||
| chr12:14381929
|
A | G | 2 | a0002c0002t0001g0246a0013c0016t0039g0245 | 2 | HG02683.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-8+16102A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14381929 | ||||||
| chr12:14382066
|
G | A | 1 | a0002c0002t0001g0297 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-8+16239G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382066 | ||||||
| chr12:14382201
|
A | G | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+16374A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382201 | ||||||
| chr12:14382328
|
T | C | 1 | a0001c0001t0006g0076 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-8+16501T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382328 | ||||||
| chr12:14382373
|
C | T | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+16546C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382373 | ||||||
| chr12:14382531
|
T | A | 1 | a0001c0001t0002g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-8+16704T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382531 | ||||||
| chr12:14382617
|
A | G | 104 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-8+16790A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382617 | ||||||
| chr12:14382945
|
G | A | 184 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(181): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-8+17118G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382945 | ||||||
| chr12:14382974
|
T | G | 141 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(138): Show | 141 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-8+17147T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382974 | ||||||
| chr12:14383071
|
C | G | 180 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(177): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-8+17244C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383071 | ||||||
| chr12:14383105
|
G | A | 1 | a0001c0001t0003g0086 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8+17278G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383105 | ||||||
| chr12:14383115
|
A | T | 1 | a0008c0011t0024g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-8+17288A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383115 | ||||||
| chr12:14383116
|
C | T | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+17289C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383116 | ||||||
| chr12:14383350
|
G | T | 1 | a0001c0001t0002g0063 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-8+17523G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383350 | ||||||
| chr12:14383416
|
G | A | 9 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(6): Show | 11 | HG00099.hp1 HG00280.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+17589G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383416 | ||||||
| chr12:14383472
|
C | G | 1 | a0001c0001t0003g0008 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-8+17645C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383472 | ||||||
| chr12:14383503
|
A | G | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+17676A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383503 | ||||||
| chr12:14383613
|
A | G | 13 | a0002c0002t0001g0225a0002c0006t0008g0208a0002c0006t0008g0217others(10): Show | 13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+17786A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383613 | ||||||
| chr12:14383724
|
T | A | 104 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-8+17897T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383724 | ||||||
| chr12:14383732
|
T | G | 142 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(139): Show | 142 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.-8+17905T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383732 | ||||||
| chr12:14383778
|
T | G | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-8+17951T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383778 | ||||||
| chr12:14383808
|
C | T | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-8+17981C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383808 | ||||||
| chr12:14383817
|
C | T | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-8+17990C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383817 | ||||||
| chr12:14383939
|
A | G | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+18112A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383939 | ||||||
| chr12:14384101
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-8+18274G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14384101 | ||||||
| chr12:14384330
|
C | G | 1 | a0001c0001t0003g0079 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-8+18503C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14384330 | ||||||
| chr12:14384331
|
C | A | 1 | a0001c0001t0003g0079 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-8+18504C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14384331 | ||||||
| chr12:14384379
|
A | C | 1 | a0002c0002t0001g0310 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-8+18552A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14384379 | ||||||
| chr12:14384578
|
T | C | 1 | a0001c0001t0002g0058 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-8+18751T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14384578 | ||||||
| chr12:14384787
|
TAATC | T | 8 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(5): Show | 8 | HG02486.hp2 NA18946.hp2 NA19003.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+18967_-8+18970d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14384787 | |||||
| chr12:14384841
|
G | A | 1 | a0002c0002t0001g0205 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-8+19014G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14384841 | ||||||
| chr12:14384872
|
T | TA | 252 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(249): Show | 252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.-8+19059dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14384872 | |||||
| chr12:14384872
|
T | TAA | 7 | a0001c0001t0003g0090a0001c0001t0003g0091a0001c0001t0006g0132others(4): Show | 7 | HG01243.hp2 HG02083.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+19058_-8+19059d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14384872 | |||||
| chr12:14384872
|
TA | T | 18 | a0003c0003t0005g0316a0003c0003t0013g0159a0003c0003t0013g0160others(15): Show | 19 | HG00609.hp2 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-8+19059delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14384872 | |||||
| chr12:14384906
|
C | CT | 7 | a0001c0001t0014g0125a0001c0001t0016g0075a0001c0001t0016g0126others(4): Show | 8 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+19094dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14384906 | |||||
| chr12:14384988
|
A | C | 13 | a0002c0002t0001g0225a0002c0006t0008g0208a0002c0006t0008g0217others(10): Show | 13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+19161A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14384988 | ||||||
| chr12:14385001
|
C | G | 4 | a0001c0001t0002g0084a0001c0001t0003g0083a0001c0001t0022g0081others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+19174C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385001 | ||||||
| chr12:14385140
|
C | T | 3 | a0002c0002t0009g0287a0002c0002t0009g0288a0002c0002t0009g0289 | 3 | HG02622.hp2 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-8+19313C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385140 | ||||||
| chr12:14385195
|
C | T | 1 | a0002c0002t0001g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-8+19368C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385195 | ||||||
| chr12:14385431
|
A | G | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-8+19604A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385431 | ||||||
| chr12:14385453
|
A | G | 1 | a0002c0004t0001g0243 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-8+19626A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385453 | ||||||
| chr12:14385557
|
A | G | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+19730A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385557 | ||||||
| chr12:14385683
|
G | T | 3 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0059 | 3 | NA18612.hp2 NA18993.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-8+19856G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385683 | ||||||
| chr12:14385782
|
G | C | 4 | a0002c0004t0001g0230a0002c0004t0001g0231a0002c0004t0001g0232others(1): Show | 4 | HG01074.hp2 HG01175.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+19955G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385782 | ||||||
| chr12:14385797
|
T | C | 1 | a0002c0002t0001g0207 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-8+19970T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385797 | ||||||
| chr12:14386385
|
C | CTTA | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+20558_-8+20559i others(5): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386385 | ||||||
| chr12:14386387
|
G | A | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+20560G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386387 | ||||||
| chr12:14386390
|
CCTG | C | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+20564_-8+20566d others(5): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386390 | ||||||
| chr12:14386438
|
G | A | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+20611G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386438 | ||||||
| chr12:14386443
|
G | A | 1 | a0003c0003t0034g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-8+20616G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386443 | ||||||
| chr12:14386469
|
A | G | 11 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+20642A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386469 | ||||||
| chr12:14386616
|
A | C | 1 | a0003c0003t0011g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-8+20789A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386616 | ||||||
| chr12:14386774
|
C | T | 3 | a0002c0002t0009g0287a0002c0002t0009g0288a0002c0002t0009g0289 | 3 | HG02622.hp2 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-8+20947C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386774 | ||||||
| chr12:14386797
|
G | A | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+20970G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386797 | ||||||
| chr12:14386945
|
A | C | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-8+21118A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386945 | ||||||
| chr12:14386972
|
A | T | 2 | a0003c0003t0012g0001a0003c0003t0012g0179 | 4 | HG02630.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+21145A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386972 | ||||||
| chr12:14386972
|
AT | A | 6 | a0001c0001t0003g0085a0001c0001t0003g0092a0001c0001t0003g0128others(3): Show | 6 | HG00741.hp1 HG01993.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+21153delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14386972 | |||||
| chr12:14387023
|
A | G | 4 | a0002c0002t0001g0225a0002c0006t0008g0223a0002c0006t0008g0224others(1): Show | 4 | NA18977.hp2 NA18981.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+21196A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387023 | ||||||
| chr12:14387070
|
C | T | 1 | a0003c0005t0041g0337 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-8+21243C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387070 | ||||||
| chr12:14387153
|
C | T | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+21326C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387153 | ||||||
| chr12:14387203
|
A | C | 186 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.-8+21376A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387203 | ||||||
| chr12:14387207
|
AAAAAAG | A | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+21392_-8+21397d others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14387207 | |||||
| chr12:14387245
|
A | C | 2 | a0003c0003t0011g0184a0003c0003t0028g0183 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-8+21418A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387245 | ||||||
| chr12:14387478
|
T | G | 2 | a0003c0005t0038g0331a0003c0005t0041g0337 | 2 | HG01934.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-8+21651T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387478 | ||||||
| chr12:14387561
|
G | C | 186 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.-8+21734G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387561 | ||||||
| chr12:14387646
|
T | A | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+21819T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387646 | ||||||
| chr12:14387694
|
G | A | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8+21867G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387694 | ||||||
| chr12:14387760
|
G | A | 1 | a0001c0001t0002g0021 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-8+21933G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387760 | ||||||
| chr12:14388014
|
CT | C | 174 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-8+22203delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14388014 | |||||
| chr12:14388077
|
T | G | 180 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(177): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-8+22250T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388077 | ||||||
| chr12:14388078
|
T | A | 180 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(177): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-8+22251T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388078 | ||||||
| chr12:14388104
|
C | T | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+22277C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388104 | ||||||
| chr12:14388123
|
C | G | 2 | a0004c0008t0005g0280a0004c0008t0005g0283 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-8+22296C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388123 | ||||||
| chr12:14388174
|
C | T | 4 | a0004c0008t0005g0003a0004c0008t0005g0279a0004c0008t0005g0293others(1): Show | 4 | HG01123.hp1 HG01361.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+22347C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388174 | ||||||
| chr12:14388229
|
T | C | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | NA18980.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-8+22402T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388229 | ||||||
| chr12:14388294
|
C | T | 1 | a0002c0002t0001g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-8+22467C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388294 | ||||||
| chr12:14388297
|
G | A | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+22470G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388297 | ||||||
| chr12:14388471
|
C | T | 1 | a0002c0002t0001g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-8+22644C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388471 | ||||||
| chr12:14388589
|
C | T | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+22762C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388589 | ||||||
| chr12:14388590
|
G | A | 1 | a0003c0005t0038g0331 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-8+22763G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388590 | ||||||
| chr12:14388669
|
C | T | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+22842C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388669 | ||||||
| chr12:14388739
|
G | C | 1 | a0003c0003t0011g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+22912G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388739 | ||||||
| chr12:14388828
|
C | T | 1 | a0002c0002t0001g0307 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-8+23001C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388828 | ||||||
| chr12:14389033
|
A | G | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+23206A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389033 | ||||||
| chr12:14389045
|
T | C | 1 | a0007c0010t0002g0022 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-8+23218T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389045 | ||||||
| chr12:14389142
|
T | G | 1 | a0003c0003t0018g0153 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-8+23315T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389142 | ||||||
| chr12:14389194
|
A | G | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+23367A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389194 | ||||||
| chr12:14389315
|
G | A | 1 | a0002c0002t0001g0285 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-8+23488G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389315 | ||||||
| chr12:14389607
|
A | G | 180 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(177): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-8+23780A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389607 | ||||||
| chr12:14389697
|
G | A | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+23870G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389697 | ||||||
| chr12:14389764
|
T | A | 180 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(177): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-8+23937T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389764 | ||||||
| chr12:14389866
|
C | T | 1 | a0001c0001t0003g0124 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-8+24039C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389866 | ||||||
| chr12:14390053
|
C | T | 4 | a0001c0001t0003g0012a0001c0001t0003g0121a0001c0001t0003g0122others(1): Show | 4 | HG01074.hp1 HG01168.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+24226C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390053 | ||||||
| chr12:14390081
|
C | T | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+24254C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390081 | ||||||
| chr12:14390112
|
G | A | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-8+24285G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390112 | ||||||
| chr12:14390113
|
C | T | 114 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.-8+24286C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390113 | ||||||
| chr12:14390114
|
G | A | 1 | a0006c0009t0005g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-8+24287G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390114 | ||||||
| chr12:14390137
|
T | TTA | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+24311_-8+24312d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14390137 | |||||
| chr12:14390282
|
A | G | 1 | a0005c0007t0010g0322 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-8+24455A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390282 | ||||||
| chr12:14390316
|
T | A | 1 | a0002c0006t0008g0256 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-8+24489T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390316 | ||||||
| chr12:14390371
|
A | G | 1 | a0003c0003t0005g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-8+24544A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390371 | ||||||
| chr12:14390386
|
G | A | 1 | a0001c0001t0002g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-8+24559G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390386 | ||||||
| chr12:14390624
|
C | G | 5 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0023g0151others(2): Show | 5 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+24797C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390624 | ||||||
| chr12:14391142
|
A | G | 13 | a0002c0002t0001g0225a0002c0006t0008g0208a0002c0006t0008g0217others(10): Show | 13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+25315A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14391142 | ||||||
| chr12:14391391
|
T | C | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+25564T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14391391 | ||||||
| chr12:14391484
|
C | G | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-8+25657C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14391484 | ||||||
| chr12:14391778
|
A | G | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-8+25951A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14391778 | ||||||
| chr12:14391806
|
C | T | 28 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(25): Show | 28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8+25979C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14391806 | ||||||
| chr12:14391871
|
G | A | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8+26044G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14391871 | ||||||
| chr12:14391911
|
G | A | 1 | a0003c0003t0028g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-8+26084G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14391911 | ||||||
| chr12:14392044
|
T | C | 2 | a0003c0003t0011g0184a0003c0003t0028g0183 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-8+26217T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392044 | ||||||
| chr12:14392082
|
T | G | 1 | a0001c0020t0036g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-8+26255T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392082 | ||||||
| chr12:14392224
|
C | CT | 31 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(28): Show | 31 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8+26407dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14392224 | |||||
| chr12:14392227
|
TTTTTTTT others(1): Show |
T | 11 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+26408_-8+26415d others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14392227 | |||||
| chr12:14392472
|
C | G | 1 | a0002c0002t0001g0306 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-8+26645C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392472 | ||||||
| chr12:14392534
|
A | G | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+26707A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392534 | ||||||
| chr12:14392541
|
G | T | 1 | a0001c0001t0002g0055 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-8+26714G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392541 | ||||||
| chr12:14392646
|
T | C | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+26819T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392646 | ||||||
| chr12:14392776
|
A | C | 1 | a0002c0002t0001g0312 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-8+26949A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392776 | ||||||
| chr12:14392809
|
A | G | 1 | a0003c0003t0011g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+26982A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392809 | ||||||
| chr12:14392870
|
A | G | 1 | a0002c0004t0001g0233 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-8+27043A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392870 | ||||||
| chr12:14392906
|
C | G | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-8+27079C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392906 | ||||||
| chr12:14393013
|
G | A | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+27186G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393013 | ||||||
| chr12:14393239
|
A | T | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+27412A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393239 | ||||||
| chr12:14393262
|
T | C | 1 | a0001c0001t0003g0080 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-8+27435T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393262 | ||||||
| chr12:14393419
|
T | C | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-8+27592T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393419 | ||||||
| chr12:14393423
|
A | G | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+27596A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393423 | ||||||
| chr12:14393435
|
C | G | 4 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(1): Show | 6 | HG02630.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+27608C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393435 | ||||||
| chr12:14393537
|
TAA | T | 15 | a0002c0004t0001g0216a0002c0004t0001g0229a0002c0004t0001g0230others(12): Show | 15 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8+27711_-8+27712d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393537 | ||||||
| chr12:14393774
|
G | A | 1 | a0001c0001t0003g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-8+27947G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393774 | ||||||
| chr12:14394447
|
A | G | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+28620A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14394447 | ||||||
| chr12:14394704
|
G | C | 1 | a0001c0001t0002g0342 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-8+28877G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14394704 | ||||||
| chr12:14394768
|
A | G | 1 | a0001c0020t0036g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-8+28941A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14394768 | ||||||
| chr12:14394958
|
G | A | 26 | a0002c0002t0001g0209a0002c0002t0001g0210a0002c0002t0001g0218others(23): Show | 26 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7-28951G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14394958 | ||||||
| chr12:14395074
|
A | G | 1 | a0002c0002t0001g0278 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-7-28835A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14395074 | ||||||
| chr12:14395318
|
T | TG | 342 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(339): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.-7-28589dupG | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14395318 | |||||
| chr12:14395380
|
A | C | 181 | a0001c0001t0002g0067a0002c0002t0001g0004a0002c0002t0001g0205others(178): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.-7-28529A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14395380 | ||||||
| chr12:14395471
|
G | T | 1 | a0002c0002t0001g0206 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-7-28438G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14395471 | ||||||
| chr12:14395891
|
C | A | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-7-28018C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14395891 | ||||||
| chr12:14395934
|
TA | T | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-27974delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14395934 | ||||||
| chr12:14396050
|
A | G | 1 | a0002c0002t0037g0237 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-7-27859A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396050 | ||||||
| chr12:14396066
|
G | A | 3 | a0003c0003t0004g0198a0003c0003t0004g0199a0003c0003t0004g0200 | 3 | HG02970.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-7-27843G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396066 | ||||||
| chr12:14396172
|
G | A | 1 | a0003c0003t0011g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-27737G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396172 | ||||||
| chr12:14396250
|
CTT | C | 19 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(16): Show | 19 | HG00733.hp2 HG01123.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-7-27657_-7-27656d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14396250 | |||||
| chr12:14396287
|
C | G | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7-27622C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396287 | ||||||
| chr12:14396380
|
G | C | 1 | a0001c0001t0003g0087 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-7-27529G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396380 | ||||||
| chr12:14396434
|
A | G | 1 | a0003c0003t0004g0202 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-7-27475A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396434 | ||||||
| chr12:14396437
|
T | TA | 13 | a0003c0003t0005g0316a0003c0003t0013g0159a0003c0003t0013g0160others(10): Show | 14 | HG00609.hp2 HG00639.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7-27461dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14396437 | |||||
| chr12:14396438
|
A | T | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7-27471A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396438 | ||||||
| chr12:14396901
|
C | T | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-27008C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396901 | ||||||
| chr12:14396926
|
C | T | 3 | a0002c0002t0001g0277a0002c0002t0001g0284a0002c0002t0001g0285 | 3 | HG00099.hp2 HG00733.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-7-26983C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396926 | ||||||
| chr12:14396971
|
A | C | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-26938A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396971 | ||||||
| chr12:14396998
|
T | A | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-26911T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396998 | ||||||
| chr12:14397118
|
C | T | 1 | a0002c0002t0001g0205 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-7-26791C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14397118 | ||||||
| chr12:14397617
|
TTCTG | T | 5 | a0002c0002t0001g0207a0002c0002t0001g0254a0002c0002t0001g0257others(2): Show | 5 | HG02083.hp1 NA18942.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-26282_-7-26279d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14397617 | |||||
| chr12:14397659
|
A | G | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-26250A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14397659 | ||||||
| chr12:14397660
|
T | A | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-26249T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14397660 | ||||||
| chr12:14397718
|
AAATATC | A | 91 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.-7-26184_-7-26179d others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14397718 | |||||
| chr12:14398037
|
A | G | 4 | a0002c0002t0001g0207a0002c0002t0001g0257a0002c0002t0001g0258others(1): Show | 4 | NA18942.hp1 NA18973.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-25872A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398037 | ||||||
| chr12:14398066
|
C | T | 13 | a0002c0002t0001g0225a0002c0006t0008g0208a0002c0006t0008g0217others(10): Show | 13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-25843C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398066 | ||||||
| chr12:14398091
|
T | C | 196 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(193): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-7-25818T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398091 | ||||||
| chr12:14398276
|
C | A | 2 | a0003c0014t0013g0163a0003c0014t0013g0164 | 2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-7-25633C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398276 | ||||||
| chr12:14398387
|
G | GT | 125 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-7-25511dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14398387 | |||||
| chr12:14398431
|
T | A | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-25478T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398431 | ||||||
| chr12:14398474
|
GT | G | 150 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.-7-25423delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14398474 | |||||
| chr12:14398476
|
T | G | 1 | a0003c0003t0015g0165 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-7-25433T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398476 | ||||||
| chr12:14398551
|
G | A | 188 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-7-25358G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398551 | ||||||
| chr12:14398592
|
C | T | 1 | a0001c0001t0031g0009 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-7-25317C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398592 | ||||||
| chr12:14398676
|
T | C | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-7-25233T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398676 | ||||||
| chr12:14398757
|
A | G | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-25152A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398757 | ||||||
| chr12:14398948
|
C | T | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7-24961C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398948 | ||||||
| chr12:14399185
|
CTTATAT | C | 17 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(14): Show | 17 | HG01123.hp2 HG02257.hp1 HG02970.hp2 others(14): Show |
intron_variant | MODIFIER | c.-7-24717_-7-24712d others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14399185 | |||||
| chr12:14399258
|
C | T | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-24651C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399258 | ||||||
| chr12:14399340
|
GT | G | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-24559delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14399340 | |||||
| chr12:14399556
|
G | T | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-7-24353G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399556 | ||||||
| chr12:14399586
|
T | A | 1 | a0003c0003t0011g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-7-24323T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399586 | ||||||
| chr12:14399593
|
C | T | 1 | a0001c0001t0003g0120 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-7-24316C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399593 | ||||||
| chr12:14399786
|
T | A | 1 | a0003c0003t0011g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-7-24123T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399786 | ||||||
| chr12:14399786
|
T | C | 27 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(24): Show | 27 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.-7-24123T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399786 | ||||||
| chr12:14399809
|
T | A | 1 | a0002c0002t0001g0292 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-7-24100T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399809 | ||||||
| chr12:14399836
|
A | G | 1 | a0003c0005t0038g0331 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-7-24073A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399836 | ||||||
| chr12:14399911
|
G | C | 141 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(138): Show | 141 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-7-23998G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399911 | ||||||
| chr12:14400441
|
T | C | 7 | a0001c0001t0003g0080a0001c0001t0003g0087a0001c0001t0003g0088others(4): Show | 7 | HG00597.hp1 NA18959.hp1 NA19010.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-23468T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14400441 | ||||||
| chr12:14400466
|
AT | A | 342 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(339): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.-7-23441delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14400466 | |||||
| chr12:14400569
|
A | AT | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-23330dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14400569 | |||||
| chr12:14400777
|
C | T | 190 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(187): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.-7-23132C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14400777 | ||||||
| chr12:14400784
|
C | T | 12 | a0001c0001t0006g0070a0001c0001t0006g0076a0001c0001t0006g0129others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7-23125C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14400784 | ||||||
| chr12:14400920
|
T | G | 2 | a0005c0007t0010g0317a0005c0007t0010g0318 | 2 | HG01346.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-7-22989T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14400920 | ||||||
| chr12:14401100
|
T | G | 1 | a0001c0001t0002g0342 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-7-22809T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401100 | ||||||
| chr12:14401157
|
A | G | 1 | a0002c0006t0019g0222 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-7-22752A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401157 | ||||||
| chr12:14401193
|
G | A | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-22716G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401193 | ||||||
| chr12:14401282
|
G | A | 91 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.-7-22627G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401282 | ||||||
| chr12:14401288
|
TG | T | 190 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(187): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.-7-22617delG | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14401288 | |||||
| chr12:14401291
|
G | A | 2 | a0003c0003t0011g0314a0003c0003t0011g0315 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-7-22618G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401291 | ||||||
| chr12:14401358
|
G | A | 1 | a0002c0004t0001g0239 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-7-22551G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401358 | ||||||
| chr12:14401471
|
A | G | 2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-7-22438A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401471 | ||||||
| chr12:14401570
|
ATT | A | 4 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0260others(1): Show | 4 | NA18947.hp1 NA18979.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-22338_-7-22337d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401570 | ||||||
| chr12:14401573
|
C | A | 4 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0260others(1): Show | 4 | NA18947.hp1 NA18979.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-22336C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401573 | ||||||
| chr12:14401583
|
CT | C | 52 | a0001c0001t0002g0140a0001c0001t0003g0012a0001c0001t0003g0071others(49): Show | 52 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.-7-22315delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14401583 | |||||
| chr12:14401604
|
A | G | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-22305A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401604 | ||||||
| chr12:14401714
|
C | CT | 33 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0039others(30): Show | 33 | HG01175.hp1 HG01358.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.-7-22174dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14401714 | |||||
| chr12:14401714
|
CT | C | 180 | a0001c0001t0002g0020a0001c0001t0003g0086a0001c0001t0003g0097others(177): Show | 183 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.-7-22174delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14401714 | |||||
| chr12:14401714
|
CTT | C | 8 | a0002c0002t0001g0277a0002c0002t0001g0284a0002c0002t0001g0285others(5): Show | 8 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-22175_-7-22174d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14401714 | |||||
| chr12:14401739
|
A | G | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7-22170A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401739 | ||||||
| chr12:14401756
|
C | T | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-22153C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401756 | ||||||
| chr12:14401841
|
G | A | 1 | a0002c0002t0001g0298 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-7-22068G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401841 | ||||||
| chr12:14401931
|
C | T | 3 | a0005c0007t0010g0319a0005c0007t0010g0320a0005c0007t0010g0322 | 3 | HG00609.hp2 HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-7-21978C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401931 | ||||||
| chr12:14401963
|
C | T | 1 | a0004c0008t0005g0294 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-7-21946C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401963 | ||||||
| chr12:14401971
|
A | C | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7-21938A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401971 | ||||||
| chr12:14402044
|
A | G | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-21865A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14402044 | ||||||
| chr12:14402118
|
T | C | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-21791T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14402118 | ||||||
| chr12:14402127
|
C | CT | 65 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0014others(62): Show | 65 | HG01175.hp1 HG01243.hp1 HG01257.hp1 others(62): Show |
intron_variant | MODIFIER | c.-7-21764dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14402127 | |||||
| chr12:14402127
|
CT | C | 155 | a0001c0001t0003g0087a0001c0001t0003g0099a0001c0001t0014g0125others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-7-21764delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14402127 | |||||
| chr12:14402127
|
CTT | C | 22 | a0002c0002t0001g0257a0002c0002t0001g0286a0002c0006t0008g0219others(19): Show | 22 | HG00438.hp1 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7-21765_-7-21764d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14402127 | |||||
| chr12:14402218
|
C | G | 1 | a0003c0003t0011g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-21691C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14402218 | ||||||
| chr12:14402367
|
A | G | 3 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0003g0128 | 3 | HG03239.hp1 NA18955.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-7-21542A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14402367 | ||||||
| chr12:14402608
|
AT | A | 300 | a0001c0001t0002g0007a0001c0001t0002g0013a0001c0001t0002g0014others(297): Show | 303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.-7-21283delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14402608 | |||||
| chr12:14402608
|
ATT | A | 31 | a0002c0002t0001g0308a0003c0003t0004g0185a0003c0003t0004g0186others(28): Show | 31 | HG00733.hp2 HG01099.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.-7-21284_-7-21283d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14402608 | |||||
| chr12:14402637
|
C | G | 3 | a0003c0003t0011g0314a0003c0003t0011g0315a0003c0003t0011g0324 | 3 | HG02280.hp1 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-7-21272C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14402637 | ||||||
| chr12:14402711
|
C | T | 2 | a0001c0001t0006g0070a0001c0001t0006g0138 | 2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-7-21198C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14402711 | ||||||
| chr12:14402766
|
T | C | 1 | a0003c0003t0011g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-7-21143T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14402766 | ||||||
| chr12:14403104
|
G | T | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-7-20805G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403104 | ||||||
| chr12:14403214
|
T | C | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-20695T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403214 | ||||||
| chr12:14403324
|
G | A | 2 | a0003c0003t0004g0195a0003c0003t0004g0201 | 2 | HG01123.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-7-20585G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403324 | ||||||
| chr12:14403386
|
G | A | 1 | a0001c0001t0003g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-7-20523G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403386 | ||||||
| chr12:14403460
|
A | G | 2 | a0003c0005t0007g0327a0003c0005t0007g0336 | 2 | HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-7-20449A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403460 | ||||||
| chr12:14403500
|
G | A | 2 | a0001c0001t0003g0074a0001c0001t0040g0139 | 2 | HG02165.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-7-20409G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403500 | ||||||
| chr12:14403550
|
G | A | 1 | a0002c0002t0001g0261 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-7-20359G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403550 | ||||||
| chr12:14403967
|
A | T | 1 | a0004c0018t0005g0276 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7-19942A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403967 | ||||||
| chr12:14404019
|
A | AT | 10 | a0001c0001t0002g0056a0003c0003t0005g0316a0005c0007t0010g0002others(7): Show | 11 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7-19879dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14404019 | |||||
| chr12:14404132
|
C | CT | 177 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0207others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.-7-19763dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14404132 | |||||
| chr12:14404132
|
CT | C | 141 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(138): Show | 141 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-7-19763delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14404132 | |||||
| chr12:14404158
|
C | T | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-7-19751C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404158 | ||||||
| chr12:14404162
|
C | T | 1 | a0001c0001t0016g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-7-19747C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404162 | ||||||
| chr12:14404175
|
A | G | 4 | a0003c0003t0004g0191a0003c0003t0004g0192a0003c0003t0004g0193others(1): Show | 4 | NA18955.hp2 NA18968.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-19734A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404175 | ||||||
| chr12:14404435
|
A | G | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-19474A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404435 | ||||||
| chr12:14404597
|
G | T | 2 | a0002c0002t0001g0312a0011c0019t0001g0313 | 2 | NA19002.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.-7-19312G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404597 | ||||||
| chr12:14404630
|
G | A | 1 | a0011c0019t0001g0313 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-7-19279G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404630 | ||||||
| chr12:14404746
|
C | T | 114 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.-7-19163C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404746 | ||||||
| chr12:14404834
|
A | AT | 104 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-7-19072dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14404834 | |||||
| chr12:14404838
|
G | T | 104 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-7-19071G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404838 | ||||||
| chr12:14404839
|
A | T | 104 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-7-19070A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404839 | ||||||
| chr12:14404994
|
T | G | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-7-18915T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404994 | ||||||
| chr12:14404996
|
T | G | 1 | a0003c0005t0007g0333 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-7-18913T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404996 | ||||||
| chr12:14405032
|
C | T | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7-18877C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405032 | ||||||
| chr12:14405165
|
G | GTAGTAGA others(2): Show |
5 | a0002c0002t0001g0298a0002c0002t0001g0299a0002c0002t0001g0307others(2): Show | 5 | HG01167.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-18742_-7-18734d others(11): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405165 | |||||
| chr12:14405232
|
T | G | 1 | a0002c0002t0001g0205 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-7-18677T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405232 | ||||||
| chr12:14405272
|
A | G | 1 | a0005c0007t0010g0322 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-7-18637A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405272 | ||||||
| chr12:14405403
|
C | CT | 41 | a0001c0001t0002g0017a0001c0001t0002g0035a0001c0001t0002g0037others(38): Show | 41 | HG00597.hp1 HG01099.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.-7-18477dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | |||||
| chr12:14405403
|
CT | C | 6 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(3): Show | 6 | HG01496.hp1 HG01981.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-18477delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | |||||
| chr12:14405403
|
CTTT | C | 21 | a0002c0002t0001g0236a0002c0002t0001g0246a0002c0002t0001g0275others(18): Show | 21 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-18479_-7-18477d others(5): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | |||||
| chr12:14405403
|
CTTTT | C | 115 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(112): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-7-18480_-7-18477d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | |||||
| chr12:14405403
|
CTTTTT | C | 24 | a0002c0002t0001g0225a0002c0002t0009g0005a0002c0002t0009g0006others(21): Show | 24 | HG00673.hp2 HG01109.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.-7-18481_-7-18477d others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | |||||
| chr12:14405403
|
CTTTTTT | C | 18 | a0001c0001t0003g0078a0003c0003t0005g0316a0003c0003t0025g0171others(15): Show | 18 | HG00099.hp1 HG00280.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.-7-18482_-7-18477d others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | |||||
| chr12:14405403
|
CTTTTTTT | C | 11 | a0001c0001t0003g0074a0001c0001t0003g0079a0001c0001t0003g0128others(8): Show | 12 | HG00609.hp2 HG01934.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7-18483_-7-18477d others(9): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | |||||
| chr12:14405403
|
CTTTTTTT others(3): Show |
C | 9 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(6): Show | 9 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-18486_-7-18477d others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | |||||
| chr12:14405403
|
CTTTTTTT others(4): Show |
C | 10 | a0001c0001t0006g0070a0001c0001t0006g0076a0001c0001t0006g0132others(7): Show | 10 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-18487_-7-18477d others(13): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | |||||
| chr12:14405505
|
C | T | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-18404C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405505 | ||||||
| chr12:14405546
|
C | T | 12 | a0001c0001t0003g0012a0001c0001t0003g0085a0001c0001t0003g0092others(9): Show | 12 | HG00140.hp2 HG00735.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-18363C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405546 | ||||||
| chr12:14405622
|
G | A | 152 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(149): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.-7-18287G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405622 | ||||||
| chr12:14405673
|
C | G | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-18236C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405673 | ||||||
| chr12:14405739
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-7-18170C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405739 | ||||||
| chr12:14405767
|
G | A | 28 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(25): Show | 28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7-18142G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405767 | ||||||
| chr12:14405784
|
G | C | 1 | a0001c0001t0003g0087 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-7-18125G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405784 | ||||||
| chr12:14406130
|
C | T | 1 | a0003c0003t0014g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-7-17779C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406130 | ||||||
| chr12:14406173
|
A | G | 1 | a0002c0004t0001g0242 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-7-17736A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406173 | ||||||
| chr12:14406256
|
G | A | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-17653G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406256 | ||||||
| chr12:14406318
|
C | T | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-7-17591C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406318 | ||||||
| chr12:14406373
|
A | T | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-17536A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406373 | ||||||
| chr12:14406447
|
C | T | 1 | a0001c0001t0003g0085 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-7-17462C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406447 | ||||||
| chr12:14406493
|
GA | G | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-17415delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406493 | ||||||
| chr12:14406514
|
G | C | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7-17395G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406514 | ||||||
| chr12:14406543
|
T | C | 1 | a0003c0005t0007g0327 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-7-17366T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406543 | ||||||
| chr12:14406552
|
G | A | 143 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(140): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-7-17357G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406552 | ||||||
| chr12:14406565
|
A | G | 2 | a0005c0007t0010g0319a0005c0007t0010g0320 | 2 | HG00609.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.-7-17344A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406565 | ||||||
| chr12:14406592
|
TA | T | 10 | a0001c0001t0002g0118a0001c0001t0003g0105a0002c0002t0001g0292others(7): Show | 12 | HG00735.hp1 HG02630.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7-17304delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14406592 | |||||
| chr12:14406665
|
G | GT | 17 | a0001c0001t0002g0034a0001c0001t0002g0037a0001c0001t0002g0038others(14): Show | 17 | HG02135.hp1 HG02486.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.-7-17227dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14406665 | |||||
| chr12:14406721
|
A | G | 1 | a0002c0002t0001g0306 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-7-17188A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406721 | ||||||
| chr12:14406749
|
C | T | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-17160C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406749 | ||||||
| chr12:14407035
|
T | C | 1 | a0004c0008t0005g0252 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-7-16874T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407035 | ||||||
| chr12:14407257
|
A | G | 28 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(25): Show | 28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7-16652A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407257 | ||||||
| chr12:14407333
|
T | C | 1 | a0002c0002t0001g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-7-16576T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407333 | ||||||
| chr12:14407585
|
A | G | 1 | a0003c0003t0015g0165 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-7-16324A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407585 | ||||||
| chr12:14407672
|
T | C | 2 | a0003c0003t0004g0196a0003c0003t0004g0197 | 2 | HG00733.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-7-16237T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407672 | ||||||
| chr12:14407752
|
CT | C | 11 | a0001c0001t0006g0070a0001c0001t0006g0076a0001c0001t0006g0129others(8): Show | 11 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7-16156delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407752 | ||||||
| chr12:14407769
|
T | A | 11 | a0001c0001t0006g0070a0001c0001t0006g0076a0001c0001t0006g0129others(8): Show | 11 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7-16140T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407769 | ||||||
| chr12:14407847
|
T | TAAAAAAA others(321): Show |
1 | a0002c0002t0001g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-7-16045_-7-16044i others(330): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14407847 | |||||
| chr12:14407942
|
T | C | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-15967T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407942 | ||||||
| chr12:14408116
|
G | GCA | 168 | a0001c0001t0002g0007a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(165): Show |
intron_variant | MODIFIER | c.-7-15768_-7-15767d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408116 | |||||
| chr12:14408116
|
G | GCACA | 127 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0003g0111others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.-7-15770_-7-15767d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408116 | |||||
| chr12:14408116
|
G | GCACACA | 17 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0260others(14): Show | 18 | HG00609.hp2 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.-7-15772_-7-15767d others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408116 | |||||
| chr12:14408116
|
G | GCACACAC others(5): Show |
3 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0182 | 5 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-15778_-7-15767d others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408116 | |||||
| chr12:14408116
|
G | GCACACAC others(7): Show |
2 | a0003c0003t0012g0180a0003c0003t0012g0181 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-7-15780_-7-15767d others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408116 | |||||
| chr12:14408141
|
C | CACAA | 9 | a0003c0003t0014g0170a0003c0003t0015g0165a0003c0003t0015g0166others(6): Show | 9 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-15767_-7-15766i others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408141 | |||||
| chr12:14408168
|
C | T | 1 | a0001c0001t0003g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-7-15741C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408168 | ||||||
| chr12:14408211
|
A | G | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-15698A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408211 | ||||||
| chr12:14408296
|
GT | G | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-15608delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408296 | |||||
| chr12:14408369
|
A | G | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-15540A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408369 | ||||||
| chr12:14408477
|
T | C | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-7-15432T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408477 | ||||||
| chr12:14408485
|
A | G | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-7-15424A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408485 | ||||||
| chr12:14408518
|
A | G | 1 | a0008c0011t0024g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-7-15391A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408518 | ||||||
| chr12:14408581
|
T | C | 1 | a0003c0003t0014g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-7-15328T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408581 | ||||||
| chr12:14408592
|
G | A | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7-15317G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408592 | ||||||
| chr12:14408714
|
G | GT | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-15191dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408714 | |||||
| chr12:14409040
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7-14869T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409040 | ||||||
| chr12:14409064
|
A | G | 2 | a0010c0013t0020g0115a0010c0013t0020g0117 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-7-14845A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409064 | ||||||
| chr12:14409165
|
A | G | 1 | a0002c0004t0001g0232 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-7-14744A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409165 | ||||||
| chr12:14409317
|
A | G | 1 | a0001c0020t0036g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-7-14592A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409317 | ||||||
| chr12:14409487
|
G | A | 7 | a0003c0003t0011g0341a0006c0009t0005g0173a0006c0009t0005g0174others(4): Show | 7 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-14422G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409487 | ||||||
| chr12:14409733
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-7-14176A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409733 | ||||||
| chr12:14409790
|
A | C | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-14119A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409790 | ||||||
| chr12:14409908
|
T | A | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-14001T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409908 | ||||||
| chr12:14409915
|
T | C | 1 | a0001c0001t0002g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-7-13994T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409915 | ||||||
| chr12:14410038
|
C | T | 3 | a0002c0002t0009g0287a0002c0002t0009g0288a0002c0002t0009g0289 | 3 | HG02622.hp2 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-7-13871C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410038 | ||||||
| chr12:14410175
|
C | T | 1 | a0003c0003t0011g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-13734C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410175 | ||||||
| chr12:14410177
|
C | T | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-13732C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410177 | ||||||
| chr12:14410195
|
C | G | 1 | a0003c0003t0004g0202 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-7-13714C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410195 | ||||||
| chr12:14410228
|
C | T | 7 | a0003c0003t0011g0341a0006c0009t0005g0173a0006c0009t0005g0174others(4): Show | 7 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-13681C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410228 | ||||||
| chr12:14410240
|
T | G | 13 | a0002c0002t0001g0225a0002c0006t0008g0208a0002c0006t0008g0217others(10): Show | 13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-13669T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410240 | ||||||
| chr12:14410271
|
A | G | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-7-13638A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410271 | ||||||
| chr12:14410373
|
C | T | 2 | a0001c0001t0003g0110a0001c0001t0003g0111 | 2 | HG01106.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-7-13536C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410373 | ||||||
| chr12:14410375
|
G | T | 1 | a0001c0001t0002g0052 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-7-13534G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410375 | ||||||
| chr12:14410387
|
T | G | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-13522T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410387 | ||||||
| chr12:14410393
|
C | T | 1 | a0001c0001t0002g0055 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-7-13516C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410393 | ||||||
| chr12:14410461
|
G | A | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-13448G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410461 | ||||||
| chr12:14410660
|
G | C | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-13249G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410660 | ||||||
| chr12:14410714
|
A | G | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-7-13195A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410714 | ||||||
| chr12:14410715
|
A | G | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-13194A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410715 | ||||||
| chr12:14410721
|
T | C | 1 | a0002c0002t0001g0286 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-7-13188T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410721 | ||||||
| chr12:14410725
|
G | C | 1 | a0001c0001t0003g0106 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-7-13184G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410725 | ||||||
| chr12:14410744
|
A | AATGT | 28 | a0001c0020t0036g0131a0003c0003t0004g0185a0003c0003t0004g0186others(25): Show | 28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7-13146_-7-13143d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14410744 | |||||
| chr12:14410777
|
A | G | 114 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.-7-13132A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410777 | ||||||
| chr12:14410908
|
T | C | 187 | a0001c0020t0036g0131a0002c0002t0001g0004a0002c0002t0001g0205others(184): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-7-13001T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410908 | ||||||
| chr12:14411069
|
C | T | 1 | a0003c0005t0007g0332 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-7-12840C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411069 | ||||||
| chr12:14411274
|
A | C | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-7-12635A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411274 | ||||||
| chr12:14411277
|
G | A | 27 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(24): Show | 27 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.-7-12632G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411277 | ||||||
| chr12:14411545
|
T | A | 2 | a0002c0002t0001g0261a0002c0002t0001g0298 | 2 | HG01167.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-7-12364T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411545 | ||||||
| chr12:14411570
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7-12339A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411570 | ||||||
| chr12:14411607
|
T | G | 1 | a0003c0003t0011g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-12302T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411607 | ||||||
| chr12:14411634
|
T | C | 1 | a0003c0005t0007g0330 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-12275T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411634 | ||||||
| chr12:14411711
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-7-12198C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411711 | ||||||
| chr12:14411730
|
C | G | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-12179C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411730 | ||||||
| chr12:14411778
|
T | A | 3 | a0007c0010t0002g0011a0007c0010t0002g0022a0007c0010t0002g0049 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-7-12131T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411778 | ||||||
| chr12:14411812
|
T | C | 7 | a0003c0003t0011g0341a0006c0009t0005g0173a0006c0009t0005g0174others(4): Show | 7 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-12097T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411812 | ||||||
| chr12:14411857
|
T | C | 28 | a0001c0020t0036g0131a0003c0003t0004g0185a0003c0003t0004g0186others(25): Show | 28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7-12052T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411857 | ||||||
| chr12:14411976
|
G | A | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-11933G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411976 | ||||||
| chr12:14412000
|
T | A | 2 | a0003c0014t0013g0163a0003c0014t0013g0164 | 2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-7-11909T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412000 | ||||||
| chr12:14412090
|
C | A | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-11819C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412090 | ||||||
| chr12:14412170
|
C | T | 2 | a0003c0003t0004g0188a0003c0003t0004g0190 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-7-11739C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412170 | ||||||
| chr12:14412307
|
T | C | 1 | a0001c0020t0036g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-7-11602T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412307 | ||||||
| chr12:14412369
|
AAG | A | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-11537_-7-11536d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14412369 | |||||
| chr12:14412420
|
C | A | 12 | a0002c0002t0001g0207a0002c0002t0001g0250a0002c0002t0001g0254others(9): Show | 12 | HG02083.hp1 NA18942.hp1 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-11489C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412420 | ||||||
| chr12:14412760
|
T | A | 1 | a0003c0003t0005g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-7-11149T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412760 | ||||||
| chr12:14412798
|
G | A | 114 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.-7-11111G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412798 | ||||||
| chr12:14412843
|
G | A | 2 | a0002c0006t0019g0222a0003c0003t0014g0170 | 2 | HG02717.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-7-11066G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412843 | ||||||
| chr12:14412912
|
G | T | 1 | a0001c0001t0022g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-7-10997G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412912 | ||||||
| chr12:14412918
|
G | A | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-10991G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412918 | ||||||
| chr12:14413065
|
C | T | 1 | a0002c0002t0001g0261 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-7-10844C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413065 | ||||||
| chr12:14413079
|
T | A | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-10830T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413079 | ||||||
| chr12:14413107
|
G | A | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-7-10802G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413107 | ||||||
| chr12:14413277
|
A | G | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-10632A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413277 | ||||||
| chr12:14413437
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-7-10472A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413437 | ||||||
| chr12:14413495
|
G | A | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-10414G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413495 | ||||||
| chr12:14413686
|
G | T | 28 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(25): Show | 28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7-10223G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413686 | ||||||
| chr12:14413714
|
A | G | 28 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(25): Show | 28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7-10195A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413714 | ||||||
| chr12:14413726
|
G | C | 1 | a0001c0001t0002g0010 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-7-10183G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413726 | ||||||
| chr12:14413852
|
C | T | 1 | a0003c0003t0034g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-7-10057C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413852 | ||||||
| chr12:14414082
|
G | A | 1 | a0002c0002t0001g0254 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-7-9827G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14414082 | ||||||
| chr12:14414316
|
T | C | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-9593T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14414316 | ||||||
| chr12:14414458
|
A | G | 1 | a0001c0001t0003g0109 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-7-9451A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14414458 | ||||||
| chr12:14414580
|
T | C | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-9329T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14414580 | ||||||
| chr12:14415408
|
C | G | 1 | a0003c0003t0005g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-7-8501C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415408 | ||||||
| chr12:14415518
|
G | A | 177 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.-7-8391G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415518 | ||||||
| chr12:14415573
|
C | T | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-8336C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415573 | ||||||
| chr12:14415691
|
G | GT | 221 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(218): Show | 224 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(221): Show |
intron_variant | MODIFIER | c.-7-8203dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14415691 | |||||
| chr12:14415691
|
G | GTT | 111 | a0001c0001t0003g0120a0001c0001t0031g0009a0002c0002t0001g0004others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.-7-8204_-7-8203dup others(2): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14415691 | |||||
| chr12:14415792
|
A | G | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-7-8117A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415792 | ||||||
| chr12:14415857
|
G | A | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-8052G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415857 | ||||||
| chr12:14415893
|
A | G | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-8016A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415893 | ||||||
| chr12:14415917
|
T | G | 1 | a0001c0001t0003g0110 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-7-7992T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415917 | ||||||
| chr12:14415950
|
T | C | 1 | a0002c0002t0001g0255 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-7-7959T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415950 | ||||||
| chr12:14416008
|
A | C | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7-7901A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416008 | ||||||
| chr12:14416242
|
G | A | 4 | a0003c0003t0004g0191a0003c0003t0004g0192a0003c0003t0004g0193others(1): Show | 4 | NA18955.hp2 NA18968.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-7667G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416242 | ||||||
| chr12:14416259
|
G | C | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-7650G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416259 | ||||||
| chr12:14416270
|
TTATTTAA | T | 105 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.-7-7630_-7-7624del others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14416270 | |||||
| chr12:14416343
|
G | T | 19 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(16): Show | 19 | HG00733.hp2 HG01123.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-7-7566G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416343 | ||||||
| chr12:14416399
|
AATGCCTT others(4): Show |
A | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-7508_-7-7498del others(11): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14416399 | |||||
| chr12:14416553
|
T | C | 13 | a0002c0002t0001g0225a0002c0006t0008g0208a0002c0006t0008g0217others(10): Show | 13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-7356T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416553 | ||||||
| chr12:14416741
|
G | A | 1 | a0003c0003t0011g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-7-7168G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416741 | ||||||
| chr12:14416819
|
G | T | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7-7090G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416819 | ||||||
| chr12:14416937
|
G | A | 1 | a0002c0004t0001g0239 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-7-6972G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416937 | ||||||
| chr12:14417142
|
T | G | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-6767T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417142 | ||||||
| chr12:14417296
|
C | G | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-6613C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417296 | ||||||
| chr12:14417370
|
C | A | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-6539C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417370 | ||||||
| chr12:14417500
|
A | G | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-7-6409A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417500 | ||||||
| chr12:14417517
|
G | A | 171 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(168): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.-7-6392G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417517 | ||||||
| chr12:14417645
|
A | G | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-6264A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417645 | ||||||
| chr12:14417705
|
T | C | 105 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.-7-6204T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417705 | ||||||
| chr12:14417832
|
T | C | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-6077T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417832 | ||||||
| chr12:14418022
|
T | G | 3 | a0001c0001t0002g0084a0001c0001t0002g0118a0001c0001t0002g0119 | 3 | HG02818.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-7-5887T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418022 | ||||||
| chr12:14418126
|
A | C | 8 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0260others(5): Show | 8 | NA18612.hp1 NA18945.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-5783A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418126 | ||||||
| chr12:14418185
|
C | T | 3 | a0003c0003t0004g0192a0003c0003t0004g0193a0003c0003t0004g0194 | 3 | NA18968.hp1 NA19007.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.-7-5724C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418185 | ||||||
| chr12:14418211
|
T | C | 178 | a0001c0020t0036g0131a0002c0002t0001g0004a0002c0002t0001g0205others(175): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.-7-5698T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418211 | ||||||
| chr12:14418295
|
C | G | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-7-5614C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418295 | ||||||
| chr12:14418497
|
C | G | 154 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(151): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.-7-5412C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418497 | ||||||
| chr12:14418539
|
T | C | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-5370T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418539 | ||||||
| chr12:14418563
|
A | C | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-5346A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418563 | ||||||
| chr12:14418737
|
A | G | 2 | a0003c0003t0011g0184a0003c0003t0028g0183 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-7-5172A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418737 | ||||||
| chr12:14418795
|
A | G | 1 | a0002c0002t0001g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-7-5114A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418795 | ||||||
| chr12:14418880
|
G | A | 180 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(177): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-7-5029G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418880 | ||||||
| chr12:14419025
|
C | A | 1 | a0012c0017t0001g0266 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-7-4884C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14419025 | ||||||
| chr12:14419056
|
A | G | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-4853A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14419056 | ||||||
| chr12:14419294
|
CAGAGTTC others(63): Show |
C | 1 | a0002c0002t0001g0250 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-7-4581_-7-4512del others(70): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14419294 | |||||
| chr12:14419333
|
A | G | 17 | a0001c0001t0002g0014a0001c0001t0002g0025a0001c0001t0002g0026others(14): Show | 17 | HG01257.hp1 HG01258.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.-7-4576A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14419333 | ||||||
| chr12:14419496
|
C | T | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-4413C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14419496 | ||||||
| chr12:14419685
|
C | T | 1 | a0003c0003t0004g0202 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-7-4224C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14419685 | ||||||
| chr12:14419956
|
C | A | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-7-3953C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14419956 | ||||||
| chr12:14419959
|
T | C | 1 | a0008c0011t0024g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-7-3950T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14419959 | ||||||
| chr12:14420427
|
A | G | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-3482A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14420427 | ||||||
| chr12:14420565
|
C | G | 107 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-7-3344C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14420565 | ||||||
| chr12:14420569
|
C | T | 2 | a0003c0003t0011g0184a0003c0003t0028g0183 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-7-3340C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14420569 | ||||||
| chr12:14420585
|
C | T | 1 | a0002c0002t0001g0235 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-7-3324C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14420585 | ||||||
| chr12:14420586
|
G | A | 2 | a0010c0013t0020g0115a0010c0013t0020g0117 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-7-3323G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14420586 | ||||||
| chr12:14420634
|
GA | G | 171 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(168): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.-7-3265delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14420634 | |||||
| chr12:14420851
|
TTTTC | T | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-3048_-7-3045del others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14420851 | |||||
| chr12:14420874
|
G | T | 2 | a0001c0001t0002g0113a0001c0001t0027g0023 | 2 | HG02735.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-7-3035G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14420874 | ||||||
| chr12:14420908
|
A | G | 2 | a0001c0001t0003g0074a0001c0001t0040g0139 | 2 | HG02165.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-7-3001A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14420908 | ||||||
| chr12:14421342
|
G | T | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-2567G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14421342 | ||||||
| chr12:14421459
|
C | T | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-2450C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14421459 | ||||||
| chr12:14421584
|
C | T | 2 | a0003c0003t0011g0184a0003c0003t0028g0183 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-7-2325C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14421584 | ||||||
| chr12:14422225
|
C | G | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-1684C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14422225 | ||||||
| chr12:14422248
|
G | A | 1 | a0001c0001t0030g0040 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-7-1661G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14422248 | ||||||
| chr12:14422312
|
T | TAC | 28 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0051others(25): Show | 28 | HG00099.hp1 HG00741.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7-1553_-7-1552dup others(2): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | |||||
| chr12:14422312
|
T | TACAC | 15 | a0001c0001t0003g0080a0001c0001t0003g0090a0001c0001t0003g0091others(12): Show | 15 | HG01099.hp1 HG01109.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7-1555_-7-1552dup others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | |||||
| chr12:14422312
|
T | TACACAC | 3 | a0001c0001t0002g0055a0002c0002t0009g0213a0003c0003t0014g0170 | 3 | HG02615.hp1 HG02717.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-7-1557_-7-1552dup others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | |||||
| chr12:14422312
|
T | TACACACA others(1): Show |
3 | a0001c0001t0003g0116a0002c0002t0009g0005a0002c0002t0009g0006 | 3 | HG01109.hp2 HG03540.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-7-1559_-7-1552dup others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | |||||
| chr12:14422312
|
TAC | T | 55 | a0001c0001t0002g0013a0001c0001t0002g0024a0001c0001t0002g0028others(52): Show | 55 | HG00140.hp2 HG01074.hp1 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.-7-1553_-7-1552del others(2): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | |||||
| chr12:14422312
|
TACAC | T | 57 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0025others(54): Show | 57 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.-7-1555_-7-1552del others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | |||||
| chr12:14422312
|
TACACAC | T | 94 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0037others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-7-1557_-7-1552del others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | |||||
| chr12:14422312
|
TACACACA others(1): Show |
T | 22 | a0001c0001t0003g0096a0002c0002t0009g0211a0002c0002t0009g0212others(19): Show | 22 | HG00597.hp1 HG00733.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7-1559_-7-1552del others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | |||||
| chr12:14422312
|
TACACACA others(3): Show |
T | 7 | a0002c0002t0001g0254a0002c0002t0009g0214a0003c0003t0011g0314others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-1561_-7-1552del others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | |||||
| chr12:14422312
|
TACACACA others(5): Show |
T | 12 | a0003c0003t0011g0184a0003c0003t0012g0001a0003c0003t0012g0179others(9): Show | 14 | HG02630.hp1 HG02723.hp1 HG02896.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-1563_-7-1552del others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | |||||
| chr12:14422312
|
TACACACA others(7): Show |
T | 9 | a0003c0003t0011g0204a0003c0003t0012g0182a0005c0007t0010g0002others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-1565_-7-1552del others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | |||||
| chr12:14422312
|
TACACACA others(9): Show |
T | 2 | a0003c0003t0012g0180a0003c0005t0007g0328 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-7-1567_-7-1552del others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | |||||
| chr12:14422312
|
TACACACA others(11): Show |
T | 2 | a0003c0003t0014g0149a0003c0003t0018g0153 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-7-1569_-7-1552del others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | |||||
| chr12:14422378
|
A | T | 16 | a0001c0001t0006g0070a0001c0001t0006g0076a0001c0001t0006g0129others(13): Show | 16 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7-1531A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14422378 | ||||||
| chr12:14422525
|
A | G | 181 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(178): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.-7-1384A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14422525 | ||||||
| chr12:14422579
|
A | G | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-7-1330A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14422579 | ||||||
| chr12:14422814
|
G | C | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7-1095G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14422814 | ||||||
| chr12:14423029
|
A | G | 1 | a0008c0011t0024g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-7-880A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423029 | ||||||
| chr12:14423102
|
T | A | 2 | a0002c0002t0026g0272a0002c0002t0026g0273 | 2 | NA18945.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-7-807T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423102 | ||||||
| chr12:14423293
|
T | C | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-616T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423293 | ||||||
| chr12:14423548
|
T | C | 150 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(147): Show | 150 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.-7-361T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423548 | ||||||
| chr12:14423574
|
C | CT | 124 | a0001c0001t0002g0037a0001c0001t0002g0054a0001c0001t0002g0140others(121): Show | 125 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-7-311dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14423574 | |||||
| chr12:14423574
|
C | CTT | 23 | a0001c0001t0016g0127a0002c0002t0001g0205a0002c0002t0001g0218others(20): Show | 23 | HG00621.hp1 HG00621.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-7-312_-7-311dupTT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14423574 | |||||
| chr12:14423574
|
CT | C | 10 | a0001c0001t0002g0020a0001c0001t0003g0100a0003c0003t0004g0191others(7): Show | 12 | HG01167.hp1 HG01168.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-311delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14423574 | |||||
| chr12:14423574
|
CTTTTT | C | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-315_-7-311delTT others(3): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14423574 | |||||
| chr12:14423651
|
A | T | 1 | a0001c0001t0029g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-7-258A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423651 | ||||||
| chr12:14423655
|
G | GA | 22 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(19): Show | 24 | HG00099.hp1 HG00280.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.-7-245dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14423655 | |||||
| chr12:14423719
|
A | T | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-190A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423719 | ||||||
| chr12:14423788
|
A | G | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-121A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423788 | ||||||
| chr12:14423809
|
A | G | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-7-100A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423809 | ||||||
| chr12:14425545
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1558+72A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14425545 | ||||||
| chr12:14425585
|
G | A | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1558+112G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14425585 | ||||||
| chr12:14425640
|
G | A | 2 | a0005c0007t0010g0317a0005c0007t0010g0318 | 2 | HG01346.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1558+167G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14425640 | ||||||
| chr12:14425918
|
A | G | 1 | a0002c0002t0001g0303 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1558+445A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14425918 | ||||||
| chr12:14425947
|
T | C | 9 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(6): Show | 11 | HG00099.hp1 HG00280.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1558+474T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14425947 | ||||||
| chr12:14426035
|
A | G | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1558+562A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426035 | ||||||
| chr12:14426079
|
A | G | 1 | a0013c0016t0039g0245 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1558+606A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426079 | ||||||
| chr12:14426084
|
C | A | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1558+611C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426084 | ||||||
| chr12:14426164
|
T | A | 2 | a0002c0006t0008g0208a0002c0006t0008g0295 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1558+691T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426164 | ||||||
| chr12:14426301
|
A | C | 187 | a0001c0020t0036g0131a0002c0002t0001g0004a0002c0002t0001g0205others(184): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1558+828A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426301 | ||||||
| chr12:14426319
|
G | C | 1 | a0003c0005t0007g0333 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1558+846G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426319 | ||||||
| chr12:14426464
|
A | G | 1 | a0001c0001t0002g0030 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1558+991A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426464 | ||||||
| chr12:14426529
|
C | CT | 26 | a0001c0001t0002g0017a0001c0001t0002g0027a0001c0001t0002g0028others(23): Show | 26 | HG01261.hp1 HG01358.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.1558+1071dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14426529 | |||||
| chr12:14426637
|
G | C | 1 | a0001c0001t0002g0025 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1558+1164G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426637 | ||||||
| chr12:14426653
|
C | G | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558+1180C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426653 | ||||||
| chr12:14426686
|
C | T | 2 | a0004c0008t0005g0280a0004c0008t0005g0283 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1558+1213C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426686 | ||||||
| chr12:14426712
|
G | C | 29 | a0001c0020t0036g0131a0003c0003t0004g0185a0003c0003t0004g0186others(26): Show | 29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1558+1239G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426712 | ||||||
| chr12:14426788
|
T | C | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1558+1315T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426788 | ||||||
| chr12:14426823
|
C | CAAAAAAA others(3): Show |
1 | a0003c0014t0013g0163 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1558+1368_1558+137 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14426823 | |||||
| chr12:14426823
|
C | CAAAAAAA others(4): Show |
1 | a0003c0014t0013g0164 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1558+1367_1558+137 others(15): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14426823 | |||||
| chr12:14426823
|
C | CAAAAAAA others(5): Show |
1 | a0003c0003t0013g0161 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1558+1366_1558+137 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14426823 | |||||
| chr12:14426847
|
AAAAG | A | 15 | a0002c0002t0009g0006a0002c0002t0009g0212a0002c0002t0009g0213others(12): Show | 15 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1558+1375_1558+137 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426847 | ||||||
| chr12:14426848
|
AAAG | A | 104 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0207others(101): Show | 107 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.1558+1376_1558+137 others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426848 | ||||||
| chr12:14426849
|
AAG | A | 34 | a0002c0002t0001g0206a0002c0002t0001g0218a0002c0002t0001g0255others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.1558+1377_1558+137 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426849 | ||||||
| chr12:14426850
|
AG | A | 130 | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0014others(127): Show | 130 | HG00280.hp2 HG00673.hp1 HG00733.hp2 others(127): Show |
intron_variant | MODIFIER | c.1558+1379delG | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14426850 | |||||
| chr12:14426851
|
G | A | 59 | a0001c0001t0002g0007a0001c0001t0002g0024a0001c0001t0002g0030others(56): Show | 59 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.1558+1378G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426851 | ||||||
| chr12:14426881
|
A | G | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558+1408A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426881 | ||||||
| chr12:14426887
|
C | A | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1558+1414C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426887 | ||||||
| chr12:14426973
|
C | T | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1558+1500C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426973 | ||||||
| chr12:14427106
|
C | CAT | 29 | a0001c0020t0036g0131a0003c0003t0004g0185a0003c0003t0004g0186others(26): Show | 29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1558+1634_1558+163 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14427106 | |||||
| chr12:14427204
|
C | T | 105 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1558+1731C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427204 | ||||||
| chr12:14427213
|
T | C | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558+1740T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427213 | ||||||
| chr12:14427232
|
C | G | 7 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(4): Show | 9 | HG00099.hp1 HG00280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558+1759C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427232 | ||||||
| chr12:14427332
|
C | T | 1 | a0003c0005t0007g0325 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1558+1859C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427332 | ||||||
| chr12:14427358
|
T | C | 29 | a0001c0020t0036g0131a0003c0003t0004g0185a0003c0003t0004g0186others(26): Show | 29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1558+1885T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427358 | ||||||
| chr12:14427394
|
G | A | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558+1921G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427394 | ||||||
| chr12:14427479
|
A | T | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1558+2006A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427479 | ||||||
| chr12:14427514
|
C | T | 1 | a0002c0002t0001g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1558+2041C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427514 | ||||||
| chr12:14427515
|
G | A | 3 | a0001c0001t0002g0084a0001c0001t0002g0118a0001c0001t0002g0119 | 3 | HG02818.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1558+2042G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427515 | ||||||
| chr12:14427656
|
G | A | 2 | a0001c0001t0003g0086a0001c0001t0003g0097 | 2 | HG01081.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1558+2183G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427656 | ||||||
| chr12:14427749
|
C | G | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1558+2276C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427749 | ||||||
| chr12:14427755
|
T | C | 29 | a0001c0020t0036g0131a0003c0003t0004g0185a0003c0003t0004g0186others(26): Show | 29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1558+2282T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427755 | ||||||
| chr12:14427804
|
T | A | 1 | a0014c0015t0003g0094 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1558+2331T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427804 | ||||||
| chr12:14427915
|
A | G | 13 | a0001c0001t0002g0024a0001c0001t0003g0071a0001c0001t0003g0072others(10): Show | 13 | HG00609.hp1 HG00673.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.1558+2442A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427915 | ||||||
| chr12:14427954
|
A | T | 1 | a0003c0003t0014g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1558+2481A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427954 | ||||||
| chr12:14427975
|
C | T | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1558+2502C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427975 | ||||||
| chr12:14428183
|
A | G | 2 | a0004c0008t0005g0280a0004c0008t0005g0283 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1558+2710A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428183 | ||||||
| chr12:14428245
|
G | A | 1 | a0001c0001t0003g0077 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1558+2772G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428245 | ||||||
| chr12:14428515
|
C | T | 143 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(140): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1558+3042C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428515 | ||||||
| chr12:14428681
|
A | G | 3 | a0002c0002t0001g0302a0002c0002t0001g0303a0002c0002t0001g0304 | 3 | NA18943.hp1 NA18949.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1558+3208A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428681 | ||||||
| chr12:14428753
|
T | G | 4 | a0001c0001t0014g0125a0001c0001t0016g0075a0001c0001t0016g0126others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558+3280T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428753 | ||||||
| chr12:14428805
|
C | T | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1558+3332C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428805 | ||||||
| chr12:14428817
|
CTATTTTA others(4): Show |
C | 1 | a0002c0006t0019g0222 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1558+3347_1558+335 others(15): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14428817 | |||||
| chr12:14428831
|
C | G | 1 | a0002c0006t0019g0222 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1558+3358C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428831 | ||||||
| chr12:14428831
|
C | T | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558+3358C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428831 | ||||||
| chr12:14428855
|
A | C | 7 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(4): Show | 9 | HG00099.hp1 HG00280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558+3382A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428855 | ||||||
| chr12:14429173
|
C | T | 1 | a0004c0008t0005g0279 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1558+3700C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429173 | ||||||
| chr12:14429183
|
A | T | 1 | a0012c0017t0001g0266 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1558+3710A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429183 | ||||||
| chr12:14429207
|
A | G | 26 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(23): Show | 26 | HG00733.hp2 HG01123.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1558+3734A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429207 | ||||||
| chr12:14429213
|
A | G | 3 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0311 | 3 | NA18947.hp1 NA18979.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1558+3740A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429213 | ||||||
| chr12:14429403
|
G | A | 1 | a0002c0002t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1558+3930G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429403 | ||||||
| chr12:14429906
|
A | G | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1559-4431A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429906 | ||||||
| chr12:14429941
|
T | G | 1 | a0001c0001t0003g0109 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1559-4396T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429941 | ||||||
| chr12:14429966
|
A | G | 1 | a0002c0004t0001g0240 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1559-4371A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429966 | ||||||
| chr12:14430176
|
G | A | 36 | a0001c0001t0002g0014a0001c0001t0002g0025a0001c0001t0002g0026others(33): Show | 36 | HG01175.hp1 HG01257.hp1 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.1559-4161G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14430176 | ||||||
| chr12:14430556
|
T | C | 7 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(4): Show | 9 | HG00099.hp1 HG00280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1559-3781T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14430556 | ||||||
| chr12:14430654
|
A | G | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1559-3683A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14430654 | ||||||
| chr12:14430776
|
A | G | 1 | a0002c0002t0001g0297 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1559-3561A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14430776 | ||||||
| chr12:14430947
|
T | C | 1 | a0002c0002t0001g0286 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1559-3390T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14430947 | ||||||
| chr12:14431062
|
A | G | 1 | a0006c0009t0005g0174 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1559-3275A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431062 | ||||||
| chr12:14431165
|
A | G | 3 | a0003c0003t0004g0198a0003c0003t0004g0199a0003c0003t0004g0200 | 3 | HG02970.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1559-3172A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431165 | ||||||
| chr12:14431196
|
C | G | 1 | a0003c0003t0011g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1559-3141C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431196 | ||||||
| chr12:14431258
|
T | G | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1559-3079T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431258 | ||||||
| chr12:14431318
|
A | G | 3 | a0007c0010t0002g0011a0007c0010t0002g0022a0007c0010t0002g0049 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1559-3019A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431318 | ||||||
| chr12:14431359
|
A | G | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1559-2978A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431359 | ||||||
| chr12:14431398
|
C | CT | 31 | a0002c0002t0037g0237a0003c0003t0004g0185a0003c0003t0004g0186others(28): Show | 31 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1559-2925dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14431398 | |||||
| chr12:14431420
|
C | A | 179 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(176): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1559-2917C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431420 | ||||||
| chr12:14431420
|
C | T | 4 | a0001c0001t0014g0125a0001c0001t0016g0075a0001c0001t0016g0126others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1559-2917C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431420 | ||||||
| chr12:14431445
|
A | G | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1559-2892A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431445 | ||||||
| chr12:14431457
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1559-2880C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431457 | ||||||
| chr12:14431504
|
C | T | 1 | a0001c0001t0003g0077 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1559-2833C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431504 | ||||||
| chr12:14431604
|
C | G | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1559-2733C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431604 | ||||||
| chr12:14431640
|
C | T | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1559-2697C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431640 | ||||||
| chr12:14431669
|
T | C | 151 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(148): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1559-2668T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431669 | ||||||
| chr12:14431673
|
T | C | 151 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(148): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1559-2664T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431673 | ||||||
| chr12:14431678
|
G | A | 151 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(148): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1559-2659G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431678 | ||||||
| chr12:14431683
|
C | T | 151 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(148): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1559-2654C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431683 | ||||||
| chr12:14431684
|
A | G | 151 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(148): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1559-2653A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431684 | ||||||
| chr12:14431686
|
A | G | 151 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(148): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1559-2651A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431686 | ||||||
| chr12:14431689
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1559-2648C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431689 | ||||||
| chr12:14431722
|
T | G | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1559-2615T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431722 | ||||||
| chr12:14431899
|
G | A | 4 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0278others(1): Show | 4 | HG02132.hp1 NA18941.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1559-2438G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431899 | ||||||
| chr12:14431914
|
T | A | 1 | a0001c0001t0002g0034 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1559-2423T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431914 | ||||||
| chr12:14431953
|
C | T | 1 | a0002c0002t0001g0298 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1559-2384C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431953 | ||||||
| chr12:14432145
|
G | A | 186 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1559-2192G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432145 | ||||||
| chr12:14432150
|
T | C | 341 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(338): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1559-2187T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432150 | ||||||
| chr12:14432257
|
C | G | 1 | a0001c0001t0002g0056 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1559-2080C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432257 | ||||||
| chr12:14432269
|
G | A | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1559-2068G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432269 | ||||||
| chr12:14432395
|
G | C | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1559-1942G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432395 | ||||||
| chr12:14432400
|
C | G | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1559-1937C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432400 | ||||||
| chr12:14432549
|
T | C | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1559-1788T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432549 | ||||||
| chr12:14432559
|
G | A | 1 | a0001c0001t0002g0140 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1559-1778G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432559 | ||||||
| chr12:14432584
|
G | A | 1 | a0003c0003t0005g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1559-1753G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432584 | ||||||
| chr12:14432899
|
T | C | 17 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(14): Show | 17 | HG01123.hp2 HG02257.hp1 HG02970.hp2 others(14): Show |
intron_variant | MODIFIER | c.1559-1438T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432899 | ||||||
| chr12:14432970
|
G | A | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1559-1367G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432970 | ||||||
| chr12:14433007
|
A | G | 3 | a0002c0002t0001g0209a0002c0002t0001g0210a0002c0002t0037g0237 | 3 | HG01256.hp1 HG01258.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1559-1330A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433007 | ||||||
| chr12:14433086
|
G | A | 2 | a0003c0003t0011g0184a0003c0003t0028g0183 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1559-1251G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433086 | ||||||
| chr12:14433106
|
C | T | 13 | a0002c0006t0008g0208a0002c0006t0008g0217a0002c0006t0008g0219others(10): Show | 13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1559-1231C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433106 | ||||||
| chr12:14433211
|
A | G | 1 | a0013c0016t0039g0245 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1559-1126A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433211 | ||||||
| chr12:14433319
|
A | G | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1559-1018A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433319 | ||||||
| chr12:14433420
|
G | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1559-917G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433420 | ||||||
| chr12:14433424
|
G | C | 1 | a0003c0003t0011g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1559-913G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433424 | ||||||
| chr12:14433466
|
C | T | 2 | a0003c0003t0004g0196a0003c0003t0004g0197 | 2 | HG00733.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1559-871C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433466 | ||||||
| chr12:14433538
|
C | T | 1 | a0001c0001t0003g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1559-799C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433538 | ||||||
| chr12:14433641
|
G | T | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1559-696G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433641 | ||||||
| chr12:14433748
|
G | T | 1 | a0001c0001t0002g0034 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1559-589G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433748 | ||||||
| chr12:14433937
|
C | T | 7 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1559-400C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433937 | ||||||
| chr12:14434083
|
T | A | 179 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(176): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1559-254T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14434083 | ||||||
| chr12:14434474
|
G | A | 1 | a0002c0002t0009g0214 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1645+51G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14434474 | ||||||
| chr12:14434513
|
A | G | 2 | a0001c0001t0003g0110a0001c0001t0003g0111 | 2 | HG01106.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1645+90A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14434513 | ||||||
| chr12:14434678
|
G | T | 12 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0077others(9): Show | 12 | HG00609.hp1 HG00673.hp1 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.1645+255G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14434678 | ||||||
| chr12:14434793
|
C | T | 170 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1645+370C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14434793 | ||||||
| chr12:14434939
|
T | A | 1 | a0003c0005t0041g0337 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1645+516T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14434939 | ||||||
| chr12:14435116
|
A | G | 1 | a0002c0004t0001g0242 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1645+693A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435116 | ||||||
| chr12:14435117
|
C | G | 1 | a0002c0004t0001g0242 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1645+694C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435117 | ||||||
| chr12:14435122
|
AGGAAGGA others(4): Show |
A | 3 | a0002c0002t0001g0301a0003c0014t0013g0163a0003c0014t0013g0164 | 3 | NA18984.hp2 NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1645+709_1645+719d others(13): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 14435122 | |||||
| chr12:14435133
|
G | GGGAA | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1645+727_1645+730d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 14435133 | |||||
| chr12:14435151
|
G | A | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1645+728G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435151 | ||||||
| chr12:14435276
|
T | C | 1 | a0011c0019t0001g0313 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1646-830T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435276 | ||||||
| chr12:14435436
|
T | C | 1 | a0003c0003t0004g0191 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1646-670T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435436 | ||||||
| chr12:14435457
|
A | C | 4 | a0003c0003t0014g0170a0003c0003t0023g0151a0003c0003t0023g0152others(1): Show | 4 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1646-649A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435457 | ||||||
| chr12:14435470
|
C | G | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1646-636C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435470 | ||||||
| chr12:14435507
|
A | G | 1 | a0014c0015t0003g0094 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1646-599A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435507 | ||||||
| chr12:14435877
|
C | T | 42 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(39): Show | 42 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.1646-229C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435877 | ||||||
| chr12:14436063
|
A | G | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1646-43A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14436063 | ||||||
| chr12:14436582
|
C | T | 1 | a0002c0002t0001g0271 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1791+331C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14436582 | ||||||
| chr12:14436599
|
G | A | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1791+348G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14436599 | ||||||
| chr12:14436640
|
C | T | 1 | a0001c0001t0003g0087 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1791+389C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14436640 | ||||||
| chr12:14436782
|
CT | C | 167 | a0001c0001t0002g0031a0001c0001t0003g0008a0001c0001t0003g0072others(164): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1791+544delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 14436782 | |||||
| chr12:14436793
|
T | A | 2 | a0006c0009t0005g0173a0006c0009t0005g0174 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1791+542T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14436793 | ||||||
| chr12:14436794
|
T | A | 7 | a0002c0002t0001g0257a0006c0009t0005g0173a0006c0009t0005g0174others(4): Show | 7 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1791+543T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14436794 | ||||||
| chr12:14436795
|
T | A | 111 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1791+544T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14436795 | ||||||
| chr12:14437055
|
G | A | 170 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1791+804G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437055 | ||||||
| chr12:14437585
|
G | A | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1792-545G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437585 | ||||||
| chr12:14437674
|
G | A | 1 | a0002c0004t0001g0242 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1792-456G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437674 | ||||||
| chr12:14437797
|
T | C | 1 | a0001c0001t0002g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1792-333T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437797 | ||||||
| chr12:14437829
|
G | A | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1792-301G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437829 | ||||||
| chr12:14437878
|
C | A | 1 | a0002c0002t0001g0286 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1792-252C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437878 | ||||||
| chr12:14437910
|
G | A | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1792-220G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437910 | ||||||
| chr12:14437916
|
A | G | 2 | a0001c0001t0021g0033a0001c0001t0021g0036 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1792-214A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437916 | ||||||
| chr12:14437926
|
G | A | 4 | a0003c0003t0014g0170a0003c0003t0023g0151a0003c0003t0023g0152others(1): Show | 4 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1792-204G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437926 | ||||||
| chr12:14437929
|
T | G | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1792-201T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437929 | ||||||
| chr12:14437977
|
C | T | 1 | a0001c0001t0006g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1792-153C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437977 | ||||||
| chr12:14437978
|
G | A | 11 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1792-152G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437978 | ||||||
| chr12:14438047
|
T | C | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1792-83T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14438047 | ||||||
| chr12:14438052
|
C | T | 1 | a0001c0001t0003g0078 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1792-78C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14438052 | ||||||
| chr12:14438286
|
G | A | 177 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1929+19G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14438286 | ||||||
| chr12:14438779
|
G | T | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1929+512G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14438779 | ||||||
| chr12:14439272
|
T | C | 4 | a0001c0001t0003g0085a0001c0001t0003g0092a0001c0001t0033g0093others(1): Show | 4 | HG00741.hp1 HG01993.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1929+1005T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439272 | ||||||
| chr12:14439325
|
C | T | 1 | a0001c0001t0003g0109 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1929+1058C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439325 | ||||||
| chr12:14439539
|
C | T | 5 | a0001c0001t0003g0074a0001c0001t0003g0078a0001c0001t0003g0079others(2): Show | 5 | HG02165.hp1 HG03239.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.1929+1272C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439539 | ||||||
| chr12:14439583
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1929+1316C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439583 | ||||||
| chr12:14439593
|
G | T | 2 | a0001c0001t0003g0074a0001c0001t0040g0139 | 2 | HG02165.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1929+1326G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439593 | ||||||
| chr12:14439840
|
A | AATCC | 44 | a0001c0001t0002g0014a0001c0001t0002g0034a0001c0001t0002g0035others(41): Show | 45 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1929+1618_1929+162 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14439840 | |||||
| chr12:14439840
|
A | AATCCATC others(1): Show |
13 | a0001c0001t0002g0038a0001c0001t0002g0041a0001c0001t0002g0042others(10): Show | 13 | HG01175.hp1 HG01358.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1929+1614_1929+162 others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14439840 | |||||
| chr12:14439840
|
AATCC | A | 128 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0015others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1929+1618_1929+162 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14439840 | |||||
| chr12:14439840
|
AATCCATC others(5): Show |
A | 14 | a0001c0001t0002g0084a0001c0001t0002g0118a0001c0001t0002g0119others(11): Show | 14 | HG01167.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1929+1610_1929+162 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14439840 | |||||
| chr12:14439840
|
AATCCATC others(13): Show |
A | 1 | a0002c0006t0008g0219 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1929+1602_1929+162 others(24): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14439840 | |||||
| chr12:14439840
|
AATCCATC others(17): Show |
A | 7 | a0002c0002t0001g0301a0003c0003t0013g0159a0003c0003t0013g0160others(4): Show | 7 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1929+1598_1929+162 others(28): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14439840 | |||||
| chr12:14439889
|
T | A | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1929+1622T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439889 | ||||||
| chr12:14439909
|
A | G | 94 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1929+1642A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439909 | ||||||
| chr12:14439945
|
A | G | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1929+1678A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439945 | ||||||
| chr12:14440086
|
G | A | 177 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1929+1819G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14440086 | ||||||
| chr12:14440140
|
A | G | 1 | a0003c0005t0041g0337 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1929+1873A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14440140 | ||||||
| chr12:14440239
|
A | G | 13 | a0001c0001t0002g0024a0001c0001t0003g0071a0001c0001t0003g0072others(10): Show | 13 | HG00609.hp1 HG00673.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.1929+1972A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14440239 | ||||||
| chr12:14440353
|
C | G | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1929+2086C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14440353 | ||||||
| chr12:14440636
|
AC | A | 104 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1929+2371delC | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14440636 | |||||
| chr12:14440751
|
G | A | 2 | a0003c0003t0011g0184a0003c0003t0028g0183 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1929+2484G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14440751 | ||||||
| chr12:14440968
|
T | C | 81 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1929+2701T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14440968 | ||||||
| chr12:14441007
|
C | G | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1929+2740C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441007 | ||||||
| chr12:14441035
|
T | C | 1 | a0002c0006t0019g0222 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1929+2768T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441035 | ||||||
| chr12:14441054
|
T | G | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1929+2787T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441054 | ||||||
| chr12:14441108
|
T | C | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1929+2841T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441108 | ||||||
| chr12:14441143
|
A | G | 1 | a0003c0003t0013g0161 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1929+2876A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441143 | ||||||
| chr12:14441283
|
A | G | 1 | a0003c0003t0005g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1929+3016A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441283 | ||||||
| chr12:14441421
|
AT | A | 4 | a0003c0003t0014g0170a0003c0003t0023g0151a0003c0003t0023g0152others(1): Show | 4 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1929+3157delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14441421 | |||||
| chr12:14441487
|
C | CT | 95 | a0001c0001t0002g0007a0001c0001t0002g0013a0001c0001t0002g0016others(92): Show | 97 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1929+3240dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14441487 | |||||
| chr12:14441487
|
CTTTTTTT others(3): Show |
C | 8 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0260others(5): Show | 8 | NA18612.hp1 NA18945.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.1929+3231_1929+324 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14441487 | |||||
| chr12:14441591
|
G | A | 2 | a0003c0003t0004g0196a0003c0003t0004g0197 | 2 | HG00733.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1929+3324G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441591 | ||||||
| chr12:14441678
|
A | T | 1 | a0003c0003t0005g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1929+3411A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441678 | ||||||
| chr12:14441800
|
A | C | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1929+3533A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441800 | ||||||
| chr12:14441806
|
C | T | 170 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1929+3539C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441806 | ||||||
| chr12:14441870
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1929+3603G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441870 | ||||||
| chr12:14442127
|
T | C | 4 | a0003c0003t0011g0204a0003c0003t0011g0314a0003c0003t0011g0315others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1929+3860T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442127 | ||||||
| chr12:14442136
|
A | G | 13 | a0002c0006t0008g0208a0002c0006t0008g0217a0002c0006t0008g0219others(10): Show | 13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1929+3869A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442136 | ||||||
| chr12:14442235
|
A | G | 1 | a0002c0002t0001g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1929+3968A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442235 | ||||||
| chr12:14442406
|
A | G | 28 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(25): Show | 28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1929+4139A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442406 | ||||||
| chr12:14442459
|
C | T | 4 | a0001c0001t0014g0125a0001c0001t0016g0075a0001c0001t0016g0126others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1929+4192C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442459 | ||||||
| chr12:14442522
|
G | A | 179 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(176): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1929+4255G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442522 | ||||||
| chr12:14442677
|
A | G | 1 | a0003c0005t0007g0328 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1930-4311A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442677 | ||||||
| chr12:14442822
|
G | A | 141 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(138): Show | 141 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.1930-4166G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442822 | ||||||
| chr12:14443032
|
G | C | 1 | a0003c0003t0011g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1930-3956G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443032 | ||||||
| chr12:14443255
|
A | T | 1 | a0010c0013t0020g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1930-3733A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443255 | ||||||
| chr12:14443382
|
G | GA | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1930-3599dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14443382 | |||||
| chr12:14443414
|
A | C | 1 | a0002c0002t0001g0307 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1930-3574A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443414 | ||||||
| chr12:14443568
|
G | A | 1 | a0002c0002t0037g0237 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1930-3420G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443568 | ||||||
| chr12:14443592
|
G | C | 1 | a0002c0002t0001g0301 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1930-3396G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443592 | ||||||
| chr12:14443691
|
G | A | 11 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1930-3297G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443691 | ||||||
| chr12:14443697
|
T | G | 1 | a0003c0003t0034g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1930-3291T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443697 | ||||||
| chr12:14443846
|
T | G | 1 | a0002c0002t0001g0275 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1930-3142T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443846 | ||||||
| chr12:14444022
|
A | G | 2 | a0001c0001t0003g0086a0001c0001t0003g0097 | 2 | HG01081.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1930-2966A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444022 | ||||||
| chr12:14444221
|
T | A | 1 | a0002c0002t0001g0300 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1930-2767T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444221 | ||||||
| chr12:14444508
|
A | AAAT | 7 | a0002c0002t0001g0205a0002c0002t0001g0225a0002c0002t0001g0255others(4): Show | 7 | HG00099.hp2 HG00621.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.1930-2479_1930-247 others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14444508 | |||||
| chr12:14444533
|
A | T | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1930-2455A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444533 | ||||||
| chr12:14444542
|
C | T | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1930-2446C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444542 | ||||||
| chr12:14444755
|
C | A | 2 | a0003c0003t0004g0196a0003c0003t0004g0197 | 2 | HG00733.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1930-2233C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444755 | ||||||
| chr12:14444841
|
C | T | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1930-2147C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444841 | ||||||
| chr12:14444901
|
T | C | 1 | a0001c0001t0002g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1930-2087T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444901 | ||||||
| chr12:14444987
|
C | G | 2 | a0003c0003t0011g0184a0003c0003t0028g0183 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1930-2001C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444987 | ||||||
| chr12:14444990
|
G | GT | 32 | a0001c0001t0003g0120a0001c0001t0006g0129a0003c0003t0004g0185others(29): Show | 32 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.1930-1979dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14444990 | |||||
| chr12:14444995
|
T | G | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1930-1993T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444995 | ||||||
| chr12:14445041
|
G | C | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1930-1947G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445041 | ||||||
| chr12:14445054
|
C | A | 1 | a0001c0001t0003g0109 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1930-1934C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445054 | ||||||
| chr12:14445055
|
G | A | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1930-1933G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445055 | ||||||
| chr12:14445060
|
C | T | 2 | a0003c0003t0011g0184a0003c0003t0028g0183 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1930-1928C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445060 | ||||||
| chr12:14445107
|
C | T | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1930-1881C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445107 | ||||||
| chr12:14445116
|
G | A | 140 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(137): Show | 140 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.1930-1872G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445116 | ||||||
| chr12:14445153
|
G | A | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1930-1835G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445153 | ||||||
| chr12:14445165
|
A | G | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1930-1823A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445165 | ||||||
| chr12:14445222
|
CT | C | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1930-1764delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14445222 | |||||
| chr12:14445298
|
G | T | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1930-1690G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445298 | ||||||
| chr12:14445393
|
C | CT | 14 | a0003c0003t0005g0316a0003c0003t0012g0001a0003c0003t0012g0179others(11): Show | 17 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1930-1585dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14445393 | |||||
| chr12:14445793
|
A | T | 3 | a0003c0003t0004g0192a0003c0003t0004g0193a0003c0003t0004g0194 | 3 | NA18968.hp1 NA19007.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1930-1195A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445793 | ||||||
| chr12:14445927
|
C | T | 1 | a0005c0007t0010g0322 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1930-1061C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445927 | ||||||
| chr12:14446155
|
G | GT | 8 | a0002c0006t0019g0228a0003c0003t0012g0180a0006c0009t0005g0173others(5): Show | 8 | HG02135.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1930-823dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14446155 | |||||
| chr12:14446158
|
T | C | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1930-830T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446158 | ||||||
| chr12:14446195
|
T | G | 13 | a0002c0006t0008g0208a0002c0006t0008g0217a0002c0006t0008g0219others(10): Show | 13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1930-793T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446195 | ||||||
| chr12:14446208
|
C | T | 1 | a0003c0003t0011g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1930-780C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446208 | ||||||
| chr12:14446210
|
C | T | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1930-778C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446210 | ||||||
| chr12:14446374
|
T | A | 1 | a0002c0002t0009g0215 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1930-614T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446374 | ||||||
| chr12:14446835
|
A | C | 1 | a0003c0003t0011g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1930-153A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446835 | ||||||
| chr12:14446906
|
T | C | 1 | a0003c0003t0005g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1930-82T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446906 | ||||||
| chr12:14446912
|
A | G | 1 | a0002c0002t0001g0286 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1930-76A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446912 | ||||||
| chr12:14446921
|
G | GT | 11 | a0001c0001t0002g0140a0002c0002t0009g0005a0002c0002t0009g0006others(8): Show | 11 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1930-56dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14446921 | |||||
| chr12:14446921
|
GT | G | 8 | a0002c0002t0001g0296a0002c0002t0001g0301a0003c0005t0007g0325others(5): Show | 8 | HG02145.hp2 HG02451.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1930-56delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14446921 | |||||
| chr12:14446970
|
C | CT | 309 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0025others(306): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
splice_region_variant&intron_variant | LOW | c.1930-4dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14446970 | |||||
| chr12:14446970
|
C | CTT | 29 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0015others(26): Show | 29 | HG00639.hp1 HG01243.hp1 HG01261.hp2 others(26): Show |
splice_region_variant&intron_variant | LOW | c.1930-5_1930-4dupTT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14446970 | |||||
| chr12:14447067
|
A | G | 1 | a0003c0003t0011g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1995+14A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447067 | ||||||
| chr12:14447281
|
CT | C | 182 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(179): Show | 182 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(179): Show |
intron_variant | MODIFIER | c.1995+248delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14447281 | |||||
| chr12:14447281
|
CTT | C | 53 | a0001c0001t0002g0030a0001c0001t0002g0056a0001c0001t0002g0069others(50): Show | 56 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1995+247_1995+248d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14447281 | |||||
| chr12:14447281
|
CTTT | C | 92 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(89): Show | 92 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1995+246_1995+248d others(5): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14447281 | |||||
| chr12:14447502
|
G | A | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995+449G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447502 | ||||||
| chr12:14447508
|
C | T | 1 | a0003c0005t0041g0337 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995+455C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447508 | ||||||
| chr12:14447591
|
T | C | 4 | a0003c0003t0011g0204a0003c0003t0011g0314a0003c0003t0011g0315others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1995+538T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447591 | ||||||
| chr12:14447629
|
A | T | 29 | a0001c0020t0036g0131a0003c0003t0004g0185a0003c0003t0004g0186others(26): Show | 29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1995+576A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447629 | ||||||
| chr12:14447698
|
C | T | 1 | a0002c0002t0001g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1995+645C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447698 | ||||||
| chr12:14447745
|
A | G | 27 | a0001c0020t0036g0131a0003c0003t0004g0185a0003c0003t0004g0186others(24): Show | 27 | HG00733.hp2 HG01123.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1995+692A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447745 | ||||||
| chr12:14447815
|
A | G | 2 | a0003c0003t0004g0185a0003c0003t0004g0186 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1995+762A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447815 | ||||||
| chr12:14448044
|
T | C | 1 | a0001c0001t0002g0342 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1995+991T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14448044 | ||||||
| chr12:14448060
|
AT | A | 142 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(139): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1995+1015delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14448060 | |||||
| chr12:14448316
|
T | C | 3 | a0002c0004t0001g0239a0002c0004t0001g0240a0002c0004t0001g0243 | 3 | HG01934.hp2 HG02148.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1995+1263T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14448316 | ||||||
| chr12:14448466
|
C | T | 1 | a0003c0003t0014g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1995+1413C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14448466 | ||||||
| chr12:14448725
|
C | G | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1995+1672C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14448725 | ||||||
| chr12:14448804
|
C | T | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1995+1751C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14448804 | ||||||
| chr12:14448998
|
C | T | 1 | a0002c0002t0001g0271 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1995+1945C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14448998 | ||||||
| chr12:14449058
|
CTT | C | 9 | a0003c0003t0035g0343a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1995+2006_1995+200 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14449058 | ||||||
| chr12:14449427
|
T | C | 1 | a0002c0002t0001g0205 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1995+2374T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14449427 | ||||||
| chr12:14449495
|
T | C | 1 | a0002c0002t0001g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1995+2442T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14449495 | ||||||
| chr12:14449529
|
A | G | 1 | a0001c0001t0003g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1995+2476A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14449529 | ||||||
| chr12:14449791
|
G | C | 4 | a0003c0003t0011g0204a0003c0003t0011g0314a0003c0003t0011g0315others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1995+2738G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14449791 | ||||||
| chr12:14449965
|
TG | T | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1995+2913delG | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14449965 | ||||||
| chr12:14450011
|
G | A | 1 | a0001c0001t0002g0013 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1995+2958G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14450011 | ||||||
| chr12:14450045
|
T | C | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995+2992T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14450045 | ||||||
| chr12:14450159
|
CT | C | 94 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1995+3111delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14450159 | |||||
| chr12:14450212
|
A | C | 11 | a0001c0001t0006g0070a0001c0001t0006g0076a0001c0001t0006g0129others(8): Show | 11 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1995+3159A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14450212 | ||||||
| chr12:14450585
|
AT | A | 7 | a0002c0002t0001g0301a0003c0003t0013g0159a0003c0003t0013g0160others(4): Show | 7 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1995+3533delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14450585 | ||||||
| chr12:14450758
|
T | C | 7 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1995+3705T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14450758 | ||||||
| chr12:14451086
|
T | C | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1995+4033T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451086 | ||||||
| chr12:14451222
|
T | C | 1 | a0002c0002t0001g0274 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1995+4169T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451222 | ||||||
| chr12:14451285
|
T | C | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1995+4232T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451285 | ||||||
| chr12:14451518
|
C | T | 2 | a0002c0002t0009g0005a0002c0002t0009g0006 | 2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1995+4465C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451518 | ||||||
| chr12:14451619
|
G | GT | 8 | a0001c0001t0031g0009a0002c0002t0001g0301a0003c0003t0013g0159others(5): Show | 8 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1995+4577dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14451619 | |||||
| chr12:14451706
|
A | G | 1 | a0001c0020t0036g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1995+4653A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451706 | ||||||
| chr12:14451891
|
A | G | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1996-4670A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451891 | ||||||
| chr12:14451967
|
A | G | 28 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(25): Show | 28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1996-4594A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451967 | ||||||
| chr12:14451978
|
G | T | 94 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1996-4583G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451978 | ||||||
| chr12:14452190
|
T | C | 1 | a0001c0001t0003g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1996-4371T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14452190 | ||||||
| chr12:14452288
|
A | C | 7 | a0002c0002t0001g0301a0003c0003t0013g0159a0003c0003t0013g0160others(4): Show | 7 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1996-4273A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14452288 | ||||||
| chr12:14452308
|
G | A | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1996-4253G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14452308 | ||||||
| chr12:14453209
|
G | A | 1 | a0002c0004t0001g0239 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1996-3352G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453209 | ||||||
| chr12:14453384
|
G | T | 3 | a0005c0007t0010g0002a0005c0007t0010g0321a0005c0007t0010g0323 | 4 | HG03490.hp2 HG03492.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1996-3177G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453384 | ||||||
| chr12:14453452
|
G | A | 1 | a0003c0003t0014g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1996-3109G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453452 | ||||||
| chr12:14453599
|
C | T | 1 | a0003c0003t0011g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1996-2962C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453599 | ||||||
| chr12:14453676
|
G | A | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1996-2885G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453676 | ||||||
| chr12:14453788
|
C | G | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1996-2773C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453788 | ||||||
| chr12:14453850
|
C | T | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1996-2711C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453850 | ||||||
| chr12:14453871
|
C | T | 1 | a0003c0003t0011g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1996-2690C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453871 | ||||||
| chr12:14453872
|
G | T | 1 | a0003c0003t0004g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1996-2689G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453872 | ||||||
| chr12:14454208
|
T | C | 29 | a0001c0020t0036g0131a0003c0003t0004g0185a0003c0003t0004g0186others(26): Show | 29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1996-2353T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454208 | ||||||
| chr12:14454423
|
A | G | 3 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0059 | 3 | NA18612.hp2 NA18993.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1996-2138A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454423 | ||||||
| chr12:14454498
|
G | A | 1 | a0003c0003t0018g0153 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1996-2063G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454498 | ||||||
| chr12:14454552
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1996-2009G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454552 | ||||||
| chr12:14454637
|
G | C | 178 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(175): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1996-1924G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454637 | ||||||
| chr12:14454697
|
A | G | 28 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(25): Show | 28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1996-1864A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454697 | ||||||
| chr12:14454787
|
C | A | 141 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.1996-1774C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454787 | ||||||
| chr12:14454892
|
A | G | 3 | a0002c0004t0001g0240a0002c0004t0001g0243a0003c0003t0014g0149 | 3 | HG01934.hp2 HG02148.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1996-1669A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454892 | ||||||
| chr12:14455000
|
A | G | 186 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1996-1561A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455000 | ||||||
| chr12:14455036
|
G | A | 3 | a0001c0001t0003g0099a0001c0001t0003g0100a0001c0001t0003g0101 | 3 | HG01069.hp1 HG01071.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1996-1525G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455036 | ||||||
| chr12:14455125
|
C | G | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1996-1436C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455125 | ||||||
| chr12:14455138
|
G | A | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1996-1423G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455138 | ||||||
| chr12:14455182
|
C | CA | 16 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0058others(13): Show | 16 | HG00741.hp1 HG01099.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1996-1360dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14455182 | |||||
| chr12:14455182
|
CA | C | 26 | a0001c0001t0003g0095a0001c0001t0003g0105a0001c0001t0003g0146others(23): Show | 27 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.1996-1360delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14455182 | |||||
| chr12:14455439
|
A | G | 4 | a0001c0001t0003g0083a0001c0001t0003g0114a0001c0001t0022g0081others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1996-1122A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455439 | ||||||
| chr12:14455468
|
A | C | 1 | a0003c0003t0011g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1996-1093A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455468 | ||||||
| chr12:14455741
|
C | T | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1996-820C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455741 | ||||||
| chr12:14455789
|
G | A | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | NA18612.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1996-772G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455789 | ||||||
| chr12:14455865
|
G | A | 151 | a0001c0001t0002g0017a0002c0002t0001g0004a0002c0002t0001g0205others(148): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1996-696G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455865 | ||||||
| chr12:14456148
|
G | C | 190 | a0001c0001t0003g0116a0001c0020t0036g0131a0002c0002t0001g0004others(187): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1996-413G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14456148 | ||||||
| chr12:14456319
|
AT | A | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1996-240delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14456319 | |||||
| chr12:14456410
|
A | T | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1996-151A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14456410 | ||||||
| chr12:14456645
|
A | G | 1 | a0001c0001t0002g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2069+11A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 7/14 | chr12 | 14456645 | ||||||
| chr12:14457160
|
C | G | 2 | a0003c0014t0013g0163a0003c0014t0013g0164 | 2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2070-47C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 7/14 | chr12 | 14457160 | ||||||
| chr12:14457505
|
A | G | 186 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.2158+210A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457505 | ||||||
| chr12:14457536
|
A | T | 1 | a0003c0003t0011g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2158+241A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457536 | ||||||
| chr12:14457628
|
T | C | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.2158+333T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457628 | ||||||
| chr12:14457657
|
A | G | 1 | a0001c0001t0003g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2158+362A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457657 | ||||||
| chr12:14457726
|
G | T | 114 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2158+431G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457726 | ||||||
| chr12:14457740
|
G | A | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.2158+445G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457740 | ||||||
| chr12:14457772
|
A | T | 1 | a0002c0002t0001g0248 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2158+477A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457772 | ||||||
| chr12:14457870
|
G | A | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.2158+575G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457870 | ||||||
| chr12:14458045
|
G | A | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2158+750G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458045 | ||||||
| chr12:14458055
|
C | T | 2 | a0001c0001t0003g0077a0001c0001t0003g0102 | 2 | NA18949.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2158+760C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458055 | ||||||
| chr12:14458095
|
CA | C | 8 | a0002c0004t0001g0229a0003c0003t0013g0159a0003c0003t0013g0160others(5): Show | 8 | HG00639.hp1 HG00741.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.2158+811delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 14458095 | |||||
| chr12:14458106
|
AT | A | 7 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2158+812delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458106 | ||||||
| chr12:14458107
|
T | A | 13 | a0002c0002t0009g0287a0002c0002t0009g0288a0002c0002t0009g0289others(10): Show | 14 | HG00609.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2158+812T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458107 | ||||||
| chr12:14458150
|
C | G | 4 | a0001c0001t0003g0083a0001c0001t0003g0114a0001c0001t0022g0081others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2158+855C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458150 | ||||||
| chr12:14458372
|
T | A | 7 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(4): Show | 9 | HG00099.hp1 HG00280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2158+1077T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458372 | ||||||
| chr12:14458547
|
C | T | 3 | a0003c0003t0023g0151a0003c0003t0023g0152a0003c0003t0034g0150 | 3 | HG01099.hp1 HG02300.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2158+1252C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458547 | ||||||
| chr12:14458588
|
C | T | 140 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(137): Show | 140 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.2158+1293C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458588 | ||||||
| chr12:14458920
|
A | G | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2159-1575A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458920 | ||||||
| chr12:14458970
|
A | G | 1 | a0002c0002t0001g0304 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2159-1525A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458970 | ||||||
| chr12:14459020
|
A | G | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2159-1475A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459020 | ||||||
| chr12:14459032
|
T | C | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2159-1463T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459032 | ||||||
| chr12:14459096
|
A | G | 1 | a0001c0001t0002g0113 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2159-1399A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459096 | ||||||
| chr12:14459282
|
G | C | 1 | a0001c0001t0002g0342 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2159-1213G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459282 | ||||||
| chr12:14459332
|
T | TA | 28 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(25): Show | 28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.2159-1162dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 14459332 | |||||
| chr12:14459389
|
A | G | 142 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(139): Show | 142 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.2159-1106A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459389 | ||||||
| chr12:14459452
|
T | G | 1 | a0001c0001t0016g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2159-1043T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459452 | ||||||
| chr12:14459505
|
C | G | 1 | a0001c0001t0003g0109 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2159-990C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459505 | ||||||
| chr12:14459570
|
T | A | 186 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.2159-925T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459570 | ||||||
| chr12:14459672
|
C | T | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.2159-823C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459672 | ||||||
| chr12:14459695
|
T | G | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2159-800T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459695 | ||||||
| chr12:14459780
|
T | C | 12 | a0002c0002t0001g0275a0003c0005t0007g0325a0003c0005t0007g0326others(9): Show | 12 | HG00621.hp1 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2159-715T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459780 | ||||||
| chr12:14459938
|
G | A | 1 | a0002c0006t0019g0228 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2159-557G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459938 | ||||||
| chr12:14459958
|
A | G | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2159-537A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459958 | ||||||
| chr12:14459961
|
G | C | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2159-534G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459961 | ||||||
| chr12:14459997
|
A | C | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2159-498A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459997 | ||||||
| chr12:14460244
|
C | T | 1 | a0003c0003t0011g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2159-251C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14460244 | ||||||
| chr12:14460271
|
C | A | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2159-224C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14460271 | ||||||
| chr12:14460311
|
T | C | 3 | a0003c0003t0023g0151a0003c0003t0023g0152a0003c0003t0034g0150 | 3 | HG01099.hp1 HG02300.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2159-184T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14460311 | ||||||
| chr12:14460457
|
TAACCATT others(2): Show |
T | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2159-34_2159-26del others(9): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 14460457 | |||||
| chr12:14460463
|
T | A | 1 | a0001c0001t0003g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2159-32T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14460463 | ||||||
| chr12:14460469
|
C | A | 1 | a0001c0001t0003g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2159-26C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14460469 | ||||||
| chr12:14461210
|
A | G | 1 | a0003c0005t0007g0335 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2797+77A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461210 | ||||||
| chr12:14461270
|
T | A | 11 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2797+137T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461270 | ||||||
| chr12:14461290
|
A | G | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2797+157A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461290 | ||||||
| chr12:14461397
|
T | C | 2 | a0003c0003t0011g0184a0003c0003t0028g0183 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2797+264T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461397 | ||||||
| chr12:14461413
|
G | A | 1 | a0003c0003t0018g0153 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2797+280G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461413 | ||||||
| chr12:14461453
|
C | T | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2797+320C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461453 | ||||||
| chr12:14461543
|
C | G | 12 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0260others(9): Show | 12 | HG02132.hp1 NA18612.hp1 NA18941.hp1 others(9): Show |
intron_variant | MODIFIER | c.2797+410C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461543 | ||||||
| chr12:14461546
|
T | C | 3 | a0001c0001t0002g0043a0001c0001t0002g0052a0001c0001t0002g0053 | 3 | HG02602.hp1 HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2797+413T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461546 | ||||||
| chr12:14461982
|
C | T | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2797+849C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461982 | ||||||
| chr12:14462159
|
CTA | C | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2797+1027_2797+102 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14462159 | ||||||
| chr12:14462192
|
A | G | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2797+1059A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14462192 | ||||||
| chr12:14462743
|
T | C | 1 | a0001c0001t0002g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2797+1610T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14462743 | ||||||
| chr12:14462931
|
G | A | 1 | a0001c0001t0003g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2797+1798G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14462931 | ||||||
| chr12:14463103
|
T | C | 4 | a0003c0003t0011g0204a0003c0003t0011g0314a0003c0003t0011g0315others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2797+1970T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463103 | ||||||
| chr12:14463346
|
T | C | 1 | a0002c0002t0001g0255 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2797+2213T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463346 | ||||||
| chr12:14463497
|
T | C | 2 | a0003c0014t0013g0163a0003c0014t0013g0164 | 2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2797+2364T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463497 | ||||||
| chr12:14463625
|
T | G | 1 | a0001c0001t0002g0113 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2797+2492T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463625 | ||||||
| chr12:14463845
|
T | C | 1 | a0003c0003t0012g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2798-2681T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463845 | ||||||
| chr12:14463960
|
C | T | 2 | a0003c0014t0013g0163a0003c0014t0013g0164 | 2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2798-2566C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463960 | ||||||
| chr12:14463979
|
T | A | 330 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.2798-2547T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463979 | ||||||
| chr12:14463979
|
T | G | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2798-2547T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463979 | ||||||
| chr12:14464226
|
G | A | 11 | a0002c0006t0008g0217a0002c0006t0008g0219a0002c0006t0008g0220others(8): Show | 11 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.2798-2300G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464226 | ||||||
| chr12:14464433
|
C | T | 1 | a0002c0002t0001g0301 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2798-2093C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464433 | ||||||
| chr12:14464435
|
A | G | 2 | a0001c0001t0002g0038a0001c0001t0002g0042 | 2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2798-2091A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464435 | ||||||
| chr12:14464511
|
G | A | 1 | a0005c0007t0010g0322 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2798-2015G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464511 | ||||||
| chr12:14464527
|
G | A | 2 | a0001c0001t0003g0074a0001c0001t0040g0139 | 2 | HG02165.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2798-1999G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464527 | ||||||
| chr12:14464534
|
A | G | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2798-1992A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464534 | ||||||
| chr12:14464610
|
T | C | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2798-1916T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464610 | ||||||
| chr12:14464703
|
G | C | 1 | a0003c0003t0028g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2798-1823G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464703 | ||||||
| chr12:14465041
|
G | A | 1 | a0003c0003t0014g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2798-1485G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465041 | ||||||
| chr12:14465253
|
T | C | 2 | a0010c0013t0020g0115a0010c0013t0020g0117 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2798-1273T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465253 | ||||||
| chr12:14465300
|
A | G | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2798-1226A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465300 | ||||||
| chr12:14465304
|
T | G | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2798-1222T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465304 | ||||||
| chr12:14465345
|
A | G | 3 | a0001c0001t0003g0012a0001c0001t0003g0122a0001c0001t0003g0123 | 3 | HG01074.hp1 HG01168.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.2798-1181A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465345 | ||||||
| chr12:14465489
|
A | C | 1 | a0003c0003t0011g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2798-1037A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465489 | ||||||
| chr12:14465499
|
C | T | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2798-1027C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465499 | ||||||
| chr12:14465548
|
T | A | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2798-978T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465548 | ||||||
| chr12:14465579
|
G | A | 300 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(297): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.2798-947G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465579 | ||||||
| chr12:14465667
|
C | T | 1 | a0008c0011t0024g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2798-859C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465667 | ||||||
| chr12:14465726
|
GTTTAAC | G | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.2798-797_2798-792d others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 14465726 | |||||
| chr12:14465738
|
G | T | 1 | a0004c0008t0005g0294 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2798-788G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465738 | ||||||
| chr12:14466034
|
T | C | 1 | a0003c0003t0015g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2798-492T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14466034 | ||||||
| chr12:14466138
|
C | G | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-388C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14466138 | ||||||
| chr12:14466161
|
G | T | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-365G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14466161 | ||||||
| chr12:14466163
|
C | A | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-363C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14466163 | ||||||
| chr12:14466165
|
T | A | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-361T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14466165 | ||||||
| chr12:14466387
|
G | A | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2798-139G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14466387 | ||||||
| chr12:14466507
|
G | A | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2798-19G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14466507 | ||||||
| chr12:14466697
|
T | A | 1 | a0003c0003t0025g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2862+107T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14466697 | ||||||
| chr12:14467165
|
G | A | 4 | a0002c0004t0001g0230a0002c0004t0001g0231a0002c0004t0001g0232others(1): Show | 4 | HG01074.hp2 HG01175.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2862+575G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14467165 | ||||||
| chr12:14467364
|
C | T | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2862+774C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14467364 | ||||||
| chr12:14467414
|
A | C | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2862+824A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14467414 | ||||||
| chr12:14467443
|
G | C | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.2862+853G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14467443 | ||||||
| chr12:14467486
|
G | T | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.2862+896G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14467486 | ||||||
| chr12:14467672
|
G | GT | 97 | a0001c0001t0003g0110a0001c0001t0003g0111a0002c0002t0001g0004others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.2862+1095dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14467672 | |||||
| chr12:14467844
|
A | AAAT | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.2862+1256_2862+125 others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14467844 | |||||
| chr12:14467990
|
G | A | 17 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(14): Show | 17 | HG01123.hp2 HG02257.hp1 HG02970.hp2 others(14): Show |
intron_variant | MODIFIER | c.2862+1400G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14467990 | ||||||
| chr12:14467995
|
G | A | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2862+1405G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14467995 | ||||||
| chr12:14468101
|
T | C | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2862+1511T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468101 | ||||||
| chr12:14468272
|
C | CA | 19 | a0001c0001t0003g0074a0002c0002t0001g0209a0002c0002t0001g0210others(16): Show | 22 | HG00609.hp2 HG01256.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2862+1699dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14468272 | |||||
| chr12:14468272
|
CA | C | 10 | a0002c0004t0001g0230a0002c0004t0001g0291a0002c0006t0008g0217others(7): Show | 10 | HG01069.hp2 HG01993.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2862+1699delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14468272 | |||||
| chr12:14468276
|
A | G | 1 | a0001c0001t0002g0017 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2862+1686A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468276 | ||||||
| chr12:14468289
|
A | G | 1 | a0003c0003t0011g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2862+1699A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468289 | ||||||
| chr12:14468384
|
T | G | 3 | a0001c0001t0003g0099a0001c0001t0003g0100a0001c0001t0003g0101 | 3 | HG01069.hp1 HG01071.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2862+1794T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468384 | ||||||
| chr12:14468398
|
T | G | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2862+1808T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468398 | ||||||
| chr12:14468401
|
G | A | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.2862+1811G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468401 | ||||||
| chr12:14468439
|
G | A | 3 | a0005c0007t0010g0319a0005c0007t0010g0320a0005c0007t0010g0322 | 3 | HG00609.hp2 HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2862+1849G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468439 | ||||||
| chr12:14468444
|
C | G | 16 | a0003c0003t0025g0171a0003c0003t0025g0172a0003c0003t0035g0343others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.2862+1854C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468444 | ||||||
| chr12:14468476
|
A | G | 1 | a0002c0002t0001g0299 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2862+1886A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468476 | ||||||
| chr12:14468493
|
TA | T | 233 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(230): Show | 236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.2862+1918delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14468493 | |||||
| chr12:14468493
|
TAA | T | 105 | a0001c0001t0006g0076a0002c0002t0001g0004a0002c0002t0001g0205others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.2862+1917_2862+191 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14468493 | |||||
| chr12:14468607
|
G | T | 2 | a0005c0007t0010g0317a0005c0007t0010g0318 | 2 | HG01346.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.2862+2017G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468607 | ||||||
| chr12:14468783
|
A | C | 105 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.2862+2193A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468783 | ||||||
| chr12:14468785
|
A | G | 95 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.2862+2195A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468785 | ||||||
| chr12:14468801
|
A | G | 1 | a0003c0003t0014g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2862+2211A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468801 | ||||||
| chr12:14468810
|
T | C | 4 | a0002c0006t0008g0223a0002c0006t0008g0224a0002c0006t0008g0226others(1): Show | 4 | NA18977.hp2 NA18981.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.2862+2220T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468810 | ||||||
| chr12:14468995
|
A | T | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.2862+2405A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468995 | ||||||
| chr12:14469052
|
T | C | 1 | a0002c0002t0001g0236 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2862+2462T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469052 | ||||||
| chr12:14469068
|
A | G | 62 | a0001c0001t0002g0013a0001c0001t0002g0024a0001c0001t0002g0140others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.2862+2478A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469068 | ||||||
| chr12:14469330
|
A | G | 3 | a0007c0010t0002g0011a0007c0010t0002g0022a0007c0010t0002g0049 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2862+2740A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469330 | ||||||
| chr12:14469346
|
C | G | 1 | a0001c0001t0003g0105 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2862+2756C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469346 | ||||||
| chr12:14469362
|
CA | C | 192 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(189): Show | 193 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(190): Show |
intron_variant | MODIFIER | c.2862+2793delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14469362 | |||||
| chr12:14469362
|
CAA | C | 124 | a0001c0001t0002g0020a0001c0001t0003g0074a0001c0001t0003g0078others(121): Show | 126 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2862+2792_2862+279 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14469362 | |||||
| chr12:14469368
|
A | C | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2862+2778A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469368 | ||||||
| chr12:14469378
|
A | C | 1 | a0003c0003t0034g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2862+2788A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469378 | ||||||
| chr12:14469383
|
A | C | 82 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.2862+2793A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469383 | ||||||
| chr12:14469420
|
G | A | 1 | a0003c0005t0007g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2862+2830G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469420 | ||||||
| chr12:14469540
|
TTTA | T | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2862+2954_2862+295 others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14469540 | |||||
| chr12:14469587
|
AAAAC | A | 4 | a0003c0003t0014g0170a0003c0003t0023g0151a0003c0003t0023g0152others(1): Show | 4 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2862+3001_2862+300 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14469587 | |||||
| chr12:14470054
|
C | G | 1 | a0001c0001t0002g0024 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2862+3464C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470054 | ||||||
| chr12:14470128
|
A | C | 1 | a0002c0002t0001g0205 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2862+3538A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470128 | ||||||
| chr12:14470198
|
C | A | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2862+3608C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470198 | ||||||
| chr12:14470241
|
C | T | 1 | a0003c0003t0014g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2862+3651C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470241 | ||||||
| chr12:14470327
|
C | T | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2862+3737C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470327 | ||||||
| chr12:14470370
|
A | T | 109 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(106): Show | 109 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.2862+3780A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470370 | ||||||
| chr12:14470381
|
A | G | 1 | a0001c0001t0003g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2862+3791A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470381 | ||||||
| chr12:14470435
|
G | A | 1 | a0001c0001t0002g0058 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2862+3845G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470435 | ||||||
| chr12:14470490
|
C | T | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2862+3900C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470490 | ||||||
| chr12:14470646
|
G | A | 11 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2862+4056G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470646 | ||||||
| chr12:14470653
|
T | C | 1 | a0003c0003t0011g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2862+4063T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470653 | ||||||
| chr12:14470771
|
A | G | 314 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2862+4181A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470771 | ||||||
| chr12:14471072
|
G | A | 2 | a0003c0003t0004g0203a0003c0003t0014g0149 | 2 | NA19056.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2862+4482G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471072 | ||||||
| chr12:14471385
|
C | T | 1 | a0001c0001t0003g0080 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2863-4505C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471385 | ||||||
| chr12:14471640
|
A | C | 143 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(140): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.2863-4250A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471640 | ||||||
| chr12:14471837
|
T | C | 1 | a0001c0001t0003g0074 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2863-4053T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471837 | ||||||
| chr12:14471842
|
G | A | 1 | a0002c0006t0008g0295 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2863-4048G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471842 | ||||||
| chr12:14471877
|
C | G | 1 | a0001c0001t0002g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2863-4013C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471877 | ||||||
| chr12:14471919
|
G | A | 3 | a0001c0001t0003g0104a0001c0001t0003g0107a0001c0001t0032g0103 | 3 | HG00673.hp1 NA19060.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.2863-3971G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471919 | ||||||
| chr12:14471955
|
A | G | 10 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(7): Show | 10 | NA18939.hp1 NA18955.hp2 NA18967.hp2 others(7): Show |
intron_variant | MODIFIER | c.2863-3935A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471955 | ||||||
| chr12:14472044
|
G | T | 2 | a0003c0003t0004g0196a0003c0003t0004g0197 | 2 | HG00733.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2863-3846G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472044 | ||||||
| chr12:14472119
|
TA | T | 149 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(146): Show | 149 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.2863-3770delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472119 | ||||||
| chr12:14472214
|
A | T | 1 | a0008c0011t0024g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2863-3676A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472214 | ||||||
| chr12:14472308
|
GAAAAGCA others(3): Show |
G | 4 | a0003c0003t0011g0204a0003c0003t0011g0314a0003c0003t0011g0315others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2863-3571_2863-356 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14472308 | |||||
| chr12:14472337
|
T | G | 4 | a0003c0003t0004g0191a0003c0003t0004g0192a0003c0003t0004g0193others(1): Show | 4 | NA18955.hp2 NA18968.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2863-3553T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472337 | ||||||
| chr12:14472350
|
C | T | 4 | a0001c0001t0003g0083a0001c0001t0003g0114a0001c0001t0022g0081others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2863-3540C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472350 | ||||||
| chr12:14472480
|
A | G | 1 | a0001c0001t0002g0059 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2863-3410A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472480 | ||||||
| chr12:14472609
|
C | G | 1 | a0003c0003t0004g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2863-3281C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472609 | ||||||
| chr12:14472618
|
G | A | 1 | a0002c0002t0001g0205 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2863-3272G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472618 | ||||||
| chr12:14472624
|
T | C | 1 | a0014c0015t0003g0094 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2863-3266T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472624 | ||||||
| chr12:14472637
|
C | A | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2863-3253C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472637 | ||||||
| chr12:14472694
|
C | T | 2 | a0003c0014t0013g0163a0003c0014t0013g0164 | 2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2863-3196C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472694 | ||||||
| chr12:14472718
|
C | G | 1 | a0001c0001t0002g0044 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2863-3172C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472718 | ||||||
| chr12:14472722
|
G | A | 2 | a0001c0001t0003g0086a0001c0001t0003g0097 | 2 | HG01081.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.2863-3168G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472722 | ||||||
| chr12:14472729
|
T | G | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2863-3161T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472729 | ||||||
| chr12:14472777
|
T | A | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.2863-3113T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472777 | ||||||
| chr12:14472820
|
G | GCA | 161 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(158): Show | 161 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(158): Show |
intron_variant | MODIFIER | c.2863-3058_2863-305 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14472820 | |||||
| chr12:14472820
|
G | GCACA | 3 | a0001c0001t0029g0060a0003c0003t0018g0153a0003c0003t0018g0155 | 3 | HG01243.hp1 HG01891.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2863-3060_2863-305 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14472820 | |||||
| chr12:14472871
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2863-3019C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472871 | ||||||
| chr12:14473081
|
A | T | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2863-2809A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473081 | ||||||
| chr12:14473200
|
C | G | 2 | a0003c0003t0018g0153a0003c0003t0018g0155 | 2 | HG01891.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2863-2690C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473200 | ||||||
| chr12:14473274
|
C | T | 1 | a0003c0003t0012g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2863-2616C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473274 | ||||||
| chr12:14473275
|
GCT | G | 56 | a0001c0001t0003g0012a0001c0001t0003g0071a0001c0001t0003g0072others(53): Show | 56 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2863-2600_2863-259 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473275 | |||||
| chr12:14473277
|
T | G | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2863-2613T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473277 | ||||||
| chr12:14473280
|
C | CTG | 10 | a0001c0001t0002g0013a0003c0003t0005g0158a0003c0003t0013g0159others(7): Show | 10 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.2863-2609_2863-260 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473280 | |||||
| chr12:14473282
|
C | G | 108 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0014others(105): Show | 108 | HG01099.hp1 HG01099.hp2 HG01123.hp1 others(105): Show |
intron_variant | MODIFIER | c.2863-2608C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473282 | ||||||
| chr12:14473284
|
C | G | 52 | a0001c0001t0003g0012a0001c0001t0003g0071a0001c0001t0003g0072others(49): Show | 52 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2863-2606C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473284 | ||||||
| chr12:14473288
|
C | CTGTA | 29 | a0001c0001t0002g0024a0001c0001t0002g0030a0001c0001t0006g0070others(26): Show | 29 | HG00735.hp2 HG01099.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | |||||
| chr12:14473288
|
C | CTGTATG | 58 | a0001c0001t0002g0010a0001c0001t0002g0018a0001c0001t0002g0068others(55): Show | 58 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | |||||
| chr12:14473288
|
C | CTGTATGT others(1): Show |
68 | a0001c0001t0002g0007a0001c0001t0002g0015a0001c0001t0002g0016others(65): Show | 68 | HG00438.hp1 HG01071.hp1 HG01074.hp2 others(65): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | |||||
| chr12:14473288
|
C | CTGTATGT others(3): Show |
29 | a0001c0001t0002g0014a0001c0001t0002g0029a0001c0001t0002g0037others(26): Show | 29 | HG01361.hp1 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | |||||
| chr12:14473288
|
C | CTGTATGT others(5): Show |
23 | a0001c0001t0002g0057a0001c0001t0002g0061a0001c0001t0002g0063others(20): Show | 23 | HG00438.hp2 HG00673.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | |||||
| chr12:14473288
|
C | CTGTATGT others(7): Show |
6 | a0002c0006t0008g0217a0002c0006t0008g0220a0003c0003t0018g0153others(3): Show | 6 | HG01515.hp2 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | |||||
| chr12:14473288
|
C | CTGTATGT others(9): Show |
7 | a0001c0001t0002g0028a0003c0003t0011g0315a0003c0003t0015g0165others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(20): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | |||||
| chr12:14473288
|
C | CTGTATGT others(11): Show |
1 | a0003c0003t0011g0314 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2863-2601_2863-260 others(22): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | |||||
| chr12:14473288
|
C | CTGTG | 4 | a0003c0003t0004g0196a0003c0003t0004g0197a0009c0012t0011g0338others(1): Show | 4 | HG00733.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | |||||
| chr12:14473288
|
C | G | 12 | a0001c0001t0002g0013a0003c0003t0005g0158a0003c0003t0013g0159others(9): Show | 12 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.2863-2602C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473288 | ||||||
| chr12:14473288
|
CTCTG | C | 5 | a0001c0001t0002g0140a0001c0001t0003g0074a0001c0001t0027g0023others(2): Show | 5 | HG00597.hp2 HG02735.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.2863-2600_2863-259 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | |||||
| chr12:14473288
|
CTCTGTG | C | 6 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0003g0109others(3): Show | 6 | HG01099.hp2 HG03239.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2863-2600_2863-259 others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | |||||
| chr12:14473288
|
CTCTGTGT others(1): Show |
C | 11 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2863-2600_2863-259 others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | |||||
| chr12:14473288
|
CTCTGTGT others(3): Show |
C | 11 | a0003c0003t0011g0184a0003c0003t0012g0001a0003c0003t0012g0179others(8): Show | 13 | HG00099.hp1 HG00280.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.2863-2600_2863-259 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | |||||
| chr12:14473290
|
C | A | 11 | a0001c0001t0002g0013a0003c0003t0005g0158a0003c0003t0013g0159others(8): Show | 11 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.2863-2600C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473290 | ||||||
| chr12:14473290
|
C | G | 241 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0014others(238): Show | 242 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(239): Show |
intron_variant | MODIFIER | c.2863-2600C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473290 | ||||||
| chr12:14473292
|
G | A | 13 | a0001c0001t0003g0098a0001c0001t0003g0111a0001c0001t0003g0112others(10): Show | 14 | HG00140.hp1 HG00609.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.2863-2598G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473292 | ||||||
| chr12:14473294
|
G | A | 56 | a0001c0001t0003g0012a0001c0001t0003g0071a0001c0001t0003g0072others(53): Show | 56 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2863-2596G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473294 | ||||||
| chr12:14473296
|
G | A | 5 | a0001c0001t0002g0140a0001c0001t0003g0074a0001c0001t0027g0023others(2): Show | 5 | HG00597.hp2 HG02735.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.2863-2594G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473296 | ||||||
| chr12:14473298
|
G | A | 6 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0003g0109others(3): Show | 6 | HG01099.hp2 HG03239.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2863-2592G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473298 | ||||||
| chr12:14473300
|
G | A | 11 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2863-2590G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473300 | ||||||
| chr12:14473302
|
G | A | 6 | a0003c0003t0011g0184a0003c0003t0025g0171a0003c0003t0025g0172others(3): Show | 6 | HG00099.hp1 HG00280.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2863-2588G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473302 | ||||||
| chr12:14473330
|
T | G | 2 | a0001c0001t0002g0013a0001c0001t0003g0008 | 2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2863-2560T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473330 | ||||||
| chr12:14473332
|
T | G | 2 | a0001c0001t0002g0013a0001c0001t0003g0008 | 2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2863-2558T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473332 | ||||||
| chr12:14473487
|
A | C | 164 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(161): Show | 164 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(161): Show |
intron_variant | MODIFIER | c.2863-2403A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473487 | ||||||
| chr12:14473512
|
A | T | 1 | a0003c0005t0041g0337 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2863-2378A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473512 | ||||||
| chr12:14473586
|
C | A | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2863-2304C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473586 | ||||||
| chr12:14473632
|
T | C | 1 | a0001c0001t0003g0078 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2863-2258T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473632 | ||||||
| chr12:14473648
|
A | G | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2863-2242A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473648 | ||||||
| chr12:14473681
|
C | T | 1 | a0001c0001t0003g0089 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2863-2209C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473681 | ||||||
| chr12:14473734
|
T | C | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2863-2156T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473734 | ||||||
| chr12:14473804
|
A | AG | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2863-2084dupG | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473804 | |||||
| chr12:14473806
|
G | A | 4 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0181others(1): Show | 6 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2863-2084G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473806 | ||||||
| chr12:14473807
|
T | G | 308 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(305): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.2863-2083T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473807 | ||||||
| chr12:14473808
|
T | G | 1 | a0002c0002t0001g0305 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2863-2082T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473808 | ||||||
| chr12:14473913
|
C | T | 3 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0059 | 3 | NA18612.hp2 NA18993.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2863-1977C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473913 | ||||||
| chr12:14473983
|
T | C | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2863-1907T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473983 | ||||||
| chr12:14474078
|
T | G | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2863-1812T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474078 | ||||||
| chr12:14474211
|
T | G | 2 | a0003c0003t0018g0153a0003c0003t0018g0155 | 2 | HG01891.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2863-1679T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474211 | ||||||
| chr12:14474214
|
C | T | 3 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0189 | 3 | NA18967.hp2 NA19090.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2863-1676C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474214 | ||||||
| chr12:14474259
|
C | T | 1 | a0003c0003t0011g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2863-1631C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474259 | ||||||
| chr12:14474387
|
A | G | 1 | a0001c0001t0029g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2863-1503A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474387 | ||||||
| chr12:14474403
|
A | AT | 12 | a0001c0001t0003g0077a0002c0002t0001g0235a0003c0003t0004g0185others(9): Show | 12 | HG00140.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.2863-1472dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14474403 | |||||
| chr12:14474456
|
A | G | 19 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(16): Show | 19 | HG00733.hp2 HG01123.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2863-1434A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474456 | ||||||
| chr12:14474459
|
C | T | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2863-1431C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474459 | ||||||
| chr12:14474475
|
A | T | 4 | a0002c0002t0009g0211a0002c0002t0009g0212a0002c0002t0009g0214others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2863-1415A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474475 | ||||||
| chr12:14474510
|
C | A | 1 | a0002c0002t0001g0307 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2863-1380C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474510 | ||||||
| chr12:14474521
|
C | T | 2 | a0001c0001t0002g0038a0001c0001t0002g0042 | 2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2863-1369C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474521 | ||||||
| chr12:14474680
|
C | T | 342 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(339): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.2863-1210C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474680 | ||||||
| chr12:14474838
|
A | T | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2863-1052A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474838 | ||||||
| chr12:14475055
|
C | T | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2863-835C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475055 | ||||||
| chr12:14475092
|
G | A | 1 | a0002c0006t0008g0295 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2863-798G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475092 | ||||||
| chr12:14475111
|
A | G | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2863-779A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475111 | ||||||
| chr12:14475135
|
A | G | 114 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2863-755A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475135 | ||||||
| chr12:14475195
|
A | G | 1 | a0003c0003t0005g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2863-695A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475195 | ||||||
| chr12:14475212
|
A | G | 4 | a0003c0003t0014g0170a0003c0003t0023g0151a0003c0003t0023g0152others(1): Show | 4 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2863-678A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475212 | ||||||
| chr12:14475313
|
C | T | 1 | a0002c0002t0001g0269 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2863-577C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475313 | ||||||
| chr12:14475478
|
G | C | 4 | a0003c0003t0014g0170a0003c0003t0023g0151a0003c0003t0023g0152others(1): Show | 4 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2863-412G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475478 | ||||||
| chr12:14475511
|
C | T | 105 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.2863-379C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475511 | ||||||
| chr12:14475543
|
A | G | 1 | a0002c0002t0001g0297 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2863-347A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475543 | ||||||
| chr12:14475591
|
C | T | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2863-299C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475591 | ||||||
| chr12:14475610
|
C | G | 313 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(310): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2863-280C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475610 | ||||||
| chr12:14475761
|
C | A | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2863-129C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475761 | ||||||
| chr12:14475771
|
A | G | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.2863-119A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475771 | ||||||
| chr12:14475839
|
C | T | 148 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(145): Show | 148 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.2863-51C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475839 | ||||||
| chr12:14475842
|
A | G | 5 | a0003c0003t0015g0165a0003c0003t0015g0166a0003c0003t0015g0167others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2863-48A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475842 | ||||||
| chr12:14475985
|
T | C | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2941+17T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14475985 | ||||||
| chr12:14476229
|
C | T | 3 | a0002c0002t0001g0205a0002c0002t0001g0225a0002c0002t0001g0269 | 3 | HG00621.hp2 HG02155.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2941+261C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14476229 | ||||||
| chr12:14476230
|
G | A | 1 | a0003c0003t0011g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2941+262G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14476230 | ||||||
| chr12:14476239
|
C | A | 2 | a0003c0003t0004g0195a0003c0003t0004g0201 | 2 | HG01123.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.2941+271C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14476239 | ||||||
| chr12:14476241
|
G | A | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2941+273G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14476241 | ||||||
| chr12:14476411
|
CA | C | 33 | a0001c0001t0002g0030a0001c0001t0002g0034a0001c0001t0002g0069others(30): Show | 34 | HG00609.hp2 HG00733.hp2 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.2941+467delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 14476411 | |||||
| chr12:14476411
|
CAA | C | 254 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2941+466_2941+467d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 14476411 | |||||
| chr12:14476411
|
CAAA | C | 34 | a0001c0001t0002g0051a0001c0001t0003g0072a0001c0001t0003g0085others(31): Show | 34 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.2941+465_2941+467d others(5): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 14476411 | |||||
| chr12:14476411
|
CAAAA | C | 11 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(8): Show | 11 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2941+464_2941+467d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 14476411 | |||||
| chr12:14476706
|
C | T | 342 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(339): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.2941+738C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14476706 | ||||||
| chr12:14476724
|
G | A | 2 | a0003c0014t0013g0163a0003c0014t0013g0164 | 2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2941+756G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14476724 | ||||||
| chr12:14476726
|
A | G | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2941+758A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14476726 | ||||||
| chr12:14477075
|
G | A | 1 | a0003c0003t0005g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2941+1107G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14477075 | ||||||
| chr12:14477330
|
C | T | 1 | a0002c0002t0001g0307 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2942-987C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14477330 | ||||||
| chr12:14477374
|
ATTATCTC others(12): Show |
A | 1 | a0001c0001t0003g0083 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2942-922_2942-904d others(21): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 14477374 | |||||
| chr12:14477383
|
A | G | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2942-934A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14477383 | ||||||
| chr12:14477762
|
C | A | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2942-555C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14477762 | ||||||
| chr12:14477779
|
GTTTT | G | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2942-536_2942-533d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 14477779 | |||||
| chr12:14477862
|
A | G | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2942-455A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14477862 | ||||||
| chr12:14477922
|
G | A | 169 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(166): Show | 169 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.2942-395G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14477922 | ||||||
| chr12:14477966
|
T | C | 2 | a0010c0013t0020g0115a0010c0013t0020g0117 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2942-351T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14477966 | ||||||
| chr12:14478050
|
T | C | 1 | a0003c0003t0011g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2942-267T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14478050 | ||||||
| chr12:14478093
|
C | T | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2942-224C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14478093 | ||||||
| chr12:14478127
|
A | G | 1 | a0002c0002t0009g0289 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2942-190A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14478127 | ||||||
| chr12:14478177
|
T | C | 164 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(161): Show | 164 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(161): Show |
intron_variant | MODIFIER | c.2942-140T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14478177 | ||||||
| chr12:14478249
|
A | G | 1 | a0002c0002t0001g0258 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2942-68A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14478249 | ||||||
| chr12:14478264
|
G | A | 1 | a0003c0003t0015g0165 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2942-53G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14478264 | ||||||
| chr12:14478558
|
A | G | 1 | a0003c0005t0007g0326 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3097+86A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14478558 | ||||||
| chr12:14478576
|
G | T | 1 | a0003c0005t0007g0326 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3097+104G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14478576 | ||||||
| chr12:14478599
|
T | C | 1 | a0001c0001t0002g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3097+127T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14478599 | ||||||
| chr12:14478612
|
G | A | 1 | a0001c0001t0002g0140 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3097+140G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14478612 | ||||||
| chr12:14478819
|
G | C | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3097+347G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14478819 | ||||||
| chr12:14478994
|
C | T | 3 | a0001c0001t0003g0104a0001c0001t0003g0107a0001c0001t0032g0103 | 3 | HG00673.hp1 NA19060.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.3097+522C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14478994 | ||||||
| chr12:14478995
|
G | A | 1 | a0001c0001t0003g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3097+523G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14478995 | ||||||
| chr12:14479272
|
T | C | 1 | a0002c0002t0001g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3097+800T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479272 | ||||||
| chr12:14479323
|
C | T | 105 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.3097+851C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479323 | ||||||
| chr12:14479368
|
A | G | 1 | a0002c0002t0001g0306 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3097+896A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479368 | ||||||
| chr12:14479405
|
A | G | 14 | a0003c0003t0005g0316a0003c0003t0012g0001a0003c0003t0012g0179others(11): Show | 17 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3097+933A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479405 | ||||||
| chr12:14479516
|
T | A | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3097+1044T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479516 | ||||||
| chr12:14479559
|
A | T | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3097+1087A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479559 | ||||||
| chr12:14479571
|
G | A | 314 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.3097+1099G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479571 | ||||||
| chr12:14479671
|
T | G | 5 | a0001c0001t0003g0074a0001c0001t0003g0078a0001c0001t0003g0079others(2): Show | 5 | HG02165.hp1 HG03239.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.3097+1199T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479671 | ||||||
| chr12:14479672
|
AG | A | 5 | a0001c0001t0003g0074a0001c0001t0003g0078a0001c0001t0003g0079others(2): Show | 5 | HG02165.hp1 HG03239.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.3097+1201delG | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479672 | ||||||
| chr12:14479778
|
C | T | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3098-1225C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479778 | ||||||
| chr12:14480050
|
C | T | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3098-953C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480050 | ||||||
| chr12:14480115
|
C | T | 1 | a0003c0003t0005g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3098-888C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480115 | ||||||
| chr12:14480122
|
T | C | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3098-881T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480122 | ||||||
| chr12:14480289
|
A | G | 105 | a0001c0001t0019g0062a0002c0002t0001g0004a0002c0002t0001g0205others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.3098-714A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480289 | ||||||
| chr12:14480511
|
A | T | 27 | a0001c0020t0036g0131a0003c0003t0004g0185a0003c0003t0004g0186others(24): Show | 27 | HG00733.hp2 HG01123.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.3098-492A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480511 | ||||||
| chr12:14480653
|
A | G | 11 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3098-350A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480653 | ||||||
| chr12:14480806
|
T | C | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3098-197T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480806 | ||||||
| chr12:14480973
|
T | C | 1 | a0002c0002t0001g0267 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3098-30T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480973 | ||||||
| chr12:14481296
|
T | A | 43 | a0001c0020t0036g0131a0003c0003t0004g0185a0003c0003t0004g0186others(40): Show | 43 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.3280+111T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481296 | ||||||
| chr12:14481332
|
C | T | 1 | a0001c0001t0003g0146 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3280+147C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481332 | ||||||
| chr12:14481454
|
A | G | 1 | a0003c0003t0013g0162 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3280+269A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481454 | ||||||
| chr12:14481458
|
C | CAGTT | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.3280+275_3280+276i others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14481458 | |||||
| chr12:14481458
|
C | T | 1 | a0003c0003t0013g0162 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3280+273C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481458 | ||||||
| chr12:14481489
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3280+304A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481489 | ||||||
| chr12:14481498
|
A | T | 1 | a0001c0001t0003g0109 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3280+313A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481498 | ||||||
| chr12:14481738
|
A | G | 9 | a0003c0003t0005g0316a0005c0007t0010g0002a0005c0007t0010g0317others(6): Show | 10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+553A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481738 | ||||||
| chr12:14481758
|
G | A | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.3280+573G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481758 | ||||||
| chr12:14481758
|
G | T | 3 | a0002c0002t0001g0255a0002c0002t0001g0296a0002c0002t0001g0297 | 3 | HG00597.hp2 HG02080.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.3280+573G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481758 | ||||||
| chr12:14481794
|
A | C | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+609A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481794 | ||||||
| chr12:14481876
|
TAAAG | T | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3280+696_3280+699d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14481876 | |||||
| chr12:14481888
|
G | C | 1 | a0001c0001t0002g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3280+703G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481888 | ||||||
| chr12:14481923
|
C | CATATGTT others(4): Show |
188 | a0001c0001t0019g0062a0001c0020t0036g0131a0002c0002t0001g0004others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.3280+739_3280+749d others(13): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14481923 | |||||
| chr12:14482078
|
C | T | 1 | a0001c0001t0014g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3280+893C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482078 | ||||||
| chr12:14482183
|
A | G | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+998A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482183 | ||||||
| chr12:14482336
|
A | G | 14 | a0003c0003t0035g0343a0003c0005t0007g0325a0003c0005t0007g0326others(11): Show | 14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.3280+1151A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482336 | ||||||
| chr12:14482388
|
G | C | 4 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0328others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3280+1203G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482388 | ||||||
| chr12:14482576
|
C | G | 1 | a0001c0001t0006g0135 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3280+1391C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482576 | ||||||
| chr12:14482601
|
T | C | 1 | a0002c0006t0008g0220 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3280+1416T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482601 | ||||||
| chr12:14482696
|
A | T | 5 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(2): Show | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.3280+1511A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482696 | ||||||
| chr12:14482721
|
T | G | 4 | a0004c0008t0005g0003a0004c0008t0005g0279a0004c0008t0005g0293others(1): Show | 4 | HG01123.hp1 HG01361.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3280+1536T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482721 | ||||||
| chr12:14482869
|
A | G | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3280+1684A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482869 | ||||||
| chr12:14482937
|
A | C | 1 | a0002c0002t0001g0275 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3280+1752A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482937 | ||||||
| chr12:14482987
|
G | A | 1 | a0003c0003t0012g0180 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3280+1802G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482987 | ||||||
| chr12:14483088
|
A | G | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.3280+1903A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483088 | ||||||
| chr12:14483152
|
T | C | 1 | a0001c0001t0017g0032 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3280+1967T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483152 | ||||||
| chr12:14483180
|
C | A | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3280+1995C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483180 | ||||||
| chr12:14483292
|
A | G | 1 | a0003c0003t0004g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3280+2107A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483292 | ||||||
| chr12:14483348
|
G | A | 1 | a0003c0003t0011g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3280+2163G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483348 | ||||||
| chr12:14483384
|
C | T | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3280+2199C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483384 | ||||||
| chr12:14483389
|
C | G | 2 | a0003c0003t0004g0195a0003c0003t0004g0201 | 2 | HG01123.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3280+2204C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483389 | ||||||
| chr12:14483422
|
G | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3280+2237G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483422 | ||||||
| chr12:14483441
|
A | G | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3280+2256A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483441 | ||||||
| chr12:14483447
|
G | T | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3280+2262G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483447 | ||||||
| chr12:14483507
|
G | A | 1 | a0002c0002t0001g0270 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3280+2322G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483507 | ||||||
| chr12:14483620
|
G | A | 2 | a0003c0014t0013g0163a0003c0014t0013g0164 | 2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3280+2435G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483620 | ||||||
| chr12:14483622
|
T | C | 2 | a0003c0014t0013g0163a0003c0014t0013g0164 | 2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3280+2437T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483622 | ||||||
| chr12:14483810
|
T | G | 2 | a0003c0003t0011g0184a0003c0003t0028g0183 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3280+2625T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483810 | ||||||
| chr12:14483899
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3280+2714G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483899 | ||||||
| chr12:14483976
|
G | C | 1 | a0002c0002t0001g0206 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3280+2791G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483976 | ||||||
| chr12:14484089
|
C | A | 106 | a0001c0001t0019g0062a0002c0002t0001g0004a0002c0002t0001g0205others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.3280+2904C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484089 | ||||||
| chr12:14484091
|
C | T | 11 | a0001c0001t0006g0070a0001c0001t0006g0076a0001c0001t0006g0129others(8): Show | 11 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.3280+2906C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484091 | ||||||
| chr12:14484476
|
C | G | 3 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0189 | 3 | NA18967.hp2 NA19090.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3280+3291C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484476 | ||||||
| chr12:14484528
|
T | G | 189 | a0001c0001t0019g0062a0001c0001t0040g0139a0001c0020t0036g0131others(186): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.3280+3343T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484528 | ||||||
| chr12:14484626
|
A | C | 5 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0212others(2): Show | 5 | HG01109.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3280+3441A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484626 | ||||||
| chr12:14484652
|
G | C | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3280+3467G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484652 | ||||||
| chr12:14484656
|
C | G | 2 | a0003c0005t0007g0327a0003c0005t0007g0336 | 2 | HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3280+3471C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484656 | ||||||
| chr12:14484720
|
C | G | 341 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(338): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.3280+3535C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484720 | ||||||
| chr12:14484852
|
G | A | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.3280+3667G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484852 | ||||||
| chr12:14484929
|
A | T | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+3744A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484929 | ||||||
| chr12:14485060
|
G | A | 187 | a0001c0001t0019g0062a0002c0002t0001g0004a0002c0002t0001g0205others(184): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.3280+3875G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485060 | ||||||
| chr12:14485223
|
A | C | 4 | a0003c0003t0011g0204a0003c0003t0011g0314a0003c0003t0011g0315others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3280+4038A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485223 | ||||||
| chr12:14485470
|
T | C | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3280+4285T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485470 | ||||||
| chr12:14485473
|
G | A | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3280+4288G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485473 | ||||||
| chr12:14485479
|
T | C | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3280+4294T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485479 | ||||||
| chr12:14485511
|
C | T | 3 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0044 | 3 | NA18957.hp1 NA19057.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.3280+4326C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485511 | ||||||
| chr12:14485570
|
C | G | 1 | a0002c0002t0001g0246 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3280+4385C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485570 | ||||||
| chr12:14485571
|
C | T | 1 | a0002c0002t0001g0246 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3280+4386C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485571 | ||||||
| chr12:14485607
|
G | A | 1 | a0003c0003t0004g0191 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3280+4422G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485607 | ||||||
| chr12:14485724
|
C | T | 139 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(136): Show | 139 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.3280+4539C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485724 | ||||||
| chr12:14485741
|
C | T | 3 | a0001c0001t0003g0104a0001c0001t0003g0107a0001c0001t0032g0103 | 3 | HG00673.hp1 NA19060.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.3280+4556C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485741 | ||||||
| chr12:14485807
|
A | G | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0003c0003t0011g0341 | 3 | HG03486.hp1 NA18980.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.3280+4622A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485807 | ||||||
| chr12:14485920
|
C | T | 82 | a0002c0002t0001g0004a0002c0002t0001g0205a0002c0002t0001g0206others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.3280+4735C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485920 | ||||||
| chr12:14485922
|
C | T | 1 | a0002c0002t0001g0250 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3280+4737C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485922 | ||||||
| chr12:14485958
|
TCTC | T | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.3280+4777_3280+477 others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14485958 | |||||
| chr12:14486003
|
T | C | 2 | a0002c0002t0001g0236a0006c0009t0005g0175 | 2 | HG03516.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.3280+4818T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486003 | ||||||
| chr12:14486063
|
C | T | 31 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.3280+4878C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486063 | ||||||
| chr12:14486081
|
A | G | 1 | a0003c0003t0034g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3280+4896A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486081 | ||||||
| chr12:14486109
|
T | G | 1 | a0001c0001t0003g0104 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3280+4924T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486109 | ||||||
| chr12:14486165
|
T | G | 14 | a0003c0003t0005g0316a0003c0003t0012g0001a0003c0003t0012g0179others(11): Show | 17 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3280+4980T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486165 | ||||||
| chr12:14486188
|
T | G | 3 | a0001c0001t0003g0080a0001c0001t0003g0090a0001c0001t0003g0091 | 3 | NA18959.hp1 NA19010.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.3280+5003T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486188 | ||||||
| chr12:14486261
|
T | G | 1 | a0001c0001t0003g0124 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3280+5076T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486261 | ||||||
| chr12:14486499
|
A | C | 1 | a0001c0001t0002g0058 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3280+5314A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486499 | ||||||
| chr12:14486618
|
A | G | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+5433A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486618 | ||||||
| chr12:14486815
|
G | C | 1 | a0003c0003t0011g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3280+5630G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486815 | ||||||
| chr12:14486818
|
C | G | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5633C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486818 | ||||||
| chr12:14486826
|
A | G | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5641A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486826 | ||||||
| chr12:14486827
|
A | C | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5642A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486827 | ||||||
| chr12:14486828
|
G | A | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5643G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486828 | ||||||
| chr12:14486829
|
G | A | 1 | a0002c0002t0001g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3280+5644G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486829 | ||||||
| chr12:14486835
|
A | G | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5650A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486835 | ||||||
| chr12:14486837
|
C | T | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5652C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486837 | ||||||
| chr12:14486838
|
G | A | 21 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(18): Show | 21 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.3280+5653G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486838 | ||||||
| chr12:14486853
|
C | T | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5668C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486853 | ||||||
| chr12:14486858
|
A | T | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5673A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486858 | ||||||
| chr12:14486881
|
A | T | 1 | a0002c0002t0001g0298 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3280+5696A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486881 | ||||||
| chr12:14486887
|
C | G | 1 | a0002c0006t0008g0221 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3280+5702C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486887 | ||||||
| chr12:14486946
|
C | T | 3 | a0006c0009t0005g0176a0006c0009t0005g0177a0006c0009t0005g0178 | 3 | HG02723.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3280+5761C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486946 | ||||||
| chr12:14486951
|
C | G | 1 | a0002c0002t0001g0301 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3280+5766C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486951 | ||||||
| chr12:14487125
|
C | CT | 147 | a0001c0001t0019g0062a0001c0001t0040g0139a0002c0002t0001g0004others(144): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.3280+5949dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14487125 | |||||
| chr12:14487125
|
C | CTT | 31 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(28): Show | 31 | HG00733.hp2 HG01123.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.3280+5948_3280+594 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14487125 | |||||
| chr12:14487125
|
C | T | 1 | a0003c0005t0041g0337 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3280+5940C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487125 | ||||||
| chr12:14487215
|
T | C | 105 | a0001c0001t0019g0062a0001c0001t0040g0139a0002c0002t0001g0004others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.3280+6030T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487215 | ||||||
| chr12:14487222
|
C | T | 1 | a0001c0001t0040g0139 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3280+6037C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487222 | ||||||
| chr12:14487224
|
T | C | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6039T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487224 | ||||||
| chr12:14487233
|
T | C | 15 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(12): Show | 15 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.3280+6048T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487233 | ||||||
| chr12:14487253
|
C | T | 107 | a0001c0001t0019g0062a0001c0001t0040g0139a0002c0002t0001g0004others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.3280+6068C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487253 | ||||||
| chr12:14487266
|
C | T | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6081C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487266 | ||||||
| chr12:14487267
|
T | C | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6082T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487267 | ||||||
| chr12:14487270
|
G | A | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6085G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487270 | ||||||
| chr12:14487278
|
T | A | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6093T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487278 | ||||||
| chr12:14487282
|
G | T | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6097G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487282 | ||||||
| chr12:14487284
|
A | G | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6099A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487284 | ||||||
| chr12:14487290
|
G | A | 13 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(10): Show | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6105G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487290 | ||||||
| chr12:14487307
|
C | T | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3280+6122C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487307 | ||||||
| chr12:14487382
|
G | T | 2 | a0001c0001t0003g0012a0001c0001t0003g0122 | 2 | HG01074.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.3280+6197G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487382 | ||||||
| chr12:14487542
|
A | G | 1 | a0001c0001t0003g0106 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3280+6357A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487542 | ||||||
| chr12:14487543
|
T | C | 107 | a0001c0001t0019g0062a0001c0001t0040g0139a0002c0002t0001g0004others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.3280+6358T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487543 | ||||||
| chr12:14487570
|
G | C | 1 | a0002c0002t0001g0205 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3280+6385G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487570 | ||||||
| chr12:14487576
|
G | A | 1 | a0002c0002t0001g0282 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3280+6391G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487576 | ||||||
| chr12:14487742
|
G | A | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.3280+6557G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487742 | ||||||
| chr12:14487773
|
T | G | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3280+6588T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487773 | ||||||
| chr12:14487899
|
G | A | 1 | a0003c0003t0004g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3280+6714G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487899 | ||||||
| chr12:14488114
|
C | T | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3280+6929C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488114 | ||||||
| chr12:14488241
|
TA | T | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3280+7057delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488241 | ||||||
| chr12:14488308
|
A | G | 3 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089 | 3 | NA19056.hp2 NA19066.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.3280+7123A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488308 | ||||||
| chr12:14488332
|
G | A | 1 | a0001c0001t0003g0096 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3280+7147G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488332 | ||||||
| chr12:14488378
|
C | G | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3280+7193C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488378 | ||||||
| chr12:14488461
|
G | A | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3280+7276G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488461 | ||||||
| chr12:14488594
|
G | T | 28 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(25): Show | 28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.3280+7409G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488594 | ||||||
| chr12:14488659
|
G | A | 1 | a0012c0017t0001g0266 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3280+7474G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488659 | ||||||
| chr12:14488677
|
A | G | 28 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(25): Show | 28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.3280+7492A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488677 | ||||||
| chr12:14489009
|
C | A | 2 | a0003c0003t0011g0314a0003c0003t0011g0315 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3281-7222C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489009 | ||||||
| chr12:14489069
|
AGTG | A | 14 | a0001c0001t0019g0062a0002c0006t0008g0208a0002c0006t0008g0217others(11): Show | 14 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.3281-7159_3281-715 others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14489069 | |||||
| chr12:14489138
|
C | T | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-7093C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489138 | ||||||
| chr12:14489248
|
A | G | 1 | a0001c0001t0003g0105 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3281-6983A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489248 | ||||||
| chr12:14489291
|
G | T | 10 | a0003c0003t0014g0149a0003c0003t0014g0170a0003c0003t0015g0165others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3281-6940G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489291 | ||||||
| chr12:14489372
|
T | C | 6 | a0006c0009t0005g0173a0006c0009t0005g0174a0006c0009t0005g0175others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3281-6859T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489372 | ||||||
| chr12:14489454
|
C | A | 2 | a0003c0003t0025g0171a0003c0003t0025g0172 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.3281-6777C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489454 | ||||||
| chr12:14489481
|
A | C | 14 | a0003c0003t0005g0316a0003c0003t0012g0001a0003c0003t0012g0179others(11): Show | 17 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3281-6750A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489481 | ||||||
| chr12:14489701
|
G | A | 66 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(63): Show | 66 | HG01175.hp1 HG01243.hp1 HG01257.hp1 others(63): Show |
intron_variant | MODIFIER | c.3281-6530G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489701 | ||||||
| chr12:14489729
|
A | G | 1 | a0003c0003t0005g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3281-6502A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489729 | ||||||
| chr12:14489793
|
G | A | 2 | a0002c0002t0001g0246a0013c0016t0039g0245 | 2 | HG02683.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3281-6438G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489793 | ||||||
| chr12:14489993
|
A | C | 1 | a0002c0002t0001g0206 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3281-6238A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489993 | ||||||
| chr12:14490084
|
T | G | 1 | a0001c0001t0003g0104 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3281-6147T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490084 | ||||||
| chr12:14490147
|
T | C | 15 | a0003c0003t0025g0171a0003c0003t0025g0172a0003c0005t0007g0325others(12): Show | 15 | HG00099.hp1 HG00280.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.3281-6084T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490147 | ||||||
| chr12:14490539
|
T | G | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.3281-5692T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490539 | ||||||
| chr12:14490567
|
G | C | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.3281-5664G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490567 | ||||||
| chr12:14490576
|
T | G | 182 | a0001c0001t0019g0062a0001c0001t0040g0139a0001c0020t0036g0131others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.3281-5655T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490576 | ||||||
| chr12:14490594
|
T | C | 188 | a0001c0001t0019g0062a0001c0001t0040g0139a0001c0020t0036g0131others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.3281-5637T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490594 | ||||||
| chr12:14490596
|
C | T | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3281-5635C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490596 | ||||||
| chr12:14490614
|
A | C | 2 | a0001c0001t0002g0010a0001c0001t0002g0018 | 2 | HG02083.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.3281-5617A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490614 | ||||||
| chr12:14490639
|
C | A | 14 | a0003c0003t0005g0316a0003c0003t0012g0001a0003c0003t0012g0179others(11): Show | 17 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3281-5592C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490639 | ||||||
| chr12:14490676
|
C | G | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3281-5555C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490676 | ||||||
| chr12:14490783
|
T | G | 188 | a0001c0001t0019g0062a0001c0001t0040g0139a0001c0020t0036g0131others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.3281-5448T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490783 | ||||||
| chr12:14490806
|
A | G | 1 | a0002c0002t0001g0246 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3281-5425A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490806 | ||||||
| chr12:14490821
|
C | G | 29 | a0001c0020t0036g0131a0003c0003t0004g0185a0003c0003t0004g0186others(26): Show | 29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.3281-5410C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490821 | ||||||
| chr12:14490953
|
C | A | 1 | a0004c0008t0005g0253 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3281-5278C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490953 | ||||||
| chr12:14490954
|
T | G | 1 | a0004c0008t0005g0253 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3281-5277T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490954 | ||||||
| chr12:14491012
|
G | A | 13 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(10): Show | 16 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.3281-5219G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491012 | ||||||
| chr12:14491236
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3281-4995A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491236 | ||||||
| chr12:14491298
|
C | G | 2 | a0010c0013t0020g0115a0010c0013t0020g0117 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3281-4933C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491298 | ||||||
| chr12:14491349
|
A | G | 29 | a0001c0020t0036g0131a0003c0003t0004g0185a0003c0003t0004g0186others(26): Show | 29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.3281-4882A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491349 | ||||||
| chr12:14491408
|
A | T | 1 | a0003c0003t0011g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3281-4823A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491408 | ||||||
| chr12:14491519
|
A | G | 11 | a0001c0001t0006g0070a0001c0001t0006g0076a0001c0001t0006g0129others(8): Show | 11 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.3281-4712A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491519 | ||||||
| chr12:14491885
|
A | G | 29 | a0001c0020t0036g0131a0003c0003t0004g0185a0003c0003t0004g0186others(26): Show | 29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.3281-4346A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491885 | ||||||
| chr12:14491947
|
G | A | 1 | a0002c0002t0001g0286 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3281-4284G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491947 | ||||||
| chr12:14492069
|
T | C | 1 | a0004c0008t0005g0279 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3281-4162T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492069 | ||||||
| chr12:14492092
|
G | A | 2 | a0003c0003t0011g0314a0003c0003t0011g0315 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3281-4139G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492092 | ||||||
| chr12:14492145
|
G | C | 66 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(63): Show | 66 | HG01175.hp1 HG01243.hp1 HG01257.hp1 others(63): Show |
intron_variant | MODIFIER | c.3281-4086G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492145 | ||||||
| chr12:14492149
|
A | G | 1 | a0001c0001t0002g0030 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3281-4082A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492149 | ||||||
| chr12:14492171
|
G | T | 1 | a0003c0003t0013g0161 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3281-4060G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492171 | ||||||
| chr12:14492183
|
T | C | 2 | a0002c0002t0001g0246a0003c0003t0013g0161 | 2 | HG00741.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3281-4048T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492183 | ||||||
| chr12:14492187
|
C | T | 14 | a0003c0003t0005g0316a0003c0003t0012g0001a0003c0003t0012g0179others(11): Show | 17 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3281-4044C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492187 | ||||||
| chr12:14492240
|
T | C | 3 | a0003c0003t0023g0151a0003c0003t0023g0152a0003c0003t0034g0150 | 3 | HG01099.hp1 HG02300.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.3281-3991T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492240 | ||||||
| chr12:14492241
|
G | C | 3 | a0003c0003t0023g0151a0003c0003t0023g0152a0003c0003t0034g0150 | 3 | HG01099.hp1 HG02300.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.3281-3990G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492241 | ||||||
| chr12:14492243
|
A | G | 3 | a0003c0003t0023g0151a0003c0003t0023g0152a0003c0003t0034g0150 | 3 | HG01099.hp1 HG02300.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.3281-3988A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492243 | ||||||
| chr12:14492332
|
A | G | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3281-3899A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492332 | ||||||
| chr12:14492335
|
G | A | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3281-3896G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492335 | ||||||
| chr12:14492341
|
T | C | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3281-3890T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492341 | ||||||
| chr12:14492347
|
G | C | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3281-3884G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492347 | ||||||
| chr12:14492350
|
A | G | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3281-3881A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492350 | ||||||
| chr12:14492416
|
A | G | 188 | a0001c0001t0019g0062a0001c0001t0040g0139a0001c0020t0036g0131others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.3281-3815A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492416 | ||||||
| chr12:14492455
|
G | A | 1 | a0001c0001t0029g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3281-3776G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492455 | ||||||
| chr12:14492457
|
C | T | 11 | a0003c0005t0007g0325a0003c0005t0007g0326a0003c0005t0007g0327others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3281-3774C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492457 | ||||||
| chr12:14492473
|
T | C | 10 | a0002c0002t0009g0005a0002c0002t0009g0006a0002c0002t0009g0211others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.3281-3758T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492473 | ||||||
| chr12:14492494
|
A | G | 182 | a0001c0001t0019g0062a0001c0001t0040g0139a0001c0020t0036g0131others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.3281-3737A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492494 | ||||||
| chr12:14492513
|
AATTG | A | 138 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(135): Show | 138 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.3281-3712_3281-370 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14492513 | |||||
| chr12:14492525
|
G | A | 1 | a0003c0003t0011g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3281-3706G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492525 | ||||||
| chr12:14492558
|
C | T | 3 | a0001c0001t0002g0007a0001c0001t0002g0016a0001c0001t0002g0019 | 3 | NA18943.hp2 NA19074.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.3281-3673C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492558 | ||||||
| chr12:14492578
|
A | C | 2 | a0003c0003t0005g0158a0003c0003t0014g0156 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3281-3653A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492578 | ||||||
| chr12:14492650
|
A | G | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3281-3581A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492650 | ||||||
| chr12:14492800
|
G | A | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-3431G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492800 | ||||||
| chr12:14492836
|
G | A | 1 | a0003c0003t0025g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3281-3395G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492836 | ||||||
| chr12:14492855
|
AGAGTC | A | 13 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(10): Show | 16 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.3281-3372_3281-336 others(9): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14492855 | |||||
| chr12:14492882
|
G | A | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-3349G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492882 | ||||||
| chr12:14492952
|
G | A | 1 | a0001c0001t0029g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3281-3279G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492952 | ||||||
| chr12:14492952
|
G | C | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-3279G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492952 | ||||||
| chr12:14493064
|
T | A | 1 | a0003c0003t0005g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3281-3167T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493064 | ||||||
| chr12:14493078
|
A | G | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-3153A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493078 | ||||||
| chr12:14493344
|
A | G | 13 | a0003c0003t0012g0001a0003c0003t0012g0179a0003c0003t0012g0180others(10): Show | 16 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.3281-2887A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493344 | ||||||
| chr12:14493446
|
A | C | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.3281-2785A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493446 | ||||||
| chr12:14493550
|
G | A | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3281-2681G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493550 | ||||||
| chr12:14493592
|
C | T | 1 | a0001c0001t0031g0009 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3281-2639C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493592 | ||||||
| chr12:14493720
|
C | G | 1 | a0001c0001t0002g0035 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3281-2511C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493720 | ||||||
| chr12:14493821
|
A | G | 3 | a0002c0006t0008g0223a0002c0006t0008g0224a0002c0006t0008g0226 | 3 | NA18977.hp2 NA18981.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.3281-2410A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493821 | ||||||
| chr12:14493929
|
A | G | 1 | a0003c0003t0004g0199 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3281-2302A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493929 | ||||||
| chr12:14494124
|
T | C | 1 | a0001c0001t0003g0120 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3281-2107T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494124 | ||||||
| chr12:14494234
|
C | A | 1 | a0001c0020t0036g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3281-1997C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494234 | ||||||
| chr12:14494284
|
A | AAT | 15 | a0001c0001t0002g0038a0001c0001t0002g0042a0001c0001t0002g0043others(12): Show | 15 | HG00140.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.3281-1898_3281-189 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
A | AATAT | 11 | a0001c0001t0002g0018a0001c0001t0002g0026a0001c0001t0002g0027others(8): Show | 11 | HG00673.hp1 HG00735.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.3281-1900_3281-189 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
A | AATATAT | 8 | a0001c0001t0002g0017a0001c0001t0002g0143a0001c0001t0002g0342others(5): Show | 8 | HG01516.hp1 HG01993.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.3281-1902_3281-189 others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
A | AATATATA others(1): Show |
11 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0035others(8): Show | 11 | HG00597.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.3281-1904_3281-189 others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
A | AATATATA others(3): Show |
3 | a0001c0001t0003g0071a0001c0001t0003g0123a0014c0015t0003g0094 | 3 | HG01168.hp2 HG03239.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.3281-1906_3281-189 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
A | AATATATA others(5): Show |
3 | a0001c0001t0002g0065a0001c0001t0003g0072a0003c0003t0011g0184 | 3 | HG03579.hp2 NA18981.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.3281-1908_3281-189 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
A | AATATATA others(7): Show |
7 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0050others(4): Show | 7 | HG03453.hp2 HG03490.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.3281-1910_3281-189 others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AAT | A | 26 | a0001c0001t0002g0007a0001c0001t0002g0016a0001c0001t0002g0019others(23): Show | 26 | HG00099.hp2 HG00280.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.3281-1898_3281-189 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AATAT | A | 21 | a0001c0001t0002g0024a0001c0001t0003g0089a0001c0001t0003g0090others(18): Show | 21 | HG00140.hp1 HG00639.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.3281-1900_3281-189 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AATATAT | A | 36 | a0001c0001t0002g0055a0001c0001t0002g0118a0001c0001t0003g0091others(33): Show | 36 | HG00621.hp2 HG00733.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.3281-1902_3281-189 others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AATATATA others(1): Show |
A | 12 | a0001c0001t0002g0059a0002c0002t0001g0304a0002c0002t0009g0212others(9): Show | 14 | HG01496.hp2 HG02572.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.3281-1904_3281-189 others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AATATATA others(3): Show |
A | 18 | a0001c0001t0002g0054a0001c0001t0002g0061a0001c0001t0002g0063others(15): Show | 18 | HG00639.hp1 HG00741.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.3281-1906_3281-189 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AATATATA others(5): Show |
A | 5 | a0001c0001t0002g0025a0002c0002t0009g0005a0002c0002t0009g0288others(2): Show | 5 | HG01109.hp2 HG01496.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3281-1908_3281-189 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AATATATA others(7): Show |
A | 11 | a0001c0001t0002g0113a0001c0001t0002g0145a0001c0001t0003g0077others(8): Show | 11 | HG02257.hp2 HG02630.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3281-1910_3281-189 others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AATATATA others(9): Show |
A | 5 | a0001c0001t0002g0144a0001c0001t0003g0120a0001c0001t0016g0127others(2): Show | 5 | HG01346.hp1 HG01884.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.3281-1912_3281-189 others(20): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AATATATA others(11): Show |
A | 1 | a0001c0001t0016g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3281-1914_3281-189 others(22): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AATATATA others(13): Show |
A | 3 | a0001c0001t0006g0136a0001c0001t0014g0125a0001c0001t0016g0126 | 3 | HG02109.hp1 HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3281-1916_3281-189 others(24): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AATATATA others(15): Show |
A | 13 | a0001c0001t0003g0141a0001c0001t0006g0070a0001c0001t0006g0076others(10): Show | 13 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.3281-1918_3281-189 others(26): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AATATATA others(17): Show |
A | 1 | a0002c0002t0001g0207 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3281-1920_3281-189 others(28): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AATATATA others(21): Show |
A | 6 | a0001c0001t0003g0142a0003c0003t0015g0165a0003c0003t0015g0166others(3): Show | 6 | HG00609.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-1924_3281-189 others(32): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AATATATA others(23): Show |
A | 1 | a0001c0001t0003g0121 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3281-1926_3281-189 others(34): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494284
|
AATATATA others(27): Show |
A | 4 | a0003c0003t0025g0171a0003c0003t0025g0172a0008c0011t0024g0147others(1): Show | 4 | HG00099.hp1 HG00280.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.3281-1930_3281-189 others(38): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | |||||
| chr12:14494309
|
ATATATAT others(19): Show |
A | 2 | a0003c0003t0004g0195a0003c0003t0004g0201 | 2 | HG01123.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3281-1920_3281-189 others(30): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494309 | |||||
| chr12:14494319
|
ATATATAT others(9): Show |
A | 1 | a0003c0003t0004g0203 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3281-1910_3281-189 others(20): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494319 | |||||
| chr12:14494323
|
A | G | 3 | a0002c0004t0001g0231a0002c0004t0001g0238a0002c0004t0001g0247 | 3 | HG01175.hp2 HG01261.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3281-1908A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494323 | ||||||
| chr12:14494325
|
A | ATG | 4 | a0002c0004t0001g0216a0002c0004t0001g0230a0002c0004t0001g0243others(1): Show | 4 | HG01071.hp1 HG01993.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.3281-1905_3281-190 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494325 | |||||
| chr12:14494325
|
A | G | 13 | a0002c0004t0001g0229a0002c0004t0001g0231a0002c0004t0001g0232others(10): Show | 13 | HG00639.hp2 HG01069.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.3281-1906A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494325 | ||||||
| chr12:14494325
|
ATATATAT others(3): Show |
A | 1 | a0003c0003t0004g0187 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3281-1904_3281-189 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494325 | |||||
| chr12:14494327
|
A | G | 38 | a0002c0002t0001g0209a0002c0002t0001g0210a0002c0002t0001g0218others(35): Show | 38 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.3281-1904A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494327 | ||||||
| chr12:14494329
|
A | ATGTGTG | 3 | a0002c0004t0001g0239a0002c0004t0001g0240a0002c0004t0001g0242 | 3 | HG01106.hp2 HG01934.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.3281-1901_3281-190 others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494329 | |||||
| chr12:14494329
|
A | G | 107 | a0001c0001t0040g0139a0002c0002t0001g0004a0002c0002t0001g0205others(104): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.3281-1902A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494329 | ||||||
| chr12:14494331
|
A | G | 128 | a0001c0001t0040g0139a0002c0002t0001g0004a0002c0002t0001g0205others(125): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.3281-1900A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494331 | ||||||
| chr12:14494331
|
ATATG | A | 4 | a0003c0003t0004g0188a0003c0003t0004g0190a0003c0003t0004g0193others(1): Show | 4 | HG03491.hp1 HG03492.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.3281-1898_3281-189 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494331 | |||||
| chr12:14494333
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0017g0046 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(26): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATATAT others(7): Show |
1 | a0007c0010t0002g0049 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATATAT others(5): Show |
5 | a0001c0001t0003g0087a0001c0001t0017g0032a0001c0001t0017g0048others(2): Show | 5 | HG01516.hp2 HG01517.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.3281-1897_3281-189 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATATAT others(7): Show |
1 | a0005c0007t0010g0320 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATATAT others(9): Show |
1 | a0002c0006t0008g0226 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(20): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0003g0106 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATATAT others(5): Show |
1 | a0005c0007t0010g0322 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATATAT others(7): Show |
1 | a0002c0006t0008g0221 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATATAT others(5): Show |
2 | a0002c0006t0008g0223a0005c0007t0010g0319 | 2 | HG00609.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.3281-1897_3281-189 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATATAT others(7): Show |
1 | a0003c0005t0007g0334 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATATGT others(3): Show |
4 | a0002c0006t0008g0224a0002c0006t0008g0227a0002c0006t0008g0256others(1): Show | 4 | HG00438.hp2 HG02135.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.3281-1897_3281-189 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATATGT others(5): Show |
3 | a0003c0005t0007g0325a0003c0005t0007g0333a0003c0005t0007g0335 | 3 | HG02451.hp2 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3281-1897_3281-189 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATG | 3 | a0001c0001t0003g0122a0001c0001t0022g0081a0001c0001t0022g0082 | 3 | HG01256.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3281-1897_3281-189 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATGTG | 2 | a0005c0007t0010g0002a0005c0007t0010g0321 | 3 | HG03490.hp2 HG03492.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3281-1897_3281-189 others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATGTGT others(1): Show |
5 | a0002c0002t0001g0275a0002c0006t0008g0217a0002c0006t0019g0222others(2): Show | 5 | HG00621.hp1 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.3281-1897_3281-189 others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATATGTGT others(5): Show |
1 | a0003c0005t0007g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATGTGTGT others(3): Show |
1 | a0003c0005t0041g0337 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3281-1896_3281-188 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | ATGTGTGT others(11): Show |
1 | a0003c0003t0005g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3281-1887_3281-188 others(22): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | |||||
| chr12:14494333
|
A | G | 149 | a0001c0001t0002g0025a0001c0001t0002g0051a0001c0001t0002g0118others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.3281-1898A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494333 | ||||||
| chr12:14494335
|
G | A | 2 | a0003c0003t0004g0189a0003c0003t0004g0191 | 2 | NA18955.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.3281-1896G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494335 | ||||||
| chr12:14494345
|
A | G | 1 | a0003c0003t0035g0343 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3281-1886A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494345 | ||||||
| chr12:14494440
|
A | G | 6 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-1791A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494440 | ||||||
| chr12:14494520
|
A | G | 106 | a0001c0001t0019g0062a0002c0002t0001g0004a0002c0002t0001g0205others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.3281-1711A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494520 | ||||||
| chr12:14494716
|
T | G | 28 | a0003c0003t0004g0185a0003c0003t0004g0186a0003c0003t0004g0187others(25): Show | 28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.3281-1515T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494716 | ||||||
| chr12:14494751
|
C | T | 3 | a0001c0001t0003g0099a0001c0001t0003g0100a0001c0001t0003g0101 | 3 | HG01069.hp1 HG01071.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.3281-1480C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494751 | ||||||
| chr12:14494908
|
G | A | 3 | a0003c0003t0005g0158a0003c0003t0014g0156a0003c0003t0014g0157 | 3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3281-1323G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494908 | ||||||
| chr12:14494932
|
C | CA | 9 | a0003c0003t0004g0193a0003c0003t0004g0201a0003c0003t0015g0165others(6): Show | 9 | HG01169.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.3281-1276dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494932 | |||||
| chr12:14494932
|
CA | C | 149 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(146): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.3281-1276delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494932 | |||||
| chr12:14494932
|
CAA | C | 126 | a0001c0001t0002g0031a0001c0001t0002g0039a0001c0001t0003g0099others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.3281-1277_3281-127 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494932 | |||||
| chr12:14495051
|
G | C | 1 | a0002c0006t0008g0219 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3281-1180G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495051 | ||||||
| chr12:14495115
|
G | A | 2 | a0001c0001t0022g0081a0001c0001t0022g0082 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3281-1116G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495115 | ||||||
| chr12:14495213
|
ATC | A | 8 | a0005c0007t0010g0002a0005c0007t0010g0317a0005c0007t0010g0318others(5): Show | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.3281-1014_3281-101 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14495213 | |||||
| chr12:14495375
|
T | C | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3281-856T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495375 | ||||||
| chr12:14495536
|
C | T | 1 | a0001c0020t0036g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3281-695C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495536 | ||||||
| chr12:14495566
|
A | G | 340 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.3281-665A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495566 | ||||||
| chr12:14495652
|
G | T | 1 | a0003c0003t0014g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3281-579G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495652 | ||||||
| chr12:14495807
|
C | A | 2 | a0003c0003t0004g0195a0003c0003t0004g0201 | 2 | HG01123.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3281-424C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495807 | ||||||
| chr12:14495846
|
C | T | 2 | a0001c0001t0002g0066a0001c0001t0002g0068 | 2 | HG01175.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.3281-385C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495846 | ||||||
| chr12:14495876
|
A | C | 2 | a0009c0012t0011g0338a0009c0012t0011g0339 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3281-355A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495876 | ||||||
| chr12:14495938
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3281-293G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495938 | ||||||
| chr12:14495996
|
AGAAAGGG others(28): Show |
A | 1 | a0001c0001t0002g0027 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3281-233_3281-199d others(37): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14495996 | |||||
| chr12:14496038
|
A | G | 1 | a0001c0001t0003g0098 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3281-193A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14496038 | ||||||
| chr12:14496088
|
C | T | 2 | a0003c0003t0011g0314a0003c0003t0011g0315 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3281-143C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14496088 | ||||||
| chr12:14496217
|
T | G | 2 | a0003c0003t0011g0314a0003c0003t0011g0315 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3281-14T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14496217 | ||||||
| chr12:14496458
|
G | C | 1 | a0003c0003t0011g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3393+115G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14496458 | ||||||
| chr12:14496525
|
GATCATTT others(19): Show |
G | 1 | a0002c0002t0001g0312 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3393+183_3393+208d others(28): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14496525 | ||||||
| chr12:14496679
|
G | A | 1 | a0003c0003t0005g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3393+336G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14496679 | ||||||
| chr12:14496773
|
C | T | 1 | a0003c0003t0012g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3393+430C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14496773 | ||||||
| chr12:14496910
|
A | G | 2 | a0008c0011t0024g0147a0008c0011t0024g0148 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3393+567A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14496910 | ||||||
| chr12:14497044
|
T | C | 4 | a0003c0003t0013g0159a0003c0003t0013g0160a0003c0003t0013g0161others(1): Show | 4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.3394-610T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14497044 | ||||||
| chr12:14497138
|
T | C | 75 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(72): Show | 75 | HG00280.hp2 HG01081.hp1 HG01123.hp1 others(72): Show |
intron_variant | MODIFIER | c.3394-516T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14497138 | ||||||
| chr12:14497279
|
T | C | 180 | a0001c0001t0019g0062a0001c0001t0040g0139a0001c0020t0036g0131others(177): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3394-375T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14497279 | ||||||
| chr12:14497533
|
T | G | 2 | a0001c0001t0002g0037a0001c0001t0002g0039 | 2 | NA18957.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.3394-121T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14497533 |